118 results
Search Results
2. Finding our way in the In Vitro Diagnostic Medical Devices Regulation: a discussion paper from the European Bioanalysis Forum.
- Author
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Timmerman P, Laurén A, Nelson R, and Barfield M
- Subjects
- Europe, Reagent Kits, Diagnostic, Biological Assay
- Published
- 2024
- Full Text
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3. High-Throughput Bioassay for Detection of Latent Fungi in Postharvest Produce.
- Author
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Ayarnah K, Kaur M, Duanis-Assaf D, Alkan N, and Eltzov E
- Subjects
- High-Throughput Screening Assays methods, Solanum lycopersicum microbiology, Fruit microbiology, Plant Diseases microbiology, Colletotrichum genetics, Biological Assay
- Abstract
Enormous fresh agricultural produce is wasted annually due to rots caused by pathogenic microorganisms. Most pathogenic fungi attack the harvested produce by penetrating the fruit at the field and remaining quiescent or latent until the fruit ripens or senescence. In this work, a recently developed simple, cost-effective, and high-throughput 96-well plate-based assay was applied to determine the presence of pathogenic fungi in their latent stage. The surface strands immobilized on the 96-well plate, only with the presence of the complementary RNA marker (enoyl-CoA hydratase (ECH)) of the latent fungal-pathogen Colletotrichum gloeosporioides will create a complex with the target and reporter (labeled with the horseradish peroxidase (HRP) enzyme) strands for positive signal generation. The developed assay demonstrated 3.1-fold higher specificity for the latent marker (ECH) of C. gloeosporioides compared to latent markers of other pathogenic fungi. A 2 nM detection limit of target strands was demonstrated, showing a high plate sensitivity, and was further validated with biological samples extracted from latent infection in tomato fruit. The developed assay provides a new economical tool for detecting the presence of latent RNA markers of pathogenic fungi in agricultural produce, ultimately improving postharvest decision-making and reducing postharvest losses., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Published
- 2024
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4. Extrapolation of cytotoxic masked effects in planar in vitro assays.
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Rosenberger T, Bell AM, Reifferscheid G, Smith KEC, Schäffer A, Ternes TA, and Buchinger S
- Subjects
- Chromatography, Thin Layer methods, Phenols toxicity, Phenols analysis, Phenols chemistry, Benzhydryl Compounds toxicity, Benzhydryl Compounds analysis, Benzhydryl Compounds chemistry, Estrogens analysis, Estrogens toxicity, Biological Assay methods
- Abstract
The masking of specific effects in in vitro assays by cytotoxicity is a commonly known phenomenon. This may result in a partial or complete loss of effect signals. For common in vitro assays, approaches for identifying and quantifying cytotoxic masking are partly available. However, a quantification of cytotoxicity-affected signals is not possible. As an alternative, planar bioassays that combine high-performance thin layer chromatography with in vitro assays, such as the planar yeast estrogen screen (p-YES), might allow for a quantification of cytotoxically affected signals. Affected signals form a typical ring structure with a supressed or completely lacking centre that results in a double peak chromatogram. This study investigates whether these double peaks can be used for fitting a peak function to extrapolate the theoretical, unaffected signals. The precision of the modelling was evaluated for four individual peak functions, using 42 ideal, undistorted peaks from estrogenic model compounds in the p-YES. Modelled ED
50 -values from bisphenol A (BPA) experiments with cytotoxically disturbed signals were 13 times higher than for the apparent data without compensation for cytotoxicity (320 ± 63 ng versus 24 ± 17 ng). This finding has a high relevance for the modelling of mixture effects according to concentration addition that requires unaffected, complete dose-response relationships. Finally, we applied the approach to results of a p-YES assay on leachate samples of an elastomer material used in water engineering. In summary, the fitting approach enables the quantitative evaluation of cytotoxically affected signals in planar in vitro assays and also has applications for other fields of chemical analysis like distorted chromatography signals., (© 2024. The Author(s).)- Published
- 2024
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5. Light-field flow cytometry for high-resolution, volumetric and multiparametric 3D single-cell analysis.
- Author
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Hua X, Han K, Mandracchia B, Radmand A, Liu W, Kim H, Yuan Z, Ehrlich SM, Li K, Zheng C, Son J, Silva Trenkle AD, Kwong GA, Zhu C, Dahlman JE, and Jia S
- Subjects
- Flow Cytometry, Microfluidics, Single-Cell Analysis, Biological Assay, Biomedical Research
- Abstract
Imaging flow cytometry (IFC) combines flow cytometry and fluorescence microscopy to enable high-throughput, multiparametric single-cell analysis with rich spatial details. However, current IFC techniques remain limited in their ability to reveal subcellular information with a high 3D resolution, throughput, sensitivity, and instrumental simplicity. In this study, we introduce a light-field flow cytometer (LFC), an IFC system capable of high-content, single-shot, and multi-color acquisition of up to 5,750 cells per second with a near-diffraction-limited resolution of 400-600 nm in all three dimensions. The LFC system integrates optical, microfluidic, and computational strategies to facilitate the volumetric visualization of various 3D subcellular characteristics through convenient access to commonly used epi-fluorescence platforms. We demonstrate the effectiveness of LFC in assaying, analyzing, and enumerating intricate subcellular morphology, function, and heterogeneity using various phantoms and biological specimens. The advancement offered by the LFC system presents a promising methodological pathway for broad cell biological and translational discoveries, with the potential for widespread adoption in biomedical research., (© 2024. The Author(s).)
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- 2024
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6. Multiplex paper-based electrochemical immunosensor for the simultaneous monitoring of blood biomarkers in Alzheimer's disease.
- Author
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Gu, Jinyu, Wang, Liming, Zhao, Li, Zuo, Yingchun, Gao, Shuai, Gu, Hui, Wang, Yinan, and Yu, Yanyan
- Subjects
- *
ALZHEIMER'S disease , *MESOPOROUS silica , *ALPHA fetoproteins , *SILICA nanoparticles , *TRANSGENIC mice , *BIOLOGICAL assay - Abstract
Joint analysis of varied biomarkers in blood sample will provide more accurate results for the monitoring and management of Alzheimer's disease (AD). In addition to the known β-amyloid protein (Aβ) used as a reliable clinical marker for AD diagnosis, Fetuin B also demonstrates a strong correlation with AD progression. Especially, for medical diagnostics, on-site detection of multi-analyte is quite important and therefore, it is desirable to develop a rapid and portable, multiplex electrochemical assay for simultaneous detection of Aβ and Fetuin B, which has been seldomly reported before. To achieve this goal, a multiplex paper-based electrode was prepared via vacuum filtration, by which, single-walled carbon nanotubes (SWCNTs) and AuNPs were sequentially filtered through cellulose paper with a five-electrode pattern to form a conductive underlay and electrical connections. A nanocomposite of AuNPs-loaded dendritic mesoporous silica nanoparticles (dmSiO 2 -Au) was firstly synthesized and further deposited thionine (Thi) for signal amplification. An immunosensor was correspondingly fabricated, which involved a combination of multiplex electrodes and dmSiO 2 -Au-Thi nanocomposite to facilitate simultaneous monitoring of Aβo and Fetuin B. Additionally, ferrocene (F c) was applied onto a separate working electrode to perform a ratiometric electrochemistry for enhancing accuracy. The outcomes demonstrated high specificity, sensitivity, and stability, and no obvious cross-talking between three working electrodes. Application of this sensor resulted in a successful determination of Aβo and Fetuin B levels in serum and brain tissue of transgenic AD mice. Overall, the presented electrochemical immunosensors for performing multiplex diagnostics may facilitate to the exploration of more AD-related blood markers. • A multiplex paper-based electrode was prepared. • A sandwich-based immunosensor enabled simultaneous monitoring of Aβo and Fetuin B. • Ferrocene was applied onto electrode to construct a ratiometric electrochemistry. • Analysis of Aβo and Fetuin B in APP/PS1 transgenic AD mice was realized. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Versatility of reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) from diagnosis of early pathological infection to mutation detection in organisms.
- Author
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Sen S, Bhowmik P, Tiwari S, Peleg Y, and Bandyopadhyay B
- Subjects
- Mutation, DNA, RNA-Directed DNA Polymerase, Biological Assay, Nucleic Acid Amplification Techniques, Molecular Diagnostic Techniques
- Abstract
Loop-mediated isothermal amplification (LAMP) is a rapid, state-of-the-art DNA amplification technology, used primarily for the quick diagnosis and early identification of microbial infection, caused by pathogens such as virus, bacteria and malaria. A target DNA can be amplified within 30 min using the LAMP reaction, taking place at a steady temperature. The LAMP method uses four or six primers to bind eight regions of a target DNA and has a very high specificity. The devices used for conducting LAMP are usually simple since the LAMP method is an isothermal process. When LAMP is coupled with Reverse Transcription (RT), it allows direct detection of RNA in a sample. This greatly enhances the efficiency of diagnosis of RNA viruses in a sample. Recently, the rampant spread of COVID-19 demanded such a rapid, simple, and cost-effective Point of Care Test (PoCT) for the accurate diagnosis of this pandemic. Loop-mediated isothermal amplification (LAMP) assays are not only used for the detection of microbial pathogens, but there are various other applications such as detection of genetic mutations in food and various organisms. In this review, various implementations of RT-LAMP techniques would be discussed., (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)
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- 2024
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8. Adaption and application of cell-based bioassays to whole-water samples.
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Johnson M, Finlayson K, van de Merwe JP, and Leusch FDL
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- Solid Phase Extraction methods, Animals, Toxicity Tests methods, Biological Assay methods, Water Pollutants, Chemical analysis, Water Pollutants, Chemical toxicity, Environmental Monitoring methods, Wastewater chemistry
- Abstract
The increasing presence of contaminants of emerging concern in wastewater and their potential environmental risks require improved monitoring and analysis methods. Direct toxicity assessment (DTA) using bioassays can complement chemical analysis of wastewater discharge, but traditional in vivo tests have ethical considerations and are expensive, low-throughput, and limited to apical endpoints (mortality, reproduction, development, and growth). In vitro bioassays offer an alternative approach that is cheaper, faster, and more ethical, and can provide higher sensitivity for some environmentally relevant endpoints. This study explores the potential benefits of using whole water samples of wastewater and environmental surface water instead of traditional solid phase extraction (SPE) methods for in vitro bioassays testing. Whole water samples produced a stronger response in most bioassays, likely due to the loss or alteration of contaminants during SPE sample extraction. In addition, there was no notable difference in results for most bioassays after freezing whole water samples, which allows for increased flexibility in testing timelines and cost savings. These findings highlight the potential advantages of using whole water samples in DTA and provide a framework for future research in this area., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2024
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9. Development of a reliable cell-based reporter gene assay to measure the bioactivity of anti-HER2 therapeutic antibodies.
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Zhao X, Qian W, Hou S, Wu Y, Guo H, Xu J, Zhang D, Li J, Fu R, Xu M, and Wang F
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- Humans, Cell Line, Tumor, Breast Neoplasms drug therapy, Breast Neoplasms immunology, Breast Neoplasms genetics, Female, Antineoplastic Agents, Immunological pharmacology, Reproducibility of Results, Response Elements, Receptor, ErbB-2 genetics, Receptor, ErbB-2 immunology, Receptor, ErbB-2 antagonists & inhibitors, Genes, Reporter, Antibodies, Monoclonal, Humanized pharmacology, Biological Assay methods, Luciferases genetics, Neuregulin-1 genetics
- Abstract
Human epidermal growth factor receptor 2 (HER2) is a key player in the pathogenesis and progression of breast cancer and is currently a primary target for breast cancer immunotherapy. Bioactivity determination is necessary to guarantee the safety and efficacy of therapeutic antibodies targeting HER2. Nevertheless, currently available bioassays for measuring the bioactivity of anti-HER2 mAbs are either not representative or have high variability. Here, we established a reliable reporter gene assay (RGA) based on T47D-SRE-Luc cell line that expresses endogenous HER2 and luciferase controlled by serum response element (SRE) to measure the bioactivity of anti-HER2 antibodies. Neuregulin-1 (NRG-1) can lead to the heterodimerization of HER2 on the cell membrane and induce the expression of downstream SRE-controlled luciferase, while pertuzumab can dose-dependently reverse the reaction, resulting in a good dose-response curve reflecting the activity of the antibody. After optimizing the relevant assay parameters, the established RGA was fully validated based on ICH-Q2 (R1), which demonstrated that the method had excellent specificity, accuracy, precision, linearity, and stability. In summary, this robust and innovative bioactivity determination assay can be applied in the development and screening, release control, biosimilar assessment and stability studies of anti-HER2 mAbs., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)
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- 2024
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10. Concept of a six-fold multiplex planar bioassay to distinguish endocrine agonist, antagonist, cytotoxic and false-positive responses.
- Author
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Meyer D and Morlock GE
- Subjects
- Humans, Endocrine Disruptors analysis, Endocrine Disruptors pharmacology, False Positive Reactions, Phenols analysis, Phenols chemistry, Phenols pharmacology, Benzhydryl Compounds analysis, Benzhydryl Compounds pharmacology, Benzhydryl Compounds chemistry, Androgens analysis, Androgens metabolism, Androgen Antagonists analysis, Androgen Antagonists pharmacology, Biological Assay methods
- Abstract
To analyze a complex sample for endocrine activity, different tests must be performed to clarify androgen/estrogen agonism, antagonism, cytotoxicity, anti-cytotoxicity, and corresponding false-positive reactions. This means a large amount of work. Therefore, a six-fold planar multiplex bioassay concept was developed to evaluate up to the mentioned six endpoints or mechanisms simultaneously in the same sample analysis. Separation of active constituents from interfering matrix via high-performance thin-layer chromatography and effect differentiation via four vertical stripes (of agonists and end-products of the respective enzyme-substrate reaction) applied along each separated sample track were key to success. First, duplex endocrine bioassay versions were established. For the androgen/anti-androgen bioassay applied via piezoelectric spraying, the mean limit of biological detection of bisphenol A was 14 ng/band and its mean half maximal inhibitory concentration IC
50 was 116 ng/band. Applied to trace analysis of six migrate samples from food packaging materials, 19 compound zones with agonistic or antagonistic estrogen/androgen activities were detected, with up to seven active compound zones within one migrate. For the first time, the S9 metabolism of endocrine effective compounds was studied on the same surface and revealed partial deactivation. Coupled to high-resolution mass spectrometry, molecular formulas were tentatively assigned to compounds, known to be present in packaging materials or endocrine active or previously unknown. Finally, the detection of cytotoxicity/anti-cytotoxicity and false-positives was integrated into the duplex androgen/anti-androgen bioassay. The resulting six-fold multiplex planar bioassay was evaluated with positive control standards and successfully applied to one migrate sample. The streamlined stripe concept for multiplex planar bioassays made it possible to assign different mechanisms to individual active compounds in a complex sample. The concept is generic and can be transferred to other assays., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)- Published
- 2024
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11. Optimization of a bovine cytokine multiplex assay using a new bovine and cross-reactive equine monoclonal antibodies.
- Author
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Sipka A, Babasyan S, Asbie S, Freer H, and Wagner B
- Subjects
- Cattle, Tumor Necrosis Factor-alpha metabolism, Inflammation, Tetradecanoylphorbol Acetate, Recombinant Proteins genetics, Antibodies, Monoclonal immunology, Mice, Horses, Mice, Inbred BALB C, Cell Line, Tumor, Interleukin-10 genetics, Interleukin-10 metabolism, Interferon-gamma metabolism, Biological Assay, Cytokines metabolism
- Abstract
Cytokines are important markers for immune activation, regulation, and homeostasis. The lack of monoclonal antibodies (mAbs) and sensitive assays to evaluate cytokine secretion has hindered research of bovine inflammation and immune regulation. We recently developed a fluorescent bead-based multiplex assay (multiplex assay) for bovine IL-10, TNF-α, and IFN-γ. Although the original assay covers a broad concentration range for the 3 targets, analytical sensitivity for IL-10 and IFN-γ could be improved to facilitate detection of these cytokines in their physiological low pg/mL range. To optimize the multiplex assay, we generated a new bovine IL-10 mAb and explored its use for the detection of intracellular and secreted bovine IL-10. The new bovine IL-10 mAb 130 recognized recombinant bovine IL-10 fusion protein and did not react with the fusion protein tag, or the TNF-α and IFN-γ standards in the multiplex assay. For improving IFN-γ detection, we explored cross-reactivity of anti-equine IFN-γ mAbs by intracellular staining of bovine stimulated peripheral blood mononuclear cells (PBMC). Equine IFN-γ mAb 3 showed excellent cross-reactivity with bovine IFN-γ by intracellular detection. Adding IL-10 mAb 130 and IFN-γ mAb 3 to the bovine multiplex assay substantially improved the analytical sensitivity with lower limits of detection in the low pg/mL range for all analytes. The detection ranges for the optimized multiplex assay were determined as 2 - 134,000 pg/mL for IL-10, 8 - 127,000 pg/mL for IFN-γ, and 12 - 193,000 pg/mL for TNF-α. The assay was next used to measure cytokine concentrations in cell culture supernatants from PBMC stimulated in plasma from whole blood stimulation to confirm native IL-10, TNF-α, and IFN-γ recognition and to explore the upper detection limits of the assay. In PBMC stimulation with a mix of phorbol myristate acetate (PMA) and ionomycin resulted in highest cytokine concentrations, while in plasma from whole blood stimulation, highest concentrations were observed in samples stimulated with a mix of lipopolysaccharide (LPS), phytohemagglutinin (PHA), and the TLR-2/6 agonist Pam2Csk4. PBMC and whole blood stimulation protocols showed that the optimized multiplex assay covers a wide linear detection range for measuring cytokine concentrations in bovine samples. For whole blood stimulation, a cocktail of pathogen associated molecular patterns elicited a stronger cytokine response than a mix of PMA and ionomycin, but response varied considerably between individual cattle. In conclusion, optimizing the bovine cytokine assay with new reagents improved the lower detection limits and widened the linear detection ranges while lowering the background of the multiplex assay., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
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- 2024
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12. Glycosaminoglycan microarrays for studying glycosaminoglycan-protein systems.
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Chittum JE, Thompson A, and Desai UR
- Subjects
- Binding, Competitive, Microarray Analysis, Research, Glycosaminoglycans, Biological Assay
- Abstract
More than 3000 proteins are now known to bind to glycosaminoglycans (GAGs). Yet, GAG-protein systems are rather poorly understood in terms of selectivity of recognition, molecular mechanism of action, and translational promise. High-throughput screening (HTS) technologies are critically needed for studying GAG biology and developing GAG-based therapeutics. Microarrays, developed within the past two decades, have now improved to the point of being the preferred tool in the HTS of biomolecules. GAG microarrays, in which GAG sequences are immobilized on slides, while similar to other microarrays, have their own sets of challenges and considerations. GAG microarrays are rapidly becoming the first choice in studying GAG-protein systems. Here, we review different modalities and applications of GAG microarrays presented to date. We discuss advantages and disadvantages of this technology, explain covalent and non-covalent immobilization strategies using different chemically reactive groups, and present various assay formats for qualitative and quantitative interpretations, including selectivity screening, binding affinity studies, competitive binding studies etc. We also highlight recent advances in implementing this technology, cataloging of data, and project its future promise. Overall, the technology of GAG microarray exhibits enormous potential of evolving into more than a mere screening tool for studying GAG - protein systems., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Umesh R. Desai reports financial support was provided by National Institutes of Health. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)
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- 2024
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13. Application of in vitro bioassays to monitor pharmaceuticals in water: A synthesis of chronological analysis, mode of action, and practical insights.
- Author
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Tanveer R, Neale PA, Melvin SD, and Leusch FDL
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- Pharmaceutical Preparations analysis, Risk Assessment methods, Animals, Water Quality, Environmental Monitoring methods, Water Pollutants, Chemical analysis, Water Pollutants, Chemical toxicity, Biological Assay, Wastewater chemistry
- Abstract
Pharmaceutical compounds in wastewater have emerged as a significant concern for the aquatic environment. The use of in vitro bioassays represents a sustainable and cost-effective approach for assessing the potential toxicological risks of these biologically active compounds in wastewater and aligns with ethical considerations in research. It facilitates high-throughput analysis, captures mixture effects, integrates impacts of both known and unknown chemicals, and reduces reliance on animal testing. The core aim of the current review was to explore the practical application of in vitro bioassays in evaluating the environmental impacts of pharmaceuticals in wastewater. This comprehensive review strives to achieve several key objectives. First, it provides a summary categorisation of pharmaceuticals based on their mode of action, providing a structured framework for understanding their ecological significance. Second, a chronological analysis of pharmaceutical research aims to document their prevalence and trends over time, shedding light on evolving environmental challenges. Third, the review critically analyses existing bioassay applications in wastewater, while also examining bioassay coverage of representative compounds within major pharmaceutical classes. Finally, it explores the potential for developing innovative bioassays tailored for water quality monitoring of pharmaceuticals, paving the way for more robust environmental monitoring and risk assessment. Overall, adopting effect-based methods for pharmaceutical monitoring in water holds significant promise. It encompasses a broad spectrum of biological impacts, promotes standardized protocols, and supports a bioassay test battery approach indicative of different endpoints, thereby enhancing the effectiveness of environmental risk assessment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
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- 2024
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14. Pathogens of the oak processionary moth Thaumetopoea processionea: Developing a user-friendly bioassay system and metagenome analyses for microorganisms.
- Author
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Schäfer L, Jehle JA, Kleespies RG, and Wennmann JT
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- Animals, Metagenome, Quercus microbiology, Bacillus thuringiensis genetics, Moths microbiology, Biological Assay methods, Pest Control, Biological methods, Larva microbiology
- Abstract
The oak processionary moth (OPM) Thaumetopoea processionea is a pest of oak trees and poses health risks to humans due to the urticating setae of later instar larvae. For this reason, it is difficult to rear OPM under laboratory conditions, carry out bioassays or examine larvae for pathogens. Biological control targets the early larval instars and is based primarily on commercial preparations of Bacillus thuringiensis ssp. kurstaki (Btk). To test the entomopathogenic potential of other spore-forming bacteria, a user-friendly bioassay system was developed that (i) applies bacterial spore suspensions by oak bud dipping, (ii) targets first instar larvae through feeding exposure and (iii) takes into account their group-feeding behavior. A negligible mortality in the untreated control proved the functionality of the newly established bioassay system. Whereas the commercial Btk HD-1 strain was used as a bioassay standard and confirmed as being highly efficient, a Bacillus wiedmannii strain was ineffective in killing OPM larvae. Larvae, which died during the infection experiment, were further subjected to Nanopore sequencing for a metagenomic approach for entomopathogen detection. It further corroborated that B.wiedmannii was not able to infect and establish in OPM, but identified potential insect pathogenic species from the genera Serratia and Pseudomonas., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
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- 2024
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15. Terrestrial bioassays for assessing the biochemical and toxicological impact of biosolids application derived from wastewater treatment plants.
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Emmanouil C, Giannakis I, and Kyzas GZ
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- Animals, Oligochaeta drug effects, Oligochaeta physiology, Fertilizers, Plants drug effects, Soil Pollutants toxicity, Soil Pollutants analysis, Toxicity Tests, Environmental Monitoring methods, Water Pollutants, Chemical toxicity, Biological Assay, Waste Disposal, Fluid methods, Wastewater chemistry, Sewage chemistry
- Abstract
Wastewater treatment plants (WWTP) are facilities where municipal wastewater undergoes treatment so that its organic load and its pathogenic potential are minimized. Sewage sludge is a by-product of this process and when properly treated is preferentially called "biosolids". These treatments may include some or most of the following: thickening, dewatering, drying, digestion, composting, liming. Nowadays it is almost impossible to landfill biosolids, which however can well be used as crop fertilizers. Continuous or superfluous biosolids fertilization may negatively affect non-target organisms such as soil macro-organisms or even plants. These effects can be depicted through bioassays on terrestrial animals and plants. It has been shown that earthworms have been affected to various degrees on the following endpoints: pollutants' bioaccumulation, viability, reproduction, avoidance behavior, burrowing behavior. Collembola have been affected on viability, reproduction, avoidance behavior. Other terrestrial organisms such as nematodes and diplopods have also shown adverse health effects. Phytotoxicity have been caused by some biosolids regimes as measured through the following endpoints: seed germination, root length, shoot length, shoot biomass, root biomass, chlorophyll content, antioxidant enzyme activity. Very limited statistical correlations between pollutant concentrations and toxicity endpoints have been established such as between juvenile mortality (earthworms) and As or Ba concentration in the biosolids, between juvenile mortality (collembola) and Cd or S concentration in the biosolids, or between phytotoxicity and some extractable metals in leachates or aquatic extracts from the biosolids; more correlations between physicochemical characteristics and toxicity endpoints have been found such as between phytotoxicity and ammonium N in biosolids or their liquid extracts, or between phytotoxicity and salinity. An inverse correlation between earthworm/collembola mortality and stable organic matter has also been found. Basing the appropriateness of biosolids only on chemical analyses for pollutants is not cost-effective. To enable risk characterization and subsequent risk mitigation it is important to apply a battery of bioassays on soil macro-organisms and on plants, utilizing a combination of endpoints and established protocols. Through combined analytical quantification and toxicity testing, safe use of biosolids in agriculture can be achieved., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)
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- 2024
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16. Bioassay predictive values for chemical health risks in drinking water.
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Pronk TE, Hoondert RPJ, Kools SAE, Kumar V, and de Baat ML
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- Risk Assessment, Bayes Theorem, Humans, Predictive Value of Tests, Drinking Water chemistry, Biological Assay, Water Pollutants, Chemical analysis
- Abstract
Bioanalytical tools can be used for assessment of the chemical quality of drinking water and its sources. For water managers it is important to know the probability that a bioassay response above an established health-based 'effect-based trigger value' (EBT) indeed implies a harmful chemical (mixture) concentration. This study presents and applies a framework, based on Bayes' theorem, to derive such risk probabilities for bioassay responses. These were evaluated under varying (in silico) chemical mixture concentrations relevant to drinking water (sources), with toxicity data for six in vitro assays from the ToxCast database. For single chemicals and in silico mixtures, the negative predictive value (NPV) was 100 % for all assays. For water managers, this means that when a bioassay response is below the EBT, a chemical risk is reliably absent, and no further action is required. The positive predictive value (PPV) increased with increasing chemical concentrations (2 µg/L) up to 40-80 %, depending on the assay. For in silico mixtures of increasing numbers of chemicals, the PPV did not increase until higher sum concentrations (>2-10 µg/L). Hence, the ability to accurately signal a harmful chemical (mixture) using bioassays will be lowest for highly diverse, low-concentration chemical mixtures. For water managers, this means in practice that further investigations after an EBT exceedance will, in many cases, not reveal chemicals at harmful concentrations. A solution offered is to increase the trigger value for positive responses to achieve a higher PPV and maintain the EBT for negative responses to ensure an optimal NPV., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)
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- 2024
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17. How the Xenopus eleutheroembryonic thyroid assay compares to the amphibian metamorphosis assay for detecting thyroid active chemicals.
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Du Pasquier D, Salinier B, Coady KK, Jones A, Körner O, LaRocca J, Lemkine G, Robin-Duchesne B, Weltje L, Wheeler JR, and Lagadic L
- Subjects
- Animals, Xenopus laevis, Receptors, Thyroid Hormone metabolism, Receptors, Thyroid Hormone agonists, Iodide Peroxidase metabolism, Thyroid Gland drug effects, Thyroid Gland metabolism, Metamorphosis, Biological drug effects, Biological Assay methods, Endocrine Disruptors toxicity, Symporters
- Abstract
The Xenopus Eleutheroembryonic Thyroid Assay (XETA) was recently published as an OECD Test Guideline for detecting chemicals acting on the thyroid axis. However, the OECD validation did not cover all mechanisms that can potentially be detected by the XETA. This study was therefore initiated to investigate and consolidate the applicability domain of the XETA regarding the following mechanisms: thyroid hormone receptor (THR) agonism, sodium-iodide symporter (NIS) inhibition, thyroperoxidase (TPO) inhibition, deiodinase (DIO) inhibition, glucocorticoid receptor (GR) agonism, and uridine 5'-diphospho-glucuronosyltransferase (UDPGT) induction. In total, 22 chemicals identified as thyroid-active or -inactive in Amphibian Metamorphosis Assays (AMAs) were tested using the XETA OECD Test Guideline. The comparison showed that both assays are highly concordant in identifying chemicals with mechanisms of action related to THR agonism, DIO inhibition, and GR agonism. They also consistently identified the UDPGT inducers as thyroid inactive. NIS inhibition, investigated using sodium perchlorate, was not detected in the XETA. TPO inhibition requires further mechanistic investigations as the reference chemicals tested resulted in opposing response directions in the XETA and AMA. This study contributes refining the applicability domain of the XETA, thereby helping to clarify the conditions where it can be used as an ethical alternative to the AMA., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: David Du Pasquier, Benoit Salinier, Gregory Lemkine, Barbara Robin-Duchesne reports financial support was provided by CropLife Europe. Laurent Lagadic reports a relationship with Bayer CropScience AG that includes: employment. This work was supported by CropLife Europe as a Company Investment Project and research and development funds from Corteva Agriscience USA. The employment affiliation of the authors is listed on the cover page. BRD, BS, DDP and GL are affiliated to Laboratoire WatchFrog, developer of the Xenopus Eleutheroembryonic Thyroid Assay (XETA) and coordinator of the validation of OECD TG 248. AJ, JL, JRW, KKC, LL, LW and OK are affiliated to companies that manufacture agrochemicals, some of which having been used in the present study. There are no other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
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- 2024
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18. Letter to the Editors regarding "Using historical control data in bioassays for regulatory toxicology" by Kluxen et al. (2021).
- Author
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Zarn JA, Geiser HC, König SLB, Shaw HV, and Zürcher UA
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- Toxicity Tests methods, Animals, Humans, Toxicology methods, Biological Assay
- Abstract
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. The first author was member of the JMPR from 2004 to 2023.
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- 2024
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19. A portable smartphone-assisted Tb-MOF-based agar-slice probe for the rapid and on-site fluorescence assay of malachite green in aquatic products.
- Author
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Song J, Zhao B, Wang Y, Liu X, Cheng Z, Zhang X, and Feng X
- Subjects
- Agar, Electron Transport, Fluorescent Dyes, Limit of Detection, Smartphone, Biological Assay
- Abstract
In this study, a new Tb-MOF fluorescence probe was developed for the detection of malachite green (MG) in real aquatic products. Fluorescence sensing experiments revealed that MG can effectively quench the green fluorescence of Tb-MOF suspensions, and the detection process exhibits the advantages of high sensitivity, a wide linear range (0-80 μM), a low detection limit (10.8 nM) and a rapid response time. Selective detection of MG is achieved primarily through fluorescence resonance energy transfer (FRET) and photoinduced electron transfer (PET) mechanisms. Furthermore, a smartphone-assisted Tb-MOF-based agar slice detection platform was constructed for the visual and quantitative detection of MG. Additionally, the on-site detection of MG in crucian and shrimp samples was accomplished with high recoveries (99.8 %-107.99 %) and low relative standard deviations (RSD < 2.2 %). This developed detection platform introduced a low-cost, portable and user-friendly approach for MG detection., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)
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- 2024
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20. A Review of Research Progress in Microfluidic Bioseparation and Bioassay.
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Zhao, Heng, Zhang, Yanyan, and Hua, Dengxin
- Subjects
LITERATURE reviews ,BIOLOGICAL assay ,BIOTECHNOLOGY ,MICROFLUIDICS - Abstract
With the rapid development of biotechnology, the importance of microfluidic bioseparation and bioassay in biomedicine, clinical diagnosis, and other fields has become increasingly prominent. Microfluidic technology, with its significant advantages of high throughput, automated operation, and low sample consumption, has brought new breakthroughs in the field of biological separation and bioassay. In this paper, the latest research progress in microfluidic technology in the field of bioseparation and bioassay is reviewed. Then, we focus on the methods of bioseparation including active separation, passive separation, and hybrid separation. At the same time, the latest research results of our group in particle separation are introduced. Finally, some application examples or methods for bioassay after particle separation are listed, and the current challenges and future prospects of bioseparation and bioassay are discussed. [ABSTRACT FROM AUTHOR]
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- 2024
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21. Liquid Chromatography-Mass Spectrometry Analytical Methods for the Quantitation of p -Cresol Sulfate and Indoxyl Sulfate in Human Matrices: Biological Applications and Diagnostic Potentials.
- Author
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Al-Dajani, Ala'a R., Hou, Qi Kun, and Kiang, Tony K. L.
- Subjects
LIQUID chromatography-mass spectrometry ,ELUTION (Chromatography) ,GRADIENT elution (Chromatography) ,SULFATES ,AMMONIUM acetate ,BIOLOGICAL assay ,LIQUID-liquid extraction - Abstract
Indoxyl sulfate (IxS) and p-cresyl sulfate (pCS) are toxic uremic compounds with documented pathological outcomes. This review critically and comprehensively analyzes the available liquid chromatography-mass spectrometry methods quantifying IxS and pCS in human matrices and the biological applications of these validated assays. Embase, Medline, PubMed, Scopus, and Web of Science were searched until December 2023 to identify assays with complete analytical and validation data (N = 23). Subsequently, citation analysis with PubMed and Scopus was utilized to identify the biological applications for these assays (N = 45). The extraction methods, mobile phase compositions, chromatography, and ionization methods were evaluated with respect to overall assay performance (e.g., sensitivity, separation, interference). Most of the assays focused on human serum/plasma, utilizing acetonitrile or methanol (with ammonium acetate/formate or formic/acetic acid), liquid–liquid extraction, reverse phase (e.g., C18) chromatography, and gradient elution for analyte separation. Mass spectrometry conditions were also consistent in the identified papers, with negative electrospray ionization, select multiple reaction monitoring transitions and deuterated internal standards being the most common approaches. The validated biological applications indicated IxS and/or pCS were correlated with renal disease progression and cardiovascular outcomes, with limited data on central nervous system disorders. Methods for reducing IxS and/or pCS concentrations were also identified (e.g., drugs, natural products, diet, dialysis, transplantation) where inconsistent findings have been reported. The clinical monitoring of IxS and pCS is gaining significant interest, and this review will serve as a useful compendium for scientists and clinicians. [ABSTRACT FROM AUTHOR]
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- 2024
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22. Chromatographic methods and approaches for bioequivalence study, drug screening and enantioseparation of indapamide.
- Author
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Sethi, Sonika, Martens, Jürgen, and Bhushan, Ravi
- Subjects
INDAPAMIDE ,CAPILLARY electrophoresis ,ENANTIOMERS ,RACEMIC mixtures ,SUPERCRITICAL fluids ,BIOLOGICAL assay ,HIGH performance liquid chromatography - Abstract
Indapamide (Indp) and certain other diuretics have been abused in sports, therefore, having sensitive methods for its detection and assay in biological fluids (whole blood, plasma, serum, and urine) is of significant importance. The racemic mixture of Indp is being used as an active pharmaceutical ingredient among other commonly prescribed diuretics. The regulatory authorities and pharmaceutical industries demand analytical methods for successful enantioseparation of such molecules. The paper presents a critical overview of the scientific issues of the application of contemporary techniques involving various chromatographic approaches (with liquid or supercritical fluid as mobile phases) and capillary electrophoresis and method development, for drug screening, assay, bioequivalence studies and enantioseparation of indapamide with their results. It also covers the historical developments that led to significant breakthroughs in research and concise evaluations of research in the area. Different types of chromatographic methods (HPLC, CEC, SFC etc) discussed herein provide an insight and a choice to select a method to (i) screen Indp for drug abuse, (ii) separate, isolate and quantify the enantiomers of Indp and (iii) investigate their pharmacokinetics as markedly different species and not as a total drug. The article evaluates the field's status with a broad base and practical oriented approach so that the underlying principles are easily understood to help chemists and non-specialists gain useful insights into the field outside their specialization and provide experts with summaries of key developments. To the best of authors' knowledge there has been no attempt to review such methods for analysis of Indp and this is the first report of its kind. [ABSTRACT FROM AUTHOR]
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- 2024
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23. Real-Time On-Site Monitoring of Viruses in Wastewater Using Nanotrap ® Particles and RICCA Technologies.
- Author
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Sharma V, Takamura H, Biyani M, and Honda R
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- Feces, RNA, Viral, SARS-CoV-2, Wastewater, Biological Assay
- Abstract
Wastewater-based epidemiology (WBE) is an effective and efficient tool for the early detection of infectious disease outbreaks in a community. However, currently available methods are laborious, costly, and time-consuming due to the low concentration of viruses and the presence of matrix chemicals in wastewater that may interfere with molecular analyses. In the present study, we designed a highly sensitive "Quick Poop (wastewater with fecal waste) Sensor" (termed, QPsor) using a joint approach of Nanotrap microbiome particles and RICCA (RNA Isothermal Co-Assisted and Coupled Amplification). Using QPsor, the WBE study showed a strong correlation with standard PEG concentrations and the qPCR technique. Using a closed format for a paper-based lateral flow assay, we were able to demonstrate the potential of our assay as a real-time, point-of-care test by detecting the heat-inactivated SARS-CoV-2 virus in wastewater at concentrations of 100 copies/mL and within one hour. As a proof-of-concept demonstration, we analyzed the presence of viral RNA of the SARS-CoV-2 virus and PMMoV in raw wastewater samples from wastewater treatment plants on-site and within 60 min. The results show that the QPsor method can be an effective tool for disease outbreak detection by combining an AI-enabled case detection model with real-time on-site viral RNA extraction and amplification, especially in the absence of intensive clinical laboratory facilities. The lab-free, lab-quality test capabilities of QPsor for viral prevalence and transmission in the community can contribute to the efficient management of pandemic situations.
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- 2024
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24. MOF-derived porous carbon nanozyme-based flexible electrochemical sensing system for in situ and real-time monitoring of H 2 O 2 released from cells.
- Author
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Wang X, Wang Y, Liu Y, Cao X, Zhang F, Xia J, and Wang Z
- Subjects
- Humans, HeLa Cells, Porosity, Carbon, Hydrogen Peroxide, Biological Assay
- Abstract
A novel flexible electrochemical sensor based on porous carbon nanosheets (PCNSs) nanozyme has been constructed for in situ and real-time monitoring of H
2 O2 released by cells. The PCNSs are prepared with the integration of thermal transformation, thermal activation and sonochemical exfoliation by using zeolitic imidazolate frameworks as template. The PCNSs exhibit high electrical conductivity, electrochemical activity and peroxidase-like catalytic properties, which is beneficial to H2 O2 assay. With the transfer printing method, the flexible electrochemical sensor is obtained, which has excellent performances for H2 O2 electrochemical detecting with wide linear range from 1 μM to 20 mM and a low detection limit of 0.76 μM. Owing to the great biocompatibility, the flexible sensor guarantees the growth of living cells for 72 h and realizes in situ and real-time monitoring the release of H2 O2 from HeLa cells. The strategy of porous nanozyme preparation and flexible sensor construction provided a promising way for in situ and real-time assay of small molecules in the cellular microenvironment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)- Published
- 2024
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25. Selected Chromatographic Methods for Determining the Biological Activity of Substances.
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Grządka, E. and Malinowska, I.
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BIOMIMETICS ,CARRIER proteins ,BIOLOGICAL assay ,PROTEIN transport ,LIPOPHILICITY ,RF values (Chromatography) ,RECORDS management - Abstract
This paper presents various aspects of the use of chromatography to determine the biological activity of substances. On the one hand, the use of chromatography to determine the lipophilicity of a substance, a property that affects all LADME steps in various biomimetic systems, is presented, using various descriptors such as the retention factor in pure water (or buffer with physiological plasma pH), the CHI value, and Chrom logD. The use of chromatography in biomimetic systems to determine the interaction of substances with phospholipids (IAM stationary phases) and transport proteins (stationary phases with immobilised proteins) is also discussed. On the basis of the retention data obtained in these systems, the volume of distribution of the substance and the degree of binding of the substance with the proteins in question can be determined. Chromatography is also a method used to determine the interaction of substances with specific membrane receptors at their site of action using membrane chromatography (MCM). Thanks to biological detection, chromatography can also be used to determine the antimicrobial activity (bioautography) of substances and the effect of substances on biochemical reactions taking place in organisms, such as antioxidant properties and the inhibitory activity of various enzymes (biological assay). [ABSTRACT FROM AUTHOR]
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- 2024
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26. Novel Tools for Single Comparative and Unified Evaluation of Qualitative and Quantitative Bioassays: SS/PV–ROC and SS-J/PV-PSI Index–ROC Curves with Integrated Concentration Distributions, and SS-J/PV-PSI Index Cut-Off Diagrams.
- Author
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Oehr, Peter
- Subjects
BLADDER cancer ,MACHINE learning ,PLANT epidemiology ,BIOLOGICAL assay ,RECEIVER operating characteristic curves ,COMPARATIVE method - Abstract
Background: This investigation is both a study of potential non-invasive diagnostic approaches for the bladder cancer biomarker UBC
® Rapid test and a study including novel comparative methods for bioassay evaluation and comparison that uses bladder cancer as a useful example. The objective of the paper is not to investigate specific data. It is used only for demonstration, partially to compare ROC methodologies and also to show how both sensitivity/specificity and predictive values can be used in clinical diagnostics and decision making. This study includes ROC curves with integrated cut-off distribution curves for a comparison of sensitivity/specificity (SS) and positive/negative predictive values (PPV/NPV or PV), as well as SS-J index/PV-PSI index–ROC curves and SS-J/PV-PSI index cut-off diagrams (J = Youden, PSI = Predictive Summary Index) for the unified direct comparison of SS-J/PV results achieved via quantitative and/or qualitative bioassays and an identification of optimal separate or unified index cut-off points. Patients and Methods: According to the routine diagnostics, there were 91 patients with confirmed bladder cancer and 1152 patients with no evidence of bladder cancer, leading to a prevalence value of 0.073. This study performed a quantitative investigation of used-up test cassettes from the visual UBC® Rapid qualitative point-of-care assay, which had already been applied in routine diagnostics. Using a photometric reader, quantitative data could also be obtained from the test line of the used cassettes. Interrelations between SS and PV values were evaluated using cumulative distribution analysis (CAD), SS/PV–ROC curves, SS-J/PV-PSI index–ROC curves, and the SS-J/PV-PSI index cut-off diagram. The maximum unified SS-J/PV-PSI index value and its corresponding cut-off value were determined and calculated with the SS-J/PV-PSI index cut-off diagram. Results: The use of SS/PV–ROC curves with integrated cut-off concentration distribution curves provides improved diagnostic information compared to "traditional" ROC curves. The threshold distributions integrated as curves into SS/PV–ROC curves and SS-J/PV-PSI index–ROC curves run in opposite directions. In contrast to the SS–ROC curves, the PV–ROC and the novel PV-PSI index–ROC curves had neither an area under the curve (AUC) nor a range from 0% to 100%. The cut-off level of the qualitative assay was 7.5 µg/L, with a sensitivity of 65.9% and a specificity of 63.3%, and the PPV was 12.4% and the NPV was 95.9%, at a threshold value of 12.5 µg/L. Based on these set concentrations, the reader-based evaluation revealed a graphically estimated 5% increase in sensitivity and a 13% increase in specificity, as compared to the visual qualitative POC test. In the case of predictive values, there was a gain of 8% for PPV and 10% for NPV. The index values and cut-offs were as follows: visual SS-J index, 0.328 and 35 µg/L; visual PV-PSI index, 0.083 and 5.4 µg/L; maximal reader Youden index, 0.0558 and 250 µg/L; and maximal PV-PSI index, 0.459 and 250 µg/L, respectively. The maximum unified SS-J/PV-PSI index value was 0.32, and the cut-off was 43 µg/L. The reciprocal SS-J index correctly detected one out of three patients, while the reciprocal PV-PSI index gave one out of twelve patients a correct diagnosis. Conclusions: ROC curves including cut-off distribution curves supplement the information lost in "traditionally plotted" ROC curves. The novel sets of ROC and index–ROC curves and the new SS/PV index cut-off diagrams enable the simultaneous comparison of sensitivity/specificity and predictive value profiles of diagnostic tools and the identification of optimal cut-off values at maximal index values, even in a unifying SS/PV approach. Because the curves within an SS-J/PV-PSI index cut-off diagram are distributed over the complete cut-off range of a quantitative assay, this field is open for special clinical considerations, with the need to vary the mentioned clinical diagnostic parameters. Complete or partial areas over the x-axis (AOX) can be calculated for summarized quantitative or qualitative effectivity evaluations with respect to single and/or unified SS-J and PV-PSI indices and with respect to single, several, or several unified assays. The SS-J/PV-PSI index-AOX approach is a new tool providing additional joint clinical information, and the reciprocal SS-J indices can predict the number of patients with a correct diagnosis and the number of persons who need to be examined in order to correctly predict a diagnosis of the disease. These methods could be used in applications like medical or plant epidemiology, machine learning algorithms, and neural networks. [ABSTRACT FROM AUTHOR]- Published
- 2024
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27. Development of new approach methods for the identification and characterization of endocrine metabolic disruptors--a PARC project.
- Author
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Braeuning, Albert, Balaguer, Patrick, Bourguet, William, Carreras-Puigvert, Jordi, Feiertag, Katreece, Kamstra, Jorke H., Knapen, Dries, Lichtenstein, Dajana, Marx-Stoelting, Philip, Rietdijk, Jonne, Schubert, Kristin, Spjuth, Ola, Stinckens, Evelyn, Thedieck, Kathrin, van den Boom, Rik, Vergauwen, Lucia, von Bergen, Martin, Wewer, Neele, and Zalko, Daniel
- Subjects
ENDOCRINE disruptors ,PANCREATIC beta cells ,ORGANS (Anatomy) ,ENERGY metabolism ,BIOLOGICAL assay - Abstract
In past times, the analysis of endocrine disrupting properties of chemicals has mainly been focused on (anti-)estrogenic or (anti-)androgenic properties, as well as on aspects of steroidogenesis and the modulation of thyroid signaling. More recently, disruption of energy metabolism and related signaling pathways by exogenous substances, so-called metabolism-disrupting chemicals (MDCs) have come into focus. While general effects such as body and organ weight changes are routinely monitored in animal studies, there is a clear lack of mechanistic test systems to determine and characterize the metabolismdisrupting potential of chemicals. In order to contribute to filling this gap, one of the project within EU-funded Partnership for the Assessment of Risks of Chemicals (PARC) aims at developing novel in vitro methods for the detection of endocrine metabolic disruptors. Efforts will comprise projects related to specific signaling pathways, for example, involving mTOR or xenobioticsensing nuclear receptors, studies on hepatocytes, adipocytes and pancreatic beta cells covering metabolic and morphological endpoints, as well as metabolism-related zebrafish-based tests as an alternative to classic rodent bioassays. This paper provides an overview of the approaches and methods of these PARC projects and how this will contribute to the improvement of the toxicological toolbox to identify substances with endocrine disrupting properties and to decipher their mechanisms of action. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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28. Diverting the Use of Hand-Operated Tablet Press Machines to Bioassays: A Novel Protocol to Test 'Waste' Insoluble Shell Matrices.
- Author
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Lutet-Toti, Camille, Da Silva Feliciano, Marie, Debrosse, Nelly, Thomas, Jérôme, Plasseraud, Laurent, and Marin, Frédéric
- Subjects
BIOLOGICAL assay ,APPLIED sciences ,BIOACTIVE compounds ,MACHINERY ,BACTERICIDES - Abstract
To mineralize their shells, molluscs secrete a complex cocktail of proteins—collectively defined as the calcifying shell matrix—that remains occluded in the exoskeleton. Nowadays, protein extracts from shells are recognized as a potential source of bioactive substances, among which signalling molecules, bactericides or protease inhibitors offer the most tangible perspectives in applied sciences, health, and aquaculture. However, one technical obstacle in testing the activity of shell extracts lies in their high insolubility. In this paper, we present a protocol that circumvents this impediment. After an adapted shell protein extraction and the production of two organic fractions—one soluble, one insoluble—we employ a hand-operated tablet press machine to generate well-calibrated tablets composed of 100% insoluble shell matrix. FT-IR monitoring of the quality of the tablets shows that the pressure used in the press machine does not impair the molecular properties of the insoluble extracts. The produced tablets can be directly tested in different biological assays, such as the bactericidal inhibition zone assay in Petri dish, as illustrated here. Diverting the use of the hand-operated tablet press opens new perspectives in the analysis of insoluble shell matrices, for discovering novel bioactive components. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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29. Research Progress on Effect-Based Trigger Values for in vitro Bioassays of Environmental Water Samples.
- Author
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Zhang Shuo, Han Yingnan, Li Na, and Ma Mei
- Subjects
ENVIRONMENTAL sampling ,WATER sampling ,WATER quality management ,BODIES of water ,BIOLOGICAL assay - Abstract
In vitrobioassays can directly obtain the toxicity information of numerous coexisting pollutants in water environment, and has become one of the important means for toxic effect evaluations and diagnosis. However, due to the lack of toxicity effect limit standards for determining the water quality, it is difficult to use bioassays for water quality management. Therefore, more and more research is focusing on deriving the effect-based trigger values (EBTs) of in vitrobioassays. This paper reviews the establishment background and derivation principles of EBTs, and summarizes a variety of derivation methods of EBTs. At present, the methods of derivation of EBTs are divided into two categories according to the protection objectives, one is the health protection objective and the other is the ecological protection objective. EBTs for drinking water are based on the premise of protecting human health and are based on allowable daily intake (ADI), in vivo safe concentration, daily dose of 10% increase in cancer inci- dence (TD10 ) and guideline values (GV) in environmental quality standard (EQS). While, EBTs for surface water, aiming at ecological protection, were derived based on GVs values in the EQS and hazardous concentrations at the 5th percentile (HC5 ) of the species sensitivity distribution (SSD). Derivation of EBTs from GV and HC5 are two widely used frameworks. The former is dedicated to reading EBT values from GV of EQS and trying to establish derivation methods that can be widely applied to various toxicity endpoints. The latter is to obtain HC5 values of positive compounds from the species sensitivity curve. At the same time, combined with the background parameters of the water body to be measured, the EBT value of the protection ecosystem was derived. This paper compares the EBT values and characteristics derived from different methods for in vitro bioassays and summarizes the applica- tion of EBTs in water environments in order to provide theoretical basis and technical support for high-throughput in vitrobioassays for water quality assessment. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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30. Architectural Synthesis of Continuous-Flow Microfluidic Biochips with Connection Pair Optimization.
- Author
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Hu, Xu, Chen, Zhen, Chen, Zhisheng, and Liu, Genggeng
- Subjects
BIOCHIPS ,MICROFLUIDICS ,CHANNEL flow ,ROUTING algorithms ,MICROFLUIDIC devices ,BIOLOGICAL assay - Abstract
Continuous-flow microfluidic biochips are a type of biochip technology based on microfluidic channels that enable various biological experiments and analyses to be performed on a tiny chip. They have the advantages of a high throughput, high sensitivity, high precision, low cost, and quick response. In the architectural synthesis of continuous-flow microfluidic biochips (CFMBs), prior work has not considered reducing component interconnection requirements, which led to an increase in the number of connection pairs. In this paper, we propose an architectural synthesis flow for continuous-flow microfluidic biochips with connection pair optimization, which includes high-level synthesis, placement, and routing. In the high-level synthesis stage, our method reduces the need for component interconnections, which reduces the number of connection pairs. Our method performs fine-grained binding, ultimately obtaining high-quality binding and scheduling results for flow paths. Based on the high-quality binding results, we propose a port placement strategy based on port correlation and subsequently use a quadratic placer to place the components. During the routing stage, we employ a conflict-aware routing algorithm to generate flow channels to reduce conflicts between liquid transportation tasks. Experimental results on multiple benchmarks demonstrate the effectiveness of our method. Compared with the existing work, the proposed algorithm obtains average reductions of 35.34% in connection pairs, 24.30% in flow channel intersections, 21.71% in total flow channel length, and 18.39% in the execution time of bioassays. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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- View/download PDF
31. Potency Assay Variability Estimation in Practice.
- Author
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Li, Hang, Witkos, Tomasz M., Umlauf, Scott, and Thompson, Christopher
- Subjects
- *
BIOLOGICAL assay , *DRUG development - Abstract
During the drug development process, testing potency plays an important role in the quality assessment required for the manufacturing and marketing of biologics. Due to multiple operational and biological factors, higher variability is usually observed in bioassays compared with physicochemical methods. In this paper, we discuss different sources of bioassay variability and how this variability can be statistically estimated. In addition, we propose an algorithm to estimate the variability of reportable results associated with different numbers of runs and their corresponding OOS rates under a given specification. Numerical experiments are conducted on multiple assay formats to elucidate the empirical distribution of bioassay variability. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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32. Food-derived dipeptidyl peptidase IV inhibitory peptides: Production, identification, structure-activity relationship, and their potential role in glycemic regulation.
- Author
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Zhang, Mingkai, Zhu, Ling, Wu, Gangcheng, Liu, Tongtong, Qi, Xiguang, and Zhang, Hui
- Subjects
- *
CD26 antigen , *PEPTIDASE , *STRUCTURE-activity relationships , *PEPTIDES , *BIOLOGICAL assay , *PEPTIDE fractionation - Abstract
Dipeptidyl Peptidase IV (DPP-IV) inhibitory peptides are attracting increasing attention, owing to their potential role in glycemic regulation by preventing the inactivation of incretins. However, few reviews have summarized the current understanding of DPP-IV inhibitory peptides and their knowledge gaps. This paper reviews the production, identification and structure-activity relationships (SAR) of DPP-IV inhibitory peptides. Importantly, their bioavailability and hypoglycemic effects are critically discussed. Unlike the traditional method to identifying peptides after separation step by step, the bioinformatics approach identifies peptides via virtual screening that is more convenient and efficient. In addition, the bioinformatics approach was also used to investigate the SAR of peptides. Peptides with proline (Pro) or alanine (Ala) residue at the second position of N-terminal are exhibit strong DPP-IV inhibitory activity. Besides, the bioavailability of DPP-IV inhibitory peptides is related to their gastrointestinal stability and cellular permeability, and in vivo studies showed that the glucose homeostasis has been improved by these peptides. Especially, the intestinal transport of DPP-IV inhibitory peptides and cell biological assays used to evaluate their potential role in glycemic regulation are innovatively summarized. For further successful development of DPP-IV inhibitory peptides in glycemic regulation, future study should elucidate their SAR and in vivo hypoglycemic effects. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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33. Isolation of Toxoplasma gondii in cell culture: an alternative to bioassay.
- Author
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Dawant, Tania, Wang, Wei, Spriggs, Maria, Magela de Faria Junior, Geraldo, Horton, Laura, Szafranski, Nicole M., Waap, Helga, Jokelainen, Pikka, Gerhold, Richard W., and Su, Chunlei
- Subjects
- *
TOXOPLASMA gondii , *BIOLOGICAL assay , *CELL culture , *WILD turkey , *WHITE-tailed deer , *ANTIBODY titer , *ANIMAL experimentation - Abstract
[Display omitted] • We reviewed the literature on isolation of Toxoplasma gondii directly in cell culture. • Four experiments were reported to isolate T. gondii from different animals in Vero and HFF cell cultures. • We recommend an in vitro protocol to isolate T. gondii. • This method is simpler, more cost-effective, ethically more acceptable, and less time-sensitive. Toxoplasma gondii is an apicomplexan protozoan parasite that can infect mammals and birds. The infection can cause acute toxoplasmosis and death in susceptible hosts. Bioassay using cats and mice has been the standard for the isolation of T. gondii from infected hosts for the past several decades. However, bioassay is labor-intensive, expensive, and involves using laboratory animals. To search alternative approaches and o work towards replacement of animal experiments, we summarized the key literature and conducted four experiments to isolate T. gondii in vitro by cell culture. A few heart tissue samples from animals with the highest antibody titers in a given collection were used for T. gondii isolation. These experiments included samples from five out of 51 wild ducks, four of 46 wild turkeys, six of 24 white-tailed deer, as well as from six kangaroos that had died with acute toxoplasmosis in a zoo. These experiments resulted in three isolates from five chronically infected wild ducks (60%), four isolates from four chronically infected wild turkeys (100%), one isolate from six chronically infected white-tailed deer (17%), and four isolates from six kangaroos with acute toxoplasmosis (67%). In addition, five isolates from the five chronically infected wild ducks were obtained by bioassay in mice, showing a 100% success rate, which is higher than the 60% rate by direct cell culture. These T. gondii isolates were successfully propagated in human foreskin fibroblast (HFF) or Vero cells, and genotyped by multilocus PCR-RFLP markers. The results showed that it is practical to isolate T. gondii directly in cell culture. Although the cell culture approach may not be as sensitive as the bioassay, it does provide an alternative that is simple, cost-effective, ethically more acceptable, and less time-sensitive to isolate T. gondii. In this paper we propose a procedure that may be applied and further optimized for isolation of T. gondii. [ABSTRACT FROM AUTHOR]
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- 2024
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34. The Concept of Using 2D Self-Assembly of Magnetic Nanoparticles for Bioassays.
- Author
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Marć, Maciej, Wolak, Wiktor, Drzewiński, Andrzej, Mudry, Stepan, Shtablavyi, Ihor, and Dudek, Mirosław R.
- Subjects
MAGNETIC nanoparticles ,MAGNETIC fluids ,BIOLOGICAL assay ,LOW density polyethylene ,AQUEOUS solutions ,MAGNETIC nanoparticle hyperthermia - Abstract
It can be observed that magnetic iron-oxide nanoparticles are increasingly used in bioassay methods. This is due to their stability in aqueous solutions, ease of functionalization, biocompatibility and very low toxicity. Here, we show that the recent discovery of the ability of magnetic nanoparticles to self-assemble into 2D structures of ordered chains may be exploited for bioassays. This would open up the possibility of controlled immobilization of proteins, enzymes, DNA or RNA and other molecular systems on spatially ordered nanostructures. In this work, fluorescein was used as an example. Also shown is the possibility of using Raman spectroscopy to analyze material accumulated on such structures. The observed formation of regularly spaced chains of magnetic nanoparticles takes place during the drying process of a thin layer of magnetic liquid placed on an appropriately prepared low-density polyethylene (LDPE) film. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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- View/download PDF
35. Reactant and Waste Minimization during Sample Preparation on Micro-Electrode-Dot-Array Digital Microfluidic Biochips using Splitting Trees.
- Author
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Dong, Chen, Chen, Xiao, and Chen, Zhenyi
- Subjects
- *
BIOCHIPS , *BIOCHEMICAL substrates , *WASTE minimization , *BIOLOGICAL assay , *GEOMETRIC approach , *LABS on a chip - Abstract
Biological assays around "lab-on-a-chip (LoC)" are required in multiple concentration (or dilution) factors, satisfying specific sample concentrations. Unfortunately, most of them suffer from non-locality and are non-protectable, requiring a large footprint and high purchase cost. A digital geometric technique can generate arbitrary gradient profiles for digital microfluidic biochips (DMFBs). A next- generation DMFB has been proposed based on the microelectrode-dot-array (MEDA) architectures are shown to produce and disperse droplets by channel dispensing and lamination mixing. Prior work in this area must address the problem of reactant and waste minimization and concurrent sample preparation for multiple target concentrations. This paper proposes the first splitting-droplet sharing algorithm for reactant and waste minimization of multiple target concentrations on MEDAs. The proposed algorithm not only minimizes the consumption of reagents but also reduces the number of waste droplets by preparing the target concentrations concurrently. Experimental results on a sequence of exponential gradients are presented in support of the proposed method and demonstrate its effectiveness and efficiency. Compared to prior work, the proposed algorithm can achieve up to a 24.8% reduction in sample usage and reach an average of 50% reduction in waste droplets. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
36. Pathologists' perspective on the study design, analysis, and interpretation of proliferative lesions in a lifetime rodent carcinogenicity bioassay of sucralose.
- Author
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Elmore, Susan A., Rehg, Jerold E., Schoeb, Trenton R., Everitt, Jeffrey I., and Bolon, Brad
- Subjects
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SUCRALOSE , *CARCINOGENICITY , *BIOLOGICAL assay , *PATHOLOGISTS , *CARCINOGENS , *MICE - Abstract
Sucralose, a sugar substitute first approved for use in 1991, is a non-caloric sweetener regulated globally as a food additive. Based on numerous experimental animal studies (dating to the 1980s) and human epidemiology studies, international health agencies have determined that sucralose is safe when consumed as intended. A single lifetime rodent carcinogenicity bioassay conducted by the Ramazzini Institute (RI) reported that mice fed diets containing sucralose develop hematopoietic neoplasia, but controversy continues regarding the validity and relevance of these data for predicting health effects in humans. The present paper addresses the controversy by providing the perspective of experienced pathologists on sucralose-related animal toxicity and carcinogenicity data generally, and the RI carcinogenicity bioassay findings specifically, using results from publicly available papers and international regulatory authority decisions. In the authors' view, flaws in the design, methodology, data evaluation, and reporting of the RI carcinogenicity bioassay for sucralose diminish the value of the data as evidence that this agent represents a carcinogenic hazard to humans. This limitation will remain until the RI bioassay is repeated under Good Laboratory Practices and the design, data, and accuracy of the pathology diagnoses and interpretations are reviewed by qualified pathologists with experience in evaluating potential chemically-induced carcinogenic hazards. [ABSTRACT FROM AUTHOR]
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- 2024
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37. Exploring in vitro modeling in hepatocarcinogenesis research: morphological and molecular features and similarities to the corresponding human disease.
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Valente, Leticia Cardoso, Bacil, Gabriel Prata, Riechelmann-Casarin, Luana, Barbosa, Giullia Cavichiolli, Barbisan, Luís Fernando, and Romualdo, Guilherme Ribeiro
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DRUG metabolism , *HEPATOCELLULAR carcinoma , *FATTY liver , *BIOLOGICAL assay , *TRANSLATIONAL research - Abstract
The hepatocellular carcinoma (HCC) features a remarkable epidemiological burden, ranking as the third most lethal cancer worldwide. As the HCC-related molecular and cellular complexity unfolds as the disease progresses, the use of a myriad of in vitro models available is mandatory in translational preclinical research setups. In this review paper, we will compile cutting-edge information on the in vitro bioassays for HCC research, (A) emphasizing their morphological and molecular parallels with human HCC; (B) delineating the advantages and limitations of their application; and (C) offering perspectives on their prospective applications. While bidimensional (2D) (co) culture setups provide a rapid low-cost strategy for metabolism and drug screening investigations, tridimensional (3D) (co) culture bioassays - including patient-derived protocols as organoids and precision cut slices - surpass some of the 2D strategies limitations, mimicking the complex microarchitecture and cellular and non-cellular microenvironment observed in human HCC. 3D models have become invaluable tools to unveil HCC pathophysiology and targeted therapy. In both setups, the recapitulation of HCC in different etiologies/backgrounds (i.e., viral, fibrosis, and fatty liver) may be considered as a fundamental guide for obtaining translational findings. Therefore, a "multimodel" approach – encompassing the advantages of different in vitro bioassays - is encouraged to circumvent "model-biased" outcomes in preclinical HCC research. [Display omitted] [ABSTRACT FROM AUTHOR]
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- 2024
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38. The antioxidant and antimicrobial activity of ethanolic extract in roots, stems, and leaves of three commercial Cymbopogon species.
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Wahyuni, Dwi Kusuma, Kharisma, Viol Dhea, Murtadlo, Ahmad Affan Ali, Rahmawati, Cici Tya, Syukriya, Alvi Jauharotus, Prasongsuk, Sehanat, Subramaniam, Sreeramanan, Wibowo, Anjar Tri, and Purnobasuki, Hery
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IN vitro studies ,COMPUTER-assisted molecular modeling ,BACILLUS (Bacteria) ,RESEARCH funding ,ETHANOL ,PLANT stems ,DRUG resistance in microorganisms ,PLANT roots ,IMMUNODIAGNOSIS ,STAPHYLOCOCCUS aureus ,DESCRIPTIVE statistics ,ANTI-infective agents ,PLANT extracts ,METABOLITES ,GAS chromatography ,CANDIDA albicans ,ESCHERICHIA coli ,ANTIOXIDANTS ,MASS spectrometry ,LEAVES ,LEMONGRASS ,BIOLOGICAL assay ,COMPARATIVE studies ,DATA analysis software ,CELL surface antigens ,PHARMACODYNAMICS - Abstract
Background: Cymbopogon is a member of the family Poaceae and has been explored for its phytochemicals and bioactivities. Although the antimicrobial activities of Cymbopogon spp. extracts have been extensively studied, comprehensive analyses are required to identify promising compounds for the treatment of antimicrobial resistance. Therefore, this study investigated the antioxidant and antimicrobial properties of Cymbopogon spp. ethanolic extracts in every single organ. Methods: Ethanolic extracts were obtained from three Indonesian commercial species of Cymbopogon spp., namely Cymbopogon citratus (L.) Rendle, Cymbopogon nardus (DC.) Spatf., and Cymbopogon winterianus Jowitt. The leaf, stem, and root extracts were evaluated via metabolite profiling using gas chromatography-mass spectrometry (GC–MS). In silico and in vitro analyses were used to evaluate the antioxidant and antimicrobial properties of the Cymbopogon spp. ethanolic extracts. In addition, bioactivity was measured using cytotoxicity assays. Antioxidant assays were performed using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2-azino-bis [3-ethylbenzothiazoline-6-sulfonic acid (ABTS) to determine toxicity to Huh7it-1 cells using a tetrazolium bromide (MTT) assay. Finally, the antimicrobial activity of these extracts was evaluated against Candida albicans, Bacillus subtilis, Staphylococcus aureus, and Escherichia coli using a well diffusion assay. Results: GC–MS analysis revealed 53 metabolites. Of these, 2,5-bis(1,1-dimethylethyl)- phenol (27.87%), alpha-cadinol (26.76%), and 1,2-dimethoxy-4-(1-propenyl)-benzene (20.56%) were the predominant compounds. C. winterianus and C. nardus leaves exhibited the highest antioxidant activity against DPPH and ABTS, respectively. Contrastingly, the MTT assay showed low cytotoxicity. C. nardus leaf extract exhibited the highest antimicrobial activity against E. coli and S. aureus, whereas C. winterianus stem extract showed the highest activity against B. substilis. Furthermore, computational pathway analysis predicted that antimicrobial activity mechanisms were related to antioxidant activity. Conclusions: These findings demonstrate that the leaves had strong antioxidant activity, whereas both the leaves and stems showed great antimicrobial activity. Furthermore, all Cymbopogon spp. ethanolic extracts showed low toxicity. These findings provide a foundation for future studies that assess the clinical safety of Cymbopogon spp. as novel drug candidates. [ABSTRACT FROM AUTHOR]
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- 2024
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39. Insights into free radicals scavenging, α-Amylase inhibition, cytotoxic and antifibrotic activities unveiled by Peganum harmala extracts.
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Jaradat, Nidal, Hawash, Mohammed, Sharifi-Rad, Majid, Shakhshir, Ali, Sobuh, Shorooq, Hussein, Fatima, Issa, Linda, Hamamrhe, Sondos, Al-Sheikh, Eman, and Ibrahim, Alaa Naser
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ANTI-inflammatory agents ,EPITHELIAL cells ,DATA analysis ,ESSENTIAL oils ,HYPOGLYCEMIC agents ,DESCRIPTIVE statistics ,PLANT extracts ,SEEDS ,CYTOTOXINS ,FIBROSIS ,CELL lines ,FREE radical scavengers ,MEDICINAL plants ,ONE-way analysis of variance ,STATISTICS ,FLUOROURACIL ,BIOLOGICAL assay ,DATA analysis software ,AMYLASES ,PHARMACODYNAMICS ,CHEMICAL inhibitors - Abstract
Background: Peganum harmala L. is used in traditional medicine to treat several health ailments. Hence, the present work aimed to investigate the DPPH free radical scavenging, α-amylase, cytotoxic, and antifibrotic effects of the hydrophilic extract and fixed oil obtained from P. harmala seeds. Methods: The hydrophilic extract and fixed oil of P. harmala were assessed for their abilities to scavenge DPPH free radicals and inhibit α-amylase using reference bioassays. The cytotoxicity was assessed on several cancer and normal cell lines, including B16F1, Caco-2, COLO205, HeLa, Hep 3B and Hep G2, MCF-7, and HEK-293 T cells. The MTS assay was used to evaluate the antifibrotic capabilities utilizing the human hepatic stellate (LX-2) cell line. Results: P. harmala plant fixed oil has potent DPPH free radical scavenging activity with an IC
50 dose of 79.43 ± 0.08 µg/ml. Besides, the hydrophilic extract has a poor anti-α-amylase effect compared with the antidiabetic drug Acarbose, with IC50 doses of 398 ± 0.59 and 25.11 ± 1.22 µg/ml, respectively. In addition, the growth of MCF-7, Hep3B, HepG2, HeLa, COLO205, CaCo2, B16F1, and HeK293t was inhibited by P. harmala hydrophilic extract with IC50 doses of 121.34 ± 1.71, 268.3 ± 0.75, 297.20 ± 1.00, 155.60 ± 1.14, 150.01 ± 0.51, 308.35 ± 0.53, 597.93 ± 1.36, and 5.38 ± 0.99 µg/ml, respectively. In addition, at 1000 µg/ml, 5-Fluorouracil reduced fibrosis cells by 0.089%, while the hydrophilic extract decreased the number of LX-2 cells by 5.81%. Conclusion: P. harmala plant-fixed oil exhibits potential antioxidant properties. While the hydrophilic extract showed limited effectiveness as an anti-α-amylase agent and demonstrated notable cytotoxic effects against various tested cancer cell lines. Furthermore, this extract significantly reduces the number of LX-2 fibrotic cells. These findings emphasize the therapeutic potential of these products in managing various health disorders and warrant further investigation into their mechanisms of action and clinical applications. [ABSTRACT FROM AUTHOR]- Published
- 2024
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40. Influence of silver nanoparticles' size on their direct interactions with doxorubicin and its biological effects.
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Grzegorz, Gołuński, Kinga, Konkel, Barbara, Galikowska-Bogut, Patrycja, Bełdzińska, Katarzyna, Bury, Marcin, Zakrzewski, Kamila, Butowska, Rafał, Sądej, and Jacek, Piosik
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BIOACTIVE compounds ,NANOPARTICLE size ,SILVER nanoparticles ,BIOLOGICAL assay ,FLUORESCENCE spectroscopy - Abstract
Breast cancer is one of cancer's most deadly varieties. Its variability makes the development of personalized therapies very difficult. Therefore, improvement of classic chemotherapy is still one of the important challenges of cancer research. We addressed this issue applying nanotechnology to verify the influence of silver nanoparticles (AgNPs) on doxorubicin (DOX) anticancer activity and assess if the size of AgNPs affects their interactions with DOX. We employed a broad spectrum of biophysical methods, characterizing 5 and 50 nm AgNPs interactions with DOX using UV–Vis spectroscopy, dynamic light scattering, fluorescence spectroscopy, and atomic force microscopy imaging. Biological effects of observed AgNPs-DOX interactions were assessed utilizing MTT and 3D Matrigel assays on SKBR3 and MDA-MB-231 breast cancer cell lines. Obtained results indicate direct interactions between AgNPs and DOX. Furthermore, AgNPs size influences their interactions with DOX, as evidenced by differences in the heteroaggregates formation observed in biophysical experiments and further supported by in vitro biological assays. We detected reduction of tumor cell viability and/or colony sizes of the analyzed cancer cell lines, registering differences linked to the observed phenomenon. However, the effects may be limited to the outer borders of the tumor microenvironment as evidenced by the 3D model. Summing up, we observed diverse patterns of interactions and biological effects for different sizes of AgNPs with DOX providing insight how the nanoparticles' size affects their interactions with other biologically active compounds. Moreover, obtained data can be further used in experiments on the reduction of tumor size i.e. before the surgical intervention. [ABSTRACT FROM AUTHOR]
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- 2024
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41. High-risk human papillomavirus genotyping in cervical cancers in Tanzania.
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Murenzi, Gad, Vuhahula, Edda, Kimambo, Asteria, Matiku, Subira, Tuyishime, Obed, Liwa, Edwin, Habanabakize, Thomas, Rugengamanzi, Eulade, Malango, Atuganile, Kubwimana, Gallican, Anastos, Kathryn, and Castle, Philip E.
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PAPILLOMAVIRUS diseases ,RISK assessment ,CROSS-sectional method ,CERVIX uteri tumors ,WOMEN ,RESEARCH funding ,HIV-positive persons ,EARLY detection of cancer ,HOSPITALS ,CANCER patients ,AGE distribution ,DESCRIPTIVE statistics ,HUMAN papillomavirus vaccines ,BIOLOGICAL assay ,WOMEN'S health ,GENOTYPES ,GENETIC profile ,HISTOLOGY ,DISEASE risk factors ,DISEASE complications - Abstract
Background: High-risk human papillomavirus (hrHPV) infection causes almost all cervical cancer. Women living with human immunodeficiency virus (Women living with HIV: WLWHIV) are at a six-fold increased risk of developing cervical cancer. This study assessed hrHPV types in cervical cancer by HIV status and histologic subtypes at Muhimbili National Hospital (MNH) in Tanzania. Methods: This cross-sectional study used formalin-fixed paraffin-embedded (FFPE) archived tissue blocks of cervical carcinomas diagnosed in the Department of Anatomical Pathology at MNH from January to December 2020. Tissue sections were tested for 15 HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, and 68) using the Ampfire assay. The distribution of HPV genotypes was assessed and compared by HIV status and histologic subtypes. Results: The mean age ± standard deviation (N = 227, with valid HPV results) was 55 ± 12.9 years, 28.6% (n = 65) were WLWHIV, and squamous cell carcinoma (SCC) was the most common histologic subtype (91.2%). Most cervical carcinomas (81.1%, n = 184) tested positive for hrHPV with HPV16 (44.1%), HPV18 (15.9%), HPV35 (8.4%) and HPV45 (5.7%) being the most common HPV types. hrHPV was higher among older women with 64.5%, 85.1% and 81.3% among 30–40, 41–60 and ≥ 61-year-old women, respectively (p = 0.033). HPV16 was more commonly detected in SCC (47.8%) than in adenocarcinomas (5%) (p < 0.0001). There was no difference in hrHPV positivity by HIV status. Conclusions: We found a high proportion of hrHPV among cervical carcinomas diagnosed in Tanzania. Rolling out HPV vaccines that target more hrHPV types than HPV16/18, especially HPV35 and HPV45, could optimize protection against cervical cancer in Tanzania. [ABSTRACT FROM AUTHOR]
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- 2024
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42. Exploring sources of inaccuracy and irreproducibility in the CDC bottle bioassay through direct insecticide quantification.
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Peard, Evah F., Luu, Calvin, Hageman, Kimberly J., Sepesy, Rose, and Bernhardt, Scott A.
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INSECTICIDES ,BIOLOGICAL assay ,GLASS bottles ,TANDEM mass spectrometry ,BOTTLES ,COATING processes - Abstract
Background: The Centers for Disease Control and Prevention (CDC) bottle bioassay is a commonly used susceptibility test for measuring insect response to insecticide exposure. However, inconsistencies and high variability in insect response when conducting CDC bottle bioassays have been reported in previous publications. We hypothesized that the CDC bottle bioassay results may be compromised when expected and actual insecticide concentrations in the bottles are not equivalent and that inadequate bottle cleaning and/or loss during insecticide introduction and bottle storage steps could be responsible. We explored this hypothesis by quantifying insecticides using gas chromatography tandem mass spectrometry (GC-MS/MS) in bottles that had been cleaned, prepared, and stored according to the CDC guidelines. Methods: We investigated the bottle cleaning, preparation, and storage methods outlined in the CDC bottle bioassay procedure to identify sources of irreproducibility. We also investigated the effectiveness of cleaning bottles by autoclaving because this method is commonly used in insecticide assessment laboratories. The two insecticides used in this study were chlorpyrifos and lambda-cyhalothrin (λ-cyhalothrin). Insecticides were removed from glass bioassay bottles by rinsing with ethyl-acetate and n-hexane and then quantified using GC-MS/MS. Results: The CDC bottle bioassay cleaning methods did not sufficiently remove both insecticides from the glass bottles. The cleaning methods removed chlorpyrifos, which has higher water solubility, more effectively than λ-cyhalothrin. Chlorpyrifos experienced significant loss during the bottle-coating process whereas λ-cyhalothrin did not. As for bottle storage, no significant decreases in insecticide concentrations were observed for 6 h following the initial drying period for either insecticide. Conclusions: The CDC bottle bioassay protocol is susceptible to producing inaccurate results since its recommended bottle cleaning method is not sufficient and semi-volatile insecticides can volatilize from the bottle during the coating process. This can lead to the CDC bottle bioassay producing erroneous LC
50 values. High levels of random variation were also observed in our experiments, as others have previously reported. We have outlined several steps that CDC bottle bioassay users could consider that would lead to improved accuracy and reproducibility when acquiring toxicity data. [ABSTRACT FROM AUTHOR]- Published
- 2024
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43. Exploring the therapeutic potential of Thai medicinal plants: in vitro screening and in silico docking of phytoconstituents for novel anti-SARS-CoV-2 agents.
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Maikhunthod, Bussayarat, Chaipayang, Sukanya, Jittmittraphap, Akanitt, Thippornchai, Narin, Boonchuen, Pakpoom, Tittabutr, Panlada, Eumkeb, Griangsak, Sabuakham, Sahachai, Rungrotmongkol, Thanyada, Mahalapbutr, Panupong, Leaungwutiwong, Pornsawan, Teaumroong, Neung, and Tanthanuch, Waraporn
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VIRUS disease drug therapy ,COMPUTER-assisted molecular modeling ,IN vitro studies ,DIARRHEA ,LIGANDS (Biochemistry) ,LIQUID chromatography-mass spectrometry ,RESEARCH funding ,HERBAL medicine ,PHYTOCHEMICALS ,PLANTS ,DESCRIPTIVE statistics ,PLANT extracts ,ANTIVIRAL agents ,MEDICINAL plants ,DRUG efficacy ,MOLECULAR structure ,BIOLOGICAL assay ,DATA analysis software ,COVID-19 - Abstract
Background: The high virulence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), responsible for coronavirus disease 2019 (COVID-19), has triggered global health and economic concerns. The absence of specific antiviral treatments and the side effects of repurposed drugs present persistent challenges. This study explored a promising antiviral herbal extract against SARS-CoV-2 from selected Thai medicinal plants based on in vitro efficacy and evaluated its antiviral lead compounds by molecular docking. Methods: Twenty-two different ethanolic-aqueous crude extracts (CEs) were rapidly screened for their potential activity against porcine epidemic diarrhea virus (PEDV) as a surrogate using a plaque reduction assay. Extracts achieving ≥ 70% anti-PEDV efficacy proceeded to the anti-SARS-CoV-2 activity test using a 50% tissue culture infectious dose method in Vero E6 cells. Molnupiravir and extract-free media served as positive and negative controls, respectively. Potent CEs underwent water/ethyl acetate fractionation to enhance antiviral efficacy, and the fractions were tested for anti-SARS-CoV-2 performance. The fraction with the highest antiviral potency was identified using liquid chromatography–high-resolution mass spectrometry (LC–HRMS). Molecular docking analyses of these compounds against the main protease (M
pro ) of SARS-CoV-2 (6LU7) were performed to identify antiviral lead molecules. The top three hits were further evaluated for their conformational stability in the docked complex using molecular dynamics (MD) simulation. Results: The water fraction of mulberry (Morus alba Linn.) leaf CE (WF-MLCE) exhibited the most potent anti-SARS-CoV-2 efficacy with low cytotoxicity profile (CC50 of ~ 0.7 mg/mL), achieving 99.92% in pre-entry mode and 99.88% in postinfection treatment mode at 0.25 mg/mL. Flavonoids and conjugates were the predominant compounds identified in WF-MLCE. Molecular docking scores of several flavonoids against SARS-CoV-2 Mpro demonstrated their superior antiviral potency compared to molnupiravir. Remarkably, myricetin-3-O-β-D-galactopyranoside, maragrol B, and quercetin 3-O-robinobioside exhibited binding energies of ~ − 9 kcal/mol. The stability of each ligand–protein complex of these compounds with the Mpro system showed stability during MD simulation. These three molecules were pronounced as antiviral leads of WF-MLCE. Given the low cytotoxicity and high antiviral potency of WF-MLCE, it holds promise as a candidate for future therapeutic development for COVID-19 treatment, especially considering its economic and pharmacological advantages. [ABSTRACT FROM AUTHOR]- Published
- 2024
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44. Point of Care Liquid Biopsy for Cancer Treatment—Early Experience from a Community Center.
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Nicholas, Champica, Beharry, Andrea, Bendzsak, Anna M., Bisson, Kassandra R., Dadson, Keith, Dudani, Shaan, Iafolla, Marco, Irshad, Kashif, Perdrizet, Kirstin, Raskin, William, Singh, Raviya, Tsui, David Chun Cheong, Wang, Xin, Yeung, Ching, Cheema, Parneet K., and Sheffield, Brandon S.
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TUMOR treatment ,COMMUNITY health services ,RESEARCH funding ,BREAST tumors ,EVALUATION of human services programs ,BODY fluid examination ,TUMOR markers ,TREATMENT effectiveness ,RETROSPECTIVE studies ,MEDICAL records ,ACQUISITION of data ,LUNG tumors ,POINT-of-care testing ,BIOLOGICAL assay ,GENETIC mutation ,SEQUENCE analysis ,HISTOLOGY ,SENSITIVITY & specificity (Statistics) ,EPIDERMAL growth factor receptors - Abstract
Simple Summary: Cancer care is being increasingly driven by biomarker testing. Many biomarkers are traditionally measured on a sample from a patient tumor such as a biopsy. More recently, "liquid biopsy" has emerged as a blood test to complement or replace traditional tissue-based testing. In this report, we explore one of the first case series of rapid liquid biopsy performed within a hospital setting. The results include a median 3-day time to results, compared to approximately 14 days using traditional centralized reference labs. Additional details of the cohort are shared to highlight the utility of point of care liquid biopsy. Liquid biopsy is rapidly becoming an indispensable tool in the oncologist's arsenal; however, this technique remains elusive in a publicly funded healthcare system, and real-world evidence is needed to demonstrate utility and feasibility. Here, we describe the first experience of an in-house point of care liquid biopsy program at a Canadian community hospital. A retrospective review of consecutive cases that underwent plasma-based next-generation sequencing (NGS) was conducted. Liquid biopsy was initiated at the discretion of clinicians. Sequencing followed a point of care workflow using the Genexus™ integrated sequencer and the Oncomine precision assay, performed by histotechnologists. Results were reported by the attending pathologist. Eligible charts were reviewed for outcomes of interest, including the intent of the liquid biopsy, results of the liquid biopsy, and turnaround time from blood draw to results available. A total of 124 cases, with confirmed or suspected cancer, underwent liquid biopsy between January 2021 and November 2023. The median turnaround time for liquid biopsy results was 3 business days (range 1–12 days). The sensitivity of liquid biopsies was 71%, compared to tissue testing in cases with matched tissue results available for comparison. Common mutations included EGFR (29%), in 86 lung cancer patients, and PIK3CA (22%), identified in 13 breast cancer patients. Healthcare providers ordered liquid biopsies to inform diagnostic investigations and treatment decisions, and to determine progression or resistance mechanisms, as these reasons often overlapped. This study demonstrates that rapid in-house liquid biopsy using point of care methodology is feasible. The technique facilitates precision treatment and offers many additional advantages for cancer care. [ABSTRACT FROM AUTHOR]
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- 2024
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45. Antioxidant activity, cytotoxicity assay, and evaluation of bioactive compounds using GC-MS and HPTLC-based bioassay in the extracts of Osbeckia stellata var. crinita (Benth. ex Naudin) grown in Manipur, India.
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Baishya, Tania, Das, Priya, Ashraf, Gouhar Jahan, Dua, Tarun Kumar, Paul, Paramita, Nandi, Gouranga, Jajo, Honey, Dutta, Ankita, Kumar, Anoop, Bhattacharya, Malay, and Sahu, Ranabir
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CYTOTOXINS ,BIOACTIVE compounds ,PHYTOCHEMICALS ,THIN layer chromatography ,FREE radical scavengers ,BIOLOGICAL assay ,BOTANICAL chemistry - Abstract
In the present study, we aimed to investigate the antioxidant, cytotoxicity activities, and phytochemical profiling of O. stellata extracts. Qualitative phytochemical tests showed the presence of different groups of phytochemicals, mainly in polar solvents. Methanolic and hydroalcoholic extracts showed high total phenolic and flavonoid contents. The antioxidant activity was determined by using 2,2-Diphenyl-1-picrylhydrazyl (DPPH), metal chelating, and reducing power assay where methanolic (IC50: 24.76 ± 2.78 μg/mL), hydroalcoholic (IC50: 29.59 ± 3.44 μg/mL), and aqueous (IC50: 33.72 ± 1.97 μg/mL) extracts showed significantly antioxidant potential. Significant cytotoxicity activity was observed in the methanolic extract. As methanolic extract showed better activities, gas chromatography–mass spectrometry (GC-MS) analysis of methanolic extract identified 41 bioactive compounds, where 17 major compounds had medicinal value. High-performance thin layer chromatography (HPTLC) bioassay-guided assay combined with Attenuated Total Reflectance-Fourier Transform Infrared (ATRFTIR) and nuclear magnetic resonance (NMR) spectroscopy characterized gallic and caffeic acid as free radical scavengers. This study evidences that the methanolic extract of O. stellata has potent antioxidant and anti-cancer properties, which may render oxidative stress-related disease and may be used for drug development for human health benefits. [ABSTRACT FROM AUTHOR]
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- 2024
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46. Activity-based detection of synthetic cannabinoid receptor agonists in plant materials.
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Timmerman, Axelle, Balcaen, Margot, Coopman, Vera, Degreef, Maarten, Pottie, Eline, and Stove, Christophe P.
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CANNABINOID receptors ,SYNTHETIC receptors ,CANNABIS (Genus) ,DANCE festivals ,BIOLOGICAL assay - Abstract
Background: Since late 2019, fortification of 'regular' cannabis plant material with synthetic cannabinoid receptor agonists (SCRAs) has become a notable phenomenon on the drug market. As many SCRAs pose a higher health risk than genuine cannabis, recognizing SCRA-adulterated cannabis is important from a harm reduction perspective. However, this is not always an easy task as adulterated cannabis may only be distinguished from genuine cannabis by dedicated, often expensive and time-consuming analytical techniques. In addition, the dynamic nature of the SCRA market renders identification of fortified samples a challenging task. Therefore, we established and applied an in vitro cannabinoid receptor 1 (CB
1 ) activity-based procedure to screen plant material for the presence of SCRAs. Methods: The assay principle relies on the functional complementation of a split-nanoluciferase following recruitment of β-arrestin 2 to activated CB1 . A straightforward sample preparation, encompassing methanolic extraction and dilution, was optimized for plant matrices, including cannabis, spiked with 5 µg/mg of the SCRA CP55,940. Results: The bioassay successfully detected all samples of a set (n = 24) of analytically confirmed authentic Spice products, additionally providing relevant information on the 'strength' of a preparation and whether different samples may have originated from separate batches or possibly the same production batch. Finally, the methodology was applied to assess the occurrence of SCRA adulteration in a large set (n = 252) of herbal materials collected at an international dance festival. This did not reveal any positives, i.e. there were no samples that yielded a relevant CB1 activation. Conclusion: In summary, we established SCRA screening of herbal materials as a new application for the activity-based CB1 bioassay. The simplicity of the sample preparation, the rapid results and the universal character of the bioassay render it an effective and future-proof tool for evaluating herbal materials for the presence of SCRAs, which is relevant in the context of harm reduction. [ABSTRACT FROM AUTHOR]- Published
- 2024
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47. Assessing human carcinogenicity risk of agrochemicals without the rodent cancer bioassay.
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Goetz, Amber, Ryan, Natalia, Sauve-Ciencewicki, Alaina, Lord, Caleb C., Hilton, Gina M., and Wolf, Douglas C.
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CARCINOGENICITY ,BIOLOGICAL assay ,RODENTS ,AGRICULTURAL chemicals ,REPORT writing - Abstract
The rodent cancer bioassays are conducted for agrochemical safety assessment yet they often do not inform regulatory decision-making. As part of a collaborative effort, the Rethinking Carcinogenicity Assessment for Agrochemicals Project (ReCAAP) developed a reporting framework to guide a weight of evidence (WOE)-based carcinogenicity assessment that demonstrates how to fulfill the regulatory requirements for chronic risk estimation without the need to conduct lifetime rodent bioassays. The framework is the result of a multi-stakeholder collaboration that worked through an iterative process of writing case studies (in the form of waivers), technical peer reviews of waivers, and an incorporation of key learnings back into the framework to be tested in subsequent case study development. The example waivers used to develop the framework were written retrospectively for registered agrochemical active substances for which the necessary data and information could be obtained through risk assessment documents or data evaluation records from the US EPA. This exercise was critical to the development of a framework, but it lacked authenticity in that the stakeholders reviewing the waiver already knew the outcome of the rodent cancer bioassay(s). Syngenta expanded the evaluation of the ReCAAP reporting framework by writing waivers for three prospective case studies for new active substances where the data packages had not yet been submitted for registration. The prospective waivers followed the established framework considering ADME, potential exposure, subchronic toxicity, genotoxicity, immunosuppression, hormone perturbation, mode of action (MOA), and all relevant information available for read-across using a WOE assessment. The point of departure was estimated from the available data, excluding the cancer bioassay results, with a proposed use for the chronic dietary risk assessment. The read-across assessments compared data from reliable registered chemical analogues to strengthen the prediction of chronic toxicity and/or tumorigenic potential. The prospective case studies represent a range of scenarios, from a new molecule in a well-established chemical class with a known MOA to a molecule with a new pesticidal MOA (pMOA) and limited read-across to related molecules. This effort represents an important step in establishing criteria for a WOE-based carcinogenicity assessment without the rodent cancer bioassay(s) while ensuring a health protective chronic dietary risk assessment. [ABSTRACT FROM AUTHOR]
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- 2024
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48. Salvia miltiorrhiza bunge extracts: a promising source for anti-atopic dermatitis activity.
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Ryu, Da Hye, Cho, Jwa Yeong, Yu, Hyung-Seok, Kim, Jin-Woo, Kim, Jin-Chul, Son, Yang-Ju, Nho, Chu Won, Hamayun, Muhammad, and Kim, Ho-Youn
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THERAPEUTIC use of antioxidants ,PHYTOTHERAPY ,ATOPIC dermatitis ,ANTI-inflammatory agents ,IN vitro studies ,HIGH performance liquid chromatography ,PEARSON correlation (Statistics) ,STATISTICAL significance ,RESEARCH funding ,PHYTOCHEMICALS ,DESCRIPTIVE statistics ,PLANT extracts ,REACTIVE oxygen species ,METABOLITES ,GENES ,MESSENGER RNA ,MEDICINAL plants ,ANTIOXIDANTS ,MASS spectrometry ,PHENOLS ,ANALYSIS of variance ,COMPARATIVE studies ,BIOLOGICAL assay ,DATA analysis software ,PHARMACODYNAMICS - Abstract
Background: Atopic dermatitis (AD) is a chronic inflammatory condition characterized by the accumulation of reactive oxygen species and the expression of inflammatory factors. Regarding its anti-atopic activity, numerous traditional medicinal materials and secondary metabolic products play pivotal roles in modulating the associated mechanisms. Methods: This study aimed to utilize Salvia miltiorrhiza Bunge (SMB) as an anti-AD source. In-vitro activity assessments and qualitative and quantitative analyses using UPLC-TQ-MS/MS and HPLC-DAD were conducted in two cultivars ('Dasan' and 'Kosan'). Statistical analysis indicated that the profiles of their secondary metabolites contribute significantly to their pharmacological properties. Consequently, bio-guided fractionation was undertaken to figure out the distinct roles of the secondary metabolites present in SMB. Results: Comparative study of two cultivars indicated that 'Dasan', having higher salvianolic acid A and B, exhibited stronger antioxidant and anti-inflammatory activities. Meanwhile, 'Kosan', containing higher tanshinones, showed higher alleviating activities on anti-AD related genes in mRNA levels. Additionally, performed bio-guided fractionation re-confirmed that the hydrophilic compounds of SMB can prevent AD by inhibiting accumulation of ROS and suppressing inflammatory factors and the lipophilic components can directly inhibit AD. Conclusions: SMB was revealed as a good source for anti-AD activity. Several bioactive compounds were identified from the UPLC-TQ-MS/MS and different compounds content was linked to biological activities. Characterization of these compounds may be helpful to understand differential role of secondary metabolites from SMB on alleviation of AD. [ABSTRACT FROM AUTHOR]
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- 2024
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49. Citral in lemon myrtle, lemongrass, litsea, and melissa essential oils suppress the growth and invasion of breast cancer cells.
- Author
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Nagata, Takuya, Satou, Tadaaki, Hayashi, Shinichiro, Satyal, Prabodh, Watanabe, Manabu, Riggs, Brannick, and Saida, Yoshihisa
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THERAPEUTIC use of antineoplastic agents ,DATA analysis ,RESEARCH funding ,ESSENTIAL oils ,BREAST tumors ,CELL proliferation ,CHALONES ,APOPTOSIS ,IMMUNODIAGNOSIS ,CELL motility ,PLANT extracts ,CELL lines ,CELL culture ,GAS chromatography ,ONE-way analysis of variance ,STATISTICS ,LEMONGRASS ,BIOLOGICAL assay ,DATA analysis software ,COMPARATIVE studies ,LEMON balm ,CELL surface antigens - Abstract
Objective: Although cancer therapy suppresses recurrence and prolongs life, it may be accompanied by strong side effects; thus, there is a strong demand for the development effective treatments with fewer side effects. Cancer therapy using plant-derived essential oils is attracting attention as one promising method. This study investigated the antitumor effects of essential oil volatiles on breast cancer cells and identifies four essential oils that display antitumor activity. Methods: Breast cancer cells were cultured in a 96-well plate, then one of twenty essential oils was added dropwise to the central well. The plate was incubated at 37 °C for 48 h and the effect of the volatile components of each essential oil on the surrounding breast cancer cell growth ability was examined using an MTT assay. Gas chromatography was used to investigate the concentration of the transpiration components that may affect cancer cells. Results: Of the 20 essential oils, Lemongrass, Lemon myrtle, Litsea, and Melissa displayed strong anti-tumor effects. These essential oils inhibited the growth of nearby breast cancer cells, even when diluted more than 500-fold. The transpiration component of lemon Myrtle showed the strongest antitumor effect, but was the least cytotoxic to mononuclear cells in normal peripheral blood (PBMC). Each of these essential oils contained a very large amount of citral. The IC
50 against breast cancer cells when citral was volatilized from each essential oil was 1.67 µL/mL for geranial and 1.31 µL/mL for neral. Volatilized citral alone showed strong anti-proliferation and infiltration-inhibiting effects. Conclusion: The transpiration components of Lemongrass, Lemon myrtle, Litsea, and Melissa are thought to inhibit breast cancer cell proliferation due to their high levels of citral. [ABSTRACT FROM AUTHOR]- Published
- 2024
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50. Ways of enhancement of biological efficiency of copper(ii) and zinc(ii) complexes: synthetic and structural aspects, thermal properties, and antimycobacterial activity.
- Author
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Koshenskova, K. A., Baravikov, D. E., Razvorotneva, L. S., Dolgushin, F. M., Bekker, O. B., Khoroshilov, A. V., Eremenko, I. L., and Lutsenko, I. A.
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COPPER ,THERMAL properties ,ZINC ,BIOLOGICAL assay ,X-ray diffraction ,ACETATES - Abstract
The reactions of copper(ii) and zinc(ii) acetates with anions of 5-phenylfuran-2-carboxylic acid (Hphfur) and 5-nitro-1,10-phenanthroline (nphen) or 2,2′-bipyridine (2,2′-bpy) in the MeOH/MeCN system afforded mononuclear complexes of the composition [Cu(phfur)
2 (nphen)H2 O] (1) and [Zn(phfur)2 (2,2′-bpy)]•H2 O (2). The structures of these complexes were determined by X-ray diffraction analysis (XRD). According to the XRD data, the copper atom in molecular complex 1 is in a distorted square-pyramidal environment (SQ (CuN2 O3 ) = 0.68); the zinc atom in molecular complex 2, in a distorted trigonal-bipyramidal environment (SQ (ZnN2 O3 ) = 3.87). The supramolecular level of 1 is mediated by intermolecular π–π interactions between the aromatic moieties of the ligands and represents a 3D supramolecular structure. in the structure of 2, the water molecules of crystallization are involved in intermolecular hydrogen bonds, resulting in the formation of centrosymmetric hydrogen-bonded dimers. The supramolecular level of 2 is mediated by C—H⋯O and C—H⋯π interactions. According to the simultaneous thermal analysis, complexes 1 and 2 are characterized by different types of thermal destruction. Thus, the explosophoric groups in the ligands of compound 1 are responsible for an intense exothermic effect. The results of biological assays show a certain correlation between the type of the substituted moiety in the heterocycle and the activity against the non-pathogenic Mycolicibacterium smegmatis strain. [ABSTRACT FROM AUTHOR]- Published
- 2024
- Full Text
- View/download PDF
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