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A novel electrochemical sensor–based glassy carbon electrode (GCE) was fabricated and applied to simultaneous detection and degradation of tebuconazole (TBZ) for the first time. The GCE was consecutively modified by multi-walled carbon nanotubes (MWCNTs), bismuth oxybromide (BiOBr), ꞵ-cyclodextrin (ꞵ-CD), and in situ addition of tetrabutylammonium bromide (TBABr). The detection was based on the decreasing of Bi signal at its anodic potential (Epa) of 0.05 V. Under the optimum conditions, the modified electrode exhibited a linear response to TBZ in the concentration range 1–100 μg L−1 with a detection limit of 0.9 μg L−1. TBZ was firstly adsorbed on the surface of the modified electrode through host–guest molecule interactions of the ꞵ-CD. The adsorption was further enhanced by the large surface area of BiOBr and MWCNTs. The adsorbed TBZ on the electrode surface hindered the electron transfer of Bi, thus decreasing the oxidation of Bi. In addition, the in situ addition of tetrabutylammonium bromide (TBABr) enriched TBZ via electrostatic interactions, increasing its detection sensitivity. The fabricated electrochemical sensor was applied to determine TBZ in water and soil samples from rice fields with recoveries of 80.5–100.5% and 87.6–112%, respectively. Furthermore, the degradation of TBZ on the modified electrode was studied under a solar light simulator. The degradation percentage (100%) of TBZ (50 µg L−1) was achieved in 5 min owing to the excellent photocatalytic properties of BiOBr. [ABSTRACT FROM AUTHOR]

Jana K Alwattar,1,2 Mohammed M Mehanna3,4 1Department of Pharmaceutical Sciences, School of Pharmacy, Lebanese International University, Beirut, Lebanon; 2Pharmaceutical Nanotechnology Research Lab, Faculty of Pharmacy, Beirut Arab University, Beirut, Lebanon; 3Department of Pharmaceutical Sciences, School of Pharmacy, Lebanese American University, Byblos, Lebanon; 4Department of Industrial Pharmacy, Faculty of Pharmacy, Alexandria University, Alexandria, EgyptCorrespondence: Mohammed M Mehanna, Department of Pharmaceutical Sciences, School of Pharmacy, Lebanese American University, Byblos, Lebanon, Tel +96171708661, Email mohammed.mehanna@lau.edu.lb; mohamed.mehanna@alexu.edu.egBackground: Cancer ranks as the second most common cause of mortality as depicted by the World Health Organization, with one in six deaths being cancer-related mortality. Taking the lead in females, breast cancer is the most common neoplasm. Raloxifene, a selective estrogen receptor modulator, has been utilized as a chemotherapeutic agent for the treatment of breast cancer in postmenopausal women. However, its poor aqueous solubility hinders its clinical applications. Beta-cyclodextrin-based framework is a novel class of nano-vectors that used to potentiate the solubility and dissolution rate of poorly soluble drugs.Aim: The present study investigates the solubility and dissolution rate enhancement as well as the potential cytotoxic activity of raloxifene-loaded nanosponges formulation.Methods: The fabrication and optimization of cyclodextrin nanosponges crosslinked with diphenyl carbonate was portrayed through stoichiometric selection of cyclodextrin-to-crosslinker ratio. The complexation phenomenon and nanosponges formation were validated using FTIR, PXRD, TEM, and SEM examination.Results: Raloxifene-loaded nanosponges exhibited a 440± 8.5 nm particle size, a negative zeta potential of 25.18± 2.3 mV and a partial drug incorporation. Moreover, the drug loaded nanosponges demonstrated an in-vitro significantly enhanced dissolution behavior. Furthermore, the in-vitro cytotoxicity of the raloxifene-loaded nanosponges on MCF-7 breast cancer cell lines was statistically significant compared to the complex-free raloxifene.Conclusion: The cytotoxic behavior provided evidence that the incorporation of raloxifene within the nanosponges structure enhanced its anticancer activity and represents a potential nanocarrier for anticancer agent delivery.Keywords: raloxifene, nanosponges, anticancer, beta-cyclodextrin, breast cancer

The global health concern of pharmacoresistant epilepsy necessitates innovative therapeutic strategies. Drug resistance often arises due to complex pharmacokinetic challenges. Beta-cyclodextrin, known for enhancing drug solubility and stability, offers a potential solution for improving the efficacy of antiseizure medications. This study aims to investigate the impact of beta-cyclodextrin-complexed rufinamide on seizure-like activity using an in vitro model of temporal lobe epilepsy.

Background and Aim: In drug delivery, the formation of cyclodextrin complexes is a widely used strategy to overcome biopharmaceutical challenges associated with various active pharmaceutical ingredients, such as poor water solubility, initial instability, and low bioavailability. Given the anti-cancer properties of thymol, this study aimed to evaluate the effects of thymol-loaded nanoparticles in a beta-cyclodextrin complex and to assess their anti-cancer effects in melanoma skin cancer cells (A2058) by examining the expression of the VEGF and VEGFR genes. Methods: The synthesized nanoparticles were characterized using various methods, including zeta potential analysis, ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM). To determine the cytotoxicity of the synthesized nanocomplex, the MTT assay was performed with β-CD-Thymol nanoparticle concentrations ranging from 62.5 to 500 μg/ml. The Chorioallantoic Membrane (CAM) assay was conducted to evaluate the cytotoxicity of the synthesized β-CD-Thymol nanoparticles in the context of angiogenesis. Finally, the expression levels of genes involved in angiogenesis (VEGF and VEGFR) were analyzed using real-time PCR. Results: Dynamic light scattering analysis revealed that the mean size of the nanoparticles was 116.20 nm, with a zeta potential of -21.64 mV. FTIR studies indicated the presence of several biologically active functional groups in the synthesized nanoparticles. Additionally, the anti-cancer effects and inhibitory role of the β-CD-Thymol complex were confirmed by a significant reduction in the expression of angiogenesis-related genes (VEGF and VEGFR) in A2058 cells treated with the β-CD-Thymol nanoparticle complex (P < 0.001). The results from the CAM assay further supported these findings. Conclusion: The findings of this study demonstrated a significant decrease in the expression of genes involved in angiogenesis, specifically VEGF and VEGFR, indicating that the β-CD-Thymol complex effectively inhibits angiogenesis in the A2058 skin cancer cell line. Overall, in addition to inhibiting the formation of new blood vessels, the β-CD-Thymol nanostructure shows promise as an anti-angiogenic agent by modulating the expression of VEGF and VEGFR genes.

The strategic integration of multi-functionalities within a singular nanoplatform has received growing attention for enhancing treatment efficacy, particularly in chemo-photothermal therapy. This study introduces a comprehensive concept of Janus nanoparticles (JNPs) composed of Au and Fe 3 O 4 nanostructures intricately bonded with β-cyclodextrins (β-CD) to encapsulate 5-Fluorouracil (5-FU) and Ibuprofen (IBU). This strategic structure is engineered to exploit the synergistic effects of chemo-photothermal therapy, underscored by their exceptional biocompatibility and photothermal conversion efficiency (∼32.88 %). Furthermore, these β-CD-conjugated JNPs enhance photodynamic therapy by generating singlet oxygen (1O 2) species, offering a multi-modality approach to cancer eradication. Computer simulation results were in good agreement with in vitro and in vivo assays. Through these studies, we were able to prove the improved tumor ablation ability of the drug-loaded β-CD-conjugated JNPs, without inducing adverse effects in tumor-bearing nude mice. The findings underscore a formidable tumor ablation potency of β-CD-conjugated Au-Fe 3 O 4 JNPs, heralding a new era in achieving nuanced, highly effective, and side-effect-free cancer treatment modalities. The emergence of multifunctional nanoparticles marks a pivotal stride in cancer therapy research. This investigation unveils Janus nanoparticles (JNPs) amalgamating gold (Au), iron oxide (Fe 3 O 4), and β-cyclodextrins (β-CD), encapsulating 5-Fluorouracil (5-FU) and Ibuprofen (IBU) for synergistic chemo-photothermal therapy. Demonstrating both biocompatibility and potent photothermal properties (∼32.88 %), these JNPs present a promising avenue for cancer treatment. Noteworthy is their heightened photodynamic efficiency and remarkable tumor ablation capabilities observed in vitro and in vivo , devoid of adverse effects. Furthermore, computational simulations validate their interactions with cancer cells, bolstering their utility as an emerging therapeutic modality. This endeavor pioneers a secure and efficacious strategy for cancer therapy, underscoring the significance of β-CD-conjugated Au-Fe 3 O 4 JNPs as innovative nanoplatforms with profound implications for the advancement of cancer therapy. [Display omitted] [ABSTRACT FROM AUTHOR]

Objective: Pharmacoresistant epilepsy represents a significant global health challenge, necessitating novel therapeutic approaches. Despite advances in antiseizure medications, many patients remain treatment-resistant partially due to complex pharmacokinetic issues. Beta-cyclodextrin, known for enhancing drug solubility and stability, offers potential solutions by forming inclusion complexes, thereby improving anti-seizure medication’s efficacy. This study aimed to investigate the effect of beta-cyclodextrin and beta-cyclodextrin-complexed carbamazepine on epileptiform activities, using an in vitro model of temporal lobe epilepsy.

Lipid-laden foam cells within the arterial walls play a key role in the development of atherosclerotic lesions at early disease stages, and they have been recognized as attractive targets for developing targeted therapeutics in atherosclerosis. Herein, we developed mannose-conjugated beta-cyclodextrin (MAN-βCD) and evaluated its targeting ability and intracellular cholesterol efflux toward cholesterol-laden foam cells. The synthesized MAN-βCD showed effective cholesterol extraction ability in aqueous conditions. The nontoxic and cytocompatible MAN-βCD specifically targeted cholesterol-laden foam cells with positive CD206 expressions and was internalized into the cells via receptor-mediated endocytosis. Additionally, the internalized MAN-βCD exhibited effective lipid droplet (LD) reduction within the cholesterol-laden foam cells, leading to remarkable prevention of LD accumulation. Therefore, the specific delivery of MAN-βCD into CD206-expressing lipid-laden foam cells provides a promising prevention strategy in the progression of atherosclerotic plaques. [ABSTRACT FROM AUTHOR]

Thymus daenensis Celak. (T. daenensis) essential oil (TDO) was encapsulated into beta-cyclodextrin (β-CD) by co-precipitation method and incorporated into polylactic acid (PLA) films along with silver nanoparticles (AgNPs) to generate the active PLA film for extending the ground beef shelf life at 4 °C. Scanning electron microscopy (SEM) and Fourier-transformed infrared spectroscopy (FTIR) confirmed the proper dispersion of AgNPs, TDO, and β-CD/TDO throughout the PLA films. Different physical properties were observed in the active PLA films, so that the addition of β-CD/TDO in the films increased the thickness and decreased the tensile strength (TS) and elongation at break compared to TDO films. The color of the AgNP films was lightly darker than the others. The microbial evaluation of the packaged ground beef samples with active PLA films indicated that accompanying AgNPs with β-CD/TDO and TDO could synergistically inhibit total viable bacteria counts, psychrotrophic bacteria counts, and Enterobacteriaceae counts during the sample's storage for 12 days. This effectiveness was also observed in controlling changes in pH and total volatile basic nitrogen (TVB-N) in the samples. Considering the efficient entrapment of TDO in β-CD, the shelf life of samples was significantly extended, due to sustained and long-lasting release of the essential oil compounds, compared to the net TDO films. Based on the results, it can be concluded that β-CD/TDO+AgNP film can be a promising approach to extend the shelf life of ground beef. [ABSTRACT FROM AUTHOR]

The thermodynamic aspects of the process of inclusion complex formation between β-cyclodextrin (acting as a host) and gaseous substances (guests; N2O, CO2, NO2, SO2, HCN, CH4, CH3CH2CH3) are studied by employing well-calibrated and tested density functional theory (DFT) calculations. This study sheds new light on the intimate mechanism of the β-cyclodextrin/gas complex formation and answers several intriguing questions: how the polarity and size of the guest molecule influence the complexation thermodynamics; which process of encapsulation by the host macrocycle is more advantageous—insertion to the central cavity without hydration water displacement or guest binding accompanied by a displacement of water molecule(s); what the major factors governing the formation of the complex between β-cyclodextrin and gaseous substances are. The special role that the cluster of water molecules inside the host's internal cavity plays in the encapsulation process is emphasized. [ABSTRACT FROM AUTHOR]

In order to prepare polyimide (PI) films with a low dielectric constant and excellent comprehensive performance, a two-step method was employed in this study to integrate β-cyclodextrin into a semi-aromatic fluorine-containing polyimide ternary system. By introducing trifluoromethyl groups to reduce the dielectric constant, the dielectric constant was further reduced to 2.55 at 10 MHz. Simultaneously, the film exhibited noteworthy thermal stability (a glass transition temperature exceeding 300 °C) and a high coefficient of thermal expansion. The material also demonstrated outstanding mechanical properties, boasting a strength of 122 MPa and a modulus of 2.2 GPa, along with high optical transparency (transmittance reaching up to 89% at 450 nm). Moreover, the inherent high transparency of colorless polyimide (CPI) combined with good stretchability contributed to the attainment of a low dielectric constant. This strategic approach not only opens up new opportunities for novel electroactive polymers but also holds potential applications in flexible displays, circuit printing, and chip packaging. [ABSTRACT FROM AUTHOR]

A novel ternary composite (RGO-βCD-ECH) consisting of epichlorohydrin (ECH) cross-linked beta-cyclodextrin polymer (βCD-ECH) with reduced graphene oxide (RGO) as a carrier was synthesised and used for the removal of malachite green (MG) dye from water. The adsorption performance was systematically investigated in batch mode, and the optimised parameters were as follows: initial MG dye concentration 100 mg/L, solution pH 8.0, contact time 90 min, adsorbent dosage 0.4 g/L, and temperature 30°C. The adsorption data follow the Langmuir model (R2 = 0.998) and the maximum sorption capacity (qm) was 902.125 mg/g. The kinetic data of adsorption follows the pseudo-second-order kinetic model (R2 = 0.999). The positive value of ΔHo = 102.047 kJ/mol indicates the endothermic nature of the adsorption process. The effects of bed height (2–4 cm) and MG dye flow rate (5–15 mL/min) were investigated in the fixed-bed column study. The exhaustion time (te), breakthrough time (tb), and bed capacity (qbed) of the column increases with bed height increases, and the value decreases with flow rate increases. The most important feature of this adsorbent is it could efficiently and easily regenerate from the MG dye loaded composite with a negligible effect on percentage removal. These characteristics of these novel composites could exhibit a bright future in the application of MG dye removal from wastewater. [ABSTRACT FROM AUTHOR]

A new polymorph of anhydrous β-cyclodextrin (polymorph III) was obtained and characterized for the first time using powder X-ray diffraction, infrared spectroscopy, and thermal analysis. The solution enthalpy and time of dissolution in water were determined using solution calorimetry for this polymorph and compared with those of the dried commercial form of β-cyclodextrin (polymorph I), its amorphous form, and 2-hydroxypropyl-β-cyclodextrin. The specific heat capacities of polymorphs I and III were determined using differential scanning calorimetry across a wide range of temperatures, providing enthalpy and Gibbs energy values for the polymorphic transition at 298 K. The affinities of polymorph III and 2-hydroxypropyl-β-cyclodextrin for water were characterized by determining their hydration isotherms, which provided values of hydration Gibbs energy. Being energy-rich, the new-found polymorph of β-cyclodextrin has a significantly higher dissolution rate and an increased affinity for water compared with the dried commercial form of β-cyclodextrin. These properties render the new polymorph promising in industrial applications for guest inclusion in aqueous solutions and pastes, and may be a desirable alternative for water-soluble β-cyclodextrin derivatives. [ABSTRACT FROM AUTHOR]

A new polymorph of anhydrous β-cyclodextrin (polymorph III) was obtained and characterized for the first time using powder X-ray diffraction, infrared spectroscopy, and thermal analysis. The solution enthalpy and time of dissolution in water were determined using solution calorimetry for this polymorph and compared with those of the dried commercial form of β-cyclodextrin (polymorph I), its amorphous form, and 2-hydroxypropyl-β-cyclodextrin. The specific heat capacities of polymorphs I and III were determined using differential scanning calorimetry across a wide range of temperatures, providing enthalpy and Gibbs energy values for the polymorphic transition at 298 K. The affinities of polymorph III and 2-hydroxypropyl-β-cyclodextrin for water were characterized by determining their hydration isotherms, which provided values of hydration Gibbs energy. Being energy-rich, the new-found polymorph of β-cyclodextrin has a significantly higher dissolution rate and an increased affinity for water compared with the dried commercial form of β-cyclodextrin. These properties render the new polymorph promising in industrial applications for guest inclusion in aqueous solutions and pastes, and may be a desirable alternative for water-soluble β-cyclodextrin derivatives.

Purpose: The study aims to explore the potential of amorphous solid dispersion (ASD) technology in improving the solubility and bioavailability of flutamide (FLT), a poorly water-soluble drug. The introduction of beta-cyclodextrin (β-CD) is investigated as a strategy to overcome FLT's solubility limitations. Methods: The study employed various methods, including a validated UV spectrophotometric technique to assess FLT solubility and the creation of supersaturation through different β-CD and FLT combinations. Two formulation approaches, physical mixtures (PMs) and solid dispersions (SDs), were developed using freeze-drying and solvent evaporation methods. Analysis involved differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR), along with loading and release tests, including statistical analysis of dissolution profiles. Results: The FTIR analysis indicated that molecular interactions and chemical bonds remained largely unchanged. DSC results demonstrated the transformation of FLT from a crystalline to an amorphous state in the SDs. In the supersaturation test, it was evident that the solution with 30% β-CD and 70% FLT achieved a remarkable 5.69-fold increase in FLT concentration compared to the pure drug. Solid dispersion formulations exhibited varying drug release profiles, with the 30% β-CD and 70% FLT combination showing the most rapid release, reaching approximately 50% within 240 min. Conclusion: The study underscores the effectiveness of β-CD in the 30:70 β-CD to FLT combination to enhance FLT solubility and bioavailability. However, higher proportions of β-CD led to reduced drug release, potentially due to cyclodextrin aggregation, which could hinder drug interactions. [ABSTRACT FROM AUTHOR]

Novel drug delivery system was prepared and evaluated as for application in cancerous bone treatment. It had three stacked layers, including a drug-free layer, a cisplatin-loaded layer, and a curcumin-containing layer. Our previously characterized biomaterials, namely Zr-hydroxyapatite (Zr-HA) and alkaline-treated polycaprolactone (modified-PCL), were used as major components of the drug carrier. Polar-polar interactions between cisplatin and Zr-HA were modulated by the modified-PCL included, leading to increase of cisplatin release. Using β-cyclodextrin (β-CD) to entrap curcumin caused improvement of curcumin solubility and release. The 3D-construct was porous with internal interconnected pores according to SEM micrographs. Large amount of apatite was formed and proteins adsorbed on the scaffolds after immersed in physiologic buffer solution and in medium containing fetal bovine serum, respectively. Optimal concentrations of ascorbic acid and triamcinolone were used for induction of bone marrow stromal cells to become osteoblasts by expressing an enzyme marker, e.g., alkaline phosphatase. The prepared scaffolds were considered osteo-conductive and osteo-inductive. The concentrations of cisplatin and curcumin reached the IC50 of SK-ES-1 cells of osteosarcoma and MCF-7 cells of breast adenocarcinoma after 24 h and 3 days of release, respectively. These cancer cells were more sensitive to the combined cisplatin and curcumin than each of the drugs. Regeneration of new bone and execution of residential cancer cells in defected bone were proposed after replacing the lost bone by this established drug carrier. The assumption needs to be verified in the future using animal models. [ABSTRACT FROM AUTHOR]

The thermodynamic aspects of the process of inclusion complex formation between β-cyclodextrin (acting as a host) and gaseous substances (guests; N2O, CO2, NO2, SO2, HCN, CH4, CH3CH2CH3) are studied by employing well-calibrated and tested density functional theory (DFT) calculations. This study sheds new light on the intimate mechanism of the β-cyclodextrin/gas complex formation and answers several intriguing questions: how the polarity and size of the guest molecule influence the complexation thermodynamics; which process of encapsulation by the host macrocycle is more advantageous—insertion to the central cavity without hydration water displacement or guest binding accompanied by a displacement of water molecule(s); what the major factors governing the formation of the complex between β-cyclodextrin and gaseous substances are. The special role that the cluster of water molecules inside the host’s internal cavity plays in the encapsulation process is emphasized.

In this paper, beta-cyclodextrin (βCD) was designed as encapsulate carrier for geranium essential oil (GEO) and then loaded into chitosan nanoparticles (GEO/βCD-CS) to enhance GEO physicochemical characteristics. Based on this approach, the GEO's chemical composition obtained during hydrodistillation was investigated using gas chromatography coupled to mass spectrometry and gas chromatography with flame ionization detection. Additionally, the physicochemical properties of GEO/βCD, encapsulation efficiency (EE%), loading efficiency (LE%), solubility, and moisture content, were analyzed. Besides, GEO/βCD and GEO/βCD-CS were characterized by morphology, particle size, crystallinity, molecular structure, thermal stability, storage stability, and control release. The results showed that citronellol (30.03%) and geraniol (14.12%) dominate the chemical profile of GEO. Furthermore, EE%, LE%, solubility, and moisture content of GEO/βCD were 68.43%, 9.54%, 70.12%, and 5.32%, respectively. Then, it could be concluded that the formation of GEO/βCD and GEO/βCD-CS using several techniques was successful. In addition to the previous finding, the loading of GEO/βCD into chitosan nanoparticles led to a decrease in the particle sizes, which improve the thermal and storage stabilities and enhance the release control of GEO. Generally, the approach developed in this paper based on loading the inclusion complex (GEO/βCD) into chitosan nanoparticles provides a strong candidate for employment in biotechnology area. [ABSTRACT FROM AUTHOR]

Alzheimer's disease is characterized by progressive cognitive decline and neuronal loss. Amyloid beta peptide consisting of 39-42 amino acids is prone to aggregation forming oligomers and amyloid plaques which are considered causes of neurotoxicity. One of the most studied strategies for preventing betaamyloid aggregation is relying on the hypothesis that non-covalent bound substances may reduce the aggregation of beta-amyloid. Considering previous studies which demonstrate the formation of non-covalent complex between beta-amyloid (1-40) and beta-cyclodextrin using a denaturing chemical environment and considering the results regarding beta-cyclodextrin presence in the rat plasma and in organs after administration of certain medications containing beta-cyclodextrin the present study aims to evaluate the interaction of beta-cyclodextrin and beta-amyloid (1-40) at neutral pH in ammonium bicarbonate. The analysis was performed using an electrospray-triple quadrupole mass spectrometer coupled to a liquid chromatograph using the flow injection analysis technique. Additionally, the cleavage using trypsin of the beta-amyloid (1-40) peptide after non-covalent complex formation was performed for the purpose of identifying the minimal peptide sequence involved in the interaction with beta-cyclodextrin. The results indicate the formation of the non-covalent complex in the chemical environment employed. Further studies using transgenic Alzheimer's Disease mice models expressing human beta-amyloid may clarify whether oral administration of beta-cyclodextrin has beneficial effects to the health of Alzheimer's disease patients. [ABSTRACT FROM AUTHOR]

BACKGROUND: Propane dehydrogenation is an alternative way both to produce propylene and to utilize CO2. Because of the high oxygen mobility in cerium‐zirconium oxide (CexZr1‐xO2), it looks promising as a support for the chromium oxide catalysts of propane dehydrogenation with CO2. Supports of CexZr1‐xO2 on mesoporous silica were synthesized in this work to combine the high oxygen mobility of the former and the pore structure of the latter. RESULTS: Two applied synthetic approaches resulted in materials with different structure and properties. The wet impregnated catalysts demonstrated a higher activity and selectivity to propylene. At the same time, they had larger pore size distribution maxima (~9 nm) than the samples prepared by the introduction of metals simultaneously with Si‐precursor hydrolysis (~2 nm). For the chromium catalysts with the same support, the catalytic activity decreased with varying chromium loading as follows: 5% Cr > 3% Cr ≈ 7% Cr. For the catalysts with different CexZr1‐xO2 supports and equal chromium loading, the activity decreased with x changing as follows: 0.5 > 0.6 > 0.8 for the samples prepared by wet impregnation, and 0.8 ≈ 0.6 > 0.5 for the other synthetic path. CONCLUSIONS: Catalysts were tested in oxidative dehydrogenation of propane with CO2. The wet impregnation approach turned out to be much more promising in terms of catalytic activity and selectivity to propylene in the reaction of propane dehydrogenation with CO2. The selectivity achieved was ≤80% at a 40% conversion. © 2023 Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

Bismuth oxide nanoparticles with appropriate surface chemistry exhibit many interesting properties that can be utilized in a variety of applications. This paper describes a new route to the surface modification of bismuth oxide nanoparticles (Bi2O3 NPs) using functionalized beta-Cyclodextrin (β-CD) as a biocompatible system. The synthesis of Bi2O3 NP was done using PVA (poly vinyl alcohol) as the reductant and the Steglich esterification procedure for the functionalization of β-CD with biotin. Ultimately, the Bi2O3 NPs are modified using this functionalized β-CD system. The particle size of the synthesized Bi2O3 NPs is found to be in the range of 12–16 nm. The modified biocompatible systems were characterized using different characterization techniques such as Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and Differential Scanning Calorimetric analysis (DSC). Additionally, the antibacterial and anticancerous effects of the surface-modified Bi2O3 NP system were also investigated. [ABSTRACT FROM AUTHOR]

The impact of β-CD on 4 benzophenones (BPs) [namely, BP, HBP, d-HBP, t-HBP] and its resultant effect on the ultraviolet protection factor (UPF) of poplin cotton fabric are tested. Drastic enhancement in the UPF values for BPs:β-CD complexes treated fabrics is noticed (than the untreated/fabric treated with free BPs). The impact of β-CD on the tautomerism of hydroxyl substituted BPs are demonstrated by investigatingthe guest (BPs:absorbers)-host(β-CD:enhancer) process. Orientation of -OH substituted benzene towards 1° rim and positioning of C = O group of BPs in the middle of β-CD could be attributed to the steric effect driven preference of the guest molecules for achieving a rigid fit. Rigid fit rendered by β-CD improves the photostability of BPs and dissipates UVR efficiently through keto-enol tautomerization. With the highest UPF (= 51) d-HBP:β-CD complex is identified as a potential application material for producing sun-protective clothing. [ABSTRACT FROM AUTHOR]

This work was aimed at evaluating the adsorption characteristics of beta-cyclodextrin (β-CD) chars. Char was prepared by pyrolysis in a furnace at 550 °C, while spherical hydrochar was obtained through hydrothermal carbonization in a Teflon autoclave at 180 °C. Both chars are water-insoluble and were prepared without cross-linking agents. They were characterized for functional groups, thermal degradation, and surface morphology. The applicability of chars in adsorption was studied using malachite green solution at varying concentrations, contact times and temperatures. Hydrochar exhibits a better malachite green capacity of 18 mg/g. The adsorption rate and equilibrium data fitted well into pseudo-first-order and pseudo-second-order kinetics, and Langmuir and Dubinin–Radushkevich models, respectively. The thermodynamic parameters suggested that the removal process is spontaneous and endothermic in nature. [ABSTRACT FROM AUTHOR]

[Display omitted] • Symmetric 14-armed βCD-cored star amphiphilic block copolymers βCD-(PBO-PGL) 14 were obtained with tunable arm block lengths, high purity and low polydispersity. • Star copolymers βCD-(PBO-PGL) 14 have similar self-assembly behavior compared to linear analogues (PGL-PBO-PGL). • Polymersomes made from βCD-(PBO-PGL) 14 have different ion permeability behavior compared to linear analogues (PGL-PBO-PGL). For polymersome-based nanoreactor purposes, we herein present the synthesis and characterization of well-defined star amphiphilic copolymers composed of a beta -cyclodextrin (βCD) core and seven poly(butylene oxide)- block -polyglycidol (PBO-PGL) arms per side (βCD-(PBO-PGL) 14). The self-assembly behavior of 14-armed βCD-(PBO-PGL) 14 and PGL-PBO-PGL (linear analogues without the βCD segment) was investigated using scattering techniques for comparison. The morphologies, including vesicles and micelles, are governed by the hydrophobic-to-hydrophilic (weight) ratio, regardless of the polymer architecture (linear or star). Interestingly, despite notable differences in polymer conformation, the produced supramolecular structures were evidenced to be fairly similar on the structural point of view. We subsequently investigated the ion permeability of the membranes of the self-assemblies focusing on the impact of the presence of βCD. The results demonstrated that the βCD-containing vesicular membranes are less permeable to H+, compared with βCD-free vesicular membranes. The presence of βCD in planar membranes also influences the K+Cl− permeability to some extent. Thus, βCD-containing membranes can be considered as potential candidates in designing nano-containers towards applications where precise changes in environmental pH are required. [ABSTRACT FROM AUTHOR]

Cryo-induced hydrogel from cellulose is a new class of biomaterials for drug delivery, cell delivery, bone and skin tissue engineering for cell proliferation and regeneration applications. This research aimed to synthesize cryo-induced hydrogel from cellulose and carboxymethyl cellulose (CMC) produced from empty bunch's cell wall of Elaeis guineensis. First, the experiment was to produce cellulose-rich material using hot-compressed water extraction followed by alkaline delignification and bleaching with H2O2. The obtained bleached EFB cellulose was used as the substrate for CMC, and the optimal condition with the highest degree of carboxyl substitution (DS) of 0.75 was achieved when varying NaOH and monochloroacetic acid concentration as well as etherification temperature using fractional factorial design. For cryogelation study, hydrogels were synthesized from cellulose, CMC and beta-cyclodextrin (β-CD) by dissolving cellulose-based matrix in a NaOH/urea system, and the cellulose (CEL) solution was frozen spontaneously at −40 °C followed by high speed mixing to loosen cellulose fibrils. Epichlorohydrin (ECH) and Polyethylene glycol diglycidyl ether (PEGDE) were used as a cross-linker. First, the ratio of cellulose and CMC with different amounts of ECH was investigated, and subsequently the proper ratio was further studied by adding different crosslinkers and matrices, i.e., CMC and β-CD. From the result, the ECH crosslinked CMC-CEL (E-CMC-CEL) gel had the highest swelling properties of 5105% with the average pore size of lyophilized hydrogel of 300 µm. In addition, E-CMC-CEL gel had the highest loading and release capability of tetracycline in buffer solution at pH 7.4 and 3.2. At pH 7.4, tetracycline loading and release properties of E-CMC-CEL gel were 65.85 mg g−1 dry hydrogel and 46.48 mg g−1 dry hydrogel (70.6% cumulative release), respectively. However, at pH 3.2, the loading and release capabilities of Tetracycline were moderately lower at 16.25 mg g−1 dry hydrogel and 5.06 mg g−1 dry hydrogel, respectively. The findings presented that E-CMC-CEL hydrogel was a suitable material for antibiotic tetracycline drug carrying platform providing successful inhibitory effect on Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, respectively. [ABSTRACT FROM AUTHOR]

Pharmaceutical contaminants pose significant risks to ecosystems and human health, necessitating effective removal strategies. This research focuses on developing advanced adsorbents for removing pharmaceutical pollutants from the environment. Metal-organic frameworks (MOFs), specifically MIL-101(Cr) functionalized with biodegradable beta-cyclodextrin (β-CDex), were investigated as potential nanocomposite adsorbents for the removal of ketorolac (KTRK), naproxen (NPXN), and tramadol (TRML). The study employed molecular simulations and density functional theory (DFT) calculations to explore the interactions between the pollutants and adsorbents. Analyses of DFT results, including electrostatic potential, ionization energy, density of states, and molecular orbital analysis, provided insights into the reactivity of pollutants and adsorbents. Additionally, the structural properties of the adsorbents, such as fractional free volume, radius of gyration, and system energies, were thoroughly examined. Molecular dynamics (MD) and Monte Carlo (MC) simulations were used to evaluate the adsorption capacities of MIL-101(Cr) for the target pharmaceutical pollutants. The results demonstrated the superior adsorption performance of the nanocomposite adsorbent, particularly for KTRK, with an adsorption energy of −1934 kcal/mol, compared to the pristine MIL-101(Cr), which had an adsorption energy of −1916 kcal/mol. This enhanced adsorption is attributed to the optimal molecular fit, guest-host solid interactions, and the selective encapsulation capabilities of β-CDex. This research highlights the potential of MOF-based nanocomposites as effective and sustainable solutions for pharmaceutical pollution. By advancing the understanding of molecular interactions through simulations, this study contributes to developing innovative adsorbents for wastewater treatment and the protection of water resources. [Display omitted] • The study developed MIL-101(Cr) MOFs functionalized with β-CDex for removing pharmaceutical pollutants. • DFT simulations revealed key insights into the reactivity and structure of pollutants and adsorbents. • Molecular simulations confirmed MIL-101(Cr)/β-CDex's superior adsorption, especially for KTRK. • Adsorption energy of MIL-101(Cr)-βCDex with pollutants: KTRK (−1934 kcal/mol) > TRML (−1765 kcal/mol) > NPXN (−785 kcal/mol). • MOF-based nanocomposites offer sustainable solutions for pharmaceutical pollution in wastewater treatment. [ABSTRACT FROM AUTHOR]

• α-CD was more efficient than β-CD in solubilizing SDS-treated Mb aggregates. • Both α-CD and β-CD removed SDS from the SDS-Mb complex and facilitated refolding. • Understanding CD mechanisms could lead to the drug development. The formation of amyloids arises from the misfolding or unfolding of various proteins. This study investigated the impact of chemical chaperones, alpha-cyclodextrin (α-CD) and beta-cyclodextrin (β-CD), on the solubilization and defibrillation of sodium dodecyl sulfate (SDS)-induced myoglobin (Mb) amyloid fibrils. Amyloid fibril was developed in Mb in the presence of 0.8 mmol dm−3 SDS at pH 4.5. Subsequently, SDS-induced Mb amyloid was incubated with varying concentrations of α-CD and β-CD at the same pH. Our turbidity, intrinsic fluorescence, SDS-PAGE, and transmission electron microscope data showed that α-CD (2.1 mmol dm−3) was more efficiently solubilized the SDS-treated Mb aggregates than β-CD (4.0 mmol dm−3). But, another interesting phenomenon was observed with β-CD. The ThT fluorescence and far-UV CD data suggested that amyloid defibrillation by β-CD (0.6 mmol dm−3) was more effective than α-CD (0.9 mmol dm−3). The intrinsic fluorescence and far-UV CD data also showed that SDS-treated Mb regained native-like structure at lower α-CD compared to β-CD. Overall our data suggest that α-CD was more efficient in aggregate solubilization while β-CD was more effective in amyloid defibrillation. Understanding the mechanisms underlying cyclodextrins' actions may serve as a basis for identifying potential drugs to suppress amyloid fibril formation effectively. This research provides valuable insights into mitigating amyloid-related pathologies. [ABSTRACT FROM AUTHOR]

The study investigated the influence of additives on the fabrication of mixed matrix membranes comprising polyethersulfone (PES), with a specific focus on hydrophilicity, flux, morphology, and antifouling properties. Carboxymethyl modified β-cyclodextrin (CMβ-CD) was used to enhance the dispersion and hydrophilicity of graphene oxide (GO), leading to the formation of a hydrophilic and stable composite nanoparticle (CMCD@GO). The hydrophilicity (WCA <51.5°) and water flux (32.6 L m−2. h−1) of the modified PES membranes (MCDGO-x) were improved by the incorporation of CMCD@GO nanoparticles, while that of PES membrane was 79.7° and 10.6 L m−2.h−1. The rate of backscattered light intensity (ΔBS) of MCDGO-x suspensions remains stable, suggesting stable dispersion of CMCD@GO in organic solvents. Compared to the bare PES membrane, the MCDGO-x membrane exhibits a thinner active layer and a finger-like structure. The MCDGO-x membrane exhibited excellent naphthenic acids (NAs) rejection (>93.2%) due to reduced roughness and higher hydrophilicity, while the GO-modified PES membrane (MGO-5) exhibited lower NAs rejection (87.2%). Furthermore, the MCDGO-5 membrane showed higher flux recovery ratio (FRR) of 79.3% compared to MGO-5 membrane (68.5%) after three cycles, indicating the antifouling performance of MCDGO-x for NAs was significantly improved. The combination of CMβ-CD and GO enhance the flux and antifouling properties of PES ultrafiltration membranes, suggesting significant potential for applications in the purification of oil sands process water and the treatment of oily wastewater. • Antifouling membrane was prepared by carboxymethyl β-cyclodextrin and GO. • The composite membrane shows good antifouling properties. • Separation and antifouling performance were comprehensively studied. • Membrane formation and antifouling mechanisms were proposed. [ABSTRACT FROM AUTHOR]

Pineapple peel waste was used in this study as a source of ferulic acid that has antioxidant and antibacterial properties. Pineapple peel extract can be used as a bioreductor in the synthesis of silver nanoparticles (AgNPs). Beta cyclodextrins are often added as stabilizers in the synthesis of AgNPs to increase their stability. This study aimed to investigate through in silico study the efficacy of beta cyclodextrin as a stabilizer in the synthesis of AgNPs. It also investigated whether ferulic acid plays the role of a bioreductor in the stabilization mechanism of the AgNPs. Molecular docking simulation was used to investigate the efficacy of beta cyclodextrin as a stabilizer in AgNPs synthesis using MGLTools 1.5.6 with AutodockTools 4.2. The visualization of each complex was observed using BIOVIA Discovery Studio Visualizer 2020. The results of this study showed that beta cyclodextrin had better affinity by stabilizing six AgNPs atoms, which was indicated by a free binding energy value of -5.15 kJ/mol. The presence of ferulic acid in the extract which was used as a bioreductor in the synthesis of AgNPs also had a better affinity for the six AgNPs atoms which was indicated by free binding energy of -2.51 kJ/mol. It can be concluded that beta cyclodextrins play the role of being a stabilizer in AgNPs synthesis. [ABSTRACT FROM AUTHOR]

A beta‐cyclodextrin covalent organic framework coated silica composite, namely beta‐cyclodextrin covalent organic framework@SiO2, was prepared by coating the beta‐cyclodextrin covalent organic framework onto a spherical aminized silica matrix and used as the chiral stationary phase for high‐performance liquid chromatography separation in both normal‐ and reversed‐phase modes. The beta‐cyclodextrin covalent organic framework@SiO2 packed column showed good separation performance towards positional isomers such as nitrotoluene and aminophenol, and benzene homologs in the reversed‐phase high‐performance liquid chromatography mode. While chiral drug molecules including omeprazole and lansoprazole could be also enantioseparated on beta‐cyclodextrin covalent organic framework@SiO2 packed column in the normal‐phase high‐performance liquid chromatography mode. Besides, the effects of mobile phase composition, column temperature, and other factors of high‐performance liquid chromatography separation on beta‐cyclodextrin covalent organic framework@SiO2 packed column were studied in detail. Moreover, the stability test of the beta‐cyclodextrin covalent organic framework@SiO2 packed column was also investigated. The results of continuous injections and monthly detection were basically identical, suggesting the excellent durability of the obtained high‐performance liquid chromatography column. This work indicated that beta‐cyclodextrin covalent organic framework@SiO2 composite could effectively separate different compounds in high‐performance liquid chromatography normal/reversed‐phase modes, making it a promising chiral stationary phase in the field of high‐performance liquid chromatography separation. [ABSTRACT FROM AUTHOR]

A novel composite consisting reduced graphene oxide–functionalized beta-cyclodextrin epichlorohydrin polymer (RGO-βCD-ECH) was synthesized for the treatment of phenolic wastewater. Batch study of phenolic pollutants (2,4-dichlorophenol, 2-chlorophenol, and phenol) was analyzed using the synthesized composite as an adsorbent from an aqueous solution. The optimized parameters were temperature 25 °C, adsorption time 60 min, solution pH 7, and dosage 0.25 g/L. The isotherm data were more suitably fitted by the Langmuir isotherm model. The maximum uptake for 2,4-dichlorophenol, phenol, and 2-chlorophenol was 702.853, 659.475, and 674.155 mg/g, respectively, at 25 ± 1 °C. The kinetic data for all the phenolic pollutants follow the pseudo-second-order model, and the rate was controlled by film diffusion. Thermodynamic data revealed that the process of removing phenolic pollutants is spontaneous and endothermic. The composite can be used up to five cycles with a small reduction in the removal. Adsorption performance of the synthesized composite for synthetic industrial effluents shows that up to 78% removal occurred in 60 min adsorption time. Based on the remarkably rapid adsorption and high adsorption capacity, the synthesized composite can be considered an efficient adsorbent for treating phenolic pollutants from wastewater. [ABSTRACT FROM AUTHOR]

By nanotechnology entrance into the field of medicinal plants, the agricultural industry and food industry ensures an increase in the amount and quality of their products, along with the preservation of the environment. The properties of materials are changed by changing their size to nano. The use of beta-cyclodextrin nanoparticles is described as a new protection strategy of the plant and induces a plant defense response. For this purpose, to study the effect of beta-cyclodextrin nanoparticles on the physiologic indexes and biochemical activities in basil of keshkeni luvelou cultivar, an experiment was performed based on a completely randomized design with four replications at four levels of 0.10, 50, 100mg/l in the greenhouse. The results showed that different growth indices such as root and stem length and diameter, fresh and dry weight of roots, shoots, and leaf area increased by 5% compared to the control and the highest increase was reported at 50ppm. Data analysis showed that the effect of different treatments on the activity of superoxide dismutase and catalase, peroxidase enzymes, malondialdehyde content, and ion leakage of roots and leaves were significantly increased (P≤5%) compared to the control. Membrane stability index was assessed by measuring the electrolyte leakage of leaves and roots. A significant reduction (P≤5%) of ion leakage and malondialdehyde of roots and leaves was observed in the treatment of 50mg/l nano-beta cyclodextrin which indicates an increase in enzyme activity. With the entrance of nanoparticles into agriculture can minimize the scope of chemical control and disruption of environmental physiological practices. The trend of changes in physiological and biochemical parameters studied in the present study are relatively reliable indicators to introduce the best concentration of beta-cyclodextrin nanoparticles for basil.

The aim of this study was to produce innovative edible films and coatings with various combinations of materials, in order to achieve the best possible resulting properties. More specifically, the effect of cellulose nanocrystals (CNC) or beta-cyclodextrin (CD) addition to chitosan (CH) films and the development of composite CH–CNC–CD films were investigated. According to the results, most properties of both CH–CNC and CH–CD edible films were improved. The viscosity of the solutions was decreased up to 50% while the surface tension was minimally changed even at high levels of CNC or CD addition. Furthermore, oxygen and water vapor permeability of the CH–CNC and the CH–CD edible films was decreased, whereas transparency and heterogeneity were increased. On the other hand, the study of the composite CH–CNC–CD films, showed that CNC improved viscosity, supporting thus the coating procedure. Moreover, CNC led to more stable structures with enhanced mechanical properties. Finally, CD mostly contributed to the improvement of the optical properties (lighter color and increased transparency). [ABSTRACT FROM AUTHOR]

Herein, polyamide thin-film composite forward osmosis (TFC-FO) membranes were fabricated using beta-cyclodextrin-graft-poly acrylic acid (ß-CD-g-PAA), as a nature-based graft polymer. The polymer was synthesized by free radical graft polymerization and was consequently incorporated into the active layer to enhance the hydrophilicity, anti-fouling, and overall performance of the conventional TFC-FO membrane. The effect of synthesized polymer concentration on characteristic features such as roughness, morphology, and hydrophilicity of the polymer-modified membranes was thoroughly investigated using different characterization techniques. Apart from that, the separation performance of the newly developed membranes was investigated in FO and reverse osmosis (RO) filtration systems. The transport data revealed increased water flux of around 1.5 times for the membrane which was modified with 1250 ppm of ß-CD-g-PAA solution (TFC-1250) compared to pristine TFC in the FO mode. Interestingly, the mentioned membrane showed demonstrably perm-selectivity of 0.043 bar in RO filtration system. The antifouling investigations of the TFC-1250 membrane against protein and organic foulant in FO mode, not only showed minor fouling tendency, but also revealed great flux recovery ratio (FRR>98%) with a simple washing step. These observations prove the reversible characteristic of fouling in FO process. Hence, this project opens a new way to surface functionalization of TFC membranes with nature-based polymers to render selectivity as well as antifouling features to them. [Display omitted] • A novel natural-based graft polymer was utilized to fabricate novel TFC-FO membrane. • Hydrophile ß-CD-g-PAA polymer led to improved water flux in various filtration systems. • The newly developed membranes were of smooth surface and ultra-thin PA layers. • Superior anti-fouling and reverse fouling feature was observed against protein and organic foulants. [ABSTRACT FROM AUTHOR]

Megastigmatrienone (MEG) is difficult to store, which affects the stability of cigarette flavoring. In order to improve the stability of MEG and the effect of flavoring and sustained release, β-cyclodextrin (β-CD) was used as the Inclusion materials, MEG and β-CD inclusion complexes (MEC) were prepared by saturated aqueous solution method, and MEC was characterized and tested for stability. Fourier transform infrared spectroscopy (FTIR) and differential Differential scanning calorimetry (DSC) confirmed the formation of MEC. Thermogravimetric (TG) analysis showed that the thermal stability of MEG was improved after inclusion. The heating rate was 10°C/min, and the temperature increased to 262.58 At ℃, the thermal stability of MEC was 71.37% higher than that of MEG. The results of the cigarette flavoring experiment showed that the scores of aroma quality, aroma quantity, concentration, miscellaneous air, irritation and aftertaste were increased by 6.45% in the MEC treatment compared with the MEG treatment., 8.06%, 9.84%, 3.27%, 1.59% and 3.33%. The preparation and stability test of MEG and β-CD inclusion compound can provide theoretical basis for MEG storage and cigarette flavoring application. [ABSTRACT FROM AUTHOR]

Introduction: Lawsone is a phyto-constituent obtained from the leaves of the Lawsonia inermis. It has antibacterial, antifungal, antiviral, wound healing, antiparasitic, tuberculostatic, anti-fertility, analgesic, anti-inflammatory, enzyme inhibitory, nematicidal, anticoagulant, and protein glycation inhibitory activities. It has poor water solubility (hydrophobic), poor bioavailability, and poor dissolution characteristics. Aim: The purpose of this research is to improve the aqueous solubility of Lawsone by preparing the inclusion complexes of Lawsone with beta-cyclodextrin. Materials and Methods: Inclusion complexes of Lawsone were prepared by different methods such as physical mixture, kneading method and co-precipitation method. Characterization of the complexes were done by Fourier Transform Infrared (FTIR) spectroscopy and in vitro dissolution study. Differential scanning calorimetry (DSC), Nuclear Magnetic Resonance spectroscopy (NMR), and Powder X-Ray Diffraction (PXRD). were used to evaluate the co-precipitation technique inclusion complexes. Antimicrobial studies of complexes against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), Bacillus subtilis (B. subtilis), and Pseudomonas aeruginosa (P. aeruginosa ) were done by colony counting method. Results: Phase solubility study revealed the molar ratio of Lawsone to betacyclodextrin in the complex is 1:1. At the third hour, the drug release was 64%, 78%, 93%, and 97% for pure drug, physical mixture, inclusion complexes formed by kneading technique and co-precipitation technique respectively. DSC, NMR, and PXRD confirmed the formation of complexes of Lawsone. The order of antibacterial activity of inclusion complexes was E. coli > B. subtilis > P. aeruginosa > S. aureus. [ABSTRACT FROM AUTHOR]

Bismuth oxide nanoparticles with appropriate surface chemistry exhibit many interesting properties that can be utilized in a variety of applications. This paper describes a new route to the surface modification of bismuth oxide nanoparticles (Bi2O3 NPs) using functionalized beta-Cyclodextrin (β-CD) as a biocompatible system. The synthesis of Bi2O3 NP was done using PVA (poly vinyl alcohol) as the reductant and the Steglich esterification procedure for the functionalization of β-CD with biotin. Ultimately, the Bi2O3 NPs are modified using this functionalized β-CD system. The particle size of the synthesized Bi2O3 NPs is found to be in the range of 12–16 nm. The modified biocompatible systems were characterized using different characterization techniques such as Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and Differential Scanning Calorimetric analysis (DSC). Additionally, the antibacterial and anticancerous effects of the surface-modified Bi2O3 NP system were also investigated.

Polyphenols are inversely associated with the incidence of chronic diseases, but therapeutic use is limited by poor stability and bioaccessibility. Encapsulation has been shown to overcome some of these limitations. A selection of polyphenols (catechin, gallic acid, and epigallocatechin gallate) and their combinations were encapsulated in beta-cyclodextrin (βCD). Encapsulation was characterized and the thermal and storage stability was evaluated using the 2,2-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assay. The samples were then subjected to in vitro digestion using a simple digestion (SD) model (gastric and duodenal phases) and a more complex digestion (CD) model (oral, gastric, and duodenal phases). Thereafter, the chemical (oxygen radical absorbance capacity assay) and cellular (dichlorofluorescein diacetate assay in Caco-2 cells) antioxidant and antiglycation (advanced glycation end-products assay) activities were determined. Inclusion complexes formed at a 1:1 molar ratio with a high encapsulation yield and efficiency. Encapsulation altered the morphology of the samples, increased the thermal stability of some and the storage stability of all samples. Encapsulation maintained the antioxidant activity of all samples and significantly improved the antiglycation and cellular antioxidant activities of some polyphenols following SD. In conclusion, the formed inclusion complexes of βCD with polyphenols had greater storage stability, without altering the beneficial cellular effects of the polyphenols. [ABSTRACT FROM AUTHOR]

β-Cyclodextrin (β-CD), a macrocyclic oligosaccharide cavitand, is a well-known candidate for drug delivery and formulation. In this study, we extended the application of β-CD using a β-cyclodextrin sulfate (β-CDS) as a possible therapeutic for fibrotic diseases caused by excess deposition of collagen fibrils. We have strategically chosen β-CDS, which mimics the natural existence of dermatan sulfate in the extracellular matrix, for limiting collagen fibrillation. The hydrophobic nature of the inner core β-CDS is expected to form an inclusion complex with hydrophobic side chain amino acids with the simultaneous action of forming an ionic bond through a negative charge on sulfate group with positively charged amino acids side chain in collagen. Various results suggested that such dual action not only limited the collagen fibrillation but also reduced the fibril size formed in the presence of β-CDS. The contemporary results thus indicate that β-CDS can be explored as a therapeutic molecule in fibrotic diseases. [Display omitted] [ABSTRACT FROM AUTHOR]

Seafood contains compounds such as omega-3 fatty acids, fat-soluble vitamins, digestible proteins and micronutrients such as fluorine, calcium, iodine, copper, iron and zinc. Therefore, it is important to provide methods to increase the shelf life and also remove heavy metals from fish meat. In this study, using the biopolymers of chitosan (CS) and beta-cyclodextrin (β-CD), the oxidative stability of minced of commerson Scomberomorus fish during 12 days of refrigeration with chemical evaluations (acidity (pH), peroxide number (PV), and Thiobarbituric acid (TBA), water holding capacity (WHC)) and microbial (total microbial load count (TVC)) were studied. The ability of these two compounds to reduce the concentration of heavy metals during refrigeration was also investigated. According to the results, the use of CS and β-CD had a significant effect on the values ​​of all indicators compared to the control treatment (P <0.05). Therefore, it can be said that the use of CS and β-CD is effective in reducing the oxidation and growth of minced meat bacteria during storage in the refrigerator. The lowest pH value was observed in T8 and T11 treatments, the lowest PV value was observed in T8, T10 and T11 treatments, the lowest TBA value was observed in T7 treatment, the highest WHC value was observed in T8 treatment and the lowest TVC value was observed in T8 and T11 treatments. The use of CS and β-CD solutions also reduced the concentration of heavy metals in the minced meat of commerson Scomberomorus, so that T8 treatment showed the best performance in reducing cadmium, lead and mercury and against nickel removal, different treatments had almost the same performance. [ABSTRACT FROM AUTHOR]

The objective of this study was to investigate the possibility of cholesterol elimination from milk using beta-cyclodextrin at pilot station scale, because there is very little information considering this level of milk processing. β-cyclodextrin is a nontoxic, edible and chemically stable compound with affinity for nonpolar molecules like cholesterol, giving the opportunity for obtaining food products that can prevent the appearance of cardiovascular diseases. By applying of this procedure, the cholesterol reduction percentage was calculated as approximately 84 %, similar to the values reported by the specialty literature. Except fat and freezing point values, the other parameters values increased with an approximate percentage of 8, indicating a concentration phenomenon due to milk pasteurization. Fat concentration value decreased with 5.9 %, due to the cholesterol inclusion in the beta-cyclodextrin molecule and its elimination at the bottom of the centrifugal separator. However the variation of the parameters is insignificant, so this process could be considered efficient to be applied at a pilot station level.

The mechanically assisted synthesis of organic compounds has recently focused considerable attention as it may be unique in features to selectively direct the reaction pathway. In the continuation of our work on the synthesis of modified cyclodextrins (CDs) via mechanochemical activation, we sought to discriminate the contribution of supramolecular effects and grinding during the course of a reaction in the solid state. As such, we recently investigated the influence of the particle size of β-CD in the synthesis of β-CD mesitylene sulfonate (β-CDMts) in the solid state using a vibrating ball-mill. We were particularly interested in the role of the particle size on the kinetics of the reaction. In this study, we show that grinding β-CD reduces the particles size over time down to a limit of 167 nm. The granulometric composition remains rather invariant for grinding times over 1 h. Each type of β-CD particles reacted with mesitylenesulfonyl chloride (MtsCl) to produce β-CDMts. Contrary to what could be intuitively anticipated, smaller particles did not lead to the highest conversions. The impact of grinding on the conversion was limited. Interestingly, the proportion of β-CDMts mono-substituted on the primary face significantly increased over time when the reaction was carried out in the presence of KOH as a base. The data series were confronted with kinetics models to get insight in the way the reactions proceeded. The diversity of possible models suggests that multiple mechanochemical processes can account for the formation of β-CDMts in the solid state. Throughout the study, we found that the reactivity depended more upon diffusion phenomena in the crystalline parts of the material than on the increase in the surface area of the CD particles resulting from grinding.

A new method to stabilize ferulic acid (FA) in the aqueous phase by encapsulating FA into β-cyclodextrin was developed to prepare ferulic acid-β-cyclodextrin inclusion complexes (FCICs), and the potential applications of FCIC as a preservative in hairtail (Trichiurus lepturus) were tested. The antibacterial properties of specific spoilage bacteria in hairtail were analyzed. FCIC possessed significantly higher efficacy (p

Background: Allyl isothiocyanate is an excellent antimicrobial compound that has been applied in the development of active food packaging materials in the last years. However, the high volatility of this compound could prevent a lasting effect over time. In order to avoid this problem, cyclodextrin inclusion complexes have been proposed as an alternative, being beta-cyclodextrin (β-CD) as the main candidate. In addition, β-CD could act as a relative humidity-responsive nanoparticle. In this regard, the aim of this study was to develop inclusion complexes based on β-CD and AITC as relative humidity-responsive agents, which can be used in the design of active food packaging materials.Methods: Two different β-CD:AITC inclusion complexes (2:1 and 1:1 molar ratios) were obtained by the co-precipitation method. Entrapment efficiency was determined by gas chromatography, while inclusion complexes were characterized through thermal, structural, and physicochemical techniques. Antifungal capacity of inclusion complexes was determined in a headspace system. Furthermore, the AITC release from inclusion complexes to headspace at different percentages of relative humidity was evaluated by gas chromatography, and this behavior was related with molecular dynamic studies.Key Findings and Conclusions: The entrapment efficiency of inclusion complexes was over to 60%. Two coexisting structures were proposed for inclusion complexes through spectroscopic analyses and molecular dynamic simulation. The water sorption capacity of inclusion complexes depended on relative humidity, and they exhibited a strong fungicide activity against Botrytis cinerea. Furthermore, the AITC release to headspace occurred in three stages, which were related with changes in β-CD conformational structure by water sorption and the presence of the different coexisting structures. In addition, a strong influence of relative humidity on AITC release was evidenced. These findings demonstrate that β-CD:AITC inclusion complexes could be used as potential antifungal agents for the design of food packaging materials, whose activity would be able to respond to relative humidity changes.

The strategic integration of multi-functionalities within a singular nanoplatform has received growing attention for enhancing treatment efficacy, particularly in chemo-photothermal therapy. This study introduces a comprehensive concept of Janus nanoparticles (JNPs) composed of Au and Fe 3 O 4 nanostructures intricately bonded with β-cyclodextrins (β-CD) to encapsulate 5-Fluorouracil (5-FU) and Ibuprofen (IBU). This strategic structure is engineered to exploit the synergistic effects of chemo-photothermal therapy, underscored by their exceptional biocompatibility and photothermal conversion efficiency (∼32.88 %). Furthermore, these β-CD-conjugated JNPs enhance photodynamic therapy by generating singlet oxygen ( 1 O 2 ) species, offering a multi-modality approach to cancer eradication. Computer simulation results were in good agreement with in vitro and in vivo assays. Through these studies, we were able to prove the improved tumor ablation ability of the drug-loaded β-CD-conjugated JNPs, without inducing adverse effects in tumor-bearing nude mice. The findings underscore a formidable tumor ablation potency of β-CD-conjugated Au-Fe 3 O 4 JNPs, heralding a new era in achieving nuanced, highly effective, and side-effect-free cancer treatment modalities. STATEMENT OF SIGNIFICANCE: The emergence of multifunctional nanoparticles marks a pivotal stride in cancer therapy research. This investigation unveils Janus nanoparticles (JNPs) amalgamating gold (Au), iron oxide (Fe 3 O 4 ), and β-cyclodextrins (β-CD), encapsulating 5-Fluorouracil (5-FU) and Ibuprofen (IBU) for synergistic chemo-photothermal therapy. Demonstrating both biocompatibility and potent photothermal properties (∼32.88 %), these JNPs present a promising avenue for cancer treatment. Noteworthy is their heightened photodynamic efficiency and remarkable tumor ablation capabilities observed in vitro and in vivo, devoid of adverse effects. Furthermore, computational simulations validate their interactions with cancer cells, bolstering their utility as an emerging therapeutic modality. This endeavor pioneers a secure and efficacious strategy for cancer therapy, underscoring the significance of β-CD-conjugated Au-Fe 3 O 4 JNPs as innovative nanoplatforms with profound implications for the advancement of cancer therapy., 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.)

[Display omitted] Silane (sol–gel)-based coatings have been introduced as an eco-friendly system for reducing the metals' corrosion in NaCl solutions. However, due to the lack of active protection property for this type of coatings, their modification is totally recommended for achieving durable protection properties. The present study introduces Beta-cyclodextrin (β -CD) as a novel/effective organic nano-container for Benzimidazole (BM) encapsulation to obtain reliable active protection property via a controlled-release property. The chemical structure of the β -CD-BM macromolecule was explored by Fourier-transform infrared spectroscopy (FT-IR), X-Ray diffraction (XRD), and Ultraviolet–visible spectroscopy (UV–Vis). Besides, the Electrochemical Impedance Spectroscopy (EIS) and polarization (potentiodynamic) tests were carried out for investigating the inhibition impacts of the constructed containers. The exposed and unexposed samples' surfaces were analyzed by Field Emission Scanning Electron Microscope (FE-SEM), Energy Dispersive Spectroscopy (EDS)/mapping, and Grazing incidence X-ray diffraction (GIXRD) experiments. Also, the EIS test was conducted over the Silane-based composite film (SCF) for analyzing the anti-corrosion performance of the constructed composites. The EIS achievements demonstrated that by the addition of β -CD-BM complexes to the saline solution, the mild steel corrosion was mitigated by about 84%. The EIS results also displayed that the total resistance of the modified composite was enhanced from 5540 Ω.cm2 to 10967 Ω.cm2 and the intact coating provided a total resistance of 80254 Ω.cm2. The dispersion-corrected Density Functional Theory (DFT)-D explorations ascertained the inclusion capacity of benzimidazole inside the β -CD. The Monte Carlo/Molecular Dynamics (MC/MD) calculations strongly affirmed the adsorption of BM and β -CD-BM over the substrate. [ABSTRACT FROM AUTHOR]

The potential effects of deep eutectic solvents (DESs) based on eutectic mixtures of amino acids (AAs) and tetrabutylammonium bromide (TBABr) in combination with beta-cyclodextrin (β-CD) were first evaluated as chiral systems in capillary electrophoresis (CE). Three DESs: tetrabutylammonium bromide/l-arginine (TBABr/l-Arg), tetrabutylammonium bromide/l-alanine (TBABr/l-Ala) and tetrabutylammonium bromide/l-proline (TBABr/l-Pro)) were used. Markedly improved chiral discrimination for four native amino acids (dl-methionine, dl-valine, dl-serine and dl-threonine) were obtained with high resolutions ranging from 4.78 to 9.84 in the presence of TBABr/l-Arg/β-CD chiral selector. Optimal CE conditions were a BGE containing 15 mmol L−1 β-CD and 10% (v/v) TBABr/l-Arg mixed with 50 mmol L−1 borate at pH 9.5, 20 kV applied voltage and 25 °C capillary temperature. The relative standard deviations (RSDs) of intra- and inter-day variations of migration times were less than 2.2% and 3.5%, respectively. l-Arg has the highest isoelectric point (pI = 10.7 at 25 °C) among protein amino acids which is appropriate for formation of stable DES at an alkaline separation medium. Moreover, TBABr/l-Arg/β-CD possessed the lowest electroosmotic flow velocity (0.018 cm2 min−1 V−1) among the investigated chiral systems providing more opportunities for chiral recognition of analytes within 14 min. Analytical characteristics of the CE/UV developed method were evaluated and demonstrated to be adequate to apply the methodology to enantiomeric analysis of methionine in commercial dietary supplements including enantiomeric impurity of d-methionine at 0.03% level (m/m). Therefore, the proposed TBABr/l-Arg/β-CD could be used as a versatile, simple and effective selector for baseline chiral recognition in CE. [ABSTRACT FROM AUTHOR]

The gold(I)‐dithiocarbamate (dtc) complex [Au(N,N‐diethyl)dtc]2 was identified as the active cytotoxic agent in the combination treatment of sodium aurothiomalate and disulfiram on a panel of cancer cell lines. In addition to demonstrating pronounced differential cytotoxicity to these cell lines, the gold complex showed no cross‐resistance in therapy‐surviving cancer cells. In the course of a medicinal chemistry campaign on this class of poorly soluble gold(I)‐dtc complexes, >35 derivatives were synthesized and X‐ray crystallography was used to examine structural aspects of the dtc moiety. A group of hydroxy‐substituted complexes has an improved solubility profile, and it was found that these complexes form 2 : 1 host–guest inclusion complexes with β‐cyclodextrin (CD), exhibiting a rarely observed "tail‐to‐tail" arrangement of the CD cones. Formulation of a hydroxy‐substituted gold(I)‐dtc complex with excess sulfobutylether‐β‐CD prevents the induction of mitochondrial reactive oxygen species, which is a major burden in the development of metallodrugs. [ABSTRACT FROM AUTHOR]