Search

Aspergillus flavipes L-methionine γ-lyase (MGL) has been authenticated as a powerful anticancer agent towards various solid tumors, however, the catalytic efficiency and stability of this enzyme remains the main challenge for its further in vivo applications. Thus, the objective of this study was to enhance the catalytic efficiency, structural stability of A. flavipes MGL, in addition to boost their anticancer activity, via conjugation with β-cyclodextrin. The purified A. flavipes MGL was (38.1 μmol/mg/min) was conjugated with β-cyclodextrin, with immobilization yield 80%. The conjugation process of MGL with β-cyclodextrin was verified from the FTIR analysis, molecular docking analysis, ensuring the covalent conjugation process via the hydrogen, and hydrophobic interactions with the cyclodextrin hydroxyl groups and MGL surface amino acids residues. The free and CD-MGL have the same optimum reaction temperature 37 °C, reaction pH 7.5 and pH stability pH 6.5–8.0. The CD-MGL conjugates had a significant stability to proteinase K and trypsin digestion. The affinity of CD-MGL was increased by ~ 2 folds to L-methionine (KM 3.1 mM), compared to the free one (KM 7.2 mM), as well as the catalytic efficiency of MGL was increased by 1.8 folds upon cyclodextrin conjugation. The higher affinity of CD-MGL for L-methionine might be due to re-orientation of the MGL to bind with the substrate by multiple interactions hydrogen, hydrophobic and covalent bonds compared to the free one. The thermal stability of MGL was increased by ~ 2 folds for the tested treatments, upon cyclodextrin conjugation. The in vitro anticancer activity of CD-MGL was enhanced by 2 folds against the HCT-116 (IC50 value 13.9 μmol/mg/min) and MCF7 (IC50 value 9.6 μmol/mg/min), compared to the free MGL (~ 21.4 μmol/mg/min). The enzymes displayed a significant activity against the proliferation of Ehrlich ascites carcinoma in vivo, with an obvious improvement on the liver tissues, as revealed from the histopathological sections [ABSTRACT FROM AUTHOR]

Cyclodextrin‐based polyrotaxanes (CD‐PRs) are gaining attention for their dynamic sliding rings along the polymer axis, enabling various applications in molecular shuttles, drug delivery, and durable polymers with slidable cross‐links. However, the conventional synthesis of CD‐PRs with tunable threading ratios is typically laborious, time‐consuming, and complicated, which limits their scalability and cost‐effectiveness. Herein, we highlight the great potential of planetary centrifugal mixing, a process that significantly accelerates and simplifies the initial synthesis of polypseudorotaxanes (PPRs), followed by a thiol‐ene click reaction as an efficient end‐capping reaction for the synthesis of PRs. Notably, PRs synthesized with glutathione (GSH) as the end‐capping reagent are in a metastable state, where GSH act as a molecular bumper that significantly prevent de‐threading of α‐CD rings at room temperature. Moreover, the rate of ring de‐threading can be precisely controlled by heating, enabling the preparation of metastable PRs with tunable threading ratios over a wide range. The developed strategy is of great significance to the efficient synthesis of CD‐PRs, thus marking a significant step towards their practical application in advanced functional materials and devices. [ABSTRACT FROM AUTHOR]

β-Cyclodextrin (β-CD)—functionalized carbon quantum dots (CDs) loaded with curcumin (CCM) were used for ClO– sensing with high sensitivity and selectivity. This fluorescence resonance energy transfer (FRET)-based sensor was created through attaching CCM to the CDs via β-CD linker. CCM could get into the interior of β-CD triggering the FRET from CDs to CCM, providing an 'off' state of the CDs. However, the effect of FRET was weakened by the ClO–, because the o-methoxyphenol structure from CCM was oxidized to be benzoquinone. The fluorescence intensity of CDs@β-CD@CCM at 440 nm can be heightened and 520 nm from CCM can decrease along with the increased ClO–. Therefore, a ratiometric fluorescence probe for ClO– sensing is successfully constructed. It conforms to a polynomial curve equation which is I440/I520 = −0.0268 + 0.0315 CClO–+ 0.0055[CClO–]2 (R 2 = 0.9958) between 0 and 18.4 μ M ClO–. Furthermore, we also obtain excellent results using this spectrophotometric method for ClO–-sensing in pure water and commercial disinfectants, which afford potential in the environment monitoring area. We expect this sensing platform could be helpful in other analogous probes in relevant fields. [ABSTRACT FROM AUTHOR]

Biological nanopores are increasingly used in molecular sensing due to their single-molecule sensitivity. The detection of per-and polyfluoroalkyl substances (PFAS) like perfluorooctanoic acid and perfluorooctane sulfonic acid is critical due to their environmental prevalence and toxicity. Here, we investigate selective interactions between PFAS and four cyclodextrin (CD) variants (a-, β-, and 2-hydroxypropyl-1-CD) within an a-hemolysin nanopore. We demonstrate that PFAS molecules can be electrochemically sensed by interacting with a 1-CD in a nanopore. Using HP-1-CDs with increased steric resistance, we can identify homologs of the perfluoroalkyl carboxylic acid and the perfluoroalkyl sulfonic acid families and detect common PFAS in drinking water at 0.4 to 2 parts per million levels, which are further lowered to 400 parts per trillion by sample preconcentration. Molecular dynamics simulations reveal the underlying chemical mechanism of PFAS-CD interactions. These insights pave the way toward nanopore-based in situ detection with promises in environmental protection against PFAS pollution. [ABSTRACT FROM AUTHOR]

In this paper, Biocompatible supramolecular hydrogels, composed of β-cyclodextrin-modified hyaluronic acid, pluronic F127, α-cyclodextrin and doxorubicin, were constructed, which can be employed for targeted delivery system. The chemical composition and rheological properties of the obtained hydrogels were fully characterised. Considering the controlled complexation between DOX and the hydrogel skeletons, the controlled release of hydrogel G[5, 10, 5] was investigated to exhibit a better pH- and temperature-controlled release behavior. The data of DOX release kinetic was fitted well with Higuchi and Korsmeyer-Peppas models. Moreover, the cellular toxicity experiments indicated that the hydrogel DOX@G[5, 10, 5] exhibited a similar anticancer ability in comparison with free DOX. Due to the hyaluronic acid-targeted effects, the cytotoxicity of the hydrogel DOX@G[5,10,5] to HepG2 cells was lower than that to SKOV-3 cells upon increasing the concentration. Therefore, these hydrogels may act as a potential prospect for the targeting release of anticancer drugs. [ABSTRACT FROM AUTHOR]

This paper explores the development and characterization of epichlorohydrin-crosslinked β-cyclodextrin nanoparticles (βCDNPs) for drug delivery, focusing on their interaction with hydrophobic drugs and biocompatibility. We synthesized βCDNPs using β-cyclodextrin (βCD) and epichlorohydrin (ECH). Our study assessed the biocompatibility and safety of βCDNPs, particularly in avoiding nephrotoxicity commonly associated with βCD, by examining their interaction with cholesterol and conducting survival analyses in mice at various dosing concentrations. Additionally, we highlight the advantages of using diffusion-ordered NMR spectroscopy (DOSY) to determine the enhanced binding constants of βCDNPs with hydrophobic compounds, in comparison with the solubility method, Job plot analysis, and isothermal titration calorimetry (ITC). We demonstrated the enhanced binding capacity of βCDNPs compared to βCD alone and established the polymerization of βCD as a significant factor in this enhancement. Our findings suggest that βCDNPs show promise as drug delivery systems due to their improved solubility, stability, and safety profiles. [ABSTRACT FROM AUTHOR]

The [c2]daisy chain rotaxane is an attractive interlocked molecule for the development of functional materials because of its unique mechanical properties that respond to various external stimuli, resulting in extension and contraction motions along the molecular axis. The synthesis of several ‘impossible’ [2]rotaxanes that do not exhibit obvious binding motifs between their axle and wheel moieties has been achieved through further chemical modification of their axle moieties within pre‐prepared [2]rotaxanes. However, no ‘impossible’ [c2]daisy chain rotaxane has been synthesized using similar strategies until now. In this study, we investigated the hydrogenation of diarylacetylene moieties within a permethylated α‐cyclodextrin (PM α‐CD)‐based [c2]daisy chain rotaxane using Pd/C or Pd/CaCO3 under hydrogen. A new [c2]daisy chain rotaxane featuring two diarylethane moieties was successfully synthesized through the simultaneous full hydrogenation of the insulated diarylacetylene moieties under optimized conditions. The new rotaxane is classified as an ‘impossible’ [c2]daisy chain rotaxane due to the lack of obvious binding motifs between diarylethane and the PM α‐CD. This work demonstrates for the first time that the insulated axle moieties of [c2]daisy chain rotaxanes can undergo novel chemical modifications using a synthetic strategy employing transition metal‐catalyzed hydrogenation, which can potentially advance the development of nanoarchitectures with functional interlocked molecules. [ABSTRACT FROM AUTHOR]

Covalent polymer networks find wide utility in diverse engineering applications owing to their desirable stiffness and resilience. However, the rigid covalent chemical structure between crosslinking points imposes limitations on enhancing their toughness. Although the incorporation of sacrificial chemical bonds has shown promise in improving toughness through energy dissipation, composite networks struggle to maintain both rapid recovery and stiffness. Consequently, a significant challenge persists in achieving a covalent network that combines high strength, stiffness, toughness, and fast recovery performance. To address this challenge, we propose a novel sacrificial structure termed “sacrificial conformation.” In this approach, β‐cyclodextrin is covalently embedded into the network skeleton as the sacrificial conformation element. Compared to traditional covalent networks (LCN), well‐designed cyclodextrin‐embedded covalent network (CCN) exhibit a 100‐fold increase in Young's modulus and a 60‐fold increase in toughness. Importantly, CCN maintains excellent elasticity, ensuring swift recovery after deformation. This sacrificial conformational strategy enables efficient energy dissipation without necessitating the rupture of chemical bonds, thereby overcoming the limitations of traditional approaches. This advancement holds great promise for the design and fabrication of advanced elastomers and hydrogels with superior mechanical properties and dynamic behavior. [ABSTRACT FROM AUTHOR]

Synthesis of polyurethane‐type poly[3]rotaxanes is achieved by polyaddition between a cyclodextrin (CD)‐based [3]rotaxane diol and various diisocyanate species, which provide a more defined structure compared to conventional polyrotaxane syntheses. In this study, hydroxyl groups on CDs of [3]rotaxane diol are initially acetylated, and deprotected after the polyaddition to introduce polyurethane backbone structure into polyrotaxane framework. Despite a relatively complicated chemical structure, [3]rotaxane diol monomer is successfully synthesized in a high yield (overall 67%) without any taxing purification process, which is beneficial for practical applications. The polymerization itself proceeds well under a standard polyaddition reaction condition to afford corresponding polyurethanes around 80% yield with Mn > 30 kDa. The poly[3]rotaxanes show different aggregation behavior or optical properties, whether or not acetyl groups are present, and are analyzed by XRD, SEM, and fluorescence measurements. [ABSTRACT FROM AUTHOR]

Thermochromic smart windows have emerged as a focal point in energy research. In this study, a novel approach is introduced for developing thermoresponsive materials for smart windows, utilizing microscopic agglomeration of molecules to regulate incident light. The groundbreaking material, β‐CD‐Val‐IBAm4, is constructed by grafting four isobutylated valines onto natural β‐cyclodextrins. This material exhibits a unique "hand‐in‐hand" effect, resulting from the interaction of isobutylated valine side chains, which leads to molecular aggregation and reduced light transmission at elevated temperatures. The hydration–dehydration process is related to molecular aggregation rather than crosslinking, ensuring the structural integrity and uniformity of the smart windows. Molecular dynamics simulations and 2D NOESY confirm the thermal response mechanism of β‐CD‐Val‐IBAm4. When dissolve in a glycerol‐water binary solvent system, the material forms a thermochromic liquid with outstanding optical performance (ΔTsol of 1 mm liquid can reach 69.8%) and long‐term stability. This innovative approach opens new avenues for the advancement of next‐generation smart window technologies. [ABSTRACT FROM AUTHOR]

Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objective: This study aimed to investigate the feasibility of using the digital image processing technique, developed to semi-quantitatively study dermal penetration, to study corneal penetration in an ex vivo porcine eye model. Here, we investigated various formulation strategies intended to enhance dermal and corneal bioavailability of the model hydrophobic drug, curcumin. Methods: Several formulation principles were explored, including oily solutions, oily suspensions, aqueous nanosuspension, micelles, liposomes and cyclodextrins. The dermal penetration efficacy was tested using an ex vivo porcine ear model previously developed at Philipps-Universität Marburg with subsequent digital image processing. This image analysis method was further applied to study corneal penetration using an ex vivo porcine whole-eye model. Results: For dermal penetration, oily solutions, oily suspensions and nanosuspensions exhibited the least penetration, whereas liposomes and cyclodextrins showed enhanced penetration. Corneal curcumin penetration correlated with dermal penetration, with curcumin loaded into cyclodextrins penetrating the deepest. Conclusions: Overall, our study suggests that the image analysis method previously developed for ex vivo skin penetration can easily be repurposed to study corneal penetration of hydrophobic drugs. [ABSTRACT FROM AUTHOR]

Background: Encapsulation of siRNA fragments inside liposome vesicles has emerged as an effective method for delivering siRNAs in vitro and in vivo. However, the liposome's fluid-phospholipid bilayer of liposomes allows siRNA fragments to diffuse out of the liposome, decreasing the dose concentration and therefore the effectiveness of the carrier. We have previously reported that β-cyclodextrins formulated in liposomes help increase the stability of siRNAs in cell culture medium. Here, we continued that study to include α, γ, methyl-β-cyclodextrins and β-cyclodextrin-modified gold and selenium nanoparticles. Methods: We used Isothermal Titration Calorimetry to study the binding thermodynamics of siRNAs to the cyclodextrin-modified nanoparticles and to screen for the best adamantane derivative to modify the siRNA fragments, and we used gel electrophoresis to study the stabilization effect of siRNA by cyclodextrins and the nanoparticles. Results: We found that only β- and methyl-β-cyclodextrins increased siRNA serum stability. Cyclodextrin-modified selenium nanoparticles also stabilize siRNA fragments in serum, and siRNAs chemically modified with an adamantane moiety (which forms inclusion complexes with the cyclodextrin-modified-nanoparticles) show a strong stabilization effect. Conclusions: β-cyclodextrins are good additives to stabilize siRNA in cell culture medium, and the thermodynamic data we generated of the interaction between cyclodextrins and adamantane analogs (widely used in drug delivery studies), should serve as a guide for future studies where cyclodextrins are sought for the delivery and solvation of small organic molecules. [ABSTRACT FROM AUTHOR]

The current review provides a focused analysis of the application of capillary electrophoresis (CE) techniques to determine the chiral purity of pharmaceuticals, with a specific emphasis on cyclodextrin- (CD) based chiral selectors (CSs), highlighting advancements, methodologies, and trends in this area as reported in studies published from 2010 to 2024. The review emphasizes CE's evolution as a critical tool in this field, discussing its advantages, such as high efficiency, flexibility, relatively low costs, and minimal environmental impact, which make it well-suited for modern pharmaceutical applications. Additionally, it underscores the importance of CE in meeting stringent regulatory requirements for chiral drug substances. A significant shift in method optimization has occurred in the last ten years, shifting from the traditional One-Factor-at-a-Time (OFAT) strategy to the Design-of-Experiments (DoE) approach; this shift has enabled more systematic and robust method development. Furthermore, a common trend in recent years is the application of Quality-by-Design (QbD) principles in method development and optimization, ensuring higher reliability and efficiency. Additionally, there is an increasing focus on developing CE methods capable of detecting both achiral and chiral impurities simultaneously, which enhances the comprehensiveness of the analysis. This review seeks to guide future research and development in optimizing CE methodologies for pharmaceutical applications. [ABSTRACT FROM AUTHOR]

Cyclodextrin (CD) derivatives have gained significant attention in biomedical applications due to their remarkable biocompatibility, unique inclusion capabilities, and potential for functionalization. This review focuses on recent advancements in CD-based assemblies, specifically their role in improving drug delivery, emphasizing remdesivir (RMD). The review introduces CD materials and their versatile applications in self-assembly and supramolecular assembly. CD materials offer immense potential for designing drug delivery systems with enhanced activity. Their inherent inclusion capabilities enable the encapsulation of diverse therapeutic agents, including RMD, resulting in improved solubility, stability, and bioavailability. The recent advances in CD-based assemblies, focusing on their integration with RMD have been concentrated here. Various strategies for constructing these assemblies are discussed, including physical encapsulation, covalent conjugation, and surface functionalization techniques. Furthermore, exploring future directions in these fields has also been provided. Ongoing research efforts are directed toward developing novel CD derivatives with enhanced properties, such as increased encapsulation efficiency and improved release kinetics. Moreover, the integration of CD-based assemblies with advanced technologies such as nanomedicine and gene therapy holds tremendous promise for personalized medicine and precision therapeutics [ABSTRACT FROM AUTHOR]

In this study, we developed a sensitive method for monitoring α‐amylase using a fluorogenic approach based on the host‐guest complexation between an amphiphilic pyrenyl derivative (1) and γ‐cyclodextrins (γ‐CDs). The compound 1 self‐assembles into nanofibrils in aqueous solutions. Upon the introduction of γ‐CD, compound 1 forms an inclusion complex with it. This complex then participates in the formation of a 2 : 2 complex with another complex, leading to strong excimer fluorescence. Upon interaction with α‐amylase, γ‐CD undergoes hydrolysis, leading to the regeneration of nanofibrils, which is accompanied by a decrease in excimer fluorescence and an increase in monomeric fluorescence. This ratiometric fluorescence color change enables the sensitive detection of low levels of α‐amylase in human urine, offering a practical approach for early screening of pancreatic‐related diseases. [ABSTRACT FROM AUTHOR]

Considerable attention has been directed towards cyclodextrins (CDs) in the creation of co‐assembled CPL‐active materials, owing to their intrinsic chiral host cavities and synergistic host‐guest interactions. However, achieving reversed CPL emission regulation with single‐handedness CDs moiety poses a significant challenge. In this study, we have devised a series of γ‐CD‐based host‐guest complexes comprising dual pyrene imidazolium derivatives with multiple linkers, which exhibit reversed circularly polarized emission. We have uncovered that the transformation of excimer stacking within γ‐CD/pyrene complexes contributes to the inverted CPL emissions originating from a single‐handed chiral host. This research elucidates the phenomenon of (+)‐ and (−)‐circularly polarized excimer emission (CPEE) within γ‐CD, arising from right‐ and left‐handed stacking conformations, respectively. [ABSTRACT FROM AUTHOR]

Leather production for human protection has been an essential industrial activity since the start of civilization, yet classical leavering methods induce pollution of ecosystems by dyes, chromium-containing wastewater, and solid waste. Here, we review sustainable leather production using polysaccharides and modified polysaccharides, which are cheap, easy to obtain, and non-toxic. Polysaccharides include starch, chitosan, cellulose, and cyclodextrins. We discuss application for leather tanning, prevention of leather mildew, leather finishing and dyeing, and wastewater treatment. The leather properties meet the requirements of garment leathers, with tear strength higher than 18 N per mm and tensile strength higher than 6.5 MPa. [ABSTRACT FROM AUTHOR]

Paclitaxel (PCTX) is one of the most prevalently used chemotherapeutic agents. However, its use is currently beset with a host of problems: solubility issue, microplastic leaching, and drug resistance. Since drug discovery is challenging, we decided to focus on repurposing the drug itself by remedying its drawbacks and making it more effective. In this study, we have harnessed the aqueous solubility of sugars, and the high affinity of cancer cells for them, to entrap the hydrophobic PCTX within the hydrophilic shell of the carbohydrate β -cyclodextrin. We have characterized this novel drug formulation by testing its various physical and chemical parameters. Importantly, in all our in vitro assays, the conjugate performed better than the drug alone. We find that the conjugate is internalized by the cancer cells (A549) via caveolin 1-mediated endocytosis. Thereafter, it triggers apoptosis by inducing the formation of reactive oxygen species. Based on experiments on zebrafish larvae, the formulation displays lower toxicity compared to PCTX alone. Thus, our "Trojan Horse" approach, relying on minimal components and relatively faster formulation, enhances the anti-tumor potential of PCTX, while simultaneously making it more innocuous toward non-cancerous cells. The findings of this study have implications in the quest for the most cost-effective chemotherapeutic molecule. [ABSTRACT FROM AUTHOR]

This study aimed to develop and evaluate hydrogels containing a cyclodextrin complex with clove essential oil and other free volatile oils with antimicrobial properties (tea tree and rosemary essential oils), focusing on their pharmaco-technical and rheological characteristics. The formulations varied in the Carbopol 940 (a hydrophilic polymer) and volatile oils' concentrations. Rheological analysis indicated that the gels displayed pseudoplastic behavior, with the flow index (n) values below 1, ensuring appropriate consistency and handling. The results showed that increasing the Carbopol concentration significantly enhanced the yield stress, consistency index, and viscosity, with gel B, containing 1% Carbopol, 1.5% tea tree essential oil, and 1.5% rosemary essential oil, demonstrating optimal stability and rheological properties. At the same time, the concentration of volatile oils was found to modulate the gels' flow parameters, but their effect was less pronounced than that of the gel-forming polymer. Antimicrobial testing revealed that both gel B and gel E (containing 1% Carbopol, 2% tea tree essential oil, and 2% rosemary essential oil) exhibited antimicrobial activity against Gram-positive, Gram-negative bacteria, and Candida spp., with gel E showing superior efficacy against Candida tropicalis. The antimicrobial effects were likely influenced by the higher concentrations of tea tree and rosemary essential oils in gel E. Overall, the study demonstrates that the concentration of Carbopol 940 primarily determines the gel's rheological behavior, while volatile oil concentration modulates antimicrobial effectiveness. [ABSTRACT FROM AUTHOR]

Viologen, as a type of strong electron acceptor, is prone to undergo electron transfer (ET) and change color under external stimuli. However, due to the easy aggregation of viologen molecules, they usually suffer from poor fluorescence emission in the condensed phase. Herein, a new viologen derivative of VioCl2·2Cl (12+·2Cl) was designed and synthesized, in which the fluorescence was enhanced by introducing Me‐β‐CD to weaken the interactions between viologen molecules. Then a viologen‐based host–guest supramolecule of 12+@Me‐β‐CD was obtained by electrostatic interactions. Photo‐/chemo‐responded guest 12+ supplies 12+@Me‐β‐CD, a green and dark purple caused by intramolecular and intermolecular ET. Furthermore, 12+@Me‐β‐CD displays an additional thermal responsive purple color. The triple chromic behaviors all exhibit excellent reversibility and cycling stability. As expected, 12+@Me‐β‐CD exhibits strong photoluminescence (PL) in solid–liquid dual states, presenting an improved quantum yield (Φ) from 12+ (Φs = 0.37%, Φl = 16.74%) to 12+@Me‐β‐CD (Φs = 10.45%, Φl = 25.86%), and the fluorescence intensity can be dynamically modulated by light, heat, and acid/base vapors. The multi‐responsive chromism and tunable fluorescence of 12+@Me‐β‐CD allow for potential applications in information security and smart windows. [ABSTRACT FROM AUTHOR]

Hemin, a heme-like compound with significant biological activity, shows promise as an iron supplement for humans. Nonetheless, its poor solubility in water greatly impedes its absorption and utilization. To surmount this obstacle, researchers have chosen various cyclodextrins with distinct cavity sizes and derivative groups to act as hosts, forming inclusion complexes with hemin chloride. Among these, γ-cyclodextrin has been identified as the optimal carrier, based on a thorough evaluation of its encapsulation efficiency, solubility, and molecular docking. Multiple characterization techniques further confirmed the formation of these inclusion complexes. Results from IEC-6 cell experiments indicated that the cytotoxicity of the inclusion complexes was lower than that of FeSO4. Static and dynamic gastrointestinal simulation digestion systems were established, and the results showed that the bioavailability of the inclusion complex was significantly higher than that of raw hemin. Additionally, only about 0.29% of hemin chloride is digested by gastric enzymes, whereas 9.52% is digested by pancreatic enzymes in the static gastrointestinal simulation digestion system, with similar outcomes observed in the dynamic system. These findings suggest that targeted digestion in the intestine significantly enhances the bioavailability of hemin chloride by forming inclusion complexes in vitro. [ABSTRACT FROM AUTHOR]

Packaging hydrophobic drugs into polysaccharide carriers can improve their aqueous solubility, biocompatibility, tumor‐specific accumulation, and therapeutic effect. In this work, phenylboronic acid (PBA) was anchored onto the chain of biocompatible polysaccharide hyaluronic acid (HA) by an amide condensation reaction, which could be used to fabricate stimuli‐responsive targeted drug delivery systems. A series of pH‐responsive conjugated hyaluronic acid nanoparticles composed of a hydrophobic drug core and hydrophilic hyaluronic acid shell were prepared by the boronate‐crosslink of the PBA with diol‐containing anticancer drugs such as capecitabine (CAPE) and aloin (Al). Satisfactory targeted drug release behavior at acidic pH, lower cytotoxicity, and higher anticancer effect were realized by using this polysaccharide carrier. It is believed that this strategy has great potential for polysaccharide modification and anticancer‐associated applications. [ABSTRACT FROM AUTHOR]

High mechanical properties and rapid sol/gel phase transition are mutually exclusive in the hydrogels reported to date, most likely because the 3D crosslinked networks of mechanically robust hydrogels comprise bundled thick fibers that are not rapidly dissociable or formable. Herein, we report a visible light‐responsive hydrogel that showed a rapid, reversible sol/gel phase transition despite its relatively high mechanical properties (storage modulus ~103 Pa). To construct its 3D crosslinked network, we used a design strategy analogous to that employed for our highly water‐rich yet mechanically robust nanocomposite supramolecular hydrogel (“aqua material”). In this case, multiple poly(ethylene glycol) chains carrying ortho‐tetramethoxyazobenzene termini (AzoPEG) were noncovalently crosslinked by clay nanosheets (CNSs) with surface‐immobilized β‐cyclodextrin units using their seven guanidinium ion (Gu+) pendants (GuCD) via a multivalent salt‐bridge. When exposed to visible light at 625 and 450 nm, the azobenzene termini isomerized from trans‐to‐cis and cis‐to‐trans, respectively, and were detached from and attached to the surface‐immobilized GuCD units. The advantage of this CNS‐based nanocomposite supramolecular system is its simple 3D network structure, which forms and breaks rapidly without slow chain entangling and disentangling processes. [ABSTRACT FROM AUTHOR]

The regioselective radical CH trifluoromethylation of aromatic compounds have been shown to proceed in good yield and high regioselectivity when cyclodextrin (CD) is present. Yet, the reaction mechanism and the role of CD during the reaction have remained obscure. To this end, here we performed density functional theory (DFT) calculations to the conformations obtained by semiempirical quantum mechanical molecular dynamics calculations to reveal the reaction mechanism and the role of CD in controlling regioselectivity. The results show that metal salt increases the yield but do not affect the regioselectivity, which we further confirmed by an experiment. In contrast, multiple CD‐substrate complex conformations and reaction pathways were obtained, and CD was shown to contribute to improving the regioselectivity by stabilizing the intermediate state via encapsulation. The present study indicates that CDs can increase the regioselectivity by stabilizing the intermediate and product states while only marginally affecting the transition state. [ABSTRACT FROM AUTHOR]

In our work, the inclusion ability and binding pattern of flavonoids (catechin, iso‐liquiritigenin, luteolin, puerarin, rutin, and curcumin) with β‐cyclodextrin (β‐CD) and curcumin (CUR) with CDs (α‐CD, β‐CD, γ‐CD, dimethyl‐β‐CD, Hydroxypropyl‐β‐CD, and glucosyl‐β‐CD) were studied by molecular docking. The results showed that CUR among the six flavonoids was more likely to form stable inclusion complexes with β‐CD, and the HP‐β‐CD is the most suitable for CUR inclusion among the 6 types of CD. Phase solubility studies showed that CUR with β‐CD or HP‐β‐CD, respectively, could form stable inclusion complexes in a stoichiometric ratio of 1 : 1. The CUR/β‐CD and CUR/HP‐β‐CD inclusion complexes (ICs) were prepared by freeze‐drying method. The successful preparation of IC was confirmed by SEM images, FT‐IR spectra, and TG‐DSC. The results of in vitro release showed that the release of CUR from IC prepared with β‐CD or HP‐β‐CD could be improved significantly, and the release effect of HP‐β‐CD was better than that of β‐CD. The inclusion with CD could be used to improve the solubility and bioavailability of CUR. [ABSTRACT FROM AUTHOR]

Combating reactive oxygen species (ROS) and targeted drug delivery to inflammatory sites are considered effective therapeutic strategies for ulcerative colitis (UC), a refractory chronic inflammatory disease. Herein, a ROS‐responsive thioketal (TK) crosslinked cyclodextrin metal‐organic framework (TCOF) is fabricated, to which a non‐ROS‐sensitive vector, sulfur substituted by carbon chain‐crosslinked cyclodextrin metal‐organic framework (CCOF) is parallelly designed as ROS negative reference. Dexamethasone (DEX) loaded in TCOF (TCD) and CCOF (CCD) are investigated to demonstrate the advantages of precision medicine for UC. After the ROS‐induced collapse of nanoparticles, TCD selectively triggered the release of DEX. Moreover, TCD effectively protected cells from oxidative stress damage and reduced inflammation levels in vitro. Remarkably, the TK group of TCD is oxidatively broken by consuming ROS at the inflammatory site, exposing the thiol group to mucosal adhesion, which enhances the retention of TCD at colons. In vivo studies of UC treatment reveals that oral administration of TCD demonstrated excellent inflammation‐targeting properties, remarkably attenuated oxidative stress, and ameliorated both acute and chronic colitis compared to CCD. Furthermore, TCD exhibits an excellent safety profile in mice. These results instill confidence in advancing targeted drug delivery and precision therapy for UC. [ABSTRACT FROM AUTHOR]

Simple Summary: This study evaluated the impact of resveratrol-loaded cyclodextrin (RLC) on the quality of ram sperm after thawing. Our hypothesis was that resveratrol-loaded cyclodextrin, which enhances the antioxidant activity of resveratrol (RES), would improve the outcomes of freezing ram semen. Accordingly, this study investigates the effects of resveratrol at varying doses (10, 20, and 40 µg/mL), either in its pure form or loaded into methyl-β-cyclodextrin (CD), on sperm functions following the thawing of ram semen. The findings indicate that while cyclodextrin negatively affected sperm quality, particularly by increasing early capacitation and mitochondrial activity, resveratrol at a dose of 20 µg/mL effectively prevented early capacitation. Overall, both resveratrol and resveratrol-loaded cyclodextrin were generally effective and beneficial in the context of freezing ram semen. This study investigated the effects of pure and methyl-β-cyclodextrin loaded forms of resveratrol (10 µg/mL, 20 µg/mL, and 40 µg/mL) on ram sperm functions post-thawing. Semen samples were pooled and divided into ten groups: Control, RES10, RES20, RES40, CD10, CD20, CD40, RLC10, RLC20, and RLC40. The groups were pre-diluted with media containing the group-specific chemicals, followed by 15 min of incubation, dilution, and freezing. To assess the effects of the chemicals, a post-thaw sperm quality assessment was conducted. Motility and other velocity parameters were evaluated using computer-assisted semen analysis. The functional integrity of spermatozoa membranes was assessed with the hypo-osmotic swelling test, and the capacitation status of spermatozoa was determined through fluorescent microscopic evaluation. Additionally, flow cytometry was used to evaluate mitochondrial activity, oxidative stress, and the integrity of the sperm membrane and acrosome. The results indicated that cyclodextrin adversely affected sperm functions following freezing–thawing, notably increasing the rate of spermatozoa exhibiting pre-capacitation and mitochondrial activity by approximately 34% and 16%, respectively (p < 0.05). It was found that 20 µg/mL resveratrol prevented pre-capacitation (p < 0.05). Both resveratrol and resveratrol-loaded cyclodextrin groups improved post-thaw sperm qualities overall, demonstrating their utility for freezing ram semen. However, higher concentrations of resveratrol were found to negatively impact sperm functions. [ABSTRACT FROM AUTHOR]

Multiple‐step on‐line preconcentration, a combination of at least two stacking techniques has been developed to increase the sensitivity in capillary electrophoresis (CE) for analytes in various samples. It is usually conducted sequentially, or in some cases, synergistically, where different stacking modes occur simultaneously. Multiple‐step techniques allow simultaneous preconcentration and separation of various kinds of analytes in different complex samples in a single CE run. This review aims to provide recent advances in multiple‐step on‐line preconcentration techniques in CE. We critically review technical papers published for the last 7 years up until July 2024, subsequently organized according to the combination of the main stacking techniques, that is, field amplification, large volume sample stacking, transient isotachophoresis, micelle to solvent or micelle to cyclodextrin stacking, and others. The procedures, fundamental mechanism, analytical figures of merits achieved, and their feasibility for complicated sample matrices are reviewed. [ABSTRACT FROM AUTHOR]

Curcumin (CUR), a polyphenolic substance from turmeric, displays diverse medicinal properties. However, its instability poses challenges in detection. Cyclodextrin-based nanogels (CyDngs) offer a transformative solution, enhancing CUR's stability in aqueous solutions. Multisensing approaches involving fluorescence, electrochemistry, and NMR spectroscopy were employed, demonstrating CyDngs' pivotal role in CUR detection. Langmuir analysis revealed a binding constant of 1.4 × 104 M–1 for CyDngs, highlighting their effectiveness over native β-CyDs. The study emphasized CyDngs' superiority in stabilizing CUR and enabling reliable and sensitive detection with very diverse methods. [ABSTRACT FROM AUTHOR]

Desolvation processes, though common in self‐assembled biological structures, are rarely evidenced and utilized in the design of crystalline architectures. In this study, we introduce a novel approach using the [Mo8S8O8(OH)8(guest)]2− complex, formed by the self‐condensation of four [MoV2O2S2]2− fragments around a guest unit (MoVIO6H4 or oxalate), as a chaotropic scaffold for crystallizing hybrid organic‐inorganic systems with natural cyclodextrins. Our findings reveal that β‐cyclodextrin (β‐CD) facilitates the formation of host‐guest complexes, while α‐cyclodextrin (α‐CD) induces the formation of a Kagome‐type structure with significant voids. These new compounds were thoroughly characterized using X‐ray diffraction (both powder and single‐crystal), N2 adsorption, elemental and thermogravimetric analysis. Additionally, solution studies using 1H NMR titration and small‐angle X‐ray scattering (SAXS) demonstrated pre‐association of the building units in solution. These results enhance our understanding of the design principles for supramolecular structures composed of inorganic polyanions and cyclodextrins. [ABSTRACT FROM AUTHOR]

The morphological symmetry‐retaining and symmetry‐breaking of single crystals of the γ‐cyclodextrin metal‐organic framework have been achieved via introducing lower symmetric β‐cyclodextrins and α‐cyclodextrins, respectively. β‐cyclodextrins led to a morphological evolution with retained symmetry from cubic to rhombic dodecahedra, while α‐cyclodextrins resulted in the original cubic crystal missing a vertex angle presenting symmetry‐breaking behavior. The crystal structures of rhombic dodecahedra and angle‐deficient crystals were confirmed through X‐ray crystallography, and the mechanisms underlying the morphological transformation evolution were further analyzed. Our work not only provides a rare case realizing two different paths of morphological evolution in one system, but also encourages future efforts towards the evolution of artificial crystal systems in a natural way. [ABSTRACT FROM AUTHOR]

The iron‐armored chain horse is a military strategy in ancient China to enhance the combat force of the entire army, especially when individual fighters are vulnerable to being picked off one by one. Herein, this strategy is adopted to generate highly efficient metal‐free blue room temperature phosphorescence (RTP) using the world's largest production of dicarboxylate acid. By encapsulating the commercially available chemical disodium terephthalate (DTPA) within the iron armor of α‐cyclodextrin (α‐CD), and subsequently linking the iron‐armored DTPA@α‐CD horses into a crystalline array mediated by hydrogen bonds and Na+ coordination, a highly confined and segregated arrangement of DTPA is achieved, leading to heavy atom‐free deep‐blue phosphorescence with a maximum efficiency of 83.3%. Since the crystalline array of the iron‐armored chain horse DTPA@α‐CD can be facilely obtained through water evaporation, the current phosphorescent material allows for rapid, high‐throughput solution processing of deep‐blue afterglow display, offering an economic and environmentally benign approach for deep‐blue RTP materials and facilitating their application. [ABSTRACT FROM AUTHOR]

Folic acid (FA) and its structural analog, anticancer medicine methotrexate (MTX), are known to form host/guest complexes with native cyclodextrins, of which the most stable are formed with the medium-sized β-cyclodextrin. Based on our research, proving that simple sugars (D-glucose, D-galactose, and D-mannose) can form adducts with folic acid, we envisioned that combining these two types of molecular receptors (cyclodextrin and simple carbohydrates) into one may be beneficial for the complexation of FA and MTX. We designed and obtained host/guest inclusion complexes of FA and MTX with two monoderivatives of β-cyclodextrin—substituted at position 6 with monosaccharide (glucose, G-β-CD) and disaccharide (maltose, Ma-β-CD). The complexation was proved by experimental (NMR, UV-vis, IR, TG, DSC) and theoretical methods. We proved that derivatization of β-cyclodextrin with glucose and maltose has a significant impact on the complexation with FA and MTX, as the addition of one glucose subunit to the structure of the receptor significantly increases the value of association constant for both FA/G-β-CD and MTX/G-β-CD, while further extending a pendant chain (incorporation of maltose subunit) results in no additional changes. [ABSTRACT FROM AUTHOR]

Lemon is a globally cultivated citrus fruit crop that has gained a significant market share in recent years. Lemon tends to taste bitter on prolonged storage periods, leading to undesirable changes in juice quality. Therefore, the study aimed to enhance lemon juice quality by reducing bitterness through combined probe ultrasonication and ß-cyclodextrin treatment. Ultrasonic treatment of 20 kHz, an incubation period ranging from 20 to 80 minutes, was applied to the juice and its effect on pH, total titratable acidity (TA), total soluble solids (TSS), ascorbic acid, total phenolic content (TPC) and antioxidant activity was evaluated. Batch debittering of limonin was carried out by adding ß-cyclodextrin at concentrations ranging from 0.25% to 2.50% for 20, 60 and 80 minutes of sonication treatment. The study also examined the influence of sonication treatments on microbial load, revealing significant reductions corresponding to 60 minutes of sonication. The sound waves generated at 20KHz from ultrasonication, including ß-cyclodextrin, could help to break down the cyclodextrin molecules and improve the encapsulation efficiency of the target compound. Moreover, increased water-soluble polyphenolic compounds due to cyclodextrin addition can enhance the lemon juice processability at an industrial scale. The present study emphasized the development of cost-effective ß-cyclodextrin debittered lemon juice in combination with ultrasonic treatment that improved juice quality at room temperature (25 °C±1 °C). [ABSTRACT FROM AUTHOR]

Olanzapine (OLZ) is an antipsychotic drug with low aqueous solubility. Cyclodextrin (CD) complexation is a potential approach employed to improve the solubility of poorly water-soluble drugs belonging to BCS classes II and IV. The solubility of olanzapine was improved using βCD, HPβCD and methyl βCD which was reported in earlier works. In the current study, a combination of βCD and HPβCD in 1:1 molar ratio was used in the preparation of complexes along with βCD and HPβCD. Methods such as slugging, hydration and granulation which are slight modifications of conventional methods like physical mixing and slugging were used. AL type curves were obtained in phase solubility studies specifying a linear increase in the solubility of drug with increase in concentration of cyclodextrin. The values of slopes calculated for AL type plots are less than one which suggests that OLZ:CD complexes are formed in 1:1 molar ratio. The stability constants obtained were 188.98 M -1, 140.63 M -1 and 157.48 M -1 with βCD, HPβCD and βCD+HPβCD and these values indicate that stable OLZ : CD complexes are formed. The drug : cyclodextrin binary complexes demonstrated a 2.27 to 3.67 - fold increment in aqueous solubility when compared to pure drug. The percentage of drug released in 60 minutes was 46 (pure drug), 65 - 89 (OLZ-βCD complexes), 59 - 80 (OLZ-HPβCD complexes) and 61 - 84 (OLZ-βCD+HPβCD complexes). Results of DSC, XRD and SEM indicated partial inclusion complexation. The complexes prepared by hydration method showed higher solubility when compared to other methods. In hydration method, the complexes were prepared using water which does not cause any harm to individual and environment. [ABSTRACT FROM AUTHOR]

KLEPTOSE® CRYSMEB methylated cyclodextrin derivative displays less methylated group substitution than randomly methylated cyclodextrin. It has demonstrated an impact on atherosclerosis and neurological diseases, linked in part to cholesterol complexation and immune response, however, its impact on inflammatory cascade pathways is not clear. Thus, the impact of KLEPTOSE® CRYSMEB on various pharmacological targets was assessed using human umbilical vein endothelial cells under physiological and inflammatory conditions, followed by screening against twelve human primary cell-based systems designed to model complex human tissue and disease biology of the vasculature, skin, lung, and inflammatory tissues using the BioMAP® Diversity PLUS® panel. Finally, its anti-inflammatory mechanism was investigated on peripheral blood mononuclear cells to evaluate anti-inflammatory or pro-resolving properties. The results showed that KLEPTOSE® CRYSMEB can modulate the immune system in vitro and potentially manage vascular issues by stimulating the expression of molecules involved in the crosstalk between immune cells and other cell types. It showed anti-inflammatory effects that were driven by the inhibition of pro-inflammatory cytokine secretion and could have different impacts on different tissue types. Moreover, this cyclodextrin showed no clear impact on pro-resolving lipid mediators. Additionally, it appeared that the mechanism of action of KLEPTOSE® CRYSMEB seems to not be shared by other well-known anti-inflammatory molecules. Finally, KLEPTOSE® CRYSMEB may have an anti-inflammatory impact, which could be due to its effect on receptors such as TLR or direct complexation with LPS or PGE2, and conversely, this methylated cyclodextrin could stimulate a pro-inflammatory response involving lipid mediators and on proteins involved in communication with immune cells, probably via interaction with membrane cholesterol. [ABSTRACT FROM AUTHOR]

Cyclodextrins are ring-shaped sugars used as additives in medications to improve solubility, stability, and sensory characteristics. Despite being widespread, Chagas disease is neglected because of the limitations of available medications. This study aims to review the compounds used in the formation of inclusion complexes for the treatment of Chagas disease, analyzing the incorporated compounds and advancements in related studies. The databases consulted include Scielo, Scopus, ScienceDirect, PubMed, LILACS, and Embase. The keywords used were "cyclodextrin AND Chagas AND disease" and "cyclodextrin complex against Trypanosoma cruzi". Additionally, a statistical analysis of studies on Chagas disease over the last five years was conducted, highlighting the importance of research in this area. This review focused on articles that emphasize how cyclodextrins can improve the bioavailability, therapeutic action, toxicity, and solubility of medications. Initially, 380 articles were identified with the keyword "cyclodextrin AND Chagas disease"; 356 were excluded for not being directly related to the topic, using the keyword "cyclodextrin complex against Trypanosoma cruzi". Over the last five years, a total of 13,075 studies on Chagas disease treatment were found in our literature analysis. The studies also showed interest in molecules derived from natural products and vegetable oils. Research on cyclodextrins, particularly in the context of Chagas disease treatment, has advanced significantly, with studies highlighting the efficacy of molecules in cyclodextrin complexes and indicating promising advances in disease treatment. [ABSTRACT FROM AUTHOR]

Inhalable formulations with cyclodextrins (CDs) as solubility and absorption enhancers show promise for pulmonary delivery. Thiolated hydroxypropyl-β-cyclodextrin (HP-β-CD-SH) has mucoadhesive properties, enhancing drug absorption. Moreover, it has self-aggregation capability, which could further improve absorption and drug stability, as well as reduce irritation. This study aims to stabilize CD nanoaggregates using bifunctional cross-linkers and evaluate their benefits for lung drug delivery compared to pristine HP-β-CD-SH. Methods: The effectiveness of cross-linked HP-β-CD-SH nanoparticles (HP-β-CD-SH-NP) was compared to transient nanoaggregates in enhancing the activity of dexamethasone (DMS) and olive leaf extracts (OLE). DMS, a poorly soluble drug commonly used in lung treatments, and OLE, known for its antioxidant properties, were chosen. Drug-loaded HP-β-CD-SH-NP were prepared and nebulized onto a lung epithelial Air–Liquid Interface (ALI) model, assessing drug permeation and activity. Results: HP-β-CD-SH with 25% thiolation was synthesized via microwave reaction, forming 150 nm nanoaggregates and stabilized 400 nm HP-β-CD-SH-NP. All carriers showed good complexing ability with DMS and OLE and were biocompatible in the lung ALI model. HP-β-CD-SH promoted DMS absorption, while stabilized HP-β-CD-SH-NP protected against oxidative stress. Conclusion: HP-β-CD-SH is promising for lung delivery, especially as stabilized nanoaggregates, offering versatile administration for labile molecules like natural extracts. [ABSTRACT FROM AUTHOR]

The present research work reported in air synthesis of a three-dimensional polymeric network of hydrogels by grafted copolymerization technique of Moringa gum and carboxymethyl cellulose by using acrylamide as a monomer, N, N-methylenebisacrylamide and ammonium persulphate as a cross-linker-initiator system. Different reaction parameters were used to optimize the synthesized hydrogel such as backbone ratio, pH of the reaction, temperature, volume of solvent, concentration of initiator, monomer and cross-linker with respect to the percentage swelling. The maximum percentage swelling 1244% was found at volume of solvent (17 mL), backbone ratio (2:1), cross-linker concentration (0.000032 molL−1) and temperature (60 °C) and concentration of monomer (0.000042 molL−1), and pH of 7. Mechanical strength and antibacterial properties of synthesized polymer networks are also evaluated. The confirmation of the synthesized hydrogel has been accomplished by using FTIR, FESEM, EDX, XRD, TGA and DSC characterization techniques. The synthesized hydrogels were evaluated as drug delivery carriers for in vitro release of antibiotic drug amoxicillin at pH of 2, 7 and 7.4. The drug release was compared between polymer matrices loaded with drug only and the polymer matrices loaded with Inclusion complex of β-Cyclodextrin and Amoxicillin. The controlled drug release has been found that is 99.25 ppm in 24 h in inclusion complex loaded polymer matrices, while the 75.472 ppm drug is released in just 8 h in the polymer matrices loaded directly with the drug. The Peppas-Sahlin equation holds good for release of amoxicillin at pH of 2 and 7, which further confirmed the diffusion and relaxation of polymer matrix are accountable the release of amoxicillin. [ABSTRACT FROM AUTHOR]

As a cultural carrier of historical inheritance, paper has high cultural, historical and scientific research value. But with the passage of time and the change of the environment, many paper are aging and damaged. In order to protect the paper, CMC-β-CD composite material for paper protection was synthesized by carboxymethyl cellulose as substrate, epichlorohydrin (ECH) as crosslinking agent, sodium hydroxide (NaOH) as catalyst and solvent, and water as medium, β-cyclodextrin as grafter. Through single factor experiment, the synthetic condition was obtained. The structure of the synthesized materials was characterized by infrared spectroscopy; CMC-β-CD was applied to paper reinforcement. The effects of solution concentration on the tensile strength, tearing degree, folding times, whiteness and gloss of paper were tested, and the suitable conditions for coating paper were found. The results show that the mass concentration of 2 % CMC-β-CD is coated on paper, its mechanical properties are greatly improved, the gloss is slightly increased, and the whiteness is basically unchanged, which is in line with the principle of "repairing the old as the old". [ABSTRACT FROM AUTHOR]

Background: Today, biologically active additives, which contain hydrolytic enzymes (amylase, lipase, protease), are widely used in the digestive industry. These enzymes are often obtained from animal and vegetable raw materials, -for example, from the pancreas of a reindeer, the Fabricius bag of chickens, and Medusomyces Gisevii Lindau (Kombucha). However, in obtaining enzymes, the activity of amylase and lipase may decrease due to active forms --of proteases. Objective: The main goal of this research work was to evaluate the stabilizing effect of nanostructures-cyclodextrins on the activity of hydrolytic enzymes (protease, amylase, lipase) obtained from animal raw material (chicken bursa of Fabricius) and microorganism cultures (Kombucha). Identify the relationship at which the negative influence of external environmental factors is leveled and, as a result, enzymatic activity is maintained for a certain period of time. Methods: The protein concentration in the solution was determined using the Lowry method. A modified method by Rukhlyadiva was used to determine the amylolytic activity. The definition of lipolytic activity is based on modified Shibabi-Bishop method. To determine the amylolytic activity, a modified method by Rukhlyadiva was used. Results: The relationship between b-cyclodextrin and enzymes was determined, at which enzymatic activity is maintained for a certain period. Conclusion: Thus, cyclodextrins in solution stabilizes the activity of proteases, amylases, and lipases, which is of great practical importance in the food and pharmaceutical industries. [ABSTRACT FROM AUTHOR]

Anemia is a global health problem that affects both adults and children, but treatment is hampered by serious side effects, primarily associated with the gastrointestinal tract with oral administration of drugs. In this study, we aimed to develop an oral form of iron compounds using polymethylsilsesquioxane hydrogels. To boost loading efficiency and prolong release, the iron compounds (FeCl3 and ferrous D-Gluconate) are incorporated into a guest–host complex with 2-hydroxypropyl-beta-cyclodextrin. We used PRXD, SEM, EDX mapping, and FTIR to investigate the complex formation, as well as the incorporation of such complexes into hydrogels. The optimal system underlines a combination of ferrous D-Gluconate and HPCD in a 1:1 molar ratio, embedded into a hydrogel with a modest quantity of silicate crosslinks. We demonstrated the slowing of iron release in a gastric media. Mathematical investigation revealed that the Higuchi mechanism releases iron from the hydrogel. [ABSTRACT FROM AUTHOR]

Essential metal ions, such as gold, zinc, copper, cadmium, silver, titanium, and platinum, play crucial roles in maintaining physiological functions in the human body. The ability of β-cyclodextrin (β-CD) to enhance the therapeutic performance of drugs loaded onto metal and soft metal ion nanoparticles (NPs) has been highlighted, underscoring its significance in nanomedicine. This review article focuses on investigating the production process of these NPs and their potential benefits. β-CDs have emerged as desirable building blocks for creating metal and soft metal ion NPs, enhancing the solubility, stability, and bioavailability of inorganic NPs. These agents improve drug characteristics by forming inclusive compounds with drugs, effectively addressing the challenge of low drug loading capacity associated with metal and soft metal NPs. Cyclodextrins (CDs) function as stabilising agents in metal NPs during their creation, reducing agglomeration and ensuring colloidal stability. This review provides valuable insights into the potential applications of metal and soft metal ion NPs functionalized with β-CD in the biomedical domain and paves the way for advancements in NP-based drug delivery systems. [ABSTRACT FROM AUTHOR]

Nigella sativa oil (NSO) and its essential oil (NSEO) have long been used in traditional treatment for various ailments. However, in practice, these substances are limited by their limited solubility in water, instability, and low bioavailability. Encapsulation has emerged as a promising solution for addressing these issues. This review is dedicated to the chemical composition of Nigella crude and essential oils, the exploration of their encapsulation system preparation methods, and a comprehensive examination of their potential applications across the food, cosmetics, and pharmaceutical industries. This exhaustive survey serves as an invaluable resource for researchers, professionals, and students with a keen interest in the encapsulation of N. sativa using cyclodextrins and liposomes. [ABSTRACT FROM AUTHOR]

Oxidative stress (OS) occurs from excessive reactive oxygen species or a deficiency of antioxidants—primarily endogenous glutathione (GSH). There are many illnesses, from acute and post-COVID-19, diabetes, myocardial infarction to Alzheimer's disease, that are associated with OS. These dissimilar illnesses are, in order, viral infections, metabolic disorders, ischemic events, and neurodegenerative disorders. Evidence is presented that in many illnesses, (1) OS is an early initiator and significant promotor of their progressive pathophysiologic processes, (2) early reduction of OS may prevent later serious and irreversible complications, (3) GSH deficiency is associated with OS, (4) GSH can likely reduce OS and restore adaptive physiology, (5) effective administration of GSH can be accomplished with a novel nano-product, the GSH/cyclodextrin (GC) complex. OS is an overlooked pathological process of many illnesses. Significantly, with the GSH/cyclodextrin (GC) complex, therapeutic administration of GSH is now available to reduce OS. Finally, rigorous prospective studies are needed to confirm the efficacy of this therapeutic approach. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Faculty of Pharmacy of Ankara University / Ankara Üniversitesi Eczacilik Fakültesi Dergisi is the property of Ankara University and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Cyclodextrin glycosyltransferase (CGTase) catalyzes intermolecular transglycosylation through either disproportionation or cyclization‐coupling pathway. Kinetics analysis reveals that the hesperidin glycosylation process catalyzed by a CGTase variant (M1) is primarily accomplished through the disproportionation pathway. The cyclization‐coupling pathway exhibits a lower reaction rate and competitively consumes glycosyl donor and yield byproducts that impair disproportionation. Under the guidance of reaction kinetics, mutagenesis was targeted at residues in the −3, +1, and +2 subsites, known to control the selectivity between disproportionation and cyclization. A quadruple variant was identified with 2.9 times hesperidin glycosylation activity compared to M1, and 20.3 times compared to the wild‐type. Kinetic analysis reveals a fourfold improvement of kcat/KmA for disproportionation and an 85.5% reduction in kcat/Km for cyclization after mutagenesis. Binding free energy analysis further confirms that the mutagenesis favors the binding of hesperidin, and destabilizes the binding of cyclodextrin. [ABSTRACT FROM AUTHOR]

Electrospun fibers were developed using different ratios of PVA/CD crosslinked with citric acid to enhance their water resistance properties. The diameter of the fibers increased as the amount of CD increased. PVA/CD fibers loaded with vitamin E (VE) were successfully prepared in 9-1PVA/CD and 7-3PVA/CD ratios, with VE loadings of 24% and 33% respectively. The release of VE from 7-3PVA/CD fibers was faster compared to that from 9-1PVA/CD fibers. Skin permeation studies demonstrated deeper penetration of FITC-incorporated VE in 9-1PVA/CD-CL fibers into the dermis. These promising results have potential for various applications involving enhanced water resistance and topical drug delivery. [ABSTRACT FROM AUTHOR]

Aflatoxins are the most potent hepatocarcinogens of all biologically produced toxins found to date. Contaminated food and commodities are one of the most serious problems due to an irreversible damage to health. Taking advantage of biological methods to improve food safety, an aflatoxin B1 (AFB1) bioremoval study was conducted to investigate the potential of arrested fungal cells on magnetic nanoparticles. The favourable results on the degradation of AFB1 indicate a reasonable influence of the carriers on the fungal cells and the degradation process. The efficacy of degradation of AFB1 by free and immobilised fungal cells on four different magnetic nanoparticles (Fe3O4) was investigated. The degradation rate by HPLC analysis exhibited 54.97% for the free cell study, 85.85% for Fe3O4@MTMS@cell, 95.07% for Fe3O4@TEOS@cell, 84.48% for Fe3O4@SiO2-NH2@cell and 96.52% for Fe3O4@BCD@cell for the 3 μg/ml AFB1. The degradation with Fe3O4@ BCD@cell showed remarkable results even for 5 μg/ml AFB1 resulting 93.42%. [ABSTRACT FROM AUTHOR]