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The application of flavoring ingredients like menthol in the food industry is hindered by their high volatility and poor thermal stability, which lead to significant losses during processing and storage. Encapsulation of flavors into porous materials to obtain inclusion complexes (ICs) has proved to be an efficient strategy. In the present study, we synthesized a series of relatively food-safe three-dimensional anionic cyclodextrin-based covalent organic frameworks (CD-COFs) with spiroborate linkages using a facile microwave-assisted method. The high surface area and newly formed cavities of COFs significantly enhanced the encapsulation efficiency of menthol compared to native CD materials. Our findings revealed that γ-CD-COF-Li, with Li as the counterion, achieved superior encapsulation efficiency of 25.9 %, outperforming γ-CD-COF-Na, γ-CD-COF-K and α-CD-COF-Li under the same conditions. Thermal stability measurements show that the menthol/γ-CD-COF-Li-ICs effectively stabilize menthol against heat evaporation at elevated temperatures due to the strengthened interaction between menthol and γ-CD-COF-Li. The promising results of this research suggest that rapid advancements in COF technology will provide new opportunities for enhancing the stability of flavoring ingredients in the food industry.
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http://dx.doi.org/10.1002/chem.202402500 | DOI Listing |
Nanoscale
August 2025
State Key Laboratory of Geomicrobiology and Environmental Changes, Faculty of Materials Science and Chemistry, China University of Geosciences, No. 388, Lumo Road, Hongshan District, Wuhan 430074, P. R. China.
Motivated by the growing demand for rare earth elements (REEs), it is crucial to design effective adsorbents capable of separating and reclaiming REEs from acidic wastewater. Herein, a phosphorus-functionalized covalent organic polymer (β-HCCD) was successfully synthesized a straightforward nucleophilic substitution reaction, utilizing two cost-effective monomers, β-cyclodextrin (β-CD) and hexachlorocyclotriphosphazene (HCCP). Owing to the presence of abundant P-O bonds in β-HCCD and the unique cavity structure of β-CD, β-HCCD exhibits adsorption efficiency exceeding 98% for scandium ions (Sc) in an acidic solution with the hydrogen ion concentration ranging from 5 mol L to 10 mol L.
View Article and Find Full Text PDFJ Chromatogr A
August 2025
College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China. Electronic address:
Chiral separation of pharmaceuticals remains a critical challenge in analytical chemistry due to identical physicochemical properties of enantiomers. Chemically bonded Chiral Stationary Phases (CSPs) generally offer superior stability and solvent compatibility compared to physically adsorbed CSPs. Although cyclodextrin-based CSPs are widely used, chemically bonded SBE-β-CD CSPs remain unexplored.
View Article and Find Full Text PDFInt J Biol Macromol
May 2025
Aulin College, Northeast Forestry University, Harbin, Heilongjiang 150000, China; Heilongjiang Provincial Key Laboratory of Ecological Utilization of Forestry-Based Active Substances, Harbin 150040, China. Electronic address:
Multifunctional wound dressings with rapid hemostasis, antimicrobial and anti-inflammatory properties, healing promotion, pain relief, and controlled degradation hold significant clinical potential. Herein, we developed a novel hydrogel system by functionalizing oxidized regenerated cellulose (ORC) with l-lysine (L-Lys) through dynamic Schiff base linkages. This strategy endowed the hydrogel with natural antimicrobial activity and enabled controlled release of L-Lys for tissue regeneration.
View Article and Find Full Text PDFMacromolecules
April 2025
Institut des Matériaux and Institut des Sciences et Ingénierie Chimiques, Laboratoire des Polymères, Bâtiment MXD, Station 12, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
This paper describes the synthesis of supramolecular polymer brushes via surface-initiated polymerization from adamantane-functionalized initiators that are noncovalently bound to β-cyclodextrin- or cucurbit[7]uril-modified substrates. Surface-initiated atom transfer radical polymerization in aqueous media allowed the growth of various hydrophilic polymer brushes with film thicknesses of up to 40 nm from β-cyclodextrin functionalized surfaces. The adamantane moiety not only forms a host-guest complex with β-cyclodextrin, but also with cucurbit[7]uril, which provides opportunities to study the effect of the binding strength of these supramolecular motifs on the film thickness and grafting density of the resulting polymer brushes.
View Article and Find Full Text PDFACS Omega
March 2025
Department of Chemistry and Center for NanoScience, University of Munich (LMU), 81377 München, Germany.
In this work, we report on the synthesis and characterization of cyclodextrin-based nanocarriers, intended as new biogenic and biodegradable drug-delivery agents. Specifically, β-cyclodextrins were covalently cross-linked by carbonyl linkages using carbonyldiimidazole (CDI) and were colloidally stabilized via PEGylation to form β-CD-CO-PEG nanoparticles termed CD-CO NPs. The optimized synthesis results in size-controlled nanoparticles with a narrow particle size distribution and a hydrodynamic diameter around 200-300 nm in water and 100-160 nm as dried powder as observed by scanning electron microscopy.
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