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通过点击化学反应将壳聚糖和葡聚糖直接交联制备双降解性生物杂化微凝胶。

Dual-Degradable Biohybrid Microgels by Direct Cross-Linking of Chitosan and Dextran Using Azide-Alkyne Cycloaddition.

机构信息

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Worringerweg 2, 52074 Aachen, Germany.

DWI-Leibniz-Institute for Interactive Materials e.V., Forckenbeckstraße 50, 52056 Aachen, Germany.

出版信息

Biomacromolecules. 2020 Dec 14;21(12):4933-4944. doi: 10.1021/acs.biomac.0c01158. Epub 2020 Nov 19.

Abstract

In this work, biocompatible and degradable biohybrid microgels based on chitosan and dextran were synthesized for drug delivery applications. Two kinds of bio-based building blocks, alkyne-modified chitosan and azide-modified dextran, were used to fabricate microgels via single-step cross-linking in water-in-oil emulsions. The cross-linking was initiated in the presence of copper(II) without the use of any extra cross-linkers. A series of pH-responsive and degradable microgels were successfully synthesized by varying the degree of cross-links. The microgels were characterized using H NMR and FTIR spectroscopy which proved the successful cross-linking of alkyne-modified chitosan and azide-modified dextran by copper(II)-mediated click reaction. The obtained microgels exhibit polyampholyte character and can carry positive or negative charges in aqueous solutions at different pH values. Biodegradability of microgels was shown at pH 9 or in the presence of Dextranase due to the hydrolysis of carbonate esters in the microgels or 1,6-α-glucosidic linkages in dextran structure, respectively. Furthermore, the microgels could encapsulate vancomycin hydrochloride (VM), an antibiotic, with a high loading of approximately 93.67% via electrostatic interactions. The payload could be released in the presence of Dextranase or under an alkaline environment, making the microgels potential candidates for drug delivery, such as colon-specific drug release.

摘要

在这项工作中,合成了基于壳聚糖和葡聚糖的生物相容性和可降解的生物杂化微凝胶,用于药物输送应用。使用两种生物基构建块,炔基改性壳聚糖和叠氮改性葡聚糖,通过在水包油乳液中单步交联来制备微凝胶。在没有使用任何额外交联剂的情况下,在铜(II)的存在下引发交联。通过改变交联度,成功合成了一系列 pH 响应和可降解的微凝胶。使用 H NMR 和 FTIR 光谱对微凝胶进行了表征,证明了炔基改性壳聚糖和叠氮改性葡聚糖通过铜(II)介导的点击反应成功交联。所得微凝胶具有聚两性电解质的性质,在不同 pH 值的水溶液中可以带正电荷或负电荷。由于微凝胶中碳酸酯酯的水解或葡聚糖结构中 1,6-α-糖苷键的水解,微凝胶在 pH 9 或存在葡聚糖酶的情况下表现出可生物降解性。此外,微凝胶可以通过静电相互作用包封盐酸万古霉素(VM),一种抗生素,载药量约为 93.67%。在存在葡聚糖酶或在碱性环境下,有效载荷可以释放,这使得微凝胶成为药物输送的潜在候选物,例如结肠特异性药物释放。

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