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通过硫醇-烯光点击交联法简便合成壳聚糖基水凝胶和微凝胶

Facile Synthesis of Chitosan-Based Hydrogels and Microgels through Thiol-Ene Photoclick Cross-Linking.

作者信息

Michel Sarah E S, Dutertre Fabien, Denbow Mark L, Galan M Carmen, Briscoe Wuge H

机构信息

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, United Kingdom.

Fetal Medicine Unit, St Michael's Hospital, Southwell Street, Bristol BS2 8EG, United Kingdom.

出版信息

ACS Appl Bio Mater. 2019 Aug 19;2(8):3257-3268. doi: 10.1021/acsabm.9b00218. Epub 2019 Jul 16.

Abstract

Polysaccharide-based microgels are effective vectors for the delivery of biopharmaceutics and functional components in tissue engineering due to their bioactivity and biocompatibility. Currently, the synthesis of chemically cross-linked microgels typically requires long reaction times and a high-energy input and are low yielding due to low volumes of the water phase used. Herein, we report the synthesis of norbornene-derived chitosan (CS-nbn-COOH), which can undergo rapid gelation in the presence of a thiolated cross-linker through the highly efficient thiol-ene photoclick reaction. This water-soluble photo-cross-linkable derivative, synthesized on scale via a single step from native chitosan and commercially available carbic anhydride, represents the first example of a norbornene-functionalized CS to the best of our knowledge. Microgels with controlled cross-linking densities and diameters varying between 100 and 400 nm were obtained via a low-energy water-in-oil nanoemulsion templating method at room temperature, with photo-cross-linking initiated in a flow reactor powered with a domestic UV-A lamp, a method that is suitable for the scale-up synthesis of the microgels. We also demonstrate that the resulting microgels were nontoxic to human dermofibroblasts (HDF) cell lines and that residual norbornene groups could be reacted in a late stage through tetrazine ligation, highlighting the potential of these microgels as scaffolds for functional nanomaterials with biomedical applications.

摘要

基于多糖的微凝胶由于其生物活性和生物相容性,是组织工程中生物药物和功能成分递送的有效载体。目前,化学交联微凝胶的合成通常需要较长的反应时间和高能量输入,并且由于水相使用量少而产率较低。在此,我们报道了降冰片烯衍生的壳聚糖(CS-nbn-COOH)的合成,它可以在硫醇化交联剂存在下通过高效的硫醇-烯光点击反应快速凝胶化。据我们所知,这种通过天然壳聚糖和市售碳酐一步法大规模合成的水溶性光可交联衍生物,是降冰片烯功能化壳聚糖的首个实例。通过低能量的油包水纳米乳液模板法在室温下获得了具有可控交联密度且直径在100至400纳米之间变化的微凝胶,光交联在由家用UV-A灯供电的流动反应器中引发,该方法适用于微凝胶的放大合成。我们还证明了所得微凝胶对人皮肤成纤维细胞(HDF)细胞系无毒,并且残留的降冰片烯基团可以在后期通过四嗪连接反应,突出了这些微凝胶作为具有生物医学应用的功能纳米材料支架的潜力。

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