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A novel method for synthesizing PEGylated chitosan nanoparticles: strategy, preparation, and in vitro analysis

机译:一种合成聚乙二醇化壳聚糖纳米粒子的新方法:策略,制备和体外分析

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摘要

Preparation of poly (ethylene glycol) (PEG)-grafted chitosan is essential for improving the biocompatibility and water solubility of chitosan. Presently available methods for this have limitations. This article describes a new method for preparing PEGylated chitosan nanoparticles. For this chitosan was chemoselectively modified using a novel scheme at the C6 position of its repeating units by PEG. The amine groups at the C2 position of the chitosan were protected using phthalic anhydride. Sodium hydride was used to catalyze the etherification reaction between chlorinated chitosan and methyl-PEG, and PEG-grafted chitosan was successfully synthesized. Each step was characterized using 13C nuclear magnetic resonance and Fourier transform infrared. After PEGylation the phthaloylated chitosan was successfully deprotected using hydrazine monohydrate. The synthetic scheme proposed demonstrates a new method for grafting PEG onto chitosan with a moderate degree of substitution. The potential of this polymer in nanoparticle preparation using an ionic gelation method and its gene delivery potentials were investigated by complexing a fluorescently labeled control siRNA. The result showed that suitable nanoparticles can be synthesized using this polymer and that they have capacity to carry genes and provide adequate transfection efficacy with no toxicity when tested in neuronal cells.
机译:制备聚乙二醇(PEG)接枝的壳聚糖对于改善壳聚糖的生物相容性和水溶性至关重要。目前可用的方法有局限性。本文介绍了一种制备聚乙二醇化壳聚糖纳米颗粒的新方法。为此,使用新颖的方案通过PEG对其壳的重复单元的C6位置进行化学选择性修饰。使用邻苯二甲酸酐保护壳聚糖C2位的胺基。用氢化钠催化氯化壳聚糖与甲基-PEG的醚化反应,成功合成了PEG接枝的壳聚糖。每个步骤均使用13 C核磁共振和傅立叶变换红外光谱进行表征。聚乙二醇化后,邻苯二甲酰化壳聚糖使用肼一水合物成功脱保护。提出的合成方案证明了一种以中等取代度将PEG接枝到壳聚糖上的新方法。通过络合荧光标记的对照siRNA,研究了该聚合物在使用离子凝胶法制备纳米颗粒中的潜力及其基因传递潜力。结果表明,使用这种聚合物可以合成合适的纳米颗粒,并且在神经元细胞中进行测试时,它们具有携带基因的能力,并提供足够的转染功效而没有毒性。

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