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基于海藻酸钠水凝胶/壳聚糖胶束复合材料的新型控释给药系统。

A novel controlled drug delivery system based on alginate hydrogel/chitosan micelle composites.

机构信息

School of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.

School of Pharmacy, Lanzhou University, 199 Donggang West Road, Lanzhou 730000, China.

出版信息

Int J Biol Macromol. 2018 Feb;107(Pt A):855-864. doi: 10.1016/j.ijbiomac.2017.09.065. Epub 2017 Sep 19.

DOI:10.1016/j.ijbiomac.2017.09.065
PMID:28935541
Abstract

In this study, we present a novel cross-linked unimolecular micelle based on chitosan. For controlling drug delivery via oral administration, emodin (EMO) encapsulated micelles were loaded into sodium alginate hydrogel matrix to construct the pH-sensitive hydrogel/micelle composites. The optimized formulation of micelle that consists of 8.06% CaCl, 1.71% chitosan and 26.52% β-GP was obtained by the combination of Box-Behnken experimental design and response surface methodology. The morphological analysis showed that the micelles exhibited a smaller diameter of about 80nm in aqueous solution, but dilated to 100-200nm in hydrogel owing to the formation of polyelectrolyte complexes. The physical characteristics in simulated digestive fluids were investigated, demonstrating that the ratio of hydrogel to micelle distinctly affected swelling, degradation and in vitro drug release behaviors. The hydrogel/micelle (1:1) exhibited a sustained-release profile, while hydrogel/micelle (3:1) exhibited a colon-specific profile. Their corresponding release mechanisms revealed that the release of drug from these two formulations followed a complex process, in which several mechanisms were involved or occurred simultaneously. These results demonstrated that the pH-sensitive hydrogel/micelle composites constructed with biocompatible materials can be a promising sustained-release or site-specific drug delivery system for instable or hydrophobic drugs.

摘要

在这项研究中,我们提出了一种基于壳聚糖的新型交联单分子胶束。为了通过口服给药控制药物传递,将大黄素(EMO)包封的胶束载入海藻酸钠水凝胶基质中,以构建 pH 敏感的水凝胶/胶束复合材料。通过 Box-Behnken 实验设计和响应面法相结合,得到了由 8.06% CaCl、1.71%壳聚糖和 26.52%β-GP 组成的优化胶束配方。形态分析表明,胶束在水溶液中表现出约 80nm 的较小直径,但在水凝胶中膨胀至 100-200nm,这是由于形成了聚电解质复合物。在模拟消化液中的物理特性进行了研究,结果表明水凝胶与胶束的比例明显影响膨胀、降解和体外药物释放行为。水凝胶/胶束(1:1)呈现出持续释放的特征,而水凝胶/胶束(3:1)则呈现出结肠特异性的特征。它们相应的释放机制表明,这两种制剂的药物释放遵循一个复杂的过程,其中涉及或同时发生了几种机制。这些结果表明,由生物相容性材料构建的 pH 敏感水凝胶/胶束复合材料可以成为一种有前途的不稳定或疏水性药物的持续释放或定位药物传递系统。

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