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基于壳聚糖的多响应水凝胶作为药物释放载体的研究:一项临床前研究。

study of chitosan-based multi-responsive hydrogels as drug release vehicles: a preclinical study.

作者信息

Gull Nafisa, Khan Shahzad Maqsood, Zahid Butt Muhammad Taqi, Khalid Syed, Shafiq Muhammad, Islam Atif, Asim Sumreen, Hafeez Sadaf, Khan Rafi Ullah

机构信息

Department of Polymer Engineering and Technology, University of the Punjab Lahore 54590 Pakistan

College of Engineering and Emerging Technology, University of the Punjab Lahore 54590 Pakistan.

出版信息

RSC Adv. 2019 Oct 1;9(53):31078-31091. doi: 10.1039/c9ra05025f. eCollection 2019 Sep 26.

DOI:10.1039/c9ra05025f
PMID:35529386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9072301/
Abstract

Systematic administration of painkillers and anti-inflammatory drugs is routinely employed to minimize pain and bodily disorders. Controlled drug delivery has the potential to improve the outcomes of disorders by providing sustained exposure to efficacious drug concentrations. Herein, we report the fabrication of multi-responsive hydrogels using reactive and functional polymers such as chitosan and polyvinyl pyrrolidone by varying the concentration of a cleavable crosslinker, tetraethyl orthosilicate. The swelling indices of the hydrogels were evaluated in distilled water, solutions with different pH values and different electrolytes. FTIR, WAXRD and TGA were conducted to investigate the structures, crystallinities and thermal stabilities of the prepared multi-responsive hydrogels, respectively. The ultimate tensile strength and elongations at break of the fabricated hydrogels were investigated to assess their mechanical stability. Optical microscopy, biodegradation, antimicrobial and cytotoxicity analyses were further carried out to verify the magnified crosslinked and porous structures, biodegradabilities, biocompatibilities and toxic behaviour of the as-prepared hydrogels, respectively. Drug release analysis was conducted to evaluate their release behaviour in PBS, SGF, SIF and electrolyte solutions. The overall results indicate the successful development of novel, non-toxic and sustained drug deliverable hydrogels, which can be considered as a paramount success towards the fabrication of controlled drug delivery systems.

摘要

通常会系统地使用止痛药和消炎药,以尽量减轻疼痛和身体不适。控释给药有可能通过持续提供有效药物浓度来改善疾病的治疗效果。在此,我们报告了通过改变可裂解交联剂原硅酸四乙酯的浓度,使用壳聚糖和聚乙烯吡咯烷酮等反应性和功能性聚合物制备多响应水凝胶的过程。在蒸馏水中、不同pH值的溶液和不同电解质中评估了水凝胶的溶胀指数。分别进行了傅里叶变换红外光谱(FTIR)、广角X射线衍射(WAXRD)和热重分析(TGA),以研究制备的多响应水凝胶的结构、结晶度和热稳定性。研究了制备的水凝胶的极限拉伸强度和断裂伸长率,以评估其机械稳定性。进一步进行了光学显微镜、生物降解、抗菌和细胞毒性分析,以分别验证所制备水凝胶的放大交联和多孔结构、生物降解性、生物相容性和毒性行为。进行了药物释放分析,以评估它们在磷酸盐缓冲盐水(PBS)、模拟胃液(SGF)、模拟肠液(SIF)和电解质溶液中的释放行为。总体结果表明成功开发了新型、无毒且可实现持续药物递送的水凝胶,这可被视为在制备控释给药系统方面取得的一项重大成功。

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