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氧化淀粉/聚(N,N-二甲基氨基乙基甲基丙烯酸酯)半互穿网络冷冻凝胶的制备、表征及吲哚美辛的体外控释评价

Preparation and characterization of oxidized starch/poly(N,N-dimethylaminoethyl methacrylate) semi-IPN cryogels and in vitro controlled release evaluation of indomethacin.

作者信息

Apopei Loghin Diana Felicia, Biliuta Gabriela, Coseri Sergiu, Dragan Ecaterina Stela

机构信息

"Petru Poni" Institute of Macromolecular Chemistry, Grigore Ghica Voda Alley 41A, Iasi 700487, Romania.

"Petru Poni" Institute of Macromolecular Chemistry, Grigore Ghica Voda Alley 41A, Iasi 700487, Romania.

出版信息

Int J Biol Macromol. 2017 Mar;96:589-599. doi: 10.1016/j.ijbiomac.2016.12.071. Epub 2016 Dec 29.

Abstract

Fabrication of novel semi-interpenetrating polymer network (semi-IPN) cryogels by cross-linking polymerization of N,N-dimethylaminoethyl methacrylate (DMAEM) in the presence of either oxidized potato starch (OPS) or oxidized wheat starch (OWS) and their characterization are presented in the paper. The influence of the nature of entrapped polymer on the properties of the composite cryogels was evaluated by the swelling kinetics, FT-IR spectroscopy, scanning electron microscopy, and response at external stimuli such as temperature, pH, and ionic strength. Indomethacin (IDM), taken as a model anti-inflammatory drug, was easily loaded into the composite cryogels by the solvent sorption-evaporation strategy. The in vitro release of IDM from the semi-IPN cryogels was low in simulated gastric fluid at pH 1.3, irrespective of the nature of the entrapped oxidized starch, and consistent in simulated intestinal fluid (SIF) at pH 7.4, the influence of the entrapped polysaccharide being evident. The release mechanism of IDM from the composite cryogels was discussed based on two kinetic models, finding that the drug release at 37°C was pseudo-Fickian diffusion, regardless the cryogel composition.

摘要

本文介绍了通过在氧化马铃薯淀粉(OPS)或氧化小麦淀粉(OWS)存在下,使甲基丙烯酸N,N-二甲基氨基乙酯(DMAEM)交联聚合来制备新型半互穿聚合物网络(semi-IPN)冷冻凝胶及其表征。通过溶胀动力学、傅里叶变换红外光谱、扫描电子显微镜以及对温度、pH值和离子强度等外部刺激的响应,评估了包埋聚合物的性质对复合冷冻凝胶性能的影响。以消炎痛(IDM)作为模型抗炎药物,通过溶剂吸附-蒸发策略将其轻松负载到复合冷冻凝胶中。在pH 1.3的模拟胃液中,无论包埋的氧化淀粉的性质如何,IDM从semi-IPN冷冻凝胶中的体外释放量都很低,而在pH 7.4的模拟肠液(SIF)中则较为一致,包埋多糖的影响很明显。基于两种动力学模型讨论了IDM从复合冷冻凝胶中的释放机制,发现无论冷冻凝胶组成如何,37°C下药物释放均为伪菲克扩散。

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