聚n -异丙基丙烯酰胺水凝胶的溶胀动力学及其在抗糖尿病药物传递系统中的应用

Danjatau W. Dogo, H. Louis, Nkafamiya I. Iliya, Akakuru U. Ozioma, Adeleye T. Aderemi, Barminas Stware
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引用次数: 2

摘要

聚n -异丙基丙烯酰胺(pnipam)水凝胶中的charantin溶胀动力学是通过直接称重完成的,然后将凝胶在温控水浴箱内的受控温度下浸泡在流体/药物溶液中。对其作为抗糖尿病药物传递系统的应用进行了研究。在控制pH为4.5的条件下,从苦瓜果实和叶片中提取夏兰汀。通过改变丙烯酰胺在(3-12)%之间的含量来制备PNIPAM,结果表明,在蒸馏水中,低临界溶液温度(LCST)从32- 43℃升高,这表明了直接关系。从蒸馏水、胰岛素和charantin溶液中改变溶液的效果可以看出,溶液的极性越高,水凝胶的LCST越低。在浓度为52.61 μg/mL的Charantin溶液中,水凝胶N1、N2、N3和N4对Charantin的吸附量分别为(42.51、44.57、43.55和44.61)μg/mL。利用傅里叶变换红外光谱(FTIR)对水凝胶进行表征,表明水凝胶基质与charantin分子之间存在物理相互作用。水凝胶的扩散系数为1.48 × 10-10 ~ 5.08 × 10-8 M2/s,释放指数≥0.5,为非菲克扩散释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Swelling Kinetics of Poly(N-Isopropylacrylamide)-Based Hydrogel and its Application as Anti-Diabetic Drugs Delivery System
The swelling kinetics of charantin from poly (N-isopropyl acrylamide), PNIPAM–based hydrogel, is accomplished through direct weighing, before soaking the gel in fluid/drug solution at controlled temperatures inside a temperature-controlled water bath. The investigation was carried out for application as anti-diabetic drug delivery system. Charantin was extracted from bitter melon fruit and leaf under a controlled pH of 4.5. The preparation of PNIPAM was done by varying the acrylamide between (3-12)% and show increase in the lower critical solution temperature (LCST) from 32- 43℃ which indicates a direct relationship in distilled water. The effect of changing solution from distilled water, insulin, and charantin solution, shows that the higher the polarity of the solution, the lower the LCST of the hydrogel. Charantin loaded on hydrogels N1, N2, N3, and N4 were found to be (42.51, 44.57, 43.55 and 44.61)μg/mL, respectively, when soaked in charantin solution of 52.61 μg/mL. Characterization of the hydrogels using Fourier transformed infrared (FTIR) spectroscopy shows that there is physical interaction between the hydrogel matrix and the charantin molecules. The diffusivity of the hydrogels ranged from 1.48 x 10-10 to 5.08 x 10-8 M2/s and their release exponents were ≥ 0.5 indicative of non-Fickian difusional release.
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