肿胀 的
热重分析
核化学
柠檬酸
生物相容性
化学
药物输送
毒品携带者
控制释放
滴定法
高分子化学
环糊精
傅里叶变换红外光谱
细胞毒性
自愈水凝胶
极限抗拉强度
材料科学
化学工程
有机化学
体外
纳米技术
生物化学
复合材料
工程类
作者
Vishwajeet Sampatrao Ghorpade,A. V. Yadav,Remeth J. Dias,Kailas K. Mali
摘要
ABSTRACT β‐cyclodextrin grafted hydroxyethylcellulose (βCD‐ g ‐HEC) hydrogel films were prepared for the controlled release of poorly soluble model drug (ketoconazole) using citric acid as crosslinking agent. The active βCD and carboxyl content of the hydrogel films were determined by phenolphthalein assay and acid–base titration. The films were characterized by solid state 13 C NMR, ATR–FTIR, thermogravimetric analysis, and differential scanning calorimetric, and analyzed for tensile strength, swelling ratio, drug loading, release, hemocompatibility, in vitro cytotoxicity, and implantation test. An increase in the concentration of βCD in feed increased the active βCD content of the hydrogel films but reduced their extent of interpolymer crosslinking. The βCD‐ g ‐HEC hydrogel films with high active βCD content showed maximum drug loading whereas those with high crosslinking density were capable of controlling the drug release for long duration. Hemolysis assay and in vitro cytotoxicity study revealed the biocompatible nature of the hydrogel films whereas implantation test indicated their minimal inflammatory effect. From the overall results, βCD‐ g ‐HEC hydrogel films were found to be better alternative to the previously reported βCD‐HPMC and βCD‐CMC hydrogel films for enhanced loading and long‐term release, respectively, of the poorly soluble drugs. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 46452.
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