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Mechanism of Drug release from Pluronic F127-based in-situ hydrogel

机译:从Pluronic F127基地水凝胶中药物释放机制

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Objective: To investigate the drug release mechanism from Pluronic F127 hydrogel. Method: Drug release from PF127 hydrogel was systematically studied by membrane-less model. The influence of PF127 concentration (20%, 25% and 30%) and the molecular weight of model drug (F-Na, FITC-rHV2 and FITC-BSA) were evaluated. The linear relationship between drug release and gel dissolution was discussed. Results: Both drug release and gel dissolution both followed zero-order kinetics. The release rate and gel dissolution rate both depended on the concentration of PF 127. Good linear relationship was observed between drug release and gel dissolution Conclusion: The release of drug from Pluronic F127 in-situ hydrogel was controlled by the dissolution of gel.
机译:目的:探讨Pluronic F127水凝胶的药物释放机制。方法:通过薄膜模型系统地研究了来自PF127水凝胶的药物释放。评估PF127浓度(20%,25%和30%)和模型药物(F-Na,FITC-RHV2和FITC-BSA)的分子量的影响。讨论了药物释放与凝胶溶解之间的线性关系。结果:药物释放和凝胶溶解均均匀零级动力学。剥离率和凝胶溶解率均取决于PF 127的浓度。药物释放和凝胶溶解之间观察到良好的线性关系结论:通过凝胶的溶解来控制来自Pluronic F127原位水凝胶的药物的释放。

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