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Effects of formulation and technology on release profile of Ornidazole biodegradable gel

机译:配方和技术对矿石生物降解凝胶释放曲线的影响

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OBJECTIVE To study the effects of formulation and technology factors on drug release profile of Ornidazole biodegradable gel. METHODS Poly (lactic-co-glycolic acid) (PLGA) was used to fabricate the gel. HPLC was used to determine drug content in the gel and UV detection was used to determine in vitro release rate. Effects of type of PLGA and solvent, the weight ratio of PLGA to solvent, the ratio of drug to PLGA were studied. RESULTS The optimum formulation consisted of 49% PLGA (50:50 15000), 49% N-ethyl-2-pyrrolidone and 2% Ornidazole. The gel could sustain release for 7 days, the release profile during 0~5 day was conformed to zero-order kinetics (R2=0.9943). CONCLUSION The gel showed a good controlled release characteristics. The process and the formulation of oridazole gel was simple and available.
机译:目的探讨配方和技术因素对奥尼唑生物降解凝胶药物释放曲线的影响。方法采用聚(乳酸二乙醇酸)(PLGA)制造凝胶。 HPLC用于确定凝胶中的药物含量,使用UV检测来确定体外释放速率。 PLGA和溶剂类型的影响,研究了PLGA对溶剂的重量比,研究了药物与PLGA的比例。结果最佳制剂由49%PLGA(50:50 15000),49%N-乙基-2-吡咯烷酮和2%Ornidazole组成。凝胶可以维持7天的释放,释放曲线在0〜5天期间符合零级动力学(R2 = 0.9943)。结论凝胶显示出良好的控释特征。奥咪唑凝胶的方法和制剂简单且可用。

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