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作 者:陶明涛[1] 沈静[1] 王静静[1] 李人宇[1]
出 处:《药学与临床研究》2013年第6期622-624,共3页Pharmaceutical and Clinical Research
摘 要:目的:开发夫西地酸凝胶剂并研究其体外渗透。方法:加热搅拌法制备夫西地酸凝胶剂,高效液相色谱法测定其主药含量,透皮扩散考察体外释放特性。结果:凝胶剂中夫西地酸为标示含量的96.70%(RSD=0.42%),体外释放方程lnQ=0.3833lnt-0.8241(r2=0.9996)。结论:夫西地酸凝胶药物含量均匀,质量控制方法可靠,体外释放符合Ritger-Peppas方程。Objective: To develop the new gel formulation of fusidic acid and explore its in vitro transdermal permeation. Methods: The gel was prepared by heatingagitating,and the content of fusidic acid was determined by high efficiency liquid chromatography,the in vitro release characteristics was researched by transdermal diffusing. Results: The relative content of fusidic acid was 96.70%(RSD = 0.42%),the in vitro release equation was lnQ=0.3833lnt-0.8241(r2=0.9996). Conclusion: The contents of the preparation are uniform,the method of quality control is reliable,the in vitro release characteristics accords with the Ritger-Peppas equation.
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