首页> 外文期刊>The Journal of automatic chemistry >Polymorphism in Commercial Sources of Fusidic Acid: A Comparative Study of the In Vitro Release Characteristics of Forms I and III from a Marketed Pharmaceutical Cream
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Polymorphism in Commercial Sources of Fusidic Acid: A Comparative Study of the In Vitro Release Characteristics of Forms I and III from a Marketed Pharmaceutical Cream

机译:商业上的夫斯地酸来源的多态性:从市售的药膏中形式I和III的体外释放特性的比较研究。

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A comparison of the polymorphic forms of 3 commercial sources of fusidic acid using FTIR and XRPD techniques has been performed in this study. It has been demonstrated that polymorphic Forms I and III are currently available on the commercial market. The influence of the observed polymorphism on the stability of the drug substance in bulk form has been investigated through stability and stress testing according to current ICH guidelines. Significant differences were detected between commercial sources with regard to the stability of the bulk substance under photolytic and humidity stress conditions. When properly packaged in an inert atmosphere, fusidic acid from all 3 manufacturers showed a comparable stability. The effects of the observed polymorphic differences on the intrinsic dissolution rate of the drug substance and its in vitro release from the marketed drug product Fusicutan? plus Betamethasone cream have been investigated. Results indicated that the release rate of the drug substance is similar for polymorphic Forms I and III, allowing both forms to be used during manufacture without affecting the safety or efficacy of the drug product.
机译:在这项研究中,已经进行了使用FTIR和XRPD技术对3种商业化夫西地酸来源的多晶型形式的比较。已经证明,多晶型I和III目前可在商业市场上获得。根据当前的ICH指南,通过稳定性和压力测试,研究了观察到的多态性对散装原料药稳定性的影响。在散装物质在光解和湿度胁迫条件下的稳定性方面,商业来源之间发现了显着差异。当在惰性气氛中正确包装时,所有3家制造商的夫西地酸都显示出可比的稳定性。观察到的多态性差异对原料药固有溶解速率及其从市售药品Fusicutan?中体外释放的影响。加倍他米松乳膏已被研究。结果表明,多晶型形式I和III的药物释放速率相似,允许两种形式都可在生产过程中使用,而不会影响药物产品的安全性或功效。

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