Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, 3584 CG Utrecht, The Netherlands; Research and Development Department, Tiofarma B.V., Hermanus Boerhaavestraat 1, 3261 ME Oud-Beijerland, The Netherlands.
Research and Development Department, Tiofarma B.V., Hermanus Boerhaavestraat 1, 3261 ME Oud-Beijerland, The Netherlands.
Eur J Pharm Sci. 2018 May 30;117:1-7. doi: 10.1016/j.ejps.2018.02.001. Epub 2018 Feb 3.
Corticosteroids are widely used in topical formulations such as creams (aqueous) and ointments (non-aqueous). The generally used corticosteroids show large molecular resemblance, where especially the 20-keto-21-hydroxyl group bound to the 17 carbon is important for their chemical stability. Oxidation in both aqueous and non-aqueous environment occurs for triamcinolone acetonide (TCA), hydrocortisone (HC) and desoximethasone (DS). Besides the 20-keto-21-hydroxyl group, TCA, HC and DS have different other moieties attached to the same C17. These moieties are shown to influence not only the type of degradation product formed but also the degradation kinetics. Seven degradation products are found in total and a degradation mechanism is proposed. Furthermore the transesterfication of betamethasone-17-valerate to betamethasone-21-valerate is shown to occur both in aqueous and non-aqueous environment. Finally, a comprehensive scheme of degradation pathways is presented that is applicable for both aqueous and non-aqueous formulations.
皮质类固醇广泛用于乳膏(水性)和软膏(非水性)等局部制剂。一般使用的皮质类固醇显示出很大的分子相似性,特别是结合到 17 号碳的 20-酮-21-羟基对于它们的化学稳定性很重要。在水性和非水性环境中,曲安奈德(TCA)、氢化可的松(HC)和去甲泼尼龙(DS)都会发生氧化。除了 20-酮-21-羟基外,TCA、HC 和 DS 还在同一个 C17 上连接了不同的其他部分。这些部分不仅影响形成的降解产物的类型,而且影响降解动力学。总共发现了七种降解产物,并提出了一种降解机制。此外,还表明倍他米松-17-戊酸酯在水性和非水性环境中均会发生酯化转化为倍他米松-21-戊酸酯。最后,提出了一个适用于水性和非水性制剂的全面降解途径方案。