替诺昔康乳质体的处方及评价

S. M. Maru
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引用次数: 0

摘要

本研究旨在探讨表面活性剂span 60、胆固醇和磷酸二酯的不同配比对包膜替诺西康乳小体的形态、粒径分布、包封效率和体外药物释放的影响。然后使用白化大鼠的血液进行niosomes的体外稳定性研究。替诺昔康颗粒体在24 h内呈双相缓释模式。结果表明,替诺昔康颗粒体可作为透皮治疗的载体。关键词:Niosomes,替诺昔康,胆固醇,Span 60,磷酸二酯《东非和中非医药科学杂志》Vol. 8 (3) 2005: pp 62-66
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Evaluation of Tenoxicam Niosomes
This study aimed at investigating the influence of varying proportions of the surfactant span 60, cholesterol and dicetylphosphate on the morphology, particle size distribution, entrapment efficiency and in vitro drug release of encapsulated tenoxicam niosomes. In vitro stability studies of the niosomes were then performed using blood from albino rats. Drug release from the niosomes showed biphasic sustained release pattern of tenoxicam for a period of 24 h. The results obtained show that niosomes of tenoxicam can be prepared as carriers for transdermal therapy.. Keywords : Niosomes, Tenoxicam, Cholesterol, Span 60, Dicetyl phosphate The East and Central African Journal of Pharmaceutical Sciences Vol. 8 (3) 2005: pp 62-66
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