采用分数因子设计筛选吡罗昔康自纳米乳化给药系统

Septiawan Adi Nugroho, I. Kuncahyo, D. Marlina
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引用次数: 0

摘要

吡罗昔康属BCSⅱ类,溶解度低。自纳米乳化给药系统(SNEDDS)被认为是增加吡罗西康的溶解度和释放的潜在途径。本研究采用分数因子设计26-2 (FFD)筛选吡罗昔康SNEDDS的成分和成分比。吡罗西康SNEDDS的DFT开发中使用的变量是油的类型和浓度(三乙酸和油酸)、表面活性剂(kolliphor EL和Tween 60)和共表面活性剂(Transcutol和peg400)。采用不同比例的吡罗昔康SNEDDS组分进行了16趟的FFD实验,并通过乳化时间、透光率、液滴大小、载药量等关键参数对其进行了表征。采用单因素图分析确定PKM SNEDDS的组成和组成比。结果表明:三乙酸酯(油)、表面活性剂kolliphor EL、助表面活性剂Transcutol对吡罗昔康SNEDDS的形成贡献最大,油比范围为11.11 ~ 28.57%,表面活性剂44.44 ~ 77.78%,助表面活性剂11.11 ~ 44.44%;
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SCREENING OF PIROXICAM SELF-NANOEMULSIFYING DRUG DELIVERY SYSTEM (SNEDDS) USING FRACTIONAL FACTORIAL DESIGN
Piroxicam belongs to BCS class II and has low solubility. Self-nanoemulsifying drug delivery systems (SNEDDS) are considered a potential approach for increasing the solubility and release of piroxicam. This study aimed to select the components and component ratios of piroxicam SNEDDS using fractional factorial design 26-2 (FFD). The variables used in the DFT development of piroxicam SNEDDS are the type and concentration of oil (triacetin and oleic acid), surfactant (kolliphor EL and Tween 60), and co-surfactants (Transcutol and PEG 400). The FFD results showed 16 runs with different proportions of the piroxicam SNEDDS components, which were then characterized by critical parameters including emulsification time, %transmittance, droplet size, and drug loading. The components and component ratios of the PKM SNEDDS were determined using single-factor plot analysis. The results showed that triacetin (oil), kolliphor EL (surfactant), Transcutol (co-surfactant) had the greatest contribution to the formation of piroxicam SNEDDS with an oil ratio range of 11.11–28.57%, surfactant 44.44–77.78%, co-surfactant 11.11–44.44 %.
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