美洛昔康
肺表面活性物质
溶解度
溶解
化学
药物输送
色谱法
吸收(声学)
400号桩
药理学
材料科学
有机化学
医学
生物化学
复合材料
聚乙二醇
作者
Selly Harnesa Putri,Lina Winarti
出处
期刊:Pharmacy Education
[International Pharmaceutical Federation (FIP)]
日期:2023-10-10
卷期号:23 (4): 71-75
标识
DOI:10.46542/pe.2023.234.7175
摘要
Background: Meloxicam has low water solubility, which affects the dissolution and level of absorption. Objective: The study aimed to develop a self-nano-emulsifying drug delivery system (SNEDDS) based on a non-ionic surfactant combination and evaluate the release kinetics model using the DDsolver program. Methods: Oil, surfactant, and co-surfactant were selected based on the solubility of meloxicam. Results: The best formula showed that 10% of castor oil, 70% of surfactant (tween 80: chromophore RH 40 in 1:1), and 20% of PEG 400 could develop SNEDDS with the 99.84±0.04% percentage of transmittance, 15.47±0.72 sec emulsifying time, and below 50 nm droplet size. The optimised formula is also stable and resistant to various dilutions and pH The dissolution efficiency (DE0-60) reveals a 5.27-fold increase compared to non-SNEDDS meloxicam. Meloxicam follows Korsmeyer-Peppas release kinetics, while meloxicam SNEDDS follows the Hixon-Crowell model. Conclusion: The best formula of SNEDDS consisting of a surfactant combination generate improvement in vitro dissolution of meloxicam.
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