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首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Preparation and in vitro and in vivo evaluation of quercetin-loaded mixed micelles for oral delivery
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Preparation and in vitro and in vivo evaluation of quercetin-loaded mixed micelles for oral delivery

机译:制备和体外和体内评价槲皮素负载混合胶束进行口服递送

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Quercetin (QT) is a plant polyphenol with various pharmacological properties. However, the low water solubility limits its therapeutic efficacy. In the present study, QT-loaded sodium taurocholate-Pluronic P123 (QT-loaded ST/P123) mixed micelles were developed and characterized, and the effect of the formulation on improving the water solubility of QT was investigated. QT-loaded ST/P123 mixed micelles were prepared by thin film hydration-direct dissolution and optimized by uniform design. The optimal formulation possessed high drug loading (12.6%) and entrapment efficiency (95.9%) in small (16.20nm) spherically-shaped micelles. A low critical micelle concentration indicated that the micelles were stable, and they showed a sustained release pattern, as determined in vitro in simulated gastric fluid and intestinal fluid. Pharmacokinetic evaluation showed the C-max and AUC(0-24) were 1.8-fold and 1.6-fold higher than the QT suspension. The present results indicate that QT-loaded ST/P123 micelles are potential candidates to improve the solubility and oral bioavailability of QT.
机译:槲皮素(QT)是一种具有各种药理学特性的植物聚酚。然而,低水溶性限制其治疗效果。在本研究中,开发出QT加载的牛磺硫酸钠-PluronicP123(QT制备的ST / P123)混合胶束,并研究了制剂对改善QT水溶性的影响。通过薄膜水合直接溶解和​​通过均匀设计进行优化制备QT负载的ST / P123混合胶束。最佳配方具有高药物负载(12.6%)和小(16.20nm)球形胶束的夹带效率(95.9%)。低临界胶束浓度表明胶束稳定,并且它们显示出持续释放图案,如模拟胃液和肠液中的体外测定。药代动力学评价显示C-MAX和AUC(0-24)的1.8倍,比QT悬浮液高1.6倍。本结果表明,QT负载的ST / P123胶束是提高Qt的溶解度和口服生物利用度的潜在候选。

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