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巯基化维生素 E 聚乙二醇 1000 琥珀酸酯胶束增强两性霉素 B 经鼻黏膜给药用于治疗白念珠菌。

Enhanced transmucosal delivery of itraconazole by thiolated d-ɑ-tocopheryl poly(ethylene glycol) 1000 succinate micelles for the treatment of Candida albicans.

机构信息

Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand; Center of Excellence in Innovative Drug Delivery and Nanomedicine, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand.

Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand.

出版信息

Eur J Pharm Biopharm. 2017 Nov;120:107-115. doi: 10.1016/j.ejpb.2017.08.012. Epub 2017 Sep 1.

Abstract

This study aimed to investigate the transmucosal delivery of itraconazole (ITZ) by thiolated d-ɑ-tocopheryl poly(ethylene glycol) 1000 succinate (TPGS-Cys) micelles. TPGS-Cys polymer was successfully synthesized by the simple coupling between carboxyl-activated TPGS and Cys as confirmed by NMR and FTIR techniques. Afterwards, the TPGS/TPGS-Cys micelles were prepared using the blend of TPGS and TPGS-Cys at 10:0, 7:3, 5:5, 3:7 and 0:10mass ratios. All micelles had the size ranged from 8 to 10nm with narrow size distribution and showed spherical in shape. The surface of the 10:0 TPGS micelles exhibited negatively charge while, the TPGS-Cys micelles demonstrated the slightly positive surface charge. The critical micelle concentration, loading capacity and release profiles of TPGS/TPGS-Cys micelles were comparable to the TPGS micelles. The release of ITZ from all micelles was biphasic and sustained in simulated saliva fluid over 48h. The 3:7 and 0:10 TPGS/TPGS-Cys micelles had a good mucoadhesive property. Meanwhile, only 0:10 TPGS/TPGS-Cys micelles enhanced the permeability through buccal mucosa and potentiated the antifungal activity of ITZ against Candida albicans by at least 1.35 folds as compared to ITZ alone. Therefore, this formulation can be further developed for the transmucosal delivery of ITZ for the treatment of C. albicans.

摘要

本研究旨在探讨巯基化 d-α-生育酚聚乙二醇 1000 琥珀酸酯(TPGS-Cys)胶束经黏膜递药传递酮康唑(ITZ)的情况。通过羧基活化的 TPGS 与 Cys 的简单偶联,成功合成了 TPGS-Cys 聚合物,这一点通过 NMR 和 FTIR 技术得到了证实。随后,通过 TPGS 和 TPGS-Cys 以 10:0、7:3、5:5、3:7 和 0:10 的质量比混合制备 TPGS/TPGS-Cys 胶束。所有胶束的粒径均在 8 至 10nm 之间,粒径分布较窄,呈球形。10:0 TPGS 胶束的表面带负电荷,而 TPGS-Cys 胶束则带轻微正电荷。TPGS/TPGS-Cys 胶束的临界胶束浓度、载药量和释放曲线与 TPGS 胶束相当。酮康唑从所有胶束中的释放均呈两相且在模拟唾液中持续 48 小时。3:7 和 0:10 的 TPGS/TPGS-Cys 胶束具有良好的黏膜黏附性。同时,只有 0:10 的 TPGS/TPGS-Cys 胶束增强了对颊黏膜的渗透性,并使酮康唑的抗真菌活性增强至少 1.35 倍,与单独使用酮康唑相比。因此,该制剂可进一步开发用于酮康唑经黏膜递药治疗白色念珠菌。

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