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姜黄素和酮康唑负载的甲氧基聚(乙二醇)-聚(ε-己内酯)胶束联合使用时的增强效果。

Enhanced effect in combination of curcumin- and ketoconazole-loaded methoxy poly (ethylene glycol)-poly (ε-caprolactone) micelles.

作者信息

Teng Fangfang, Deng Peizong, Song Zhimei, Zhou Feilong, Feng Runliang

机构信息

School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, No. l6866 East Road of Jingshi, Jinan 250200, Shandong Province, PR China; Shandong Academy of Medical Sciences, No. 18877 Jingshi Road, Jinan 250062, Shandong Province, PR China.

School of Biological Science and Technology, University of Jinan, No. 336 West Road of Nanxinzhuang, Jinan 250022, Shandong Province, PR China.

出版信息

Biomed Pharmacother. 2017 Apr;88:43-51. doi: 10.1016/j.biopha.2017.01.033. Epub 2017 Jan 13.

DOI:10.1016/j.biopha.2017.01.033
PMID:28092844
Abstract

In order to enhance water-solubility and realize controlled release while keeping synergistic effects of ketoconazole and curcumin, drug-loaded methoxy poly (ethylene glycol)-b-poly (ε-caprolactone) micelles were prepared through thin membrane hydration method. Transmission electric microscopy and dynamitic light scattering characterization revealed the formation of ketoconazole- and curcumin-loaded micelles with an average size of 44.70nm and 39.56nm, respectively. The drug-loaded micelles endowed the two drugs' slow controlled release with water-solubility enhanced to 85 and 82000 folds higher than the corresponding raw drugs, respectively. In vitro antifungal activity test, chequerboard test and inhibition zone test indicated that efficacy of ketoconazole-loaded micelles was improved by introduction of curcumin-loaded micelles with a low fractional inhibitory concentration index (0.073). Biofilm formation inhibition assay also demonstrated that participation of curcumin-loaded micelles obviously strengthened the inhibition of fungal biofilms formation induced by ketoconazole-loaded micelles. The high synergistic activity of combinations is encouraging and the MPEG-PCL micelle is a potential drug delivery system for the combination of ketoconazole and curcumin.

摘要

为了提高水溶性并实现控释,同时保持酮康唑和姜黄素的协同作用,通过薄膜水化法制备了载药的甲氧基聚(乙二醇)-b-聚(ε-己内酯)胶束。透射电子显微镜和动态光散射表征显示,载酮康唑和载姜黄素胶束的形成,其平均粒径分别为44.70nm和39.56nm。载药胶束使两种药物实现缓慢控释,水溶性分别提高到比相应原料药高85倍和82000倍。体外抗真菌活性试验、棋盘法试验和抑菌圈试验表明,引入载姜黄素胶束可提高载酮康唑胶束的疗效,其分数抑菌浓度指数较低(0.073)。生物膜形成抑制试验也表明,载姜黄素胶束的参与明显增强了载酮康唑胶束对真菌生物膜形成的抑制作用。联合用药的高协同活性令人鼓舞。聚乙二醇-聚己内酯胶束是酮康唑和姜黄素联合用药的潜在药物递送系统。

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