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首页> 外文期刊>International Journal of Nanomedicine >A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting
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A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting

机译:一种新型的叶酸修饰的姜黄素自微乳化递药系统,用于结肠靶向

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Background: The objective of this study was to prepare, characterize, and evaluate a folate-modified self-microemulsifying drug delivery system (FSMEDDS) with the aim to improve the solubility of curcumin and its delivery to the colon, facilitating endocytosis of FSMEDDS mediated by folate receptors on colon cancer cells.Methods: Ternary phase diagrams were constructed in order to obtain the most efficient self-emulsification region, and the formulation of curcumin-loaded SMEDDS was optimized by a simplex lattice experiment design. Then, three lipophilic folate derivatives (folate-polyethylene glycol-distearoylphosphatidylethanolamine, folate-polyethylene glycol-cholesteryl hemisuccinate, and folate-polyethylene glycol-cholesterol) used as a surfactant were added to curcumin-loaded SMEDDS formulations. An in situ colon perfusion method in rats was used to optimize the formulation of FSMEDDS. Curcumin-loaded FSMEDDS was then filled into colon-targeted capsules and the in vitro release was investigated. Cytotoxicity studies and cellular uptake studies was used in this research.Results: The optimal formulation of FSMEDDS obtained with the established in situ colon perfusion method in rats was comprised of 57.5% Cremophor? EL, 32.5% Transcutol? HP, 10% Capryol? 90, and a small amount of folate-polyethylene glycol-cholesteryl hemisuccinate (the weight ratio of folate materials to Cremophor EL was 1:100). The in vitro release results indicated that the obtained formulation of curcumin could reach the colon efficiently and release the drug immediately. Cellular uptake studies analyzed with fluorescence microscopy and flow cytometry indicated that the FSMEDDS formulation could efficiently bind with the folate receptors on the surface of positive folate receptors cell lines. In addition, FSMEDDS showed greater cytotoxicity than SMEDDS in the above two cells.Conclusion: FSMEDDS-filled colon-targeted capsules are a potential carrier for colon delivery of curcumin.
机译:背景:这项研究的目的是准备,表征和评估叶酸修饰的自微乳化药物递送系统(FSMEDDS),旨在提高姜黄素的溶解度及其向结肠的递送,从而促进由姜黄素介导的FSMEDDS的内吞作用方法:构建三元相图以获得最有效的自乳化区域,并通过单晶格实验设计优化姜黄素负载型SMEDDS的配方。然后,将用作表面活性剂的三种亲脂性叶酸衍生物(叶酸-聚乙二醇-二硬脂酰磷脂酰乙醇胺,叶酸-聚乙二醇-胆固醇半琥珀酸酯和叶酸-聚乙二醇-胆固醇)添加到加载姜黄素的SMEDDS配方中。用大鼠原位结肠灌注方法优化FSMEDDS的配方。然后将姜黄素负载的FSMEDDS装入结肠靶向胶囊中,并研究了体外释放。结果:用建立的原位结肠灌注方法在大鼠中获得的FSMEDDS的最佳配方为57.5%的Cremophor? EL,32.5%Transcutol? HP,10%辛酸? 90,和少量叶酸-聚乙二醇-胆固醇半琥珀酸酯(叶酸材料与Cremophor EL的重量比为1:100)。体外释放结果表明,所获得的姜黄素制剂可以有效地到达结肠并立即释放药物。用荧光显微镜和流式细胞术分析的细胞摄取研究表明,FSMEDDS制剂可以有效地结合阳性叶酸受体细胞系表面上的叶酸受体。此外,在上述两个细胞中,FSMEDDS的细胞毒性高于SMEDDS。

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