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用于增强紫杉烷溶解性和细胞毒性的树枝状聚合物-聚乙二醇维生素E琥珀酸酯混合胶束

Dendrimer-TPGS mixed micelles for enhanced solubility and cellular toxicity of taxanes.

作者信息

Pooja Deep, Kulhari Hitesh, Singh Mayank K, Mukherjee Sudip, Rachamalla Shyam Sunder, Sistla Ramakrishna

机构信息

Medicinal Chemistry & Pharmacology Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India; Faculty of Pharmacy, College of Technology, Osmania University, Hyderabad, India.

Medicinal Chemistry & Pharmacology Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India; IICT-RMIT Research Centre, CSIR-Indan Institute of Chemical Technology, Hyderabad, India.

出版信息

Colloids Surf B Biointerfaces. 2014 Sep 1;121:461-8. doi: 10.1016/j.colsurfb.2014.06.059. Epub 2014 Jul 2.

Abstract

Taxanes are the most effective, efficient and broad spectrum anticancer drugs for the treatment of various cancers. However, poor aqueous solubility is the major problem in their delivery at higher concentrations in cancer cells. In this research work, poor solubility of taxanes is addressed by preparing dendrimer and d-α-tocopherol polyethylene glycol succinate (TPGS) mixed micelles by taking into consideration the advantages of TPGS such as solubility enhancement and P-glycoprotein inhibition. Dendrimer-TPGS mixed micelles were prepared by solvent casting method. Docetaxel (DTX) and paclitaxel (PTX) were chosen as model drugs representing the group of taxanes. Nanomicelles were characterized by DLS, FTIR, PXRD, in vitro drug release and hemolytic studies. Effects of pH and dendrimer to TPGS ratio on the solubility of taxanes were also studied. Solubility of DTX and PTX were increased by 20.36 and 34.95 folds, respectively, when formulated in dendrimer-TPGS mixed micelles. Drug release studies exhibited better release profile of encapsulated drug at acidic pH which is advantageous in enhanced intracellular drug release in cancer cells. Formulations were found to be biocompatible in hemolytic toxicity assay. Cytotoxicity studies revealed that anticancer activities of both drugs were enhanced after encapsulation in micelles against cancer cells while caused very low toxicity to normal cells. Thus, dendrimer-TPGS mixed micelles are promising alternate for delivery of poorly water-soluble drugs taxanes.

摘要

紫杉烷类是治疗各种癌症最有效、高效且广谱的抗癌药物。然而,水溶性差是其在癌细胞中高浓度递送时的主要问题。在本研究工作中,考虑到二硬脂酰磷脂酰胆碱(TPGS)具有增强溶解性和抑制P-糖蛋白等优点,通过制备树枝状聚合物与TPGS的混合胶束来解决紫杉烷类溶解性差的问题。采用溶剂浇铸法制备树枝状聚合物-TPGS混合胶束。选择多西他赛(DTX)和紫杉醇(PTX)作为代表紫杉烷类的模型药物。通过动态光散射(DLS)、傅里叶变换红外光谱(FTIR)、粉末X射线衍射(PXRD)、体外药物释放和溶血研究对纳米胶束进行了表征。还研究了pH值和树枝状聚合物与TPGS的比例对紫杉烷类溶解性的影响。当制成树枝状聚合物-TPGS混合胶束时,DTX和PTX的溶解度分别提高了20.36倍和34.95倍。药物释放研究表明,包封药物在酸性pH值下具有更好的释放曲线,这有利于增强癌细胞内的药物释放。在溶血毒性试验中发现制剂具有生物相容性。细胞毒性研究表明,两种药物包封在胶束中后对癌细胞的抗癌活性增强,而对正常细胞的毒性非常低。因此,树枝状聚合物-TPGS混合胶束有望成为递送水溶性差的药物紫杉烷类的替代物。

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