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首页> 外文期刊>Journal of Pharmacy and Pharmacology >In vitro In vitro characterization of pH‐sensitive Bletilla Striata polysaccharide copolymer micelles and enhanced tumour suppression in vivo in vivo
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In vitro In vitro characterization of pH‐sensitive Bletilla Striata polysaccharide copolymer micelles and enhanced tumour suppression in vivo in vivo

机译:体外体外体外表征pH敏感的甲状腺素串联多糖共聚物胶束,体内体内增强肿瘤抑制

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Abstract Objectives A system of stearic acid (SA)‐modified Bletilla striata polysaccharide (BSP) micelles was developed for the targeted delivery of docetaxel (DTX) as a model anticancer drug (DTX‐SA‐BSP). Methods Particle size, zeta potential and DTX release in vitro were measured in release media at different pH values. Quantitative cellular uptake, cytotoxicity assay in vitro and antitumour efficacy in vivo were also evaluated. Cell apoptosis was assessed by flow cytometry. Key findings DTX‐SA‐BSP copolymer micelles displayed pH‐dependent properties in the respects of particle size, zeta potential and in vitro release behaviour ranging from pH 5.0 to pH 7.4. DTX‐SA‐BSP copolymer micelles showed higher release rate at pH 5.0 than that at pH 6.0 and 7.4. In vitro cytotoxic effect of DTX‐SA‐BSP copolymer micelles was higher than that of DTX injection. The results of high‐performance liquid chromatography determination confirmed that DTX cellular uptake of micelles was enhanced compared with that of DTX injection. Anticancer activity in vivo further confirmed the enhanced tumour targeting and anticancer efficacy of DTX‐SA‐BSP copolymer micelles. Conclusions The above results show that DTX‐SA‐BSP copolymer micelles have pH sensitivity. SA‐BSP copolymers are a promising carrier for delivering hydrophobic anticancer drugs.
机译:摘要目的是开发了硬脂酸(SA)制定的甲状腺素施联多糖(BSP)胶束的系统,用于靶向递送多西紫杉醇(DTX)作为模型抗癌药物(DTX-SA-BSP)。方法在不同pH值的释放介质中测量体外粒径,Zeta电位和DTX释放。还评价了体外体外和抗肿瘤疗效的定量细胞吸收,细胞毒性测定。通过流式细胞术评估细胞凋亡。关键发现DTX-SA-BSP共聚物胶束在粒径,ζ电位和体外释放行为的方面显示pH依赖性,从pH5.0至pH 7.4的范围内。 DTX-SA-BSP共聚物胶束在pH5.0下显示比pH6.0和7.4在pH 5.0的更高释放速率。 DTX-SA-BSP共聚物胶束的体外细胞毒性效果高于DTX注射的效果。高效液相色谱法测定的结果证实,与DTX注射的胶束的DTX细胞摄取增强。体内抗癌活性进一步证实了DTX-SA-BSP共聚物胶束的增强肿瘤靶向和抗癌效果。结论上述结果表明,DTX-SA-BSP共聚物胶束具有pH敏感性。 SA-BSP共聚物是一种有望的载体,用于提供疏水性抗癌药物。

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