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Tissue distribution of 2-methoxyestradiol nanosuspension in rats and its antitumor activity in C57BL/6 mice bearing lewis lung carcinoma

机译:2-甲氧基雌二醇纳米悬浮液在大鼠的组织分布及其对刘易斯肺癌的C57BL / 6小鼠的抗肿瘤活性

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The purpose of the present study was to evaluate the tissue distribution and antitumor activity of 2-methoxyestradiol (2-ME) nanosuspension compared with 2-ME solution both in vitro and in vivo. 2-ME nanosuspension was made by nanoprecipitation-high-frequency ultrasonication method with the particle size of 168.4?±?3.2?nm and the zeta potential of ?29.79?±?1.89 mV. The overall targeting efficiency (TEQ) of 2-ME nanosuspension was improved from 28.71 to 51.95% in the lung of rats. MTT assay showed that 2-ME nanosuspension could significantly enhance the in vitro cytotoxicity against lewis lung carcinoma (LLC) cells compared with the 2-ME solution, the IC50 at 72?h was reduced from 6.35 μM for 2-ME solution to 3.56 μM for 2-ME nanosuspension. The antitumor activity in vivo was investigated in C57BL/6 mice bearing LLC, and the results indicated that 2-ME nanosuspension not only exhibited significant suppression of the tumor growth when compared with that of positive group or cyclophosphamide group at the same dose, but also enhanced the spleen indices. Overall, 2-ME nanosuspension could mainly deliver the drug to lungs and made the drug accumulate in the lungs, so 2-ME nanosuspension has a possible lung cancer therapeutic potential.
机译:本研究的目的是评估2-甲氧基雌二醇(2-ME)纳米混悬液与2-ME溶液在体外和体内的组织分布和抗肿瘤活性。用纳米沉淀-高频超声法制备2-ME纳米悬浮液,其粒径为168.4±3.2±nm,ζ电势为29.79±1.89mV。在大鼠肺中,2-ME纳米悬浮液的总靶向效率(TE Q )从28.71提高到51.95%。 MTT分析表明,与2-ME溶液相比,2-ME纳米悬浮液可显着增强对刘易斯肺癌(LLC)细胞的体外细胞毒性,在72?h时IC 50 降低。对于2-ME纳米悬浮液,适用于2-ME溶液的3.56μM。在带有LLC的C57BL / 6小鼠中研究了体内抗肿瘤活性,结果表明,与相同剂量的阳性组或环磷酰胺组相比,2-ME纳米混悬液不仅对肿瘤的生长具有显着抑制作用,而且增强脾脏指标。总体而言,2-ME纳米混悬剂主要可将药物递送至肺部并使药物在肺中积聚,因此2-ME纳米混悬剂具有潜在的肺癌治疗潜力。

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