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首页> 外文期刊>Drug delivery. >Tissue distribution of 2-methoxyestradiol nanosuspension in rats and its antitumor activity in C57BL/6 mice bearing lewis lung carcinoma
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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 (TE Q) 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 IC 50 at 72 h was reduced from 6.35 μ M for 2-ME solution to 3.56 μ M 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 groupat 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:本研究的目的是在体外和体内评估2-甲氧基雌二醇(2-ME)纳米混悬液与2-ME溶液相比的组织分布和抗肿瘤活性。通过纳米沉淀-高频超声法制备2-ME纳米悬浮液,粒径为168.4±3.2 nm,ζ电位为-29.79±1.89 mV。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,72 h时的IC 50从2-ME溶液的6.35μM降低至3.56 2-ME纳米悬浮液的μM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纳米混悬液不仅显示出对肿瘤生长的显着抑制,而且增强了脾脏指数。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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