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首页> 外文期刊>International Journal of Pharmaceutics >Mitoxantrone-loaded BSA nanospheres and chitosan nanospheres for local injection against breast cancer and its lymph node metastases. II: Tissue distribution and pharmacodynamics.
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Mitoxantrone-loaded BSA nanospheres and chitosan nanospheres for local injection against breast cancer and its lymph node metastases. II: Tissue distribution and pharmacodynamics.

机译:装载米托蒽醌的BSA纳米球和壳聚糖纳米球用于局部注射,可预防乳腺癌及其淋巴结转移。 II:组织分布和药效学。

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摘要

Bovine serum albumin (BSA) and chitosan (CS) nanospheres of mitoxantrone (MTO) were comparatively evaluated in terms of tissue distribution, acute toxicity and therapeutic efficiency against breast cancer and its lymph node metastases. After local injection in rats, MTO nanospheres showed a slower elimination rate and a much higher drug concentration in lymph nodes compared with MTO solution, and a lower drug concentration in other tissues. There was no observed acute toxicity to the main tissues of Kunming mice after local injection of MTO-BSA-NS. Mild toxicity to liver and lung was observed for MTO-CS-NS, but, for MTO solution, severe toxicity to liver and lung and much lower number of white blood cells were observed. Human MCF-7 breast cancer in nude mice and animal model of P388 lymph node metastases in Kunming mice were applied to investigate the therapeutic efficiency. The inhibition rate of the nanospheres against breast cancer was much higher than that of MTO solution, and lymph node metastaseswere efficiently inhibited by the nanospheres, especially MTO-BSA-NS.
机译:从组织分布,急性毒性和对乳腺癌及其淋巴结转移的治疗效率方面对米托蒽醌(MTO)的牛血清白蛋白(BSA)和壳聚糖(CS)纳米球进行了比较评估。在大鼠中局部注射后,与MTO溶液相比,MTO纳米球在淋巴结中的清除速度较慢,药物浓度更高,而在其他组织中则较低。局部注射MTO-BSA-NS后,未观察到对昆明小鼠主要组织的急性毒性。对于MTO-CS-NS,观察到对肝和肺的轻度毒性,但是对于MTO溶液,观察到对肝和肺的重度毒性,白血球数量低得多。应用裸鼠人MCF-7乳腺癌和昆明小鼠P388淋巴结转移的动物模型研究其治疗效果。纳米球对乳腺癌的抑制率远高于MTO溶液,并且纳米球尤其是MTO-BSA-NS有效抑制了淋巴结转移。

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