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含油核/两亲聚合物壳纳米胶囊改变了乳腺癌细胞内阿霉素的细胞内命运。

Oily core/amphiphilic polymer shell nanocapsules change the intracellular fate of doxorubicin in breast cancer cells.

机构信息

Faculty of Ceilandia, University of Brasilia, Brasilia 72220-900, Brazil.

Department of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia 70910-900, Brazil.

出版信息

J Mater Chem B. 2019 Oct 23;7(41):6390-6398. doi: 10.1039/c9tb00587k.

DOI:10.1039/c9tb00587k
PMID:31642844
Abstract

The aim of this work was to develop and test the in vitro biological activity of nanocapsules loaded with a doxorubicin (DOX) free base dissolved in a core of castor oil shelled by poly(methyl vinyl ether-co-maleic anhydride) conjugated to n-octadecylamine residues. This system was stable and monodisperse, with a hydrodynamic diameter of about 300 nm. These nanocapsules changed the intracellular distribution of DOX, from the nuclei to the cytoplasm, and exhibited higher toxicity towards cancer cells - 4T1 and MCF-7 - and significantly lower toxicity towards normal cells - NIH-3T3 and MCF-10A - in vitro. In conclusion, these nanocapsules are suitable DOX carriers, which remain to be studied in in vivo tumor models.

摘要

这项工作的目的是开发和测试载有游离阿霉素(DOX)的纳米胶囊的体外生物活性,该 DOX 溶解在由聚(甲基乙烯基醚-马来酸酐)接枝到正十八烷基胺残基的壳聚糖油核中。该系统稳定且单分散,水动力直径约为 300nm。这些纳米胶囊改变了 DOX 的细胞内分布,从细胞核到细胞质,并表现出对癌细胞(4T1 和 MCF-7)更高的毒性,而对正常细胞(NIH-3T3 和 MCF-10A)的毒性显著降低。总之,这些纳米胶囊是合适的 DOX 载体,有待在体内肿瘤模型中进一步研究。

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