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In vitro and in vivo effect of hyaluronic acid modified, doxorubicin and gallic acid co-delivered lipid-polymeric hybrid nano-system for leukemia therapy

机译:玻尿酸修饰,阿霉素和没食子酸共递送脂质-聚合物杂合纳米系统在白血病治疗中的体外和体内作用

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Objective: To investigate the hyaluronic acid (HA) modified, doxorubicin (DOX) and gallic acid (GA) co-delivered lipid-polymeric hybrid nano-system for leukemia therapy. Methods: We produced a kind of lipid-polymer hybrid nanoparticle (LPHN) with a core-shell structure in which DOX and GA were co-loaded. In vitro and in vivo leukemia therapeutic effects of the HA modified, DOX and GA co-delivered LPHNs (HA-DOX/GA-LPHNs) were evaluated in DOX resistant human HL-60 promyelocytic leukemia cells (HL-60/ADR cells), DOX resistant human K562 chronic myeloid leukemia cells (K562/ADR cells), and HL-60/ADR cells bearing mouse model. Results: The sizes and zeta potentials of HA modified LPHNs were about 160 nm and ?40 mV. HA-DOX/GA-LPHNs showed the most prominent cytotoxicity and the best synergistic effect was obtained when DOX/GA ratio was 2/1. In vivo studies revealed that HA-DOX/GA-LPHNs inhibited tumor growth from 956 mmsup3,/sup to 213 mm,sup3/sup with an inhibition rate of 77.7%. Conclusion: In summary, the study showed that HA-DOX/GA-LPHNs can be applied as a promising leukemia therapy system.
机译:目的:研究透明质酸(HA)修饰,阿霉素(DOX)和没食子酸(GA)共同提供的脂质-聚合物混合纳米系统用于白血病治疗。方法:我们制备了一种脂质-聚合物杂化纳米颗粒(LPHN),其具有核壳结构,其中DOX和GA共同负载。在抗DOX的人HL-60早幼粒细胞白血病细胞(HL-60 / ADR细胞)中评估了HA修饰的,DOX和GA共递送的LPHN(HA-DOX / GA-LPHN)的体外和体内白血病治疗效果,对DOX耐药的人K562慢性粒细胞白血病细胞(K562 / ADR细胞)和带有小鼠模型的HL-60 / ADR细胞。结果:HA修饰的LPHN的大小和Zeta电位约为160 nm,约为40 mV。当DOX / GA比为2/1时,HA-DOX / GA-LPHNs表现出最显着的细胞毒性,并获得最佳的协同作用。体内研究表明,HA-DOX / GA-LPHNs抑制肿瘤生长,从956 mm 3 到213 mm, 3 ,抑制率为77.7%。结论:总之,研究表明,HA-DOX / GA-LPHNs可以作为有前途的白血病治疗系统。

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