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Microencapsulated Multicellular Tumor Spheroids as a Tool to Test Novel Anticancer Nanosized Drug Delivery Systems In Vitro

机译:微囊化多细胞肿瘤球体作为测试新型抗癌纳米药物递送系统的工具

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In the study, MCF-7 human breast adenocarcinoma cells were used to study cytotoxicity of novel anticancer nanosized formulations, such as docetaxel-loaded nanoemulsion and liposomal formulation of a lipophilic methotrexate (MTX) prodrug. In vitro study of cytotoxicity was carried out in 2 models, namely using 3D in vitro model based on multicellular tumor spheroids (MTS) and 2D monolayer culture. MTS were generated by tumor cell cultivation within alginate-oligochitosan microcapsules. In the case of the monolayer culture, cell viability was found to be 25, 18 and 12% for the samples containing nanoemulsion at concentrations 20, 300 and 1000 nM of docetaxel, respectively, after 48 hs incubation. For MTS these values were higher, namely 33, 23 and 18%, respectively. Cytotoxicity of liposomal MTX prodrug-based formulation with final concentration of 1, 2, 10, 50, 100 and 1000 nM in both models was also studied. MIX liposomal formulation demonstrated lower cytotoxicity on MIS compared to intact MTX. Moreover, MIS were also more resistant to both liposomal formulation and intact MTX than the monolayer culture. Thus, at 1000 nM MTX in the liposomal form, cell viability in MTS was 1.4-fold higher than that in the nnonolayer culture. MTS could be proposed as a promising tool to test novel anticancer nanosized formulations in vitro.
机译:在这项研究中,MCF-7人乳腺癌细胞被用于研究新型抗癌纳米制剂的细胞毒性,例如载有多西他赛的纳米乳剂和亲脂性甲氨蝶呤(MTX)前药的脂质体制剂。在2种模型中进行了细胞毒性的体外研究,即使用基于多细胞肿瘤球体(MTS)和2D单层培养的3D体外模型。 MTS是通过在藻酸盐-低聚壳聚糖微胶囊中培养肿瘤细胞而产生的。在单层培养的情况下,孵育48小时后,发现含有浓度分别为20、300和1000 nM多西紫杉醇的纳米乳的样品的细胞活力分别为25%,18%和12%。对于MTS,这些值较高,分别为33%,23%和18%。还研究了两种模型中终浓度分别为1、2、10、50、100和1000 nM的脂质体MTX前药制剂的细胞毒性。与完整的MTX相比,MIX脂质体制剂对MIS的细胞毒性更低。此外,MIS也比单层培养物对脂质体制剂和完整的MTX都更有抵抗力。因此,在脂质体形式的1000 nM MTX下,MTS中的细胞存活率比在无核层培养物中高1.4倍。 MTS可以作为一种有希望的工具在体外测试新型抗癌纳米制剂。

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