叶酸受体
细胞毒性
化学
阿糖胞苷
MCF-7型
壳聚糖
药物输送
靶向给药
癌症研究
细胞凋亡
药理学
基因传递
碳二亚胺
细胞培养
体外
癌细胞
转染
生物化学
癌症
生物
医学
内科学
人体乳房
髓系白血病
有机化学
基因
遗传学
作者
Deepa Geethakumari,B.S. Anoop,Krishnapriya Raji Sathyan,M. Dhaneesha,Jisha V. Somasekharan,Sajeevan Thavarool Puthiyedathu
标识
DOI:10.1016/j.ijbiomac.2021.12.070
摘要
Anticancer drug cytarabine, has been widely used for treating haematological malignancies while it has minimal activity against solid tumours, which demands continuous infusion leading to high dose cytarabine toxicity. In this study, folate conjugated chitosan nanoparticles (FCCNP) were used for targeted delivery of cytarabine in breast adenocarcinoma cell lines by making use of the overexpressed folate receptors on the surface of MCF-7. Folate was conjugated to chitosan using carbodiimide. FCCNPs show spherical morphology with a size of<50 nm. Zeta potential of + 45.2 mV and PDI of 0.98 from DLS measurement confirms a stable monodisperse nanoformulation. Cytotoxicity was studied in folate receptor positive, MCF-7 and folate receptor negative, A-549 cell lines. Increased cellular uptake of the drug incorporated nanoparticles was confirmed in MCF-7 cells with fluorophore, squaraine 650 compared to A-549 cells. The relative fold of expression of genes involved in apoptosis such as bax, cyt c and cas 9 were upregulated. The present in vitro study confirms improved cytotoxicity of cytarabine folate conjugated chitosan nanoparticles in MCF-7 cells.
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