化学
药理学
尼罗替尼
生物利用度
体外
渗透
Zeta电位
细胞毒性
体内
药代动力学
聚乙二醇化
分散性
药品
生物制药
IC50型
穿心莲内酯
脂质体
色谱法
离体
粒径
毒品携带者
酪氨酸激酶
阿霉素
膜透性
治疗指标
差示扫描量热法
药物输送
细胞凋亡
作者
Dilpreet Singh,Amritpal Singh,Harinder Singh
摘要
cm/s) relative to the pure drug. Biological evaluation using MCF-7 breast cancer cells demonstrated substantially improved cytotoxicity (50% inhibitory concentration = 6.7 µg/mL), enhanced reactive oxygen species generation, pronounced mitochondrial membrane depolarization, stronger apoptosis induction, and significant G0/G1-phase arrest compared with the pure drug. Collectively, these findings demonstrate that the optimized PEGylated nanoliposomal formulation significantly improves solubility, stability, intestinal permeation, and in vitro anticancer activity of nilotinib, supporting its potential as a promising preclinical formulation strategy for further in vivo and clinical evaluation.
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