阿霉素
脂质体
A549电池
化学
IC50型
细胞生长
MTT法
生长抑制
癌细胞
体外
生物物理学
分子生物学
生物化学
生物
化疗
癌症
遗传学
作者
Zhiqiang Zhang,Chunlei Zhong,Xin Zhao
出处
期刊:PubMed
日期:2015-11-01
卷期号:46 (6): 837-41
摘要
To determine the physicochemical properties of iRGD conjugated doxorubicin loaded liposome (iRGD-LP-DOX), and its effect on targeting and inhibiting growth of A549 cells.Liposomes were observed under a transmission electron microscope. Release of doxorubicin from iRGD-LP-DOX was detected by the dialysis bag method. The efficiency of cellular uptake and tumor spheroids penetration on A549 cells in vitro was determined. The anti-proliferation efficiency of iRGD-LP-DOX was evaluated by MTT assay using IC50 (50% inhibition concentration).iRGD-LP-DOX was spherical in a uniform size. Free DOX was released by 100% in 5 h, while LP-DOX and iRGD-LP-DOX were released by about 40% in 48 h. A higher level of iRGD-LP-DOX uptaken by A549 was found compared with that of LP-DOX (P<0.01). Higher fluorescence intensity was detected with iRGD-LP-DOX than with LP-DOX in tumor spheroid. The MTT assay confirmed strong inhibitory effect of iRGD-LP-DOX (P<0.01).iRGD can enhance uptake of liposomes by A549 cells and inhibit the proliferation of tumor cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI