体内
医学
紫杉醇
癌症研究
T790米
药理学
肺癌
药品
化学
联合疗法
肿瘤科
癌症
毒性
生物
表皮生长因子受体
吉非替尼
内科学
有机化学
生物技术
作者
Xin Shuai Wang,Li Zhang,Xiaocen Li,De Jiu Kong,Xiao Chen Hu,Xue Ding,Jun Yang,Meng Zhao,Yijie He,Kit S. Lam,She Gan Gao,Tzu‐Yin Lin,Yuanpei Li
出处
期刊:Nanomedicine
日期:2018-05-01
卷期号:13 (10): 1107-1120
被引量:12
标识
DOI:10.2217/nnm-2017-0355
摘要
This study aims to develop new nanoformulations of EGFR T790M targeted inhibitor AZD9291 and paclitaxel (PTX) for combination therapy of lung cancer.We prepared and characterized PTX- and AZD9291-loaded disulfide cross-linking micelles (DCMs), and evaluate their combination effect and toxicity in vitro and in lung cancer-bearing mice.Drug-loaded DCMs were relatively small in size, and possessed glutathione-responsive drug release. The combination of PTX-DCMs and AZD92921-DCMs exhibited strong synergistic effects in both cell line and in vivo without additional toxicity. Molecular studies demonstrated the synergistic modification in both IKB-α/NF-κB/Bcl-2 and EGFR/Akt pathways.The combination of DCM-loaded AZD9291 and PTX could potentially offer more effective and less toxicity treatment options for lung cancer patients.
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