Dual-responsive nanoparticles loading bevacizumab and gefitinib for molecular targeted therapy against non-small cell lung cancer
文献类型:期刊论文
作者 | Zhao, Zi-tong4,5,6; Wang, Jue4,5; Fang, Lei4,5; Qian, Xin-di4,5; Cai, Ying4,5; Cao, Hai-qiang4,5; Wang, Guan-ru4,5; He, Mei-lin3; Jiang, Yan-yan6; Wang, Dang-ge3,4,5 |
刊名 | ACTA PHARMACOLOGICA SINICA |
出版日期 | 2022-06-15 |
页码 | 11 |
ISSN号 | 1671-4083 |
关键词 | nanoparticles molecular targeted therapy non-small cell lung cancer dual-responsive controlled release |
DOI | 10.1038/s41401-022-00930-6 |
通讯作者 | Jiang, Yan-yan(yanyanjiang@fudan.edu.cn) ; Wang, Dang-ge(dgwang@simm.ac.cn) ; Li, Ya-ping(ypli@simm.ac.cn) |
英文摘要 | The combination of vascular endothelial growth factor (VEGF) inhibitors and tyrosine kinase inhibitors (TKIs) is newly available for molecular targeted therapy against non-small cell lung cancer (NSCLC) in clinic. However, the therapeutic benefits remain unsatisfying due to the poor drug delivery to targets of interest. In this study, we developed bevacizumab-coated gefitinib-loaded nanoparticles (BCGN) with dual-responsive drug release for inhibiting tumor angiogenesis and phosphorylation of epidermal growth factor receptor (EGFR). Through an exogenous corona strategy, bevacizumab is easily coated on gefitinib-loaded nanoparticles via electrostatic interaction. After intravenous injection, BCGN are efficiently accumulated in NSCLC tumors as confirmed by dual-model imaging. Bevacizumab is released from BCGN upon oxidation in tumor microenvironment, whereas gefitinib is released after being internalized by tumor cells and disassembled in reduction cytoplasm. The dual-responsive release of bevacizumab and gefitinib significantly inhibits tumor growth in both A549 and HCC827 human NSCLC models. Our approach provides a promising strategy to improve combinational molecular targeted therapy of NSCLC with precisely controlled drug release. |
WOS关键词 | GROWTH-FACTOR RECEPTOR ; TUMOR MICROENVIRONMENT ; DRUG-DELIVERY ; ANTI-VEGF ; COMBINATION ; PERSPECTIVE ; EXPRESSION ; STRATEGIES ; ANTITUMOR ; ERLOTINIB |
资助项目 | National Natural Science Foundation of China[81903548] ; National Natural Science Foundation of China[32170935] ; National Natural Science Foundation of China[32070927] ; National Natural Science Foundation of China[81690265] ; National Natural Science Foundation of China[31930066] ; National Natural Science Foundation of China[82172615] ; Youth Innovation Promotion Association of CAS[2019283] ; Shanghai Sailing Program[19YF1457300] ; Shandong Provincial Natural Science Foundation[ZR2019PH013] |
WOS研究方向 | Chemistry ; Pharmacology & Pharmacy |
语种 | 英语 |
出版者 | NATURE PUBL GROUP |
WOS记录号 | WOS:000811488100001 |
源URL | [http://119.78.100.183/handle/2S10ELR8/301483] |
专题 | 新药研究国家重点实验室 |
通讯作者 | Jiang, Yan-yan; Wang, Dang-ge; Li, Ya-ping |
作者单位 | 1.Yantai Univ, Sch Pharm, Yantai 264005, Peoples R China 2.Bohai Rim Adv Res Inst Drug Discovery, Shandong Lab Yantai Drug Discovery, Yantai 264000, Peoples R China 3.Yantai Inst Mat Med, Yantai Key Lab Nanomed & Adv Preparat, Yantai 264000, Peoples R China 4.Chinese Acad Sci, Ctr Pharmaceut, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 5.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China 6.Fudan Univ, Sch Pharm, Shanghai 201203, Peoples R China |
推荐引用方式 GB/T 7714 | Zhao, Zi-tong,Wang, Jue,Fang, Lei,et al. Dual-responsive nanoparticles loading bevacizumab and gefitinib for molecular targeted therapy against non-small cell lung cancer[J]. ACTA PHARMACOLOGICA SINICA,2022:11. |
APA | Zhao, Zi-tong.,Wang, Jue.,Fang, Lei.,Qian, Xin-di.,Cai, Ying.,...&Li, Ya-ping.(2022).Dual-responsive nanoparticles loading bevacizumab and gefitinib for molecular targeted therapy against non-small cell lung cancer.ACTA PHARMACOLOGICA SINICA,11. |
MLA | Zhao, Zi-tong,et al."Dual-responsive nanoparticles loading bevacizumab and gefitinib for molecular targeted therapy against non-small cell lung cancer".ACTA PHARMACOLOGICA SINICA (2022):11. |
入库方式: OAI收割
来源:上海药物研究所
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