Engineering a Tumor-Acidity-Responsive PEG-Sheddable Nanoassembly for Combating Drug Resistance
文献类型: 外文期刊
作者: Xie, Jin 1 ; Zhou, Mengxue 3 ; Ren, Hongyu 3 ; Dou, Rui 3 ; Zhang, Jiayu 3 ; Hu, Yi 3 ; Ouyang, Jun 2 ; Chen, Jun 3 ;
作者机构: 1.Zhengzhou Univ, Affiliated Hosp 1, Dept Biol Sample Bank, Zhengzhou 450052, Henan, Peoples R China
2.Southern Med Univ, Guangdong Engn Res Ctr Translat Med 3D Printing Ap, Natl Virtual & Real Expt Educ Ctr Med Morphol, Sch Basic Med Sci,Natl Key Discipline Human Anat,G, Guangzhou 510515, Peoples R China
3.Inst High Energy Phys, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100049, Peoples R China
4.Univ Chinese Acad Sci UCAS, Chinese Acad Sci CAS, Beijing 100049, Peoples R China
5.Chinese Acad Agr Sci, Tea Res Inst, Key Lab Tea Biol & Resource Utilizat, Minist Agr, Hangzhou 310008, Peoples R China
6.Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, State Key Lab Complex Severe & Rare Dis, Biomed Engn Facil Natl Infrastruct Translat Med, Beijing 100730, Peoples R China
关键词: core-crosslinked micellar nanoassembly; co-delivery; drug resistance; nanomedicine; tumor-acidity-responsive
期刊名称:MACROMOLECULAR CHEMISTRY AND PHYSICS ( 影响因子:2.7; 五年影响因子:2.5 )
ISSN: 1022-1352
年卷期: 2025 年 226 卷 13 期
页码:
收录情况: SCI
摘要: This study presents a simple strategy to develop a tumor-acidity responsive core-crosslinked micellar nanoassembly capable of delivering multiple drugs to combat drug resistance. Paclitaxel (PTX) nanocrystals are prepared using D-alpha-tocopherol polyethylene glycol 1000 succinate (TPGS) as an emulsifier and cross-linked with poly(beta-cyclodextrin) (PCD) to form the core. An acid-labile prodrug, poly(ethylene glycol)-doxorubicin (mPEG-DOX), is utilized as the shell, forming a core-shell nanoassembly (CSNA) via supramolecular interactions. The CSNA demonstrated high stability in aqueous and serum environments, with triggered shell-detachment in response to tumor acidity. The nanomedicine exhibited superior inhibition of drug-resistant cancer cell line MCF-7/ADR compared to DOX or PTX alone, offering potential to overcome drug resistance in chemotherapy.
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