中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Sequentially Activatable Polypeptide Nanoparticles for Combinatory Photodynamic Chemotherapy of Breast Cancer

文献类型:期刊论文

作者Zhang, Huijuan3,4; Pan, Jiaxing2,3; Wang, Tingting1; Lai, Yi3; Liu, Xiaoying3; Chen, Fangmin3; Xu, Leiming2; Qu, Xiongwei4; Hu, Xiuli4; Yu, Haijun3
刊名ACS APPLIED MATERIALS & INTERFACES
出版日期2022-08-24
页码12
ISSN号1944-8244
关键词stimulus responsive polypeptide nanoparticles photodynamic therapy breast cancer precise tumor therapy
DOI10.1021/acsami.2c09064
通讯作者Lai, Yi(laiyi@simm.ac.cn) ; Qu, Xiongwei(xwqu@hebut.edu.cn) ; Hu, Xiuli(huxiuli@hebut.edu.cn) ; Yu, Haijun(hjyu@simm.ac.cn)
英文摘要Stimuli-activatable nanomaterials hold significant promise for tumor-specific drug delivery by recognizing the internal or external stimulus. Herein, we reported a dual-responsive and biodegradable polypeptide nanoparticle (PPTP@PTX2 NP) for combinatory chemotherapy and photodynamic therapy (PDT) of breast cancer. The NPs were engineered by encapsulating diselenide bond linked dimeric prodrug of paclitaxel (PTX2) in an intracellular acidity-activatable polypeptide micelle. Specifically, the acid-responsive polypeptide was synthesized by grafting a tetraphenyl porphyrin (TPP) photosensitizer and N,N-diisopropy-lethylenediamine (DPA) onto the poly(ethylene glycol)-block- poly(glutamic acid) diblock copolymer by the amidation reaction, which self-assembled into micellar NPs and was activated inside the acidic endocytic vesicles to perform PDT. The paclitaxel dimer can be stably loaded into the polypeptide NPs and be restored by PDT inside the tumor cells. The formed PPTP@PTX2 NPs remained inert during blood circulation and passively accumulated in the tumor foci, which could be activated within the endocytic vesicles via acid-triggered protonation of DPA groups to generate fluorescence signal and release PTX(2 )in 4T1 murine breast tumor cells. Upon 660 nm laser irradiation, the activated NPs carried out PDT via TPP and chemotherapy via PTX to induce apoptosis of 4T1 cells and thereby efficiently inhibited 4T1 tumor growth and prevented metastasis of tumor cells.
WOS关键词PRODRUG NANOPARTICLES ; DRUG-RESISTANCE ; ACID ; MECHANISMS ; MICELLES
资助项目National Natural Science Foundation of China[51973213] ; Lingang Laboratory[LG-QS-202206-04] ; China Postdoctoral Science Foundation[2021M700157] ; Shanghai Post-Doctoral Excellence Program[2021424] ; e National Facility for Protein Science in Shanghai (NFPS)
WOS研究方向Science & Technology - Other Topics ; Materials Science
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000848603200001
源URL[http://119.78.100.183/handle/2S10ELR8/302147]  
专题新药研究国家重点实验室
通讯作者Lai, Yi; Qu, Xiongwei; Hu, Xiuli; Yu, Haijun
作者单位1.Tongji Univ, Shanghai Peoples Hosp 10, Ultrasound Res & Educ Inst, Sch Med,Dept Med Ultrasound, Shanghai 200072, Peoples R China
2.Shanghai Jiaotong Univ Sch Med, Xinhua Hosp, Dept Gastroenterol, Shanghai, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res & Ctr Pharmaceut, Shanghai 201203, Peoples R China
4.Hebei Univ Technol, Inst Polymer Sci & Engn, Sch Chem Engn, Tianjin 300130, Peoples R China
推荐引用方式
GB/T 7714
Zhang, Huijuan,Pan, Jiaxing,Wang, Tingting,et al. Sequentially Activatable Polypeptide Nanoparticles for Combinatory Photodynamic Chemotherapy of Breast Cancer[J]. ACS APPLIED MATERIALS & INTERFACES,2022:12.
APA Zhang, Huijuan.,Pan, Jiaxing.,Wang, Tingting.,Lai, Yi.,Liu, Xiaoying.,...&Yu, Haijun.(2022).Sequentially Activatable Polypeptide Nanoparticles for Combinatory Photodynamic Chemotherapy of Breast Cancer.ACS APPLIED MATERIALS & INTERFACES,12.
MLA Zhang, Huijuan,et al."Sequentially Activatable Polypeptide Nanoparticles for Combinatory Photodynamic Chemotherapy of Breast Cancer".ACS APPLIED MATERIALS & INTERFACES (2022):12.

入库方式: OAI收割

来源:上海药物研究所

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