Highly Stable, Coordinated Polymeric Nanoparticles Loading Copper(II) Diethyldithiocarbamate for Combinational Chemo/Chemodynamic Therapy of Cancer

被引:97
作者
Peng, Xinyu [1 ]
Pan, Qingqing [1 ]
Zhang, Boya [1 ]
Wan, Shiyu [2 ]
Li, Sai [2 ]
Luo, Kui [3 ]
Pu, Yuji [1 ]
He, Bin [1 ]
机构
[1] Sichuan Univ, Natl Engn Res Ctr Biomat, Chengdu 610064, Sichuan, Peoples R China
[2] Sichuan Univ, Sch Chem Engn, Chengdu 610065, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Radiol, Huaxi MR Res Ctr HMRRC, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
OXIDATIVE STRESS; IN-VITRO; DISULFIRAM; MICELLES; DELIVERY; DRUG; CELLS; DOXORUBICIN; APOPTOSIS; EFFICACY;
D O I
10.1021/acs.biomac.9b00367
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Disulfiram (DSF) has excellent in vitro anticancer activity in the presence of Cu(II). The anticancer mechanism studies have demonstrated that copper(II) diethyldithiocarbamate, Cu(DDC)(2), is the crucial DSF's metabolite exhibiting anticancer activity. In this paper, highly stable polymeric nanoparticles were fabricated via a coordination strategy between Cu(II) and carboxylic groups in poly(ethylene glycol)-b-poly(ester-carbonate) (PEC) for efficient loading of Cu(DDC)(2), which was generated by the in situ reaction of DSF and Cu(II). The properties of nanoparticles such as drug loading contents, sizes, and morphologies could be tuned by varying the feeding ratios of DSF, Cu(II), and PEC. These Cu(II)/DDC-loaded nanoparticles showed excellent stability in both neutral and weak acidic solutions and under dilution. In vitro anticancer study established that Cu(II)/DDC-loaded nanoparticles could enable a combination therapy of Cu(DDC)(2)-based chemotherapy and chemodynamic therapy mediated by bioavailable Cu(II) that was not in the form of Cu(DDC)(2). The in vivo antitumor results demonstrated that the Cu(II)/DDC-loaded nanoparticles showed superior antitumor efficacy to DSF/Cu(II). Our study provided a facile and effective strategy of highly stable coordination-mediated polymeric nanoparticles for combinational therapy of cancer.
引用
收藏
页码:2372 / 2383
页数:12
相关论文
共 45 条
[1]   Disulfiram (DSF) acts as a copper ionophore to induce copper-dependent oxidative stress and mediate anti-tumor efficacy in inflammatory breast cancer [J].
Allensworth, Jennifer L. ;
Evans, Myron K. ;
Bertucci, Francois ;
Aldrich, Amy J. ;
Festa, Richard A. ;
Finetti, Pascal ;
Ueno, Naoto T. ;
Safi, Rachid ;
McDonnell, Donald P. ;
Thiele, Dennis J. ;
Van Laereg, Steven ;
Devi, Gayathri R. .
MOLECULAR ONCOLOGY, 2015, 9 (06) :1155-1168
[2]   Leveraging -Glutamyl Transferase To Direct Cytotoxicity of Copper Dithiocarbamates against Prostate Cancer Cells [J].
Bakthavatsalam, Subha ;
Sleeper, Mark L. ;
Dharani, Azim ;
George, Daniel J. ;
Zhang, Tian ;
Franz, Katherine J. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (39) :12780-12784
[3]   Investigation of the key chemical structures involved in the anticancer activity of disulfiram in A549 non-small cell lung cancer cell line [J].
Butcher, Kate ;
Kannappan, Vinodh ;
Kilari, Rajagopal Sharada ;
Morris, Mark R. ;
McConville, Christopher ;
Armesilla, Angel L. ;
Wang, Weiguang .
BMC CANCER, 2018, 18
[4]   Disulfiram facilitates intracellular Cu uptake and induces apoptosis in human melanoma cells [J].
Cen, DZ ;
Brayton, D ;
Shahandeh, B ;
Meyskens, FL ;
Farmer, PJ .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (27) :6914-6920
[5]  
Cen DZ, 2002, MOL CANCER THER, V1, P197
[6]   Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity [J].
Chen, Di ;
Cui, Qiuzhi Cindy ;
Yang, Huanjie ;
Dou, Q. Ping .
CANCER RESEARCH, 2006, 66 (21) :10425-10433
[7]   Stimuli-responsive polymer-doxorubicin conjugate: Antitumor mechanism and potential as nano-prodrug [J].
Chen, Kai ;
Cai, Hao ;
Zhang, Hu ;
Zhu, Hongyan ;
Gu, Zhongwei ;
Gong, Qiyong ;
Luo, Kui .
ACTA BIOMATERIALIA, 2019, 84 :339-355
[8]   Disulfiram Copper Nanoparticles Prepared with a Stabilized Metal Ion Ligand Complex Method for Treating Drug-Resistant Prostate Cancers [J].
Chen, Wu ;
Yang, Wen ;
Chen, Pengyu ;
Huang, Yongzhuo ;
Li, Feng .
ACS APPLIED MATERIALS & INTERFACES, 2018, 10 (48) :41118-41128
[9]   The polymerization kinetics, oxidation-responsiveness, and in vitro anticancer efficacy of poly(ester-thioether)s [J].
Cheng, Furong ;
Su, Ting ;
Luo, Kui ;
Pu, Yuji ;
He, Bin .
JOURNAL OF MATERIALS CHEMISTRY B, 2019, 7 (06) :1005-1016
[10]   Mining for therapeutic gold [J].
Collins, Francis S. .
NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (06) :397-397