Recent advances in the delivery of disulfiram: a critical analysis of promising approaches to improve its pharmacokinetic profile and anticancer efficacy

被引:27
作者
Farooq, Muhammad Asim [1 ]
Aquib, Md [1 ]
Khan, Daulat Haleem [2 ]
Hussain, Zahid [3 ]
Ahsan, Anam [4 ]
Baig, Mirza Muhammad Faran Ashraf [5 ]
Wande, Dickson Pius [1 ]
Ahmad, Muhammad Masood [6 ]
Ahsan, Hafiz Muhammad [7 ]
Jiang Jiajie [1 ]
Wang, Bo [1 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Pharmaceut, Nanjing 211198, Jiangsu, Peoples R China
[2] Lahore Coll Pharmaceut Sci, Dept Pharm, Lahore, Pakistan
[3] Univ Sharjah, Coll Pharm, Dept Pharmaceut & Pharmaceut Technol, Sharjah 27272, U Arab Emirates
[4] Shanxi Agr Univ, Coll Anim Sci & Vet Med, Taigu, Peoples R China
[5] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Jiangsu, Peoples R China
[6] Jouf Univ, Coll Pharm, Dept Pharmaceut, Sakaka, Saudi Arabia
[7] CMH Inst Med Sci, Dept Pharmacol, Cantt 63100, Bahawalpur, Pakistan
关键词
Disulfiram; Polymeric nanoparticles; Cancer; Nanotechnology; Drug delivery systems; DRUG-DELIVERY; MULTIDRUG-RESISTANCE; MIXED NANOPARTICLES; PLGA NANOPARTICLES; POLYMERIC MICELLES; IN-VITRO; CANCER; COPPER; CELLS; NANOTECHNOLOGY;
D O I
10.1007/s40199-019-00308-w
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Disulfiram (DSF) has a long history of being used as a first-line promising therapy for treatment of alcoholism in human. Besides its prominence in the treatment of alcoholism, extensive investigations have been carried out to explore other biomedical and pharmacological effects of DSF. Amongst other biomedical implications, plenty researches have shown evidence of promising anticancer efficacy of this agent for treatment of wide range of cancers such as breast cancer, liver cancer and lung carcinoma. Methods Electronic databases, including Google scholar, PubMed and Web of science were searched with the keywords disulfiram, nanoparticles, cancer, drug delivery systems. Result Despite its excellent anticancer efficacy, the pharmaceutical significance and clinical applicability of DSF are hampered due to poor stability, low solubility, short plasma half-life, rapid metabolism, and early clearance from systemic circulation. Various attempts have been made to eradicate these issues. Nanotechnology based interventions have gained remarkable recognition in improving pharmacokinetic and pharmacodynamic profile of DSF by improving its stability and avoiding its degradation. Conclusion The aim of the present review is to critically analyse all recent developments in designing various nanotechnology-based delivery systems, to ponder their relevance in improving stability, pharmacokinetic and pharmacodynamic profile, and achieving target-specific delivery of this agent to cancer cells to effectively eradicate cancer and abolish its metastasis. Nanotechnology is a novel approach for overcoming such obstacles faced presently, the results obtained so far using different novel drug delivery systems seem to be very promising to increase the stability and half-life of DSF.
引用
收藏
页码:853 / 862
页数:10
相关论文
共 66 条
[1]   In Vitro Collapsing Colon Cancer Cells by Selectivity of Disulfiram-Loaded Charge Switchable Nanoparticles Against Cancer Stem Cells [J].
Abu-Serie, Marwa M. ;
El-Rashidy, Fatma H. .
RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY, 2017, 12 (03) :260-271
[2]   Drug repositioning: Identifying and developing new uses for existing drugs [J].
Ashburn, TT ;
Thor, KB .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (08) :673-683
[3]   Integrating the drug, disulfiram into the vitamin E-TPGS-modified PEGylated nanostructured lipid carriers to synergize its repurposing for anti-cancer therapy of solid tumors [J].
Banerjee, Parikshit ;
Geng, Tianjiao ;
Mahanty, Arpan ;
Li, Tiantian ;
Zong, Li ;
Wang, Bo .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2019, 557 :374-389
[4]   On firm ground: IP protection of therapeutic nanoparticles [J].
Burgess, Paul ;
Hutt, Peter Barton ;
Farokhzad, Omid C. ;
Langer, Robert ;
Minick, Scott ;
Zale, Stephen .
NATURE BIOTECHNOLOGY, 2010, 28 (12) :1267-1271
[5]   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
[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]   Targeting Malignancies with Disulfiram (Antabuse): Multidrug Resistance, Angiogenesis, and Proteasome [J].
Cvek, B. .
CURRENT CANCER DRUG TARGETS, 2011, 11 (03) :332-337
[8]   Nonprofit drugs as the salvation of the world's healthcare systems: the case of Antabuse (disulfiram) [J].
Cvek, Boris .
DRUG DISCOVERY TODAY, 2012, 17 (9-10) :409-412
[9]   Polymeric micelles: Basic research to clinical practice [J].
Deshmukh, Anand S. ;
Chauhan, Pratik N. ;
Noolvi, Malleshappa N. ;
Chaturvedi, Kiran ;
Ganguly, Kuntal ;
Shukla, Shyam S. ;
Nadagouda, Mallikarjuna N. ;
Aminabhavi, Tejraj M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 532 (01) :249-268
[10]   Inhibitory effect of Disulfiram/copper complex on non-small cell lung cancer cells [J].
Duan, Lincan ;
Shen, Hongmei ;
Zhao, Guangqiang ;
Yang, Runxiang ;
Cai, Xinyi ;
Zhang, Lijuan ;
Jin, Congguo ;
Huang, Yunchao .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 446 (04) :1010-1016