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- Publisher Website: 10.1007/s40199-019-00308-w
- Scopus: eid_2-s2.0-85075360825
- PMID: 31758497
- WOS: WOS:000498002100001
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Article: Recent advances in the delivery of disulfiram: a critical analysis of promising approaches to improve its pharmacokinetic profile and anticancer efficacy
Title | Recent advances in the delivery of disulfiram: a critical analysis of promising approaches to improve its pharmacokinetic profile and anticancer efficacy |
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Authors | |
Keywords | Polymeric nanoparticles Nanotechnology Disulfiram Cancer Drug delivery systems |
Issue Date | 2019 |
Citation | DARU Journal of Pharmaceutical Sciences, 2019, v. 27, n. 2, p. 853-862 How to Cite? |
Abstract | © 2019, Springer Nature Switzerland AG. 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. |
Persistent Identifier | http://hdl.handle.net/10722/293123 |
ISSN | 2014 Impact Factor: 1.638 2023 SCImago Journal Rankings: 0.625 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Farooq, Muhammad Asim | - |
dc.contributor.author | Aquib, Md | - |
dc.contributor.author | Khan, Daulat Haleem | - |
dc.contributor.author | Hussain, Zahid | - |
dc.contributor.author | Ahsan, Anam | - |
dc.contributor.author | Baig, Mirza Muhammad Faran Ashraf | - |
dc.contributor.author | Wande, Dickson Pius | - |
dc.contributor.author | Ahmad, Muhammad Masood | - |
dc.contributor.author | Ahsan, Hafiz Muhammad | - |
dc.contributor.author | Jiajie, Jiang | - |
dc.contributor.author | Wang, Bo | - |
dc.date.accessioned | 2020-11-19T09:02:02Z | - |
dc.date.available | 2020-11-19T09:02:02Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | DARU Journal of Pharmaceutical Sciences, 2019, v. 27, n. 2, p. 853-862 | - |
dc.identifier.issn | 1560-8115 | - |
dc.identifier.uri | http://hdl.handle.net/10722/293123 | - |
dc.description.abstract | © 2019, Springer Nature Switzerland AG. 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. | - |
dc.language | eng | - |
dc.relation.ispartof | DARU Journal of Pharmaceutical Sciences | - |
dc.subject | Polymeric nanoparticles | - |
dc.subject | Nanotechnology | - |
dc.subject | Disulfiram | - |
dc.subject | Cancer | - |
dc.subject | Drug delivery systems | - |
dc.title | Recent advances in the delivery of disulfiram: a critical analysis of promising approaches to improve its pharmacokinetic profile and anticancer efficacy | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1007/s40199-019-00308-w | - |
dc.identifier.pmid | 31758497 | - |
dc.identifier.pmcid | PMC6895293 | - |
dc.identifier.scopus | eid_2-s2.0-85075360825 | - |
dc.identifier.volume | 27 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 853 | - |
dc.identifier.epage | 862 | - |
dc.identifier.eissn | 2008-2231 | - |
dc.identifier.isi | WOS:000498002100001 | - |
dc.identifier.issnl | 1560-8115 | - |