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Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics

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dc.contributor.author Mvango, Sindisiwe
dc.contributor.author Matshe, William MR
dc.contributor.author Balogun, AO
dc.contributor.author Pilcher, LA
dc.contributor.author Balogun, Mohammed O
dc.date.accessioned 2018-11-08T08:17:32Z
dc.date.available 2018-11-08T08:17:32Z
dc.date.issued 2018-12
dc.identifier.citation Mvango, S. et al. 2018. Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics. Pharmaceutical Research, vol. 35: https://doi.org/10.1007/s11095-018-2517-z en_US
dc.identifier.issn 0724-8741
dc.identifier.issn 1573-904X
dc.identifier.uri http://link-springer-com-443.webvpn.jxutcm.edu.cn/article/10.1007%2Fs11095-018-2517-z
dc.identifier.uri https://doi.org/10.1007/s11095-018-2517-z
dc.identifier.uri http://hdl.handle.net/10204/10527
dc.description Copyright: 2018 Springer. Due to copyright restrictions, the attached PDF file only contains the abstract of the full text item. For access to the full text item, please consult the publisher's website. en_US
dc.description.abstract Malaria is one of the oldest infectious diseases that afflict humans and its history extends back for millennia. It was once prevalent throughout the globe but today it is mainly endemic to tropical regions like sub-Saharan Africa and South-east Asia. Ironically, treatment for malaria has existed for centuries yet it still exerts an enormous death toll. This contradiction is attributed in part to the rapid development of resistance by the malaria parasite to chemotherapeutic drugs. In turn, resistance has been fuelled by poor patient compliance to the relatively toxic antimalarial drugs. While drug toxicity and poor pharmacological potentials have been addressed or ameliorated with various nanomedicine drug delivery systems in diseases like cancer, no clinically significant success story has been reported for malaria. There have been several reviews on the application of nanomedicine technologies, especially drug encapsulation, to malaria treatment. Here we extend the scope of the collation of the nanomedicine research literature to polymer therapeutics technology. We first discuss the history of the disease and how a flurry of scientific breakthroughs in the latter part of the nineteenth century provided scientific understanding of the disease. This is followed by a review of the disease biology and the major antimalarial chemotherapy. The achievements of nanomedicine in cancer and other infectious diseases are discussed to draw parallels with malaria. A review of the current state of the research into malaria nanomedicines, both encapsulation and polymer therapeutics polymer-drug conjugation technologies, is covered and we conclude with a consideration of the opportunities and challenges offered by both technologies. en_US
dc.language.iso en en_US
dc.publisher Springer en_US
dc.relation.ispartofseries Worklist;21573
dc.subject Antimalarial en_US
dc.subject Malaria en_US
dc.subject Nanomedicine en_US
dc.subject Plasmodium en_US
dc.subject Polymer therapeutics en_US
dc.title Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics en_US
dc.type Article en_US
dc.identifier.apacitation Mvango, S., Matshe, W. M., Balogun, A., Pilcher, L., & Balogun, M. O. (2018). Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics. http://hdl.handle.net/10204/10527 en_ZA
dc.identifier.chicagocitation Mvango, Sindisiwe, William MR Matshe, AO Balogun, LA Pilcher, and Mohammed O Balogun "Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics." (2018) http://hdl.handle.net/10204/10527 en_ZA
dc.identifier.vancouvercitation Mvango S, Matshe WM, Balogun A, Pilcher L, Balogun MO. Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics. 2018; http://hdl.handle.net/10204/10527. en_ZA
dc.identifier.ris TY - Article AU - Mvango, Sindisiwe AU - Matshe, William MR AU - Balogun, AO AU - Pilcher, LA AU - Balogun, Mohammed O AB - Malaria is one of the oldest infectious diseases that afflict humans and its history extends back for millennia. It was once prevalent throughout the globe but today it is mainly endemic to tropical regions like sub-Saharan Africa and South-east Asia. Ironically, treatment for malaria has existed for centuries yet it still exerts an enormous death toll. This contradiction is attributed in part to the rapid development of resistance by the malaria parasite to chemotherapeutic drugs. In turn, resistance has been fuelled by poor patient compliance to the relatively toxic antimalarial drugs. While drug toxicity and poor pharmacological potentials have been addressed or ameliorated with various nanomedicine drug delivery systems in diseases like cancer, no clinically significant success story has been reported for malaria. There have been several reviews on the application of nanomedicine technologies, especially drug encapsulation, to malaria treatment. Here we extend the scope of the collation of the nanomedicine research literature to polymer therapeutics technology. We first discuss the history of the disease and how a flurry of scientific breakthroughs in the latter part of the nineteenth century provided scientific understanding of the disease. This is followed by a review of the disease biology and the major antimalarial chemotherapy. The achievements of nanomedicine in cancer and other infectious diseases are discussed to draw parallels with malaria. A review of the current state of the research into malaria nanomedicines, both encapsulation and polymer therapeutics polymer-drug conjugation technologies, is covered and we conclude with a consideration of the opportunities and challenges offered by both technologies. DA - 2018-12 DB - ResearchSpace DP - CSIR KW - Antimalarial KW - Malaria KW - Nanomedicine KW - Plasmodium KW - Polymer therapeutics LK - https://researchspace.csir.co.za PY - 2018 SM - 0724-8741 SM - 1573-904X T1 - Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics TI - Nanomedicines for malaria chemotherapy: Encapsulation vs. polymer therapeutics UR - http://hdl.handle.net/10204/10527 ER - en_ZA


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