Cisplatin is the first anticancer drug based on inorganic complexes which was discovered accidentally by Rosenberg in 1965. Cisplatin is now used to treat a wide range of cancers such as head and neck testicular, small-cell lung and non-small-cell lung, bladder, cervical and ovarian cancers. Cisplatin has become the premier in combination therapy for solid tumours such as gastric, bladder, cervical, ovarian, lung, breast, head and neck cancers and some malignant mesothelioma and some less common cancers. This review begins with an introduction to the accidental discovery of cisplatin highlighting the amazing fact of serendipity involved in drug discovery. This will follow a reviewing of chemistry of cisplatin, identification of cis and trans isomers of diamminedicholoroplatinum(II). As for the most relevance to Pharmacy the action of cisplatin is reviewed next. Highlighted there are the reasons for cisplatin toxicity and hence ways and means of reducing cytotoxicity of cisplatin to healthy cells. Finally, the work on encapsulation of cisplatin in porous calcium carbonate nanoparticles for safe and targeted delivery to cancerous cells for more effective and selective action on cancer cells will be discussed.
Published in | International Journal of Clinical Oncology and Cancer Research (Volume 2, Issue 3) |
DOI | 10.11648/j.ijcocr.20170203.13 |
Page(s) | 65-74 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2017. Published by Science Publishing Group |
Anticancer Drug, Discovery of Cisplatin, Chemistry of Cisplatin, Action of Cisplatin, Ways of Reducing Cytotoxicity, Encapsulation, Targeted-Delivery, Slow-Release
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APA Style
Rajapakse Mudiyanselage Gamini Rajapakse, Shashiprabha Punyakantha Dunuweera. (2017). Discovery, Chemistry, Anticancer Action and Targeting of Cisplatin. International Journal of Clinical Oncology and Cancer Research, 2(3), 65-74. https://doi.org/10.11648/j.ijcocr.20170203.13
ACS Style
Rajapakse Mudiyanselage Gamini Rajapakse; Shashiprabha Punyakantha Dunuweera. Discovery, Chemistry, Anticancer Action and Targeting of Cisplatin. Int. J. Clin. Oncol. Cancer Res. 2017, 2(3), 65-74. doi: 10.11648/j.ijcocr.20170203.13
@article{10.11648/j.ijcocr.20170203.13, author = {Rajapakse Mudiyanselage Gamini Rajapakse and Shashiprabha Punyakantha Dunuweera}, title = {Discovery, Chemistry, Anticancer Action and Targeting of Cisplatin}, journal = {International Journal of Clinical Oncology and Cancer Research}, volume = {2}, number = {3}, pages = {65-74}, doi = {10.11648/j.ijcocr.20170203.13}, url = {https://doi.org/10.11648/j.ijcocr.20170203.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcocr.20170203.13}, abstract = {Cisplatin is the first anticancer drug based on inorganic complexes which was discovered accidentally by Rosenberg in 1965. Cisplatin is now used to treat a wide range of cancers such as head and neck testicular, small-cell lung and non-small-cell lung, bladder, cervical and ovarian cancers. Cisplatin has become the premier in combination therapy for solid tumours such as gastric, bladder, cervical, ovarian, lung, breast, head and neck cancers and some malignant mesothelioma and some less common cancers. This review begins with an introduction to the accidental discovery of cisplatin highlighting the amazing fact of serendipity involved in drug discovery. This will follow a reviewing of chemistry of cisplatin, identification of cis and trans isomers of diamminedicholoroplatinum(II). As for the most relevance to Pharmacy the action of cisplatin is reviewed next. Highlighted there are the reasons for cisplatin toxicity and hence ways and means of reducing cytotoxicity of cisplatin to healthy cells. Finally, the work on encapsulation of cisplatin in porous calcium carbonate nanoparticles for safe and targeted delivery to cancerous cells for more effective and selective action on cancer cells will be discussed.}, year = {2017} }
TY - JOUR T1 - Discovery, Chemistry, Anticancer Action and Targeting of Cisplatin AU - Rajapakse Mudiyanselage Gamini Rajapakse AU - Shashiprabha Punyakantha Dunuweera Y1 - 2017/06/22 PY - 2017 N1 - https://doi.org/10.11648/j.ijcocr.20170203.13 DO - 10.11648/j.ijcocr.20170203.13 T2 - International Journal of Clinical Oncology and Cancer Research JF - International Journal of Clinical Oncology and Cancer Research JO - International Journal of Clinical Oncology and Cancer Research SP - 65 EP - 74 PB - Science Publishing Group SN - 2578-9511 UR - https://doi.org/10.11648/j.ijcocr.20170203.13 AB - Cisplatin is the first anticancer drug based on inorganic complexes which was discovered accidentally by Rosenberg in 1965. Cisplatin is now used to treat a wide range of cancers such as head and neck testicular, small-cell lung and non-small-cell lung, bladder, cervical and ovarian cancers. Cisplatin has become the premier in combination therapy for solid tumours such as gastric, bladder, cervical, ovarian, lung, breast, head and neck cancers and some malignant mesothelioma and some less common cancers. This review begins with an introduction to the accidental discovery of cisplatin highlighting the amazing fact of serendipity involved in drug discovery. This will follow a reviewing of chemistry of cisplatin, identification of cis and trans isomers of diamminedicholoroplatinum(II). As for the most relevance to Pharmacy the action of cisplatin is reviewed next. Highlighted there are the reasons for cisplatin toxicity and hence ways and means of reducing cytotoxicity of cisplatin to healthy cells. Finally, the work on encapsulation of cisplatin in porous calcium carbonate nanoparticles for safe and targeted delivery to cancerous cells for more effective and selective action on cancer cells will be discussed. VL - 2 IS - 3 ER -