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Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity

[Image: see text] Cisplatin is a highly toxic material used clinically as a potent chemotherapeutic. While effective against some cancers, toxicity limits widespread use and low solubility confounds delivery. To formulate a better tolerated and more water-soluble form of cisplatin, we designed a rap...

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Autores principales: Sharma, Sudhir Kumar, Al Hosani, Sumaya, Kalmouni, Mona, Nair, Anjana Ramdas, Palanikumar, Loganathan, Pasricha, Renu, Sadler, Kirsten C., Magzoub, Mazin, Jagannathan, Ramesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066560/
https://www.ncbi.nlm.nih.gov/pubmed/32175502
http://dx.doi.org/10.1021/acsomega.9b03917
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author Sharma, Sudhir Kumar
Al Hosani, Sumaya
Kalmouni, Mona
Nair, Anjana Ramdas
Palanikumar, Loganathan
Pasricha, Renu
Sadler, Kirsten C.
Magzoub, Mazin
Jagannathan, Ramesh
author_facet Sharma, Sudhir Kumar
Al Hosani, Sumaya
Kalmouni, Mona
Nair, Anjana Ramdas
Palanikumar, Loganathan
Pasricha, Renu
Sadler, Kirsten C.
Magzoub, Mazin
Jagannathan, Ramesh
author_sort Sharma, Sudhir Kumar
collection PubMed
description [Image: see text] Cisplatin is a highly toxic material used clinically as a potent chemotherapeutic. While effective against some cancers, toxicity limits widespread use and low solubility confounds delivery. To formulate a better tolerated and more water-soluble form of cisplatin, we designed a rapid expansion of supercritical solutions (RESS) technique with supercritical carbon dioxide (sc-CO(2)) to collect nanoclusters of cisplatin embedded in dry ice, in a dual-stage collection vessel cooled to liquid nitrogen temperature. These nanoclusters were solubilized in deionized water and further concentrated (up to 51.3 mM) by a Rotovap process, yielding stable cisplatin solutions with solubility up to 15 × (w/w) greater than that of normal cisplatin. Extensive material characterizations of the solutions were carried out to determine any chemical and/or structural changes of the RESS-processed cisplatin. In vitro cytotoxicity studies of these aqueous solutions showed increased cell viability and early apoptosis compared to equivalent concentrations of standard cisplatin solutions. In vivo studies using zebrafish embryos revealed that standard cisplatin solutions were acutely toxic and caused death of rapidly proliferating cells compared to RESS-processed cisplatin, which were better tolerated with reduced general cell death. Increased water solubility and matched chemical identity of RESS-processed aqueous cisplatin solutions indicate the potential to open up novel drug-delivery routes, which is beneficial for new pharmaceutical design and development.
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spelling pubmed-70665602020-03-13 Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity Sharma, Sudhir Kumar Al Hosani, Sumaya Kalmouni, Mona Nair, Anjana Ramdas Palanikumar, Loganathan Pasricha, Renu Sadler, Kirsten C. Magzoub, Mazin Jagannathan, Ramesh ACS Omega [Image: see text] Cisplatin is a highly toxic material used clinically as a potent chemotherapeutic. While effective against some cancers, toxicity limits widespread use and low solubility confounds delivery. To formulate a better tolerated and more water-soluble form of cisplatin, we designed a rapid expansion of supercritical solutions (RESS) technique with supercritical carbon dioxide (sc-CO(2)) to collect nanoclusters of cisplatin embedded in dry ice, in a dual-stage collection vessel cooled to liquid nitrogen temperature. These nanoclusters were solubilized in deionized water and further concentrated (up to 51.3 mM) by a Rotovap process, yielding stable cisplatin solutions with solubility up to 15 × (w/w) greater than that of normal cisplatin. Extensive material characterizations of the solutions were carried out to determine any chemical and/or structural changes of the RESS-processed cisplatin. In vitro cytotoxicity studies of these aqueous solutions showed increased cell viability and early apoptosis compared to equivalent concentrations of standard cisplatin solutions. In vivo studies using zebrafish embryos revealed that standard cisplatin solutions were acutely toxic and caused death of rapidly proliferating cells compared to RESS-processed cisplatin, which were better tolerated with reduced general cell death. Increased water solubility and matched chemical identity of RESS-processed aqueous cisplatin solutions indicate the potential to open up novel drug-delivery routes, which is beneficial for new pharmaceutical design and development. American Chemical Society 2020-02-24 /pmc/articles/PMC7066560/ /pubmed/32175502 http://dx.doi.org/10.1021/acsomega.9b03917 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Sharma, Sudhir Kumar
Al Hosani, Sumaya
Kalmouni, Mona
Nair, Anjana Ramdas
Palanikumar, Loganathan
Pasricha, Renu
Sadler, Kirsten C.
Magzoub, Mazin
Jagannathan, Ramesh
Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity
title Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity
title_full Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity
title_fullStr Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity
title_full_unstemmed Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity
title_short Supercritical CO(2) Processing Generates Aqueous Cisplatin Solutions with Enhanced Cancer Specificity
title_sort supercritical co(2) processing generates aqueous cisplatin solutions with enhanced cancer specificity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066560/
https://www.ncbi.nlm.nih.gov/pubmed/32175502
http://dx.doi.org/10.1021/acsomega.9b03917
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