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Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer
BACKGROUND: Although cisplatin is extensively used in the clinical field, its intrinsic toxicity limits its clinical use. We investigated nanoparticle formations of poly(acrylic acid-co-methyl methacrylate) (PAA-MMA) incorporating cisplatin and their antitumor activity in vitro and in vivo. METHODS:...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743654/ https://www.ncbi.nlm.nih.gov/pubmed/23966778 http://dx.doi.org/10.2147/IJN.S48367 |
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author | Lee, Kyung Dong Jeong, Young-Il Kim, Da Hye Lim, Gyun-Taek Choi, Ki-Choon |
author_facet | Lee, Kyung Dong Jeong, Young-Il Kim, Da Hye Lim, Gyun-Taek Choi, Ki-Choon |
author_sort | Lee, Kyung Dong |
collection | PubMed |
description | BACKGROUND: Although cisplatin is extensively used in the clinical field, its intrinsic toxicity limits its clinical use. We investigated nanoparticle formations of poly(acrylic acid-co-methyl methacrylate) (PAA-MMA) incorporating cisplatin and their antitumor activity in vitro and in vivo. METHODS: Cisplatin-incorporated nanoparticles were prepared through the ion-complex formation between acrylic acid and cisplatin. The anticancer activity of cisplatin-incorporated nanoparticles was assessed with CT26 colorectal carcinoma cells. RESULTS: Cisplatin-incorporated nanoparticles have small particle sizes of less than 200 nm with spherical shapes. Drug content was increased according to the increase of the feeding amount of cisplatin and acrylic acid content in the copolymer. The higher acrylic acid content in the copolymer induced increase of particle size and decrease of zeta potential. Cisplatin-incorporated nanoparticles showed a similar growth-inhibitory effect against CT26 tumor cells in vitro. However, cisplatin-incorporated nanoparticles showed improved antitumor activity against an animal tumor xenograft model. CONCLUSION: We suggest that PAA-MMA nanoparticles incorporating cisplatin are promising carriers for an antitumor drug-delivery system. |
format | Online Article Text |
id | pubmed-3743654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37436542013-08-21 Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer Lee, Kyung Dong Jeong, Young-Il Kim, Da Hye Lim, Gyun-Taek Choi, Ki-Choon Int J Nanomedicine Original Research BACKGROUND: Although cisplatin is extensively used in the clinical field, its intrinsic toxicity limits its clinical use. We investigated nanoparticle formations of poly(acrylic acid-co-methyl methacrylate) (PAA-MMA) incorporating cisplatin and their antitumor activity in vitro and in vivo. METHODS: Cisplatin-incorporated nanoparticles were prepared through the ion-complex formation between acrylic acid and cisplatin. The anticancer activity of cisplatin-incorporated nanoparticles was assessed with CT26 colorectal carcinoma cells. RESULTS: Cisplatin-incorporated nanoparticles have small particle sizes of less than 200 nm with spherical shapes. Drug content was increased according to the increase of the feeding amount of cisplatin and acrylic acid content in the copolymer. The higher acrylic acid content in the copolymer induced increase of particle size and decrease of zeta potential. Cisplatin-incorporated nanoparticles showed a similar growth-inhibitory effect against CT26 tumor cells in vitro. However, cisplatin-incorporated nanoparticles showed improved antitumor activity against an animal tumor xenograft model. CONCLUSION: We suggest that PAA-MMA nanoparticles incorporating cisplatin are promising carriers for an antitumor drug-delivery system. Dove Medical Press 2013 2013-08-08 /pmc/articles/PMC3743654/ /pubmed/23966778 http://dx.doi.org/10.2147/IJN.S48367 Text en © 2013 Lee et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed. |
spellingShingle | Original Research Lee, Kyung Dong Jeong, Young-Il Kim, Da Hye Lim, Gyun-Taek Choi, Ki-Choon Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
title | Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
title_full | Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
title_fullStr | Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
title_full_unstemmed | Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
title_short | Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
title_sort | cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate) copolymer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743654/ https://www.ncbi.nlm.nih.gov/pubmed/23966778 http://dx.doi.org/10.2147/IJN.S48367 |
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