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Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy
Nanoparticles are useful delivery vehicles for promising drug candidates that face obstacles for clinical applicability. Sirolimus, an inhibitor of mammalian target of rapamycin has gained attention for targeted anticancer therapy, but its clinical application has been limited by its poor solubility...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356221/ https://www.ncbi.nlm.nih.gov/pubmed/22619555 http://dx.doi.org/10.2147/IJN.S29480 |
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author | Woo, Ha Na Chung, Hye Kyung Ju, Eun Jin Jung, Joohee Kang, Hye-Won Lee, Sa-Won Seo, Min-Hyo Lee, Jin Seong Lee, Jung Shin Park, Heon Joo Song, Si Yeol Jeong, Seong-Yun Choi, Eun Kyung |
author_facet | Woo, Ha Na Chung, Hye Kyung Ju, Eun Jin Jung, Joohee Kang, Hye-Won Lee, Sa-Won Seo, Min-Hyo Lee, Jin Seong Lee, Jung Shin Park, Heon Joo Song, Si Yeol Jeong, Seong-Yun Choi, Eun Kyung |
author_sort | Woo, Ha Na |
collection | PubMed |
description | Nanoparticles are useful delivery vehicles for promising drug candidates that face obstacles for clinical applicability. Sirolimus, an inhibitor of mammalian target of rapamycin has gained attention for targeted anticancer therapy, but its clinical application has been limited by its poor solubility. This study was designed to enhance the feasibility of sirolimus for human cancer treatment. Polymeric nanoparticle (PNP)–sirolimus was developed as an injectable formulation and has been characterized by transmission electron microscopy and dynamic light scattering. Pharmacokinetic analysis revealed that PNP–sirolimus has prolonged circulation in the blood. In addition, PNP–sirolimus preserved the in vitro killing effect of free sirolimus against cancer cells, and intravenous administration displayed its potent in vivo anticancer efficacy in xenograft tumor mice. In addition, PNP–sirolimus enhanced the radiotherapeutic efficacy of sirolimus both in vitro and in vivo. Clinical application of PNP–sirolimus is a promising strategy for human cancer treatment. |
format | Online Article Text |
id | pubmed-3356221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33562212012-05-22 Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy Woo, Ha Na Chung, Hye Kyung Ju, Eun Jin Jung, Joohee Kang, Hye-Won Lee, Sa-Won Seo, Min-Hyo Lee, Jin Seong Lee, Jung Shin Park, Heon Joo Song, Si Yeol Jeong, Seong-Yun Choi, Eun Kyung Int J Nanomedicine Original Research Nanoparticles are useful delivery vehicles for promising drug candidates that face obstacles for clinical applicability. Sirolimus, an inhibitor of mammalian target of rapamycin has gained attention for targeted anticancer therapy, but its clinical application has been limited by its poor solubility. This study was designed to enhance the feasibility of sirolimus for human cancer treatment. Polymeric nanoparticle (PNP)–sirolimus was developed as an injectable formulation and has been characterized by transmission electron microscopy and dynamic light scattering. Pharmacokinetic analysis revealed that PNP–sirolimus has prolonged circulation in the blood. In addition, PNP–sirolimus preserved the in vitro killing effect of free sirolimus against cancer cells, and intravenous administration displayed its potent in vivo anticancer efficacy in xenograft tumor mice. In addition, PNP–sirolimus enhanced the radiotherapeutic efficacy of sirolimus both in vitro and in vivo. Clinical application of PNP–sirolimus is a promising strategy for human cancer treatment. Dove Medical Press 2012 2012-04-27 /pmc/articles/PMC3356221/ /pubmed/22619555 http://dx.doi.org/10.2147/IJN.S29480 Text en © 2012 Woo et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Woo, Ha Na Chung, Hye Kyung Ju, Eun Jin Jung, Joohee Kang, Hye-Won Lee, Sa-Won Seo, Min-Hyo Lee, Jin Seong Lee, Jung Shin Park, Heon Joo Song, Si Yeol Jeong, Seong-Yun Choi, Eun Kyung Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
title | Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
title_full | Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
title_fullStr | Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
title_full_unstemmed | Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
title_short | Preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
title_sort | preclinical evaluation of injectable sirolimus formulated with polymeric nanoparticle for cancer therapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356221/ https://www.ncbi.nlm.nih.gov/pubmed/22619555 http://dx.doi.org/10.2147/IJN.S29480 |
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