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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
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.
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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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