Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy

Keun Sang Oh,1,* Kyungim Kim,1,* Byeong Deok Yoon,1 Hye Jin Lee,1 Dal Yong Park,1 Eun-yeong Kim,1 Kiho Lee,1 Jae Hong Seo,2 Soon Hong Yuk1,2 1College of Pharmacy, Korea University, Sejong, 2Biomedical Research Center, Korea University Guro Hospital, Guro-gu, Seoul, Republic of Korea *These authors...

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Autores principales: Oh KS, Kim KI, Yoon BD, Lee HJ, Park DY, Kim EY, Lee K, Seo JH, Yuk SH
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Lenguaje:EN
Publicado: Dove Medical Press 2016
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Acceso en línea:https://doaj.org/article/c0130dda0bcc4482bd4c6aede607004a
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spelling oai:doaj.org-article:c0130dda0bcc4482bd4c6aede607004a2021-12-02T07:22:59ZDocetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy1178-2013https://doaj.org/article/c0130dda0bcc4482bd4c6aede607004a2016-03-01T00:00:00Zhttps://www.dovepress.com/docetaxel-loaded-multilayer-nanoparticles-with-nanodroplets-for-cancer-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Keun Sang Oh,1,* Kyungim Kim,1,* Byeong Deok Yoon,1 Hye Jin Lee,1 Dal Yong Park,1 Eun-yeong Kim,1 Kiho Lee,1 Jae Hong Seo,2 Soon Hong Yuk1,2 1College of Pharmacy, Korea University, Sejong, 2Biomedical Research Center, Korea University Guro Hospital, Guro-gu, Seoul, Republic of Korea *These authors contributed equally to this work Abstract: A mixture of docetaxel (DTX) and Solutol® HS 15 (Solutol) transiently formed nanodroplets when it was suspended in an aqueous medium. However, nanodroplets that comprised DTX and Solutol showed a rapid precipitation of DTX because of their unstable characteristics in the aqueous medium. The incorporation of nanodroplets that comprised DTX and Solutol through vesicle fusion and subsequent stabilization was designed to prepare multilayer nanoparticles (NPs) with a DTX-loaded Solutol nanodroplet (as template NPs) core for an efficient delivery of DTX as a chemotherapeutic drug. As a result, the DTX-loaded Solutol nanodroplets (~11.7 nm) were observed to have an increased average diameter (from 11.7 nm to 156.1 nm) and a good stability of the hydrated NPs without precipitation of DTX by vesicle fusion and multilayered structure, respectively. Also, a long circulation of the multilayer NPs was observed, and this was due to the presence of Pluronic F-68 on the surface of the multilayer NPs. This led to an improved antitumor efficacy based on the enhanced permeation and retention effect. Therefore, this study indicated that the multilayer NPs have a considerable potential as a drug delivery system with an enhanced therapeutic efficacy by blood circulation and with low side effects. Keywords: multilayer nanoparticles, Solutol, Pluronic F-68, docetaxel, cancer therapyOh KSKim KIYoon BDLee HJPark DYKim EYLee KSeo JHYuk SHDove Medical PressarticleMultilayer nanoparticlesSolutolPluronic F-68DocetaxelCancer therapyMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2016, Iss default, Pp 1077-1087 (2016)
institution DOAJ
collection DOAJ
language EN
topic Multilayer nanoparticles
Solutol
Pluronic F-68
Docetaxel
Cancer therapy
Medicine (General)
R5-920
spellingShingle Multilayer nanoparticles
Solutol
Pluronic F-68
Docetaxel
Cancer therapy
Medicine (General)
R5-920
Oh KS
Kim KI
Yoon BD
Lee HJ
Park DY
Kim EY
Lee K
Seo JH
Yuk SH
Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
description Keun Sang Oh,1,* Kyungim Kim,1,* Byeong Deok Yoon,1 Hye Jin Lee,1 Dal Yong Park,1 Eun-yeong Kim,1 Kiho Lee,1 Jae Hong Seo,2 Soon Hong Yuk1,2 1College of Pharmacy, Korea University, Sejong, 2Biomedical Research Center, Korea University Guro Hospital, Guro-gu, Seoul, Republic of Korea *These authors contributed equally to this work Abstract: A mixture of docetaxel (DTX) and Solutol® HS 15 (Solutol) transiently formed nanodroplets when it was suspended in an aqueous medium. However, nanodroplets that comprised DTX and Solutol showed a rapid precipitation of DTX because of their unstable characteristics in the aqueous medium. The incorporation of nanodroplets that comprised DTX and Solutol through vesicle fusion and subsequent stabilization was designed to prepare multilayer nanoparticles (NPs) with a DTX-loaded Solutol nanodroplet (as template NPs) core for an efficient delivery of DTX as a chemotherapeutic drug. As a result, the DTX-loaded Solutol nanodroplets (~11.7 nm) were observed to have an increased average diameter (from 11.7 nm to 156.1 nm) and a good stability of the hydrated NPs without precipitation of DTX by vesicle fusion and multilayered structure, respectively. Also, a long circulation of the multilayer NPs was observed, and this was due to the presence of Pluronic F-68 on the surface of the multilayer NPs. This led to an improved antitumor efficacy based on the enhanced permeation and retention effect. Therefore, this study indicated that the multilayer NPs have a considerable potential as a drug delivery system with an enhanced therapeutic efficacy by blood circulation and with low side effects. Keywords: multilayer nanoparticles, Solutol, Pluronic F-68, docetaxel, cancer therapy
format article
author Oh KS
Kim KI
Yoon BD
Lee HJ
Park DY
Kim EY
Lee K
Seo JH
Yuk SH
author_facet Oh KS
Kim KI
Yoon BD
Lee HJ
Park DY
Kim EY
Lee K
Seo JH
Yuk SH
author_sort Oh KS
title Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
title_short Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
title_full Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
title_fullStr Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
title_full_unstemmed Docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
title_sort docetaxel-loaded multilayer nanoparticles with nanodroplets for cancer therapy
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/c0130dda0bcc4482bd4c6aede607004a
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