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Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging

Paclitaxel (PTX) is used as a major antitumor agent for the treatment of recurrent and metastatic breast cancer. For the clinical application of PTX, it needs to be dissolved in an oil/detergent-based solvent due to its poor solubility in an aqueous medium. However, the formulation often causes unde...

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Autores principales: Lee, Jung Eun, Kim, Myung Goo, Jang, Yeon Lim, Lee, Min Sang, Kim, Nak Won, Yin, Yue, Lee, Jong Han, Lim, Su Yeon, Park, Ji Won, Kim, Jaeyun, Lee, Doo Sung, Kim, Sun Hwa, Jeong, Ji Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060380/
https://www.ncbi.nlm.nih.gov/pubmed/30044159
http://dx.doi.org/10.1080/10717544.2018.1489430
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author Lee, Jung Eun
Kim, Myung Goo
Jang, Yeon Lim
Lee, Min Sang
Kim, Nak Won
Yin, Yue
Lee, Jong Han
Lim, Su Yeon
Park, Ji Won
Kim, Jaeyun
Lee, Doo Sung
Kim, Sun Hwa
Jeong, Ji Hoon
author_facet Lee, Jung Eun
Kim, Myung Goo
Jang, Yeon Lim
Lee, Min Sang
Kim, Nak Won
Yin, Yue
Lee, Jong Han
Lim, Su Yeon
Park, Ji Won
Kim, Jaeyun
Lee, Doo Sung
Kim, Sun Hwa
Jeong, Ji Hoon
author_sort Lee, Jung Eun
collection PubMed
description Paclitaxel (PTX) is used as a major antitumor agent for the treatment of recurrent and metastatic breast cancer. For the clinical application of PTX, it needs to be dissolved in an oil/detergent-based solvent due to its poor solubility in an aqueous medium. However, the formulation often causes undesirable complications including hypersensitivity reactions and limited tumor distribution, resulting in a lower dose-dependent antitumor effect. Herein, we introduce a facile and oil-free method to prepare albumin-based PTX nanoparticles for efficient systemic cancer therapy using a conjugate of human serum albumin (HSA) and poly(ethyleneglycol) (PEG). PTX were efficiently incorporated in the self-assembled HSA-PEG nanoparticles (HSA-PEG/PTX) using a simple film casting and re-hydration procedure without additional processes such as application of high pressure/shear or chemical crosslinking. The spherical HSA-PEG nanoparticle with a hydrodynamic diameter of ca. 280 nm mediates efficient cellular delivery, leading to comparable or even higher cytotoxicity in various breast cancer cells than that of the commercially available Abraxane(®). When systemically administered in a mouse xenograft model for human breast cancer, the HSA-PEG-based nanoparticle formulation exhibited an extended systemic circulation for more than 96 h and enhanced intratumoral accumulation, resulting in a remarkable anticancer effect and prolonged survival of the animals.
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spelling pubmed-60603802018-08-17 Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging Lee, Jung Eun Kim, Myung Goo Jang, Yeon Lim Lee, Min Sang Kim, Nak Won Yin, Yue Lee, Jong Han Lim, Su Yeon Park, Ji Won Kim, Jaeyun Lee, Doo Sung Kim, Sun Hwa Jeong, Ji Hoon Drug Deliv Research Article Paclitaxel (PTX) is used as a major antitumor agent for the treatment of recurrent and metastatic breast cancer. For the clinical application of PTX, it needs to be dissolved in an oil/detergent-based solvent due to its poor solubility in an aqueous medium. However, the formulation often causes undesirable complications including hypersensitivity reactions and limited tumor distribution, resulting in a lower dose-dependent antitumor effect. Herein, we introduce a facile and oil-free method to prepare albumin-based PTX nanoparticles for efficient systemic cancer therapy using a conjugate of human serum albumin (HSA) and poly(ethyleneglycol) (PEG). PTX were efficiently incorporated in the self-assembled HSA-PEG nanoparticles (HSA-PEG/PTX) using a simple film casting and re-hydration procedure without additional processes such as application of high pressure/shear or chemical crosslinking. The spherical HSA-PEG nanoparticle with a hydrodynamic diameter of ca. 280 nm mediates efficient cellular delivery, leading to comparable or even higher cytotoxicity in various breast cancer cells than that of the commercially available Abraxane(®). When systemically administered in a mouse xenograft model for human breast cancer, the HSA-PEG-based nanoparticle formulation exhibited an extended systemic circulation for more than 96 h and enhanced intratumoral accumulation, resulting in a remarkable anticancer effect and prolonged survival of the animals. Taylor & Francis 2018-07-25 /pmc/articles/PMC6060380/ /pubmed/30044159 http://dx.doi.org/10.1080/10717544.2018.1489430 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lee, Jung Eun
Kim, Myung Goo
Jang, Yeon Lim
Lee, Min Sang
Kim, Nak Won
Yin, Yue
Lee, Jong Han
Lim, Su Yeon
Park, Ji Won
Kim, Jaeyun
Lee, Doo Sung
Kim, Sun Hwa
Jeong, Ji Hoon
Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging
title Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging
title_full Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging
title_fullStr Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging
title_full_unstemmed Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging
title_short Self-assembled PEGylated albumin nanoparticles (SPAN) as a platform for cancer chemotherapy and imaging
title_sort self-assembled pegylated albumin nanoparticles (span) as a platform for cancer chemotherapy and imaging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6060380/
https://www.ncbi.nlm.nih.gov/pubmed/30044159
http://dx.doi.org/10.1080/10717544.2018.1489430
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