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Recent advances in PEG–PLA block copolymer nanoparticles

Due to their small particle size and large and modifiable surface, nanoparticles have unique advantages compared with other drug carriers. As a research focus in recent years, polyethylene glycol–polylactic acid (PEG–PLA) block copolymer and its end-group derivative nanoparticles can enhance the dru...

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Detalles Bibliográficos
Autores principales: Xiao, Ren Zhong, Zeng, Zhao Wu, Zhou, Guang Lin, Wang, Jun Jie, Li, Fan Zhu, Wang, An Ming
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000205/
https://www.ncbi.nlm.nih.gov/pubmed/21170353
http://dx.doi.org/10.2147/IJN.S14912
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author Xiao, Ren Zhong
Zeng, Zhao Wu
Zhou, Guang Lin
Wang, Jun Jie
Li, Fan Zhu
Wang, An Ming
author_facet Xiao, Ren Zhong
Zeng, Zhao Wu
Zhou, Guang Lin
Wang, Jun Jie
Li, Fan Zhu
Wang, An Ming
author_sort Xiao, Ren Zhong
collection PubMed
description Due to their small particle size and large and modifiable surface, nanoparticles have unique advantages compared with other drug carriers. As a research focus in recent years, polyethylene glycol–polylactic acid (PEG–PLA) block copolymer and its end-group derivative nanoparticles can enhance the drug loading of hydrophobic drugs, reduce the burst effect, avoid being engulfed by phagocytes, increase the circulation time of drugs in blood, and improve bioavailability. Additionally, due to their smaller particle size and modified surface, these nanoparticles can accumulate in inflammation or target locations to enhance drug efficacy and reduce toxicity. Recent advances in PEG–PLA block copolymer nanoparticles, including the synthesis of PEG–PLA and the preparation of PEG–PLA nanoparticles, were introduced in this study, in particular the drug release and modifiable characteristics of PEG–PLA nanoparticles and their application in pharmaceutical preparations.
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spelling pubmed-30002052010-12-17 Recent advances in PEG–PLA block copolymer nanoparticles Xiao, Ren Zhong Zeng, Zhao Wu Zhou, Guang Lin Wang, Jun Jie Li, Fan Zhu Wang, An Ming Int J Nanomedicine Review Due to their small particle size and large and modifiable surface, nanoparticles have unique advantages compared with other drug carriers. As a research focus in recent years, polyethylene glycol–polylactic acid (PEG–PLA) block copolymer and its end-group derivative nanoparticles can enhance the drug loading of hydrophobic drugs, reduce the burst effect, avoid being engulfed by phagocytes, increase the circulation time of drugs in blood, and improve bioavailability. Additionally, due to their smaller particle size and modified surface, these nanoparticles can accumulate in inflammation or target locations to enhance drug efficacy and reduce toxicity. Recent advances in PEG–PLA block copolymer nanoparticles, including the synthesis of PEG–PLA and the preparation of PEG–PLA nanoparticles, were introduced in this study, in particular the drug release and modifiable characteristics of PEG–PLA nanoparticles and their application in pharmaceutical preparations. Dove Medical Press 2010 2010-11-26 /pmc/articles/PMC3000205/ /pubmed/21170353 http://dx.doi.org/10.2147/IJN.S14912 Text en © 2010 Xiao 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 Review
Xiao, Ren Zhong
Zeng, Zhao Wu
Zhou, Guang Lin
Wang, Jun Jie
Li, Fan Zhu
Wang, An Ming
Recent advances in PEG–PLA block copolymer nanoparticles
title Recent advances in PEG–PLA block copolymer nanoparticles
title_full Recent advances in PEG–PLA block copolymer nanoparticles
title_fullStr Recent advances in PEG–PLA block copolymer nanoparticles
title_full_unstemmed Recent advances in PEG–PLA block copolymer nanoparticles
title_short Recent advances in PEG–PLA block copolymer nanoparticles
title_sort recent advances in peg–pla block copolymer nanoparticles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000205/
https://www.ncbi.nlm.nih.gov/pubmed/21170353
http://dx.doi.org/10.2147/IJN.S14912
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