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Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy

For the treatment of malignancy, many therapeutic agents, including small molecules, photosensitizers, immunomodulators, proteins and genes, and so forth, have been loaded into nanocarriers for controllable cancer therapy. Among these nanocarriers, polymeric micelles have been considered as one of t...

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Detalles Bibliográficos
Autores principales: Wang, Jixue, Li, Shengxian, Han, Yuping, Guan, Jingjing, Chung, Shirley, Wang, Chunxi, Li, Di
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890116/
https://www.ncbi.nlm.nih.gov/pubmed/29662450
http://dx.doi.org/10.3389/fphar.2018.00202
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author Wang, Jixue
Li, Shengxian
Han, Yuping
Guan, Jingjing
Chung, Shirley
Wang, Chunxi
Li, Di
author_facet Wang, Jixue
Li, Shengxian
Han, Yuping
Guan, Jingjing
Chung, Shirley
Wang, Chunxi
Li, Di
author_sort Wang, Jixue
collection PubMed
description For the treatment of malignancy, many therapeutic agents, including small molecules, photosensitizers, immunomodulators, proteins and genes, and so forth, have been loaded into nanocarriers for controllable cancer therapy. Among these nanocarriers, polymeric micelles have been considered as one of the most promising nanocarriers, some of which have already been applied in different stages of clinical trials. The successful advantages of polymeric micelles from bench to bedside are due to their special core/shell structures, which can carry specific drugs in certain disease conditions. Particularly, poly(ethylene glycol)–polylactide (PEG–PLA) micelles have been considered as one of the most promising platforms for drug delivery. The PEG shell effectively prevents the adsorption of proteins and phagocytes, thereby evidently extending the blood circulation period. Meanwhile, the hydrophobic PLA core can effectively encapsulate many therapeutic agents. This review summarizes recent advances in PEG–PLA micelles for the treatment of malignancy. In addition, future perspectives for the development of PEG–PLA micelles as drug delivery systems are also presented.
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spelling pubmed-58901162018-04-16 Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy Wang, Jixue Li, Shengxian Han, Yuping Guan, Jingjing Chung, Shirley Wang, Chunxi Li, Di Front Pharmacol Pharmacology For the treatment of malignancy, many therapeutic agents, including small molecules, photosensitizers, immunomodulators, proteins and genes, and so forth, have been loaded into nanocarriers for controllable cancer therapy. Among these nanocarriers, polymeric micelles have been considered as one of the most promising nanocarriers, some of which have already been applied in different stages of clinical trials. The successful advantages of polymeric micelles from bench to bedside are due to their special core/shell structures, which can carry specific drugs in certain disease conditions. Particularly, poly(ethylene glycol)–polylactide (PEG–PLA) micelles have been considered as one of the most promising platforms for drug delivery. The PEG shell effectively prevents the adsorption of proteins and phagocytes, thereby evidently extending the blood circulation period. Meanwhile, the hydrophobic PLA core can effectively encapsulate many therapeutic agents. This review summarizes recent advances in PEG–PLA micelles for the treatment of malignancy. In addition, future perspectives for the development of PEG–PLA micelles as drug delivery systems are also presented. Frontiers Media S.A. 2018-03-08 /pmc/articles/PMC5890116/ /pubmed/29662450 http://dx.doi.org/10.3389/fphar.2018.00202 Text en Copyright © 2018 Wang, Li, Han, Guan, Chung, Wang and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wang, Jixue
Li, Shengxian
Han, Yuping
Guan, Jingjing
Chung, Shirley
Wang, Chunxi
Li, Di
Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy
title Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy
title_full Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy
title_fullStr Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy
title_full_unstemmed Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy
title_short Poly(Ethylene Glycol)–Polylactide Micelles for Cancer Therapy
title_sort poly(ethylene glycol)–polylactide micelles for cancer therapy
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890116/
https://www.ncbi.nlm.nih.gov/pubmed/29662450
http://dx.doi.org/10.3389/fphar.2018.00202
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