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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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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. |
format | Online Article Text |
id | pubmed-5890116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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