Recent advances in PEG-PLA block copolymer nanoparticles

被引:2
|
作者
Xiao, Ren Zhong [1 ]
Zeng, Zhao Wu [1 ,2 ]
Zhou, Guang Lin [1 ]
Wang, Jun Jie [1 ]
Li, Fan Zhu [2 ]
Wang, An Ming [1 ]
机构
[1] Hangzhou Normal Univ, Res Ctr Biomed & Hlth, Hangzhou 310012, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Pharmaceut Sci, Hangzhou, Zhejiang, Peoples R China
来源
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
PEG-PLA; block copolymer; nanoparticles; drug delivery system; IN-VITRO; DRUG-RELEASE; PEGYLATED NANOPARTICLES; LOADED POLYMERSOMES; PROTEIN ADSORPTION; TRIBLOCK COPOLYMER; BRAIN DELIVERY; MICELLES; PACLITAXEL; DEGRADATION;
D O I
10.2147/ijn.S14912
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:1057 / 1065
页数:9
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