Effects of copolymer component on the properties of phosphorylcholine micelles

Zhengzhong Wu,1 Mengtan Cai,1 Jun Cao,2 Jiaxing Zhang,1 Xianglin Luo1,3 1College of Polymer Science and Engineering, 2National Engineering Research Center for Biomaterials, 3State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, People’s Republic of China Abs...

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Autores principales: Wu Z, Cai M, Cao J, Zhang J, Luo X
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Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:46bf1aec215d420e80cd6114c6badc572021-12-02T02:41:35ZEffects of copolymer component on the properties of phosphorylcholine micelles1178-2013https://doaj.org/article/46bf1aec215d420e80cd6114c6badc572017-01-01T00:00:00Zhttps://www.dovepress.com/effects-of-copolymer-component-on-the-properties-of-phosphorylcholine--peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Zhengzhong Wu,1 Mengtan Cai,1 Jun Cao,2 Jiaxing Zhang,1 Xianglin Luo1,3 1College of Polymer Science and Engineering, 2National Engineering Research Center for Biomaterials, 3State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, People’s Republic of China Abstract: Zwitterionic polymers have unique features, such as good compatibility, and show promise in the application of drug delivery. In this study, the zwitterionic copolymers, poly(ε-caprolactone)-b-poly(2-methacryloyloxyethyl phosphorylcholine) with disulfide (PCL-ss-PMPC) or poly(ε-caprolactone)-b-poly(2-methacryloyloxyethyl phosphorylcholine) or without disulfide (PCL-PMPC) and with different block lengths in PCL-ss-PMPC, were designed. The designed copolymers were obtained by a combination of ring-opening polymerization and atom transferring radical polymerization. The crystallization properties of these polymers were investigated. The micelles were prepared based on the obtained copolymers with zwitterionic phosphorylcholine as the hydrophilic shell and PCL as the hydrophobic core. The size distributions of the blank micelles and the doxorubicin (DOX)-loaded micelles were uniform, and the micelle diameters were <100 nm. In vitro drug release and intracellular drug release results showed that DOX-loaded PCL-ss-PMPC micelles could release drugs faster responding to the reduction condition and the intracellular microenvironment in contrast to PCL-PMPC micelles. Moreover, in vitro cytotoxicity evaluation revealed that the designed copolymers possessed low cell toxicity, and the inhibiting effect of DOX-loaded phosphorylcholine micelles to tumor cells was related to the components of these copolymers. These results reveal that the reduction-responsive phosphorylcholine micelles with a suitable ratio of hydrophilic/hydrophobic units can serve as promising drug carriers. Keywords: zwitterionic, reduction-sensitive, disulfide, phosphorylcholineWu ZCai MCao JZhang JLuo XDove Medical Pressarticlezwitterionicreduction-sensitivedisulfidephosphorylcholineMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 487-500 (2017)
institution DOAJ
collection DOAJ
language EN
topic zwitterionic
reduction-sensitive
disulfide
phosphorylcholine
Medicine (General)
R5-920
spellingShingle zwitterionic
reduction-sensitive
disulfide
phosphorylcholine
Medicine (General)
R5-920
Wu Z
Cai M
Cao J
Zhang J
Luo X
Effects of copolymer component on the properties of phosphorylcholine micelles
description Zhengzhong Wu,1 Mengtan Cai,1 Jun Cao,2 Jiaxing Zhang,1 Xianglin Luo1,3 1College of Polymer Science and Engineering, 2National Engineering Research Center for Biomaterials, 3State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, People’s Republic of China Abstract: Zwitterionic polymers have unique features, such as good compatibility, and show promise in the application of drug delivery. In this study, the zwitterionic copolymers, poly(ε-caprolactone)-b-poly(2-methacryloyloxyethyl phosphorylcholine) with disulfide (PCL-ss-PMPC) or poly(ε-caprolactone)-b-poly(2-methacryloyloxyethyl phosphorylcholine) or without disulfide (PCL-PMPC) and with different block lengths in PCL-ss-PMPC, were designed. The designed copolymers were obtained by a combination of ring-opening polymerization and atom transferring radical polymerization. The crystallization properties of these polymers were investigated. The micelles were prepared based on the obtained copolymers with zwitterionic phosphorylcholine as the hydrophilic shell and PCL as the hydrophobic core. The size distributions of the blank micelles and the doxorubicin (DOX)-loaded micelles were uniform, and the micelle diameters were <100 nm. In vitro drug release and intracellular drug release results showed that DOX-loaded PCL-ss-PMPC micelles could release drugs faster responding to the reduction condition and the intracellular microenvironment in contrast to PCL-PMPC micelles. Moreover, in vitro cytotoxicity evaluation revealed that the designed copolymers possessed low cell toxicity, and the inhibiting effect of DOX-loaded phosphorylcholine micelles to tumor cells was related to the components of these copolymers. These results reveal that the reduction-responsive phosphorylcholine micelles with a suitable ratio of hydrophilic/hydrophobic units can serve as promising drug carriers. Keywords: zwitterionic, reduction-sensitive, disulfide, phosphorylcholine
format article
author Wu Z
Cai M
Cao J
Zhang J
Luo X
author_facet Wu Z
Cai M
Cao J
Zhang J
Luo X
author_sort Wu Z
title Effects of copolymer component on the properties of phosphorylcholine micelles
title_short Effects of copolymer component on the properties of phosphorylcholine micelles
title_full Effects of copolymer component on the properties of phosphorylcholine micelles
title_fullStr Effects of copolymer component on the properties of phosphorylcholine micelles
title_full_unstemmed Effects of copolymer component on the properties of phosphorylcholine micelles
title_sort effects of copolymer component on the properties of phosphorylcholine micelles
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/46bf1aec215d420e80cd6114c6badc57
work_keys_str_mv AT wuz effectsofcopolymercomponentonthepropertiesofphosphorylcholinemicelles
AT caim effectsofcopolymercomponentonthepropertiesofphosphorylcholinemicelles
AT caoj effectsofcopolymercomponentonthepropertiesofphosphorylcholinemicelles
AT zhangj effectsofcopolymercomponentonthepropertiesofphosphorylcholinemicelles
AT luox effectsofcopolymercomponentonthepropertiesofphosphorylcholinemicelles
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