Self-assembled micelles of biodegradable triblock copolymers based on poly(ethyl ethylene phosphate) and poly(ε-caprolactone) as drug carriers

被引:144
作者
Wang, Yu-Cai [3 ]
Tang, Ling-Yan [1 ,2 ]
Sun, Tian-Meng [1 ,2 ]
Li, Chang-Hua [3 ]
Xiong, Meng-Hua [3 ]
Wang, Jun [1 ,2 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Sch Life Sci, Hefei 230026, Anhui, Peoples R China
[3] Univ Sci & Technol China, Dept Polymer Sci & Engn, Hefei 230026, Anhui, Peoples R China
关键词
D O I
10.1021/bm700732g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of novel amphiphilic triblock copolymers of poly(ethyl ethylene phosphate) and poly (E-caprolactone) (PEEP-PCL-PEEP) with various PEEP and PCL block lengths were synthesized and characterized. These triblock copolymers formed micelles composed of a hydrophobic core of poly (E-caprolactone) (PCL) and a hydrophilic shell of poly(ethyl ethylene phosphate) (PEEP) in aqueous solution. The micelle morphology was spherical, determined by transmission electron microscopy. It was found that the size and critical micelle concentration values of the micelles depended on both hydrophobic PCL block length and PEEP hydrophilic block length. The in vitro degradation characteristics of the triblock copolymers were investigated in micellar form, showing that these copolymers were completely biodegradable under enzymatic catalysis of Pseudomonas lipase and phosphodiesterase I. These triblock copolymers were used for paclitaxel (PTX) encapsulation to demonstrate the potential in drug delivery. PTX was successfully loaded into the micelles, and the in vitro release profile was found to be correlative to the polymer composition. These biodegradable triblock copolymer micelles are potential as novel carriers for hydrophobic drug delivery.
引用
收藏
页码:388 / 395
页数:8
相关论文
共 39 条
[1]   Self-porating polymersomes of PEG-PLA and PEG-PCL: hydrolysis-triggered controlled release vesicles [J].
Ahmed, F ;
Discher, DE .
JOURNAL OF CONTROLLED RELEASE, 2004, 96 (01) :37-53
[2]   Micelles of methoxy poly(ethylene oxide)-b-poly(ε-caprolactone) as vehicles for the solubilization and controlled delivery of Cyclosporine A [J].
Aliabadi, HM ;
Mahmud, A ;
Sharifabadi, AD ;
Lavasanifar, A .
JOURNAL OF CONTROLLED RELEASE, 2005, 104 (02) :301-311
[3]   Formation of core-shell type biodegradable polymeric micelles from amphiphilic poly(aspartic acid)-block-polylactide diblock copolymer [J].
Arimura, H ;
Ohya, Y ;
Ouchi, T .
BIOMACROMOLECULES, 2005, 6 (02) :720-725
[4]   Cyclic nucleotide phosphodiesterases: Molecular regulation to clinical use [J].
Bender, Andrew T. ;
Beavo, Joseph A. .
PHARMACOLOGICAL REVIEWS, 2006, 58 (03) :488-520
[5]   Biodegradable nanoparticles of amphiphilic triblock copolymers based on poly(3-hydroxybutyrate) and poly(ethylene glycol) as drug carriers [J].
Chen, Cheng ;
Yu, Chung Him ;
Cheng, Yin Chung ;
Yu, Peter H. F. ;
Cheung, Man Ken .
BIOMATERIALS, 2006, 27 (27) :4804-4814
[6]   Targeted worm micelles [J].
Dalhaimer, P ;
Engler, AJ ;
Parthasarathy, R ;
Discher, DE .
BIOMACROMOLECULES, 2004, 5 (05) :1714-1719
[7]   Methoxy poly(ethylene glycol)-poly(lactide) (MPEG-PLA) nanoparticles for controlled delivery of anticancer drugs [J].
Dong, YC ;
Feng, SS .
BIOMATERIALS, 2004, 25 (14) :2843-2849
[8]   Synthesis and micellization of amphiphilic brush-coil block copolymer based on poly(ε-caprolactone) and PEGylated polyphosphoester [J].
Du, Jhi-Zhi ;
Chen, Dong-Ping ;
Wang, Yu-Cai ;
Xiao, Chun-Sheng ;
Lu, Yi-Jie ;
Wang, Jun ;
Zhang, Guang-Zhao .
BIOMACROMOLECULES, 2006, 7 (06) :1898-1903
[9]   Hydrolytic degradation of poly(ethylene oxide)-block-polycaprolactone worm micelles [J].
Geng, Y ;
Discher, DE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (37) :12780-12781
[10]   Bioresorbable vesicles formed through spontaneous self-assembly of amphiphilic poly(ethylene oxide)-block-polycaprolactone [J].
Ghoroghchian, PP ;
Li, GZ ;
Levine, DH ;
Davis, KP ;
Bates, FS ;
Hammer, DA ;
Therien, MJ .
MACROMOLECULES, 2006, 39 (05) :1673-1675