Synthesis and evaluation of a star amphiphilic block copolymer from poly(ε-caprolactone) and poly(ethylene glycol) as a potential drug delivery carrier

被引:293
作者
Wang, F
Bronich, TK
Kabanov, AV
Rauh, RD
Roovers, J
机构
[1] EIC Labs Inc, Norwood, MA 02062 USA
[2] Univ Nebraska, Med Ctr, Univ Med Ctr 986025, Dept Pharmaceut Sci, Omaha, NE USA
关键词
D O I
10.1021/bc049784m
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A star polymer composed of amphiphilic block copolymer arms has been synthesized and characterized. The core of the star polymer is polyamidoamine (PAMAM) dendrimer, the inner block in the arm is lipophilic poly(E-caprolactone) (PCL), and the outer block in the arm is hydrophilic poly(ethylene glycol) (PEG). The star-PCL polymer was synthesized first by ring-opening polymerization of E-caprolactone with a PAMAM-OH dendrimer as initiator. The PEG polymer was then attached to the PCL terminus by an ester-forming reaction. Characterization with SEC, H-1 NMR, FTIR, TGA, and DSC confirmed the star structure of the polymers. The micelle formation of the star copolymer (star-PCL-PEG) was studied by fluorescence spectroscopy. Hydrophobic dyes and drugs can be encapsulated in the micelles. A loading capacity of up to 22% (w/w) was achieved with etoposide, a hydrophobic anticancer drug. A cytotoxicity assay demonstrated that the star-PCL-PEG copolymer is nontoxic in cell culture. This type of block copolymer can be used as a drug delivery carrier.
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收藏
页码:397 / 405
页数:9
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