Novel micelle-forming block copolymer composed of poly(ε-caprolactone) and poly(vinyl pyrrolidone)

被引:63
作者
Chung, TW
Cho, KY
Lee, HC
Nah, JW
Yeo, JH
Akaike, T
Cho, CS [1 ]
机构
[1] Seoul Natl Univ, Sch Agr Biotechnol, Seoul 151742, South Korea
[2] Chonnam Natl Univ, Sch Med, Dept Microbiol, Kwangju 501190, South Korea
[3] Chonnam Natl Univ, Sch Med, Res Inst Med Sci, Kwangju 501190, South Korea
[4] Sunchon Natl Univ, Dept Polymer Sci & Engn, Sunchon 540742, South Korea
[5] Natl Inst Agr Sci & Technol, Suwon 441100, South Korea
[6] Tokyo Inst Technol, Fac Biomol Engn, Yokohama, Kanagawa 2268501, Japan
关键词
poly (epsilon-caprolactone); poly(vinyl pyrrolidone); coordination-insertion ring-opening polymerization;
D O I
10.1016/j.polymer.2003.12.074
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The well-defined poly (epsilon-caprolactone) (PCL)/poly(vinyl pyrrolidone) (PVP) diblock copolymers were synthesized through combining radical polymerization of VP and the controlled coordination-insertion ring-opening polymerization of CL using an aluminum alkoxide macroinitiator formed from the equimolar reaction of triethylaluminum with hydroxy-terminated PVP (PVP-OH). The molecular characterization of PCL/PVP diblock copolymers was confirmed through H-1 NMR spectroscopy and GPC analysis. Polymeric micelles composed of PCL as a hydrophobic core and PVP as a hydrophilic shell were prepared by a diafiltration method. The micellar properties such as sizes, shapes, and critical micelle concentrations (CMC) were investigated with a dynamic light scattering (DLS) spectrometer, transmission electron microscope (TEM) and spectrofluorimeter. The sizes of micelles ranged from 30 to 80 nm in average size. The novel micelles formed from the well-defined PCL/PVP diblock copolymers seem to be feasible as novel promising carriers in biomedical and pharmaceutical applications. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1591 / 1597
页数:7
相关论文
共 30 条
[1]   Solvent-regulated ordering in block copolymers [J].
Alexandridis, P ;
Spontak, RJ .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 1999, 4 (02) :130-139
[2]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[3]  
Barakat I, 1996, J POLYM SCI POL CHEM, V34, P497, DOI 10.1002/(SICI)1099-0518(199602)34:3<497::AID-POLA19>3.0.CO
[4]  
2-K
[5]  
BARTUS RT, 1998, SCIENCE, V58, P357
[6]  
CHASIN M, 1990, DRUG PHARM SCI, V3, P71
[7]   Novel core-shell type thermo-sensitive nanoparticles composed of poly(gamma-benzyl L-glutamate) as the core and poly(N-isopropylacrylamide) as the shell [J].
Cho, CS ;
Cheon, JB ;
Jeong, YI ;
Kim, IS ;
Kim, SH ;
Akaike, T .
MACROMOLECULAR RAPID COMMUNICATIONS, 1997, 18 (05) :361-369
[8]   Chiral recognition of bilirubin by polymeric nanoparticles [J].
Chung, TW ;
Cho, KY ;
Nah, JW ;
Akaike, T ;
Cho, CS .
LANGMUIR, 2002, 18 (16) :6462-6464
[9]   Induced circular dichroism of disperse red dye in the self-assembled nanoparticles composed of poly(γ-benzyl L-glutamate) and poly(N-isopropylacrylamide) and its phase transition by temperature [J].
Chung, TW ;
Kim, BJ ;
Park, SY ;
Akaike, T ;
Nah, JW ;
Cho, CS .
MACROMOLECULES, 2000, 33 (24) :8921-8923
[10]   The control of protein release from poly(DL-lactide co-glycolide) microparticles by variation of the external aqueous phase surfactant in the water-in oil-in water method [J].
Coombes, AGA ;
Yeh, MK ;
Lavelle, EC ;
Davis, SS .
JOURNAL OF CONTROLLED RELEASE, 1998, 52 (03) :311-320