Tri-component diblock copolymers of poly(ethylene glycol)-poly(ε-caprolactone-co-lactide):: synthesis, characterization and loading camptothecin

被引:24
作者
Zhang, Y
Wang, CC
Yang, WL
Shi, B
Fu, SK [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, Shanghai 200433, Peoples R China
[2] Minist Educ, Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[3] Anhui Univ, Modern Expt Technol Ctr, Hefei 230039, Peoples R China
[4] Fudan Univ, Sch Pharm, Shanghai 200032, Peoples R China
关键词
methoxy poly(ethylene glycol)-poly(epsilon-caprolactone-co-lactide) diblock copolymer; nano-particles; camptothecin; drug carrier;
D O I
10.1007/s00396-005-1306-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Biodegradable tri-component diblock copolymer was synthesized by bulk copolymerization of epsilon-caprolactone (CL) and D, L-lactide (LA) in the presence of methoxy poly(ethylene glycol) (MePEG), using stannous octoate as catalyst. Their chemical structure and physical properties were investigated by GPC, NMR, DSC, TGA and XRD. The increase of CL/LA ratio in the diblock copolymer leads to lower T-g, higher decomposition temperature and crystallinity. Nanoparticles formulated from MePEG-poly(CL-co-LA) (PCAE) possess spherical structure, which was characterized by dynamic light scattering (DLS) and transmission electron microscopy (TEM). The DLS results indicate that the particle size increased with the increase of CL/LA ratio and the hydrophobic fragment length in the copolymer. The drug encapsulation efficiency and the drug release behavior in vitro conditions of camptothecin were measured by high performance liquid chromatography (HPLC). The encapsulation efficiency can be achieved as high as 84.4% and the release behavior can be made well-controlled. MePEG-poly(CL-co-LA) nanoparticles might have a great potential as carriers for hydrophobic drugs.
引用
收藏
页码:1246 / 1252
页数:7
相关论文
共 35 条
[21]   Polymer-drug compatibility: A guide to the development of delivery systems for the anticancer agent, Ellipticine [J].
Liu, JB ;
Xiao, YH ;
Allen, C .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (01) :132-143
[22]   Biodegradable poly(D,L-lactic acid)-poly(ethylene glycol)-monomethyl ether diblock copolymers:: structures and surface properties relevant to their use as biomaterials [J].
Lucke, A ;
Tessmar, J ;
Schnell, E ;
Schmeer, G ;
Göpferich, A .
BIOMATERIALS, 2000, 21 (23) :2361-2370
[23]   The effect of poly(ethylene glycol)-poly(D,L-lactic acid) diblock copolymers on peptide acylation [J].
Lucke, A ;
Fustella, E ;
Tessmar, J ;
Gazzaniga, A ;
Göpferich, A .
JOURNAL OF CONTROLLED RELEASE, 2002, 80 (1-3) :157-168
[24]   Synthesis and characterization of ABA triblock and novel multiblock copolymers from ethylene glycol, L-lactide, and ε-caprolactone [J].
Mohammadi-Rovshandeh, J ;
Farnia, SMF ;
Sarbolouki, MN .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 83 (10) :2072-2081
[25]  
POTMESIL M, 1994, CANCER RES, V54, P1431
[26]  
Shin ILG, 1998, J CONTROL RELEASE, V51, P1
[27]   Incorporation and release of hydrophobic probes in biocompatible polycaprolactone-block-poly(ethylene oxide) micelles:: Implications for drug delivery [J].
Soo, PL ;
Luo, LB ;
Maysinger, D ;
Eisenberg, A .
LANGMUIR, 2002, 18 (25) :9996-10004
[28]   LONG CIRCULATING MICROPARTICULATE DRUG CARRIERS [J].
STOLNIK, S ;
ILLUM, L ;
DAVIS, SS .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :195-214
[29]  
TOBYO M, 1998, PHARM RES, V15, P270
[30]   PEG-based micelles as carriers of contrast agents for different imaging modalities [J].
Torchilin, VP .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (02) :235-252