Controlled release of proteins from degradable poly(ether-ester) multiblock copolymers

被引:21
作者
van Dijkhuizen-Radersma, R
Métairie, S
Roosma, JR
de Groot, K
Bezemer, JM
机构
[1] OctoPlus Technol BV, NL-2333 CL Leiden, Netherlands
[2] Univ Twente, Fac Chem Technol, BMTI, NL-7500 AE Enschede, Netherlands
关键词
poly(ether ester); degradable; protein release; diffusion; delayed release;
D O I
10.1016/j.jconrel.2004.08.014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new series of multiblock poly(ether-ester)s based on poly(ethylene glycol) (PEG), butylene terephthalate (BT) and butylene succinate (BS) segments were introduced as matrices for controlled release applications. The release of two model proteins, lysozyme and bovine serum albumin (BSA), from poly(ether-ester) films were evaluated and correlated to the swelling and degradation characteristics of the polymer matrices. First- and zero-order profiles were found for the release of lysozyme, depending on the composition of the polymer matrix. The initial diffusion coefficient was correlated to the swelling of the matrix, which increased with longer PEG segments and lower BT/BS ratios of the polymer. High swelling matrices released the lysozyme according to diffusion-controlled first-order release profiles. Zero-order release profiles were obtained from less swollen matrices due to a combination of diffusion and degradation of the matrix. In contrast to the release of lysozyme, BSA was released from the poly(ether-ester) matrices via delayed release profiles. Both the delay time and the release rate could be tailored by varying the matrix composition. The BSA release rate was mainly determined by the degradation, whereas the delay time was determined by a combination of the swelling and the degradation rate of the polymer matrix. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:175 / 186
页数:12
相关论文
共 47 条
[1]   An obstruction-scaling model for diffusion in homogeneous hydrogels [J].
Amsden, B .
MACROMOLECULES, 1999, 32 (03) :874-879
[2]   Solute diffusion within hydrogels. Mechanisms and models [J].
Amsden, B .
MACROMOLECULES, 1998, 31 (23) :8382-8395
[3]   Water, solute and protein diffusion in physiologically responsive hydrogels of poly(methacrylic acid-g-ethylene glycol) [J].
Bell, CL ;
Peppas, NA .
BIOMATERIALS, 1996, 17 (12) :1203-1218
[4]   Zero-order release of lysozyme from poly(ethylene glycol) poly(butylene terephthalate) matrices [J].
Bezemer, JM ;
Radersma, R ;
Grijpma, DW ;
Dijkstra, PJ ;
Feijen, J ;
van Blitterswijk, CA .
JOURNAL OF CONTROLLED RELEASE, 2000, 64 (1-3) :179-192
[5]   Microspheres for protein delivery prepared from amphiphilic multiblock copolymers 1. Influence of preparation techniques on particle characteristics and protein delivery [J].
Bezemer, JM ;
Radersma, R ;
Grijpma, DW ;
Dijkstra, PJ ;
van Blitterswijk, CA ;
Feijen, J .
JOURNAL OF CONTROLLED RELEASE, 2000, 67 (2-3) :233-248
[6]   Microspheres for protein delivery prepared from amphiphilic multiblock copolymers 2. Modulation of release rate [J].
Bezemer, JM ;
Radersma, R ;
Grijpma, DW ;
Dijkstra, PJ ;
van Blitterswijk, CA ;
Feijen, J .
JOURNAL OF CONTROLLED RELEASE, 2000, 67 (2-3) :249-260
[7]   A controlled release system for proteins based on poly(ether ester) block-copolymers: polymer network characterization [J].
Bezemer, JM ;
Grijpma, DW ;
Dijkstra, PJ ;
van Blitterswijk, CA ;
Feijen, J .
JOURNAL OF CONTROLLED RELEASE, 1999, 62 (03) :393-405
[8]   Control of protein delivery from amphiphilic poly(ether ester) multiblock copolymers by varying their water content using emulsification techniques [J].
Bezemer, JM ;
Grijpma, DW ;
Dijkstra, PJ ;
van Blitterswijk, CA ;
Feijen, J .
JOURNAL OF CONTROLLED RELEASE, 2000, 66 (2-3) :307-320
[9]   Release of recombinant human interleukin-2 from dextran-based hydrogels [J].
Cadée, JA ;
de Groot, CJ ;
Jiskoot, W ;
den Otter, W ;
Hennink, WE .
JOURNAL OF CONTROLLED RELEASE, 2002, 78 (1-3) :1-13
[10]   CORRELATION BETWEEN MESH SIZE AND EQUILIBRIUM DEGREE OF SWELLING OF POLYMERIC NETWORKS [J].
CANAL, T ;
PEPPAS, NA .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1989, 23 (10) :1183-1193