Control of vitamin B12 release from poly(ethylene glycol)/poly(butylene terephthalate) multiblock copolymers

被引:40
作者
van Dijkhuizen-Radersma, R
Péters, FLAMA
Stienstra, NA
Grijpma, DW
Feijen, J
de Groot, K
Bezemer, JM
机构
[1] IsoTis NV, NL-3720 AB Bilthoven, Netherlands
[2] Univ Twente, NL-7500 AE Enschede, Netherlands
关键词
poly(ether ester); controlled release; peptides; swelling; crystallinity;
D O I
10.1016/S0142-9612(01)00286-1
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The release of vitamin B-12 (1355 Da) from matrices based on multiblock copolymers was studied. The copolymers were composed of hydrophilic poly(ethylene glycol)-terephthalate (PEGT) blocks and hydrophobic poly(butylene terephthalate) (PBT) blocks. Vitamin B-12 loaded films were prepared by using a water-in-oil emulsion method. The copolymer properties, like permeability, could be varied by increasing the PEG-segment length from 300 up to 4000 g/mol and by changing the wt% of PEGT. From permeation and release experiments, the diffusion coefficient of vitamin B-12 through PEGT/PBT films of different compositions was determined. The diffusion coefficient of vitamin B-12 was strongly dependent on the composition of the copolymers. Although an increased wt% of PEGT (at a constant PEG-segment length) resulted in a higher diffusion coefficient, a major effect was observed at increasing PEG-segment length. By varying the copolymer composition, a complete release of vitamin B-12 in 1 day up to a constant release for over 12 weeks was obtained. The release rate could be effectively tailored by blending copolymers with different PEG-segment lengths. The swelling and the crystallinity of the matrix could explain the effect of the matrix composition on the release behavior. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1527 / 1536
页数:10
相关论文
共 37 条
[1]  
ADAMS RK, 1996, THERMOPLASTIC ELASTO, P191
[2]  
Antonsen K.P., 1992, Poly (Ethylene Glycol) Chemistry, P15, DOI [10.1007/978-1-4899-0703-5_2, DOI 10.1007/978-1-4899-0703-5_2]
[3]  
Baker R. W., 1974, Controlled Release of Biologically Active Agents, P15
[4]   BIOCOMPATIBILITY OF A POLYETHER URETHANE, POLYPROPYLENE OXIDE, AND A POLYETHER POLYESTER COPOLYMER - A QUALITATIVE AND QUANTITATIVE STUDY OF 3 ALLOPLASTIC TYMPANIC MEMBRANE MATERIALS IN THE RAT MIDDLE-EAR [J].
BAKKER, D ;
VANBLITTERSWIJK, CA ;
HESSELING, SC ;
KOERTEN, HK ;
KUIJPERS, W ;
GROTE, JJ .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1990, 24 (04) :489-515
[5]   DEGRADATIVE BEHAVIOR OF POLYMERIC MATRICES IN (SUB)DERMAL AND MUSCLE-TISSUE OF THE RAT - A QUANTITATIVE STUDY [J].
BEUMER, GJ ;
VANBLITTERSWIJK, CA ;
PONEC, M .
BIOMATERIALS, 1994, 15 (07) :551-559
[6]   CELL-SEEDING AND IN-VITRO BIOCOMPATIBILITY EVALUATION OF POLYMERIC MATRICES OF PEO PBT COPOLYMERS AND PLLA [J].
BEUMER, GJ ;
VANBLITTERSWIJK, CA ;
BAKKER, D ;
PONEC, M .
BIOMATERIALS, 1993, 14 (08) :598-604
[7]   BIOCOMPATIBILITY OF A BIODEGRADABLE MATRIX USED AS A SKIN SUBSTITUTE - AN IN-VIVO EVALUATION [J].
BEUMER, GJ ;
VANBLITTERSWIJK, CA ;
PONEC, M .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1994, 28 (05) :545-552
[8]   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
[9]   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
[10]  
BUDAVARI S, 1996, MERCK INDEX, P10152