THE RELEASE OF 5-FLUOROURACIL FROM A SWELLABLE MATRIX OF A TRIBLOCK COPOLYMER OF EPSILON-CAPROLACTONE AND ETHYLENE-OXIDE

被引:8
作者
MARTINI, LGA
COLLETT, JH
ATTWOOD, D
机构
[1] UNIV MANCHESTER,DEPT PHARM,MANCHESTER M13 9PL,LANCS,ENGLAND
[2] SCHERER DDS,SWINDON,WILTS,ENGLAND
关键词
SWELLABLE MATRICES; CONTROLLED RELEASE; HYDROPHILIC MATRIX; RELEASE MECHANISM;
D O I
10.1023/A:1016290411383
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. The purpose of this study was to investigate the influence of hydration characteristics on the in vitro release of 5-fluorouracil from a swellable matrix prepared using a novel triblock copolymer of poly(epsilon-caprolactone) and poly(oxyethylene). Methods. Matrices were prepared by dry compression of mixtures of the drug and copolymer using low compressional forces. Release studies were performed using a custom made rotating basket dissolution apparatus. The positions of the eroding and swelling fronts within the matrices during hydration were monitored using freeze fracture scanning electron microscopy. Results. Analysis of the release data revealed a predominantly diffusion controlled mechanism. Observations of the swelling characteristics of the copolymer matrices on immersion in Sorensen's buffer at pH 7.4 revealed gel formation and preferential swelling in the radial direction with visible erosion of the matrix after 4h. During hydration, a gradual increase in gel layer thickness was noted prior to the erosion and eventual dissolution of the matrix. Conclusions. This study demonstrates a means of differentiating the relative importance of the swelling characteristics in determining the release mechanism and subsequent release rate from swellable matrices.
引用
收藏
页码:1786 / 1790
页数:5
相关论文
共 12 条
[1]  
BINNS JS, 1990, P INT S CONTR REL BI, V17, P339
[2]   SWELLING CHARACTERISTICS OF HYDROPHILIC MATRICES FOR CONTROLLED RELEASE NEW DIMENSIONLESS NUMBER TO DESCRIBE THE SWELLING AND RELEASE BEHAVIOR [J].
COLOMBO, P ;
CATELLANI, PL ;
PEPPAS, NA ;
MAGGI, L ;
CONTE, U .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 88 (1-3) :99-109
[3]   SWELLING-ACTIVATED DRUG DELIVERY SYSTEMS [J].
CONTE, U ;
COLOMBO, P ;
GAZZANIGA, A ;
SANGALLI, ME ;
LAMANNA, A .
BIOMATERIALS, 1988, 9 (06) :489-493
[4]  
CONTE U, 1991, 10TH P PHARM TECH C, V3, P316
[5]  
LEE PI, 1987, ACS SYM SER, V348, P1
[6]   MICELLIZATION AND GELATION OF TRIBLOCK COPOLYMER OF ETHYLENE-OXIDE AND SIGMA-CAPROLACTONE, CLNEMCLN, IN AQUEOUS-SOLUTION [J].
MARTINI, L ;
ATTWOOD, D ;
COLLETT, JH ;
NICHOLAS, CV ;
TANODEKAEW, S ;
DENG, NJ ;
HEATLEY, F ;
BOOTH, C .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1994, 90 (13) :1961-1966
[7]  
MELIA CD, 1991, CRIT REV THER DRUG, V8, P395
[8]   PROBING THE MECHANISMS OF SWELLING OF HYDROXYPROPYLMETHYLCELLULOSE MATRICES [J].
PAPADIMITRIOU, E ;
BUCKTON, G ;
EFENTAKIS, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 98 (1-3) :57-62
[9]   A SIMPLE EQUATION FOR THE DESCRIPTION OF SOLUTE RELEASE .3. COUPLING OF DIFFUSION AND RELAXATION [J].
PEPPAS, NA ;
SAHLIN, JJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 57 (02) :169-172
[10]  
PEPPAS NA, 1992, SAFYBI, V32, P22