Controlled release of furosemide from the ethylene-vinyl acetate matrix

被引:13
作者
Cho, CW
Choi, JS
Shin, SC
机构
[1] Chonnam Natl Univ, Coll Pharm, Kwangju 500757, South Korea
[2] CJ Corp, R&D Ctr Pharmaceut, Ichonsi 467812, Gyonggido, South Korea
[3] Chosun Univ, Coll Pharm, Kwangju 501759, South Korea
关键词
furosemide; ethylene-vinyl acetate; controlled release; plasticizer; matrix;
D O I
10.1016/j.ijpharm.2005.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ethylene-vinyl acetate (EVA) matrix containing furosemide was prepared by the casting method and the release patterns were observed. The solubility of furosemide was determined as a function of volume fraction of polyethylene glycol 400. The release of drug from the matrix was studied as a function of temperature and drug concentration. Plasticizers such as the citrates and the phthalates were added for preparing the membrane to increase the flexibility of the EVA matrix. The solubility of furosemide was the highest when the concentration of PEG 400 was 40% (v/v). The release rate of drug from the EVA matrix increased with increasing temperature and drug loading doses. A linear relationship was found between the release rate and the square root of the loading dose. The activation energy (E-a) which was measured from the slope of the log P versus 1000/T plots, was 12.33 kcal/mol for the 0.5% loading dose, and 11.58 kcal/mol for the 1.0% loading dose, and 11.00 kcal/mol for the 1.5% loading dose. Among the plasticizers used such as the citrates and the phthalates groups, diethyl phthalate showed the best enhancing effects in drug release. In conclusion, the application of an EVA matrix containing a plasticizer might be useful in the development of a controlled drug delivery system. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 133
页数:7
相关论文
共 26 条
[1]   EVALUATION OF DRUG-CONTAINING POLYMER-FILMS PREPARED FROM AQUEOUS LATEXES [J].
BODMEIER, R ;
PAERATAKUL, O .
PHARMACEUTICAL RESEARCH, 1989, 6 (08) :725-730
[2]  
BRUCKS R, 1989, PHARM RES, V6, P679
[3]  
CHIEN YW, 1975, CHEM PHARM BULL, V23, P1085
[4]   COMBINED EFFECTS OF PH, COSOLVENT AND PENETRATION ENHANCERS ON THE INVITRO BUCCAL ABSORPTION OF PROPRANOLOL THROUGH EXCISED HAMSTER-CHEEK POUCH [J].
COUTELEGROS, A ;
MAITANI, Y ;
VEILLARD, M ;
MACHIDA, Y ;
NAGAI, T .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 84 (02) :117-128
[5]   ENHANCEMENT OF PERMEABILITY OF ETHYL CELLULOSE FILMS FOR DRUG PENETRATION [J].
DONBROW, M ;
FRIEDMAN, M .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1975, 27 (09) :633-646
[6]   Evaluation of high molecular weight Poly(oxyethylene) (Polyox) polymer: Studies of flow properties and release rates of furosemide and captopril from controlled-release hard gelatin capsules [J].
Efentakis, M ;
Vlachou, M .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2000, 5 (03) :339-346
[7]   DRUG RELEASE FROM METHYL ACRYLATE-METHYL METHACRYLATE COPOLYMER MATRIX .2. CONTROL OF RELEASE RATE BY EXPOSURE TO ACETONE VAPOR [J].
FARHADIEH, B ;
BORODKIN, S ;
BUDDENHAGEN, JD .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1971, 60 (02) :212-+
[8]  
GIEBISCH G, 1985, ARZNEIMITTEL-FORSCH, V35, P336
[9]  
HADGRAFT J, 1987, TRANSDERMAL DRUG DEL, P298
[10]  
HALPERN BD, 1976, CONTROLLED RELEASE P, P135