Analysis of the release process of phenylpropanolamine hydrochloride from ethylcellulose matrix granules

被引:6
作者
Fukui, A
Fujii, R
Yonezawa, Y
Sunada, H [1 ]
机构
[1] Meijo Univ, Fac Pharm, Tenpaku Ku, Nagoya, Aichi 4688503, Japan
[2] Ryukakusan Co Ltd, Chiyoda Ku, Tokyo 1010031, Japan
关键词
ethylcellulose matrix; phenylpropanolamine hydrochloride; square-root time law; cube root law; simulation;
D O I
10.1248/cpb.50.1439
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The release properties of phenylpropanolamine hydrochloride (PPA) from ethylcellulose (EC, ethylcellulose 10 cps (EC#10) and/or 100 cps (EC#100)) matrix granules prepared by the extrusion granulation method were examined. The release process could be divided into two parts, and was well analyzed by applying square-root time law and cube root law equations, respectively. The validity of the treatments was confirmed by the. fitness of the simulation curve with the measured curve. At the initial stage, PPA was released from the gel layer of swollen EC in the matrix granules. At the second stage, the drug existing below the gel layer dissolved, and was released through the gel layer. Also, the time and release ratio at the connection point of the simulation curves was examined to determine the validity of the analysis. Comparing the release properties of PPA from the two types of EC matrix granules, EC#100 showed more effective sustained release than EC#10. On the other hand, changes in the release property of the EC#10 matrix granule were relatively more clear than that of the EC#100 matrix granule. Thus, it was supposed that EC#10 is more available for controlled and sustained release formulations than EC#100.
引用
收藏
页码:1439 / 1442
页数:4
相关论文
共 21 条
[1]  
ABD E, 1993, PHARM IND, V55, P83
[2]   PREPARATION OF A NOVEL TYPE OF CONTROLLED-RELEASE CARRIER AND EVALUATION OF DRUG RELEASE FROM THE MATRIX TABLET AND ITS PHYSICAL-PROPERTIES [J].
AOKI, S ;
OHWAKI, T ;
UESUGI, K ;
TATSUISHI, K ;
OZAWA, H ;
KAYANO, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1992, 85 (1-3) :29-38
[3]   MICROENCAPSULATION STUDIES ON AMINOPHYLLINE INVOLVING SPHERICAL CRYSTALLIZATION, SPHERONIZATION AND DRUG LOADING ON TO NON-PAREIL SEEDS [J].
BOLES, MG ;
DEASY, PB ;
DONNELLAN, MF .
JOURNAL OF MICROENCAPSULATION, 1994, 11 (01) :55-67
[4]   Elaboration and evaluation of an intraoral controlled release delivering system [J].
Diarra, M ;
Pourroy, G ;
Muster, D ;
Zingraff, M ;
Boymond, C .
BIOMATERIALS, 1998, 19 (16) :1523-1527
[5]  
GUOJIE X, 1995, J CHINESE PHARM SCI, V43, P483
[8]  
Higuchi T., 1960, J SOC COSMET CHEM, V11, P85
[9]   Dependence of reaction velocity upon surface and agitation I - Theoretical consideration [J].
Hixson, AW ;
Crowell, JH .
INDUSTRIAL AND ENGINEERING CHEMISTRY, 1931, 23 :923-931
[10]   A novel positively thermosensitive controlled-release microcapsule with membrane of nano-sized poly(N-isopropylacrylamide) gel dispersed in ethylcellulose matrix [J].
Ichikawa, H ;
Fukumori, Y .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (1-2) :107-119