DISSOLUTION PROFILES OF MESALAZINE FORMULATIONS INVITRO

被引:27
|
作者
STOLK, LML [1 ]
RIETBROEK, R [1 ]
WILTINK, EH [1 ]
TUKKER, JJ [1 ]
机构
[1] STATE UNIV UTRECHT,FAC PHARM,DEPT MAKROMOLEK CHEM,3511 GH UTRECHT,NETHERLANDS
关键词
Dissolution; Mesalazine; Tablets; controlled release;
D O I
10.1007/BF01980047
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In vitro dissolution profiles of three controlled-release mesalazine formulations were determined at pH 1.0, 6.0 and 7.5. A closed-column type dissolution apparatus was used. A reproducible gradual dissolution profile was seen for Pentasa® at all pH values. Dissolution starts immediately and is complete after 20 h. Dissolution profiles at pH 1 and pH 7.5 are much alike and dissolution is faster than at pH 6. The behaviour of Asacol® at different pH values corresponds with the expectations: no release at pH 6 and pH 1, fast release at pH 7.5. Dissolution starts after 1 h and is complete after 3 h. Mesalazine release from Salofalk® tablets at pH 7.5 and pH 6.0 starts after 2 and 3 h, respectively, and is complete after 5 and 10 h. However, after a long lag-time (10 h) mesalazine is also released from Salofalksu® tablets at pH 1 and dissolution is complete after 23 h. © 1990 Royal Dutch Association for Advancement of Pharmacy.
引用
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页码:200 / 204
页数:5
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