Comparative study of aqueous and organic enteric coatings of chlorpheniramine maleate tablets

被引:7
作者
GarciaArieta, A
TorradoSantiago, D
Torrado, JJ
机构
[1] Depto. Farmacia y Tecn. Farmaceut., Facultad de Farmacia, Universidad Complutense de Madrid, 28040 Madrid, Avenida Complutense s/n
关键词
D O I
10.3109/03639049609063211
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two acrylic polymers (Eudragit(R)L 12.5 P and L 30 D) and a cellulosic polymer (cellulose acetate trimellitate, CAT) in organic and aqueous formulations were used in order to obtain an enteric coating on tablets containing clorpheniramine maleate as a water-soluble model drug. The coating of tablets was executed in a coating pan in similar conditions for each kind of solvent. The coated tablets were tested according to the delayed-release test of USP 23 (Method A). In our experimental conditions different amounts of polymers were needed to obtain an enteric coating. The lowest amount was in the case ofEudragit L 30 D (aqueous), after which appeared Eudragit L 12.5 P (organic), CAT (organic), and finally, CAT (aqueous) as the polymer that needed to be ofthe highest amount. During the dissolution test differences in the size and aspect ofthe tablets were observed according to the polymers. Acrylic polymers did not show changes in size and aspect, but CAT polymers showed a notable increase in size. The different behavior of the tablets during the dissolution test can explain the differences observed in the adjustment of the release data. The release data were tested assuming common kinetic models. In the present study it was observed that Eudragit L polymers release the drug in a first-order kinetic and that CAT releases it according to a zero-order kinetic.
引用
收藏
页码:579 / 585
页数:7
相关论文
共 14 条
[1]  
BANAKER UV, 1992, PHARM DISSOLUTION TE, P299
[2]  
BAUDOUX M, 1990, PHARM TECHNOL INT, V2, P18
[3]   TECHNOLOGICAL EVALUATION OF 3 ENTERIC COATING POLYMERS .2. WITH A SOLUBLE DRUG [J].
KANE, Y ;
RAMBAUD, J ;
MAILLOLS, H ;
LAGET, JP ;
GAUDY, D ;
DELONCA, H .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1994, 20 (06) :1021-1034
[4]  
KAWASHIMA Y, 1989, AQUEOUS POLYM COATIN, P151
[5]  
LEHMANN K, 1979, PHARM TECH INT, V2, P33
[6]  
Lehmann K, 1981, INT J PHARM TECH PRO, V2, P31
[7]  
LEHMANN K, 1979, PHARM TECH INT, V2, P55
[8]  
*MACK EAST, 1995, 23NF 18 USP, P1795
[9]   PROPERTIES OF FREE FILMS PREPARED FROM AQUEOUS POLYMERS BY A SPRAYING TECHNIQUE [J].
OBARA, S ;
MCGINITY, JW .
PHARMACEUTICAL RESEARCH, 1994, 11 (11) :1562-1567
[10]  
PLAIZIERVERCAMMEN J, 1992, EUR J PHARM BIOPHARM, V38, P145