A. Garciaarieta et al., COMPARATIVE-STUDY OF AQUEOUS AND ORGANIC ENTERIC COATINGS OF CHLORPHENIRAMINE MALEATE TABLETS, Drug development and industrial pharmacy, 22(7), 1996, pp. 579-585
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 tablet
s containing clorpheniramine maleate as a water-soluble model drug. Th
e coating of tablets was executed in a coating pan in similar conditio
ns 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 ente
ric coating. The lowest amount was in the case ofEudragit L 30 D (aque
ous), after which appeared Eudragit L 12.5 P (organic), CAT (organic),
and finally, CAT (aqueous) as the polymer that needed to be ofthe hig
hest amount. During the dissolution test differences in the size and a
spect ofthe tablets were observed according to the polymers. Acrylic p
olymers did not show changes in size and aspect, but CAT polymers show
ed a notable increase in size. The different behavior of the tablets d
uring 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 Eudr
agit L polymers release the drug in a first-order kinetic and that CAT
releases it according to a zero-order kinetic.