%0 Journal Article %T Research: FORMULATION DEVELOPMENT OF ACECLOFENAC TABLETS BY WET GRANULATION AND DIRECT COMPRESSION METHODS EMPLOYING STARCH CITRATE %A K P R Chowdary* %A Veeraiah Enturi %A Ch Achyuth Reddy %J Pharmacie Globale : International Journal of Comprehensive Pharmacy %D 2011 %I %X Aceclofenac, a widely prescribed anti inflammatory analgesic drug belongs to BCS class II and exhibit low and variable oral bioavailability due to its poor solubility and dissolution rate. The objective of the present study is to develop aceclofenac rapidly dissolving tablet formulations by wet granulation and direct compression methods employing starch citrate, a new modified starch. As per FDA guidelines on biowaivers, drug products containing weakly acidic BCS class II drugs with dissolution of >85% in 30 min are eligible for biowaiver. Hence dissolution of >85% in 30 min is taken as target dissolution to achieve in the formulation development of aceclofenac tablets. Starch citrate prepared by reacting potato starch with citric acid at elevated temperatures was insoluble in water and has good swelling (1500%) property without pasting or gelling when heated in water. In the micromeritic evaluation, the angle of repose and compressibility index values revealed the excellent flow characteristic of starch citrate prepared. All the physical properties studied indicated that starch citrate is a promising pharmaceutical excipient in tablets. Aceclofenac rapidly dissolving tablets with >85% dissolution in 30 min could be formulated employing starch citrate as directly compressible vehicle by direct compression method (BF3) and also employing aceclofenac-starch citrate (1:2) solid dispersion by wet granulation method (BF4). Formulations BF3 and BF4 respectively gave 87.57% and 94.80% dissolution in 30 min fulfilling the target dissolution requirement for biowaiver. %K Aceclofenac Tablets %K Starch citrate %K Direct Compression %K Solid Dispersion %K Biowaiver. %U http://www.pharmacie-globale.info/index.php?option=com_docman&task=doc_view&gid=175&tmpl=component&format=raw&Itemid=41