THE INFLUENCE OF POLYVINYL PYRROLIDONE (PVP) ON PIROXICAM ABSORPTION WITH EVERTED INTESTINAL SAC METHOD

ABSTRACT: Oral drug absorption was highly influenced by  dissolution rate, especially for poorly and insoluble drugs. Piroxicam is a nonsteroidal anti-inflammatory drug that is practically insoluble in water. The oral absorption rate of piroxicam is dependent on its dissolution rate in the GI tract. Polyvinyl Pyrrolidone (PVP) as surfactant can increase drug solubility by means of a micelle forming mechanism. The aim of the study was to know the influence of addition and variation of Polyvinyl Pyrrolidone (PVP) on Piroxicam absorption with everted intestinal sac method.  The concentration of piroxicam solution was prepared by PVP in  1.0, 2.0 and 3.0 % respectively.  Crane  and  Wilson  tube  containing  75  ml of  the mucosal  fluid  was taken at 370C in waterbath. Than, serosal  solution  of 1.5  ml was added to intestinal sac by turned upside down and tied to a cannula, then put into  the tube containing  the mucosal  fluid  and  constantly  flowing oxygen gas. Serosal solution of 1 ml were taken every 15 minutes and then diluted with 2 ml of Ba (OH) 2 and 2 ml of ZnSO4 then centrifuge until 25 minute. The absorbant of supernatant was  measured  by UV  spectrophotometer  and data analyse was calculated by one-way ANAVA.  PVP at 1%,2% and 3% increased piroxicam absorption from the phosphate buffer pH 7.5 compared with negative control. According to Papp, the values were 2.52 ± 0.43 cm/minute (negative control), 3.41 ± 2.17 cm/minute (1% PVP),  2.75  ± 1.14 cm/minute (2% PVP) and  4.77  ± 4.93 cm/minute (3% PVP) respectively. In conclusion. Lower doses of the surfactant (1%, 2%, and 3% PVP) significantly increased absorption of the drug by altering the membrane permeability.
Keywords: Piroxicam, absorption, in vitro, PVP
Author: Fea Prihapsara. Anif Nur Artanti, Mimiek Murrukmihadi
Journal Code: jpfarmasigg150023

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