1Department of Pharmaceutics, GES's Sir Dr. M. S. Gosavi College of Pharmaceutical Education and Research, Nashik-42205, Maharashtra, India
2Department of Pharmaceutical Chemistry, GES's Sir Dr. M. S. Gosavi College of Pharmaceutical Education and Research, Nashik-42205, Maharashtra, India
*Corresponding Author: prashant.pingale@gmail.com
Online published on 4 July, 2024.
Mouth dissolving films offer an attractive route for systemic drug delivery. MDFs are an alternative to fast dissolving tablets, Chewable tablet, due to their faster dissolution rate. Some drugs are absorbed from the mouth, pharynx and esophagus as the saliva passes down into the stomach. Fast mouth dissolving films have become popular as a new delivery system. They disintegrate or disintegrate in the oral cavity without the need to swallow or chew.The objective of the present study was to develop mouth dissolving films (MDF) of Cisapride used to treat heartburn in patients with gastroesophageal reflux disease (GERD), with fast disintegration, optimum morphological properties, and mechanical strength. Lycoat RS 720, Hydroxypropylmethyl-cellulose 3cps were used as polymers and Glycerine as plasticizer. Films were prepared by solvent casting technique. Parameters like in-vitro disintegration time, tensile strength, content uniformity, folding endurance, swelling index, and in-vitro drug release were evaluated. In-vitro dissolution studies showed that 99% of Cisapride was released within 5 min with an average disintegration time of 60 sec. UV and FTIR spectrophotometry were used to identify drug-excipient interactions. Accelerated stability studies were performed as per ICH guidelines wherein the MDFs were stable for 2 months at 40 ± 2 °C and 75 ± 5% relative humidity.
Cisapride, Mouth-dissolving film, HPMC 3cps, Lycoat RS 720, Glycerine