Sunday , 1 September 2024

Solubility Enhancement and Formulation of Lovastatin Self Emulsifying Drug Delivery System

Yernagu Sai Roopa 1, B. Venkata Ramana*2
1M. Pharm Student, Department of Pharmaceutics, Prabhath Institute of Pharmacy, Parnapally (Vil.), Bandiatmakur (MD), Nandyal Dist., Andhra Pradesh

2Associate Professor, Department of Pharmaceutics, Prabhath Institute of Pharmacy, Parnapally (Vil.), Bandiatmakur (MD), Nandyal Dist., Andhra Pradesh

ABSTRACT
Carbamazepine (CBZ) is used for epilepsy but has also been reported to have effect in treating bipolar disorder. The absorption is 75% because of first pass hepatic metabolism, Its half life is 10-20 hrs and it is a BCS – class II drug. Thus formulating an immediate release CBZ fast dissolving buccal films formulation for the speedy release of the drug was planned. FTIR analysis was done to know the compatibility of the drug with the excipients which are used in formulation of the drug. Preparation of fast dissolving buccal films by selecting various concentration of Sodium Saccharin Gel (SSG), croscarmellose and crospovidone. Coating solvent method was employed for the preparation of films. Various characteristics such as weight, thickness, surface pH, tensile strength, diffusion studies and its release kinetics were determined for the prepared film formulations. It was observed that all the films were within surface approximate, close to the neutral pH level and all of them were found to have content uniformity. The result shown here also clearly depict that the F4 formulation has higher release profile as compared to other all formulations. From the above data, it was perceived that increase in concentration of crospovidone will enhance the release profile of the formulation. It was seen that release kinetics depends on higuchi equation. Due to good tensile strength and the ability to get more than % drug release, more concentration crospovidone used film formulations was selected for the study.

Keywords: Carbamazepine, fast dissolving Buccal films, % Cumulative drug release, Epilepsy.

Scroll To Top