S. B. Waikar
Publications by S. B. Waikar
2 publications found • Active 2012-2012
2012
2 publicationsIn-vitro antioxidant activity of flavonoids rich fraction of aerial parts of Hemidesmus indicus Linn, R. BR.
The aerial parts of plant contain a number of medicinally important compounds. The present study was carried out to extract the flavonoid rich fraction from the aerial parts of Hemidesmus indicus Linn. R. Br. and identified the phytochemicals presents in the flavonoid rich fraction of aerial parts of Hemidesmus indicus Linn. R. Br. & determined the total flavonoid contents and antioxidant potential of obtained favonoid rich fraction of Hemidesmus indicus Linn. R. Br. Total flavonoid content was estimated by Aluminium Chloride colorimetric method and the flavonoid content was 0.406 % TFC (Total Flavonoids Contents) in grams of Quercetin equivalent. Antioxidant activity was evaluated by DPPH method and IC50 value of flavonoid rich fraction of aerial parts of Hemidesmus indicus Linn. was found to be 21.39 µg/ml. Key words: Total flavonoids, Aluminium chloride, Antioxidant activity, DPPH, IC50 value.
Formulation and Evaluation of Fast Dissolving Drug Delivery System of Pantoprazole Sodium by Direct Compression Technique
Fast dissolving drug delivery system offers a solution for those patients having difficulty in swallowing tablet. In the present study, an attempt has been made to formulate fast dissolving tablets of Pantoprazole Sodium Sesquihydrate using superdisintegrants such as Croscarmellose sodium (Ac‐Di‐Sol), Sodium starch glycolate (Explotab) and Crosspovidone by direct compression technique. The prepared tablets were evaluated for hardness, friability, wetting time, weight variation, in vitro disintegration time and in vitro dissolution study. The hardness of the tablets was in the range of 3.0 ‐ 4.0 Kg/cm². The percentage friability of the tablets was less than one. Weight variation test results showed that the tablets were deviating from the average weight within the permissible limits of ±7.5 %. Drug content uniformity study results showed the uniform dispersion of the drug throughout the formulation i.e. 98.54% to 101.23%. Tablets containing Crosspovidone (F9) showed better disintegrating character along with the rapid release (99.83% drug within 4 minutes). No appreciable difference was found between the formulations containing other two superdisintegrants. Crosspovidone was found to be better suited for the formulation of mouth dissolving tablet of Pantoprazole Sodium Sesquihydrate compared to other superdisintegrarnts used in the study.
