RESUMO
Background: Evaluate the anti-inflammatory property of theophylline on rat hind paw edema using carrageenan-induced acute inflammatory model. Methods: Wistar male rats (150-200 gm) were divided into 7 groups- 3 standard groups, 3 test groups and 1 control group. Each group consists of six rats. A control group was treated with 0.2ml of normal saline, 3 standard groups were treated with different doses of Diclofenac (Standard drug): 5 mg/kg, 10 mg/kg, 15 mg/kg body weight, respectively and 3 test groups were treated with different doses of Theophylline (Test drug): 5 mg/kg , 10 mg/kg and 15 mg/kg, respectively. The anti-inflammatory property was assessed by plethysmograph. Results: Theophylline demonstrated a significant anti-inflammatory property at different dose levels when compared to controls (p > 0.05). However this anti-inflammatory activity was less as compared to standard drug. Conclusions: Theophylline exhibited a dose dependent anti-inflammatory activity in a carrageenan model of inflammation.
RESUMO
Two simple, rapid, sensitive, precise and economic spectrophotometric methods have been developed for the estimation of Erlotinib in bulk and tablet formulation. During the course of study, it was observed that solution of the drug formed colored ion-pair complexes with Bromocresol Green (BCG) and Methyl Orange (MO) in phosphate buffer pH 2.5, and extracted in chloroform. This property of the drug was followed for the development of colorimetric methods for analysis of drug. The complex of etoricoxib with BCG and MO showed λ max at 418.5 nm and 424.4 nm respectively. The complex was stable up to 22 hrs and obeyed Beer's law over the concentration ranges of 10-1000 μg/ml. Correlation coefficient was found to be 0.9985. In addition we have determined the molar absorptivity, Sandell sensitivity and the optimum conditions for quantitative analysis of erlotinib. These methods were validated statistically. Recovery studies gave satisfactory results indicating that none of common additives and excipients interfere the assay method. The proposed methods are found to be simple, accurate and reproducible that was successfully applied for the analysis of tablet formulation.