Pharmaceutical preparations
Explore 2 research publications tagged with this keyword
Publications Tagged with "Pharmaceutical preparations"
2 publications found
2013
1 publicationVisible Spectrophotometric Determination of Lansoprazole in Pure and Pharmaceutical Formulations
Four simple, accurate and highly sensitive spectrophotometric methods have been developed for the determination of Lansoprazole in both pure and in pharmaceutical preparations. The method A andB are based on the ion associationcomplex formation between Lansoprazole and Supracen Violet 3B (method A) or Tropaeolin OOO (method B) the third and fourth are indirect methods where the drug is oxidsed by a known excess of Chloramine T and determining the consumed Chloramine T with decrease in colour intensity of the dye Gallocyanine (method C ) or oxidation with excess of N-Bromosuccunimide in acid medium. followed by the determination of unreacted N-Bromosuccunimide with the dye Celestin Blue - (method D) .Regreesion analysis of Beer’s law plots showed good correlation in the concentration range of 5.0 - 40 μg ml−1, 5.0 -25 μg ml−1 , 2.5 – 12.5 μg ml−1, 1.0 – 6.0μg ml−1 for methods A, B ,C and D respectively, and the corresponding molar absorptivity values are 0.9232 x 104 , 1.0857 x 104 , 7.0997 x 104 and 2.3265 x 104 1mol−1cm−1. All variables have been optimized and the results were statistically compared with those of literature methods by employing the student’s t-test and F-test. No interference was observed from excipients normally added to the tablets.
2012
1 publicationStability indicating GC-FID method for estimation of Camylofin dihydrochloride and Paracetamol in pharmaceutical dosage form
 This research paper describes simple analytical method for determination of Camylofin dihydrochloride and Paracetamol in syrup formulation by Gas chromatography method. Benzoic acid was used as internal standard. Validation was carried out in compliance with the International Conference on Harmonization guidelines. The method utilized GC (Agilent Technologies 6890N Network GC system with FID detector), and RTX-5 capillary column (Crossbond 50% diphenyl-95% dimethyl polysiloxane), 30m x 0.53mm, 1.5µm as stationary phase. Helium was used as the carrier gas. The proposed method was validated for linearity, LOD, LOQ, accuracy, precision, ruggedness and solution stability. It can be conveniently adopted for routine quality control analysis. Key Words:Validation, Gas chromatography, Pharmaceutical preparations, Camylofin dihydrochloride, Paracetamol.
