Asian Journal of Research in Pharmaceutical Sciences

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Validated First Order Derivative Spectrophotometric Method for Simultaneous Estimation of Lansoprazole and Aspirin in Tablet Dosage Forms


Affiliations
1 Department of Pharmaceutical Analysis, Care College of Pharmacy, Athamakur (Mdl), Oglapur(V), Warangal (Dist), Telangana, India
     

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The present work was aimed at method development and validation for simultaneous estimation of Lansoprazole and Aspirin by UV-Spectrophotometric method in pharmaceutical dosage form. In UV method Methanol as solvent and λmax of Lansoprazole and Aspirin were found to be 232nm and 222nm respectively. Concentration ranges were found to be 4-20μg/mL for both drugs. The R2 values were found to be 0.996 and 0.999 for Lansoprazole and Aspirin respectively. The method was validated statistically and by recovery studies. Percentage Assay and Recovery were found to be 95-105% for Lansoprazole and Aspirin. LOD and LOQ ranges were found to be 0.177 and 0.539μg/mL and 0.298 and 0.903μg/mL for Lansoprazole and Aspirin repectively. This method was validated using ICH guidelines.

Keywords

Aspirin, Lansoprazole, UV-Spectrophotometric Method, Simultaneous Equation, Validation.
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  • Validated First Order Derivative Spectrophotometric Method for Simultaneous Estimation of Lansoprazole and Aspirin in Tablet Dosage Forms

Abstract Views: 174  |  PDF Views: 2

Authors

G. Kumaraswamy
Department of Pharmaceutical Analysis, Care College of Pharmacy, Athamakur (Mdl), Oglapur(V), Warangal (Dist), Telangana, India
Repudi Lalitha
Department of Pharmaceutical Analysis, Care College of Pharmacy, Athamakur (Mdl), Oglapur(V), Warangal (Dist), Telangana, India
D. Sudheer Kumar
Department of Pharmaceutical Analysis, Care College of Pharmacy, Athamakur (Mdl), Oglapur(V), Warangal (Dist), Telangana, India

Abstract


The present work was aimed at method development and validation for simultaneous estimation of Lansoprazole and Aspirin by UV-Spectrophotometric method in pharmaceutical dosage form. In UV method Methanol as solvent and λmax of Lansoprazole and Aspirin were found to be 232nm and 222nm respectively. Concentration ranges were found to be 4-20μg/mL for both drugs. The R2 values were found to be 0.996 and 0.999 for Lansoprazole and Aspirin respectively. The method was validated statistically and by recovery studies. Percentage Assay and Recovery were found to be 95-105% for Lansoprazole and Aspirin. LOD and LOQ ranges were found to be 0.177 and 0.539μg/mL and 0.298 and 0.903μg/mL for Lansoprazole and Aspirin repectively. This method was validated using ICH guidelines.

Keywords


Aspirin, Lansoprazole, UV-Spectrophotometric Method, Simultaneous Equation, Validation.