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Development and Validation of RP-HPLC Method for the Simultaneous Estimation of Irbesartan and Atorvastatin in Synthetic Mixture


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1 Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
     

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A simple, accurate, rapid and precise reverse phase high performance liquid chromatographic method was developed for simultaneous estimation of Irbesartan and Atorvastatin in synthetic mixture. Inertsil C18, 150 mm x 4.6 mm, 5 μm particle size in gradient mode with mobile phase Acetonitrile: 0.1% Formic acid (40: 60 v/v) and pH adjusted to 3.5 ± 0.1 with orthophosphoric acid was used. The flow rate was 1.0 ml/min and absorbance of individual component was measured at 262 nm. The retention times of Irbesartan and Atorvastatin were found to be 3.993 and 7.733 min, respectively. Linearity for Irbesartan and Atorvastatin was in the range of 400 - 800 and 50- 100μg/ml with correlation coefficient values 0.9995and 0.9994, the percentage recovery obtained was 99.88and 99.70 %, respectively.

Keywords

Irbesartan, Atorvastatin, RP-HPLC, Method Validation.
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  • Development and Validation of RP-HPLC Method for the Simultaneous Estimation of Irbesartan and Atorvastatin in Synthetic Mixture

Abstract Views: 199  |  PDF Views: 2

Authors

Virani Paras
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
Sojitra Rajanit
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
Savaj Bhadresh
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
Raj Hashumati
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
Jain Vineet
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
Patel Kalpesh
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India
Sutariya Vishnu
Quality Assurance Department, Shree Dhanvantary Pharmacy College, Kim, Surat, India

Abstract


A simple, accurate, rapid and precise reverse phase high performance liquid chromatographic method was developed for simultaneous estimation of Irbesartan and Atorvastatin in synthetic mixture. Inertsil C18, 150 mm x 4.6 mm, 5 μm particle size in gradient mode with mobile phase Acetonitrile: 0.1% Formic acid (40: 60 v/v) and pH adjusted to 3.5 ± 0.1 with orthophosphoric acid was used. The flow rate was 1.0 ml/min and absorbance of individual component was measured at 262 nm. The retention times of Irbesartan and Atorvastatin were found to be 3.993 and 7.733 min, respectively. Linearity for Irbesartan and Atorvastatin was in the range of 400 - 800 and 50- 100μg/ml with correlation coefficient values 0.9995and 0.9994, the percentage recovery obtained was 99.88and 99.70 %, respectively.

Keywords


Irbesartan, Atorvastatin, RP-HPLC, Method Validation.