Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

RP-HPLC Determination of Amlodipine Besylate and Atorvastatin in Amlodipine Besilate and Atorvastatin Tablets


     

   Subscribe/Renew Journal


A simple, specific, accurate and precise high performance liquid chromatographic method was developed for the determination of Amlodipine and Atorvastatin in Amlodipine besylate and Atorvastatin tablet dosage forms. A Hypersil BDS C18 5 μm (250×4.6 mm I.D) with column temperature 30°C in isocratic mode, with mobile phase containing Acetonitrile:10 mM Ammonium acetate buffer pH 4.0 (50:50) was used. The flow rate was 1.0 mL/min and effluent was monitored at 238 nm.The retention time of Amlodipine was 2.5 min and for Atorvastatin was 4.7 min. The linearity for Amlodipine and Atorvastatin was in the range 0.02 mg/mL to 0.12 mg/mL. The proposed method is accurate, precise, specific and rapid estimation of Amlodipine and Atorvastatin in Amlodipine besilate and Atorvastatin tablets.

Keywords

HPLC, Amlodipine Besylate (AMD), Atorvastatin (ATVR), Dissolution, Assay, Validation, Isocratic Elution.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 185

PDF Views: 0




  • RP-HPLC Determination of Amlodipine Besylate and Atorvastatin in Amlodipine Besilate and Atorvastatin Tablets

Abstract Views: 185  |  PDF Views: 0

Authors

Abstract


A simple, specific, accurate and precise high performance liquid chromatographic method was developed for the determination of Amlodipine and Atorvastatin in Amlodipine besylate and Atorvastatin tablet dosage forms. A Hypersil BDS C18 5 μm (250×4.6 mm I.D) with column temperature 30°C in isocratic mode, with mobile phase containing Acetonitrile:10 mM Ammonium acetate buffer pH 4.0 (50:50) was used. The flow rate was 1.0 mL/min and effluent was monitored at 238 nm.The retention time of Amlodipine was 2.5 min and for Atorvastatin was 4.7 min. The linearity for Amlodipine and Atorvastatin was in the range 0.02 mg/mL to 0.12 mg/mL. The proposed method is accurate, precise, specific and rapid estimation of Amlodipine and Atorvastatin in Amlodipine besilate and Atorvastatin tablets.

Keywords


HPLC, Amlodipine Besylate (AMD), Atorvastatin (ATVR), Dissolution, Assay, Validation, Isocratic Elution.