Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant

Background: Amlodipine is a third generation dihydropyridine calcium antagonist, It is used in the treatment of hypertension and angina. It is formulated in IIUM pilot plant in the tablet dosage form, an analytical method is needed for the analysis of amlodipine to qualify the GMP requirements. The...

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Main Authors: Helaluddin , Abul Bashar Mohammed, Alaama, Mohammed, Mohamad, Huda Jamilah, Amiruddin , Noor Syafawati
Format: Conference or Workshop Item
Language:English
Published: 2013
Subjects:
Online Access:http://irep.iium.edu.my/34520/
http://irep.iium.edu.my/34520/1/Development_and_validation_of_a_new_RP-HPLC_method_for_the_analysis_of_amlodipine_tablet_dosage_form_manufactured_by_IIUM_pilot_plant.pdf
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spelling iium-345202014-01-20T06:59:58Z http://irep.iium.edu.my/34520/ Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant Helaluddin , Abul Bashar Mohammed Alaama, Mohammed Mohamad, Huda Jamilah Amiruddin , Noor Syafawati QD Chemistry RS Pharmacy and materia medica Background: Amlodipine is a third generation dihydropyridine calcium antagonist, It is used in the treatment of hypertension and angina. It is formulated in IIUM pilot plant in the tablet dosage form, an analytical method is needed for the analysis of amlodipine to qualify the GMP requirements. The pharmacopeia method was tested and found to be very old and non-economic as it caused the column to spoil earlier. Objective: To develop and validate new sensitive and cheap analytical method for the analysis of amlodipine in tablet dosage form. Methodology: Standards and samples were prepared by dissolving amlodipine or amlodipine tablets in mobile phase and sonicate for 5 min. Samples were analysed using Agilent 1200 Series RP-HPLC equipped with quaternary pump and auto injector. Samples were injected to C18 column and the mobile phase consisted of ammonium acetate buffer (pH=4 adjusted using glacial acetic acid) and acetonitrile in the ratio 60-40. The flow rate was 1 ml/min and UV detector was used for the detection and the wavelength was 248nm.The method was validated according to ICH guidelines. Results: The retention time was 3.4 min with the total run time of 6 min. The method was linear over the range 0.1-40 ug/ml with R2 = 0.999. The recovery was 98%, and the method showed high precision and repeatability. All validated parameters were in the accepted range of ICH requirements. Conclusion: New rapid sensitive and highly economic method was developed and validated for the analysis of amlodipine in tablet dosage form. 2013 Conference or Workshop Item PeerReviewed application/pdf en http://irep.iium.edu.my/34520/1/Development_and_validation_of_a_new_RP-HPLC_method_for_the_analysis_of_amlodipine_tablet_dosage_form_manufactured_by_IIUM_pilot_plant.pdf Helaluddin , Abul Bashar Mohammed and Alaama, Mohammed and Mohamad, Huda Jamilah and Amiruddin , Noor Syafawati (2013) Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant. In: 4th USIM Annual Health Conference 2013, 5-6 October 2013, Hotel Istana, Kuala Lumpur.
repository_type Digital Repository
institution_category Local University
institution International Islamic University Malaysia
building IIUM Repository
collection Online Access
language English
topic QD Chemistry
RS Pharmacy and materia medica
spellingShingle QD Chemistry
RS Pharmacy and materia medica
Helaluddin , Abul Bashar Mohammed
Alaama, Mohammed
Mohamad, Huda Jamilah
Amiruddin , Noor Syafawati
Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant
description Background: Amlodipine is a third generation dihydropyridine calcium antagonist, It is used in the treatment of hypertension and angina. It is formulated in IIUM pilot plant in the tablet dosage form, an analytical method is needed for the analysis of amlodipine to qualify the GMP requirements. The pharmacopeia method was tested and found to be very old and non-economic as it caused the column to spoil earlier. Objective: To develop and validate new sensitive and cheap analytical method for the analysis of amlodipine in tablet dosage form. Methodology: Standards and samples were prepared by dissolving amlodipine or amlodipine tablets in mobile phase and sonicate for 5 min. Samples were analysed using Agilent 1200 Series RP-HPLC equipped with quaternary pump and auto injector. Samples were injected to C18 column and the mobile phase consisted of ammonium acetate buffer (pH=4 adjusted using glacial acetic acid) and acetonitrile in the ratio 60-40. The flow rate was 1 ml/min and UV detector was used for the detection and the wavelength was 248nm.The method was validated according to ICH guidelines. Results: The retention time was 3.4 min with the total run time of 6 min. The method was linear over the range 0.1-40 ug/ml with R2 = 0.999. The recovery was 98%, and the method showed high precision and repeatability. All validated parameters were in the accepted range of ICH requirements. Conclusion: New rapid sensitive and highly economic method was developed and validated for the analysis of amlodipine in tablet dosage form.
format Conference or Workshop Item
author Helaluddin , Abul Bashar Mohammed
Alaama, Mohammed
Mohamad, Huda Jamilah
Amiruddin , Noor Syafawati
author_facet Helaluddin , Abul Bashar Mohammed
Alaama, Mohammed
Mohamad, Huda Jamilah
Amiruddin , Noor Syafawati
author_sort Helaluddin , Abul Bashar Mohammed
title Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant
title_short Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant
title_full Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant
title_fullStr Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant
title_full_unstemmed Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant
title_sort development and validation of new rp-hplc method for the determination of amlodipine in tablet dosage form manufactured by iium pilot plant
publishDate 2013
url http://irep.iium.edu.my/34520/
http://irep.iium.edu.my/34520/1/Development_and_validation_of_a_new_RP-HPLC_method_for_the_analysis_of_amlodipine_tablet_dosage_form_manufactured_by_IIUM_pilot_plant.pdf
first_indexed 2023-09-18T20:49:45Z
last_indexed 2023-09-18T20:49:45Z
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