IIUM Repository

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 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.

[img] PDF (Development and validation of new RP-HPLC method for the determination of Amlodipine in tablet dosage form manufactured by IIUM pilot plant) - Published Version
Restricted to Repository staff only

Download (737kB) | Request a copy

Abstract

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.

Item Type: Conference or Workshop Item (Full Paper)
Additional Information: 4478/34520
Uncontrolled Keywords: Amlodipine, RP-HPLC, ICH guidelines, validation.
Subjects: Q Science > QD Chemistry
R Medicine > RS Pharmacy and materia medica
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Pharmacy
Depositing User: Dr. A. B. M. Helal Uddin
Date Deposited: 20 Jan 2014 14:59
Last Modified: 20 Jan 2014 14:59
URI: http://irep.iium.edu.my/id/eprint/34520

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year