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Original Research Article | OPEN ACCESS

A Spectrophotometric Method for the Determination of Ramipril in Solid Dosage Forms

O E Afieroho1 , O Okorie2, TJN Okonkwo3

1Department of Medicinal Chemistry and Quality Control, National Institute for Pharmaceutical Research and Development, Abuja; 2Pharmaceutics & Pharmaceutical Technology Department; 3Department of Pharmaceutical and Medicinal Chemistry, Faculty of Pharmaceutical Sciences, University of Port Harcourt, East-West Rd, Choba, Port Harcourt, Nigeria.

For correspondence:-  O Afieroho   Email: eriarieafieroho@yahoo.com

Received: 17 December 2010        Accepted: 31 January 2012        Published: 24 April 2012

Citation: Afieroho OE, Okorie O, Okonkwo T. A Spectrophotometric Method for the Determination of Ramipril in Solid Dosage Forms. Trop J Pharm Res 2012; 11(2):275-279 doi: 10.4314/tjpr.v11i2.15

© 2012 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To develop a simple and cost effective spectrophotometer method for the determination of ACE inhibitor ramipril in dosage forms.
Methods: UV spectrophotometry was used to develop and validate a simple method for the assay of ramipril in solid dosage form at λmax of 210 nm,  as per International Conference on Harmonization (ICH) guidelines. Aqueous methanol (5 %) was used as the blank solvent. The method was validated for linearity, recovery, accuracy, precision, specificity in the presence of excipients, and also for inter-day stability under laboratory conditions.
Results: Validation results showed linearity in the range 1 – 38 µg/ml; recovery accuracy 101.55%; regression equation Y = 0.0256X + 0.0697, R² of 0.9942; precision RSD < 2.00 %; and negligible interference from common excipients and colorants. The method was accurate (95 % confidence limit) compared to standard liquid chromatography (LC) method, with comparable reproducibility when used to assay a commercial product (Ramitace®, 2 and 5 mg tablets).
Conclusion: The validated data were within allowable limits and therefore, the proposed method is recommended for routine quality control (QC) analysis.

Keywords: Ramipril, Spectrophotmetric assay, Validation, Solid dosage forms

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Thompson Reuters (ISI): 0.523 (2021)
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