Quantitative determination of captopril, perindopril erbumine, moexipril hydrochloride, and ramipril in bulk and pharmaceutical preparations by high performance liquid chromatography | ||||
Records of Pharmaceutical and Biomedical Sciences | ||||
Article 4, Volume 1, Issue 1, March 2017, Page 22-32 PDF (868.48 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/rpbs.2018.5917 | ||||
View on SCiNiTO | ||||
Authors | ||||
Mohamed Elgawish 1; Samia M. Mostafa2; Abdalla A. Elshanawane3 | ||||
1Medicinal Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia, 41522, Egypt. | ||||
2Medicinal Chemistry Department, Faculty of Pharmacy, University of Suez Canal, Ismailia 41522, Egypt | ||||
3Medicinal Chemistry Department, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt | ||||
Abstract | ||||
A high-performance liquid chromatographic method was developed for simultaneous determination of four ACE-inhibitors: captopril (CAP), perindopril erbumine (PER), moexipril hydrochloride (MOEX), and ramipril (RAM) in pharmaceutical formulations. The chromatographic separation was performed on Shim-pack cyanopropyl column with a mobile phase consisting of methanol-10mM ammonium acetate buffer (pH 6.0) in a ratio of (40: 60, v/v) at flow rate 1 ml min-1. the analysis was performed at ambient temperature using UV detector setting at 210 nm. All ACE-inhibitors were separated within seven min. The calibration curves were linear (r ≥ 0.9994) over a concentration range from 5 to 50 µg ml-1. the method was successfully applied to commercially available pharmaceutical preparations. The validity of the method was examined comparing the results obtained with official or published methods. | ||||
Keywords | ||||
Column liquid chromatography; ACE-Inhibitors; Pharmaceutical formulations | ||||
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