HPLC-UV Method development for Fixed Dose Pharmaceutical Formulations

Yadav, Sonia; Sharma, Anunny; Maratha, Sushma

ISBN 10: 6209779719 / ISBN 13: 9786209779718

Published by LAP Lambert Academic Publishing, 2026

About this Item

Seller Inventory # 26406501017

Bibliographic Details

• Title: HPLC-UV Method development for Fixed Dose Pharmaceutical Formulations
• Publisher: LAP Lambert Academic Publishing
• Publication Date: 2026
• Language: English
• ISBN 10: 6209779719
• ISBN 13: 9786209779718
• Binding: Soft cover
• Condition: New

About this title

Synopsis

Estimation of imeglimin hydrochloride in human plasma by HPLC-UV. The estimation of drugs by RP-HPLC (reverse phase chromatography) was chosen since it is advised for use with ionic and mild to non-polar compounds. Simple, specific, and superior in terms of efficiency, stability, and reproducibility is reverse phase chromatography. For the separation of imeglimin, the C18 column 250 x 4.6 mm, 5 µm particle size was chosen. In the mobile phase, various solvent solutions were tested and combined for optimum performance. Imeglimin hydrochloride (4 µg/ml) in buffer, pH 4 for Acetonitrile: Water (70:30), a concentration range (8-40 and 0.5-4 µg/ml) displaying excellent peak and a sizable resolution level. Having the mobile phase run at 1ml/min, photodiode array detectors were used to detect both analytes at 215 nm. The method was validated in different concentration ranges in human plasma. Imeglimin inter and intra-run precision was measured at less than 3.60% and had an accuracy of less than 1.869%. imeglimin in human plasma was validated by linearity, recovery matrix, and stability. The retention time of IMEG is 4.8 minutes in plasma. Suggested method denotes that it is cost-effective