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- W4384698885 abstract "The objective of this study was to develop a simple, sensitive and reproducible method for estimation of Pregabalin by Ultra Performance Liquid Chromatography (UPLC). Pregabalin was separated on Endeversil C18 ODS (2.1 x 50mm, 3µm), using 0.1% Octane Sulphonic acid buffer with pH of 3.0: Acetonitrile (30:70) at the PDA detection of 226nm. Isocratic elution of buffer and acetonitrile was used as a mobile phase with different flow rates, eventually 30:70 v/v buffer and acetonitrile was being set with the flow rate of 0.2 ml per min. Pregabalin was eluted at a run time of 2 mins. The statistical validation parameters such as linearity, accuracy, precision, inter-day and intra-day variation were checked as suggested by ICH recommendations, further the limit of detection and limit of quantification of Pregabalin concentrations were found to be 2.98µg/mL and 9.97µg/mL. Recovery and assay studies of Pregabalin were within 99 to 102% indicating that the proposed method can be adoptable for quality control analysis of Pregabalin in bulk form and Marketed Pharmaceutical dosage form." @default.
- W4384698885 created "2023-07-20" @default.
- W4384698885 date "2023-07-07" @default.
- W4384698885 modified "2023-09-28" @default.
- W4384698885 title "METHOD DEVELOPMENT AND VALIDATION FOR THE DETERMINATION OF PREGABALIN BY USING ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY IN API SUBSTANCE AND MARKETED PHARMACEUTICAL DOSAGE FORM" @default.
- W4384698885 doi "https://doi.org/10.48047/ecb/2023.12.si5a.0238" @default.
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