Amanda Kusumaning Astari
Universitas Setia Budi

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Pengembangan dan Validasi Metode KCKT Fase Terbalik untuk Analisis Senyawa Ranitidin, Simetidin, Asetosal Menggunakan Desain Faktorial Amanda Kusumaning Astari; Iswandi Iswandi; Dian Marlina
PHARMADEMICA : Jurnal Kefarmasian dan Gizi Vol 6 No 1 (2026): April - September
Publisher : LPPM-KI - POLTEKKES PIM (Formerly AKAFARMA-AKFAR PIM

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.54445/pharmademica.v6i1.186

Abstract

Differences in physicochemical properties between ranitidine, cimetidine, and acetosal such as pKa and log P values ​​can affect the analysis results in the High Performance Liquid Chromatography (HPLC) method. The purpose of this study was to determine the best chromatography system for HPLC that is optimal in separating compounds and ensuring the validation of the method. The research method used laboratory experiments in the development of a reversed phase HPLC system using a factorial design. The variables analyzed were flow rate, pH, and mobile phase buffer concentration. Method validation was carried out with selectivity, linearity, LOD, LOQ, accuracy, and precision parameters. The results showed the best conditions using a 230 nm wavelength UV detector, a flow rate of 0.5 mL/min, a mobile phase of acetonitrile: 0.05 M acetate buffer at pH 5 (20:80 v/v). Based on the analysis of interactions between variables, it showed an influence on all three variables. The validation results of the linearity test for ranitidine, cimetidine, and acetosal were 0.9989; 0.9989; and 0.999, respectively. The LOD value was 2.59 ppm and the LOQ value was 8.64 ppm. The selectivity test on the first peak with the second peak was 1.509 and on the second peak with the third peak was 5.495. The accuracy test with % recovery was 103.863% and % RSD was 1.819%. The method used was proven valid as indicated by the results that met the method validation requirements.