Lestari, Annisa Dyah and Rohman, Abdul F. and Martono, Sudibyo (2020) Analytical method validation of reversed phase HPLC for quantitative analysis of tartrazine and auramine o in powder drinks. Food Research, 4 (6). 2037 - 2041. ISSN 25502166
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This study was aimed to perform analytical method validation of high-performance liquid chromatography (HPLC) technique using photo-diode array detector for the simultaneous determination of Tartrazine (TAR) and Auramine O (AUO) in powder drink products. TAR and AUO were analysed using Waters Shield C<inf>18</inf> column (250 mm x 4.6 mm i.d., 5 µm) using PDA detector at 300-650 nm. The mobile phase used was acetonitrile-ammonium acetate 19 mM (86:14 v/v) delivered isocratically at a flow rate of 1.2 mL/ min. The optimized HPLC condition was subjected to analytical method validation by assessing some performance characteristics as guided by International Conference on Harmonization (ICH). The method was linear over the studied concentration ranges with the coefficient of determination (R<sup>2</sup>) of 0.999 and 0.997 for TAR and AUR with intercept less than 2, respectively. The developed method was sensitive with a limit of detection value of 0.0325 μg/mL and 0.1052 μg/mL for TAR and AUO, respectively. The method is also accurate and precise as indicated with acceptable recovery values of 99.0-100.7 for TAR and 102.1-106.5 for AUO with relative standard deviation (RSD) values lower than those required by Association of Official Analytical Chemists (AOAC). The developed method is simple and can be used for routine analysis of TAR and AUO for quality assurance purposes of powder drinks. © 2020 Elsevier B.V., All rights reserved.
| Item Type: | Article |
|---|---|
| Additional Information: | Cited by: 0; All Open Access; Gold Open Access |
| Uncontrolled Keywords: | auramine; tartrazine; Article; beverage; cost effectiveness analysis; drug determination; limit of detection; limit of quantitation; measurement accuracy; measurement precision; quality control; quantitative analysis; retention time; reversed phase high performance liquid chromatography; validation process; validation study |
| Subjects: | R Medicine > RS Pharmacy and materia medica |
| Divisions: | Faculty of Pharmacy |
| Depositing User: | Sri JUNANDI |
| Date Deposited: | 07 Nov 2025 01:25 |
| Last Modified: | 07 Nov 2025 01:25 |
| URI: | https://ir.lib.ugm.ac.id/id/eprint/23961 |
