An improved underivatized, cost-effective, validated method for six short-chain fatty organic acids by high-performance liquid chromatography

•A rapid low-cost underivatized HPLC-PDA method was optimized for organic acids.•The method was validated for accuracy, linearity, and repeatability.•The optimized method can be applied to aqueous samples with complex matrices. A fast analytical method for a High-Performance Liquid Chromatograph cou...

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Veröffentlicht in:Journal of Chromatography Open Jg. 7; H. C; S. 100193
Hauptverfasser: Olonimoyo, Esther A., Amradi, Naresh Kumar, Lansing, Stephanie, Asa-Awuku, Akua A., Duncan, Candice M.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Elsevier B.V 01.05.2025
Elsevier
Schlagworte:
Liquid chromatography
Method optimization
Validation, Photodiode Array Detector
Volatile fatty acids
Liquid chromatography
Method optimization
Validation, Photodiode Array Detector
Volatile fatty acids
ISSN:2772-3917, 2772-3917
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Zusammenfassung:•A rapid low-cost underivatized HPLC-PDA method was optimized for organic acids.•The method was validated for accuracy, linearity, and repeatability.•The optimized method can be applied to aqueous samples with complex matrices. A fast analytical method for a High-Performance Liquid Chromatograph coupled with a Photodiode Array detector (HPLC-PDA) for quantifying six short-chain fatty acids: formic, acetic, propionic, butyric, isovaleric, and valeric acids is optimized and validated. The improved method is compared to existing literature, does not require derivatization, and produces rapid results with relatively low chromatographic cost. Elution modes, mobile phase, pH, and column temperature are optimized to improve peak separation and shorten analysis time without derivatization. The optimized method is characterized by a gradient elution mode with flow rates ranging from 1 to 2.5 mL min −1 and a short analysis time (7.6 mins). The limits of detection for all six acids (LOD) ranged from 0.0003 to 0.068 mM, while the limits of quantification (LOQ) ranged from 0.001 to 0.226 mM. The improved method showed acceptable sensitivity, precision, and dynamic range. Validation and quantification were tested using fermentation broth samples. This optimized method is characterized by lower detection limits and a 50 % shorter analysis time and is applicable to aqueous samples with complex matrices. [Display omitted]
Bibliographie:USDOE Office of Energy Efficiency and Renewable Energy (EERE)
EE0009268
ISSN:2772-3917
2772-3917
DOI:10.1016/j.jcoa.2024.100193