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Quantitative determination of short chain organic acids by RP-HPLC/ESI(-)-MS using post column phase modification

Sarmite Katkevica1, Andreas Held1, Marcus A. Horn2
1 Atmospheric chemistry, BayCEER
2 Ecological Microbiology, BayCEER

P 2.3 in Research in its Prime: First Results of Ongoing Research

Microbial fermentation products include short chain organic acids in environmental samples. Analyses of carbon flow via microbial fermentation utilizing 13C-labelled tracers depend on a sensitive detection of short chain organic acids and their isotopic composition. Thus, a high performance liquid chromatography/mass spectrometry (HPLC-MS) method with selected ion monitoring was developed and optimized to analyze several short chain organic acids (acetic, propionic, butyric, iso-butyric, 2-methylbutyric, 3-methylbutyric, valeric, lactic, succinic, pyruvic, oxalic, and acrylic acids) in environmental samples.  Chromatographic separation and peak shape optimization require protonation of short chain organic acids by a mobile phase approximating pH 3, whereas a sensitive detection in atmospheric pressure electrospray (APS-ES) negative mode requires charged carboxylate anions occurring at higher pH. Such a dilemma was resolved by a post column phase modification of the eluent pH (i.e., the continuous addition of base in post column flow increasing the pH of the mobile phase from 3 to 9-10), maximizing the formation of carboxylate anions and thus the detection sensitivity under APS-ES negative ionization mode. Three methods for selected organic acids differing in detection sensitivity, analysis time, and chromatographic separation were developed. Baseline separation of nine organic acids was achieved at a flow rate of 0.2 mL min-1. Limits of detection (LOD) and quantification (LOQ) ranged from 0.01 to 1 µM and 0.05 to 5 µM, respectively. LODs and LOQs were highest for succinic acid. Calibration curves were linear over three orders of magnitude of organic acid concentrations. A 4-fold increase in detection sensitivity for acetic acid was achieved at a flow rate of 0.1 mL/min. Recoveries of representative organic acids in peat extracts were reduced on average by approximately 20 % due to matrix effects. Representative 13C-labelled acids were likewise quantified. This method is accurate, sensitive, simple, and can be used to analyze diverse short chain organic acids including their isotopic composition in various environmental samples.

last modified 2013-09-18