Analysis of Organic Acid Preservatives in Food With the PerkinElmer Flexar® FX-15 UHPLC System

December 1, 2010

Special Issues

Volume 0, Issue 0

In food, organic acids originate from the natural biochemistry processes or are added as preservatives, acidulants and stabilizers.

Njies Pedjie, PerkinElmer

In food, organic acids originate from the natural biochemistry processes or are added as preservatives, acidulants and stabilizers. Organic acids contribute to the sensory properties of foods by providing taste and aroma. Citric acid is widely used in soft drinks to provide them with the sour taste of citrus fruit. In the food industry, organic acids are used as antimicrobial agents: formic acid is used as a preservative agent in livestock feeds where it can kill salmonella bacteria.

Analysis of organic acids by reversed phase liquid chromatography is challenging because they have low retention factors and therefore elute close, or within the void volume.

This application note presents a robust UHPLC method for the analysis of some commonly used organic acids. In addition to the method condition, precision and linearity data for formic acid, d-isoascorbic acid, acetic acid, citric acid, fumaric acid and proprionic acid are presented. Red wine vinegar and lemon juice will be analyzed and the acid type and concentration confirmed.

Experimental

A PerkinElmer FlexarFX-15 with Flexar FX Photodiode Array detector provided the UHPLC platform for this application. The separation was achieved with a PerkinElmer Brownlee Analytical C18, 5 μm 100 × 4.6 mm column. The run time was approximately 4.5 min with a back pressure of 2,000 PSI (138 bars).

Repeatability was studied with six injections of the working standard with concentration ranging from 0.015 mg/mL for fumaric acid to 9.4 mg/mL for proprionic acid. Linearity was determined across a wide range: from 0.1–0.15 μg/mL for formic acid to 120–9400 μg/mL for proprionic acid.

Results and Discussion

Optimal resolution and retention was obtained with a pH 2.3 mobile phase. All acid peaks eluted within 5 min. The method performance was outstanding: the linearity of the analysis achieved an average r2 value of 0.9996. Precision was less than 2% relative standard deviation for each acid. A representative chromatogram of the standard solution with annotated peaks is shown in Figure 1.

Figure 1: Chromatogram from the analysis of a standard solution of organic acids.

Conclusion

The method was shown to be linear and peaks were well resolved. The red wine vinegar tested has 6.4 % acetic acid well within the requirement of not less than 4% mandated by the FDA. The lemon juice tested has 5.8% of citric acid. PerkinElmer PDA provides a rugged and accurate detection over a range of 190 nm to 700 nm encompassing UV and Vis wavelengths. PerkinElmer's Chromera® software offers many data acquisition and processing features: spectral library creation, and peak purity, spectra 3D and contour maps, which are powerful tools for interrogating the information content of a 3D photodiode array chromatogram. The spectra library search function allowed the storage of acids standard spectra that were later used for peak identification and confirmation in the samples.

References

(1) Leo M.L., Nollet, Food Analysis by HPLC, second edition, April 2000.

(2) FDA, CPG Sec.525.825 vinegar.

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