Determination of Glucuronic acid, Lactic acid and Acetic acid

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Summary

Significance of the Topic

Analysis of small carboxylic acids such as glucuronic, lactic, and acetic acids is critical in biochemical research, fermentation process monitoring, and quality control in pharmaceutical and food industries. This method provides reliable quantification of these compounds, which play key roles in metabolic pathways and product quality.

Aims and Overview of the Study

The objective was to establish a robust HPLC method (VFD0135J) using an ion-exchange column and refractive index detection to simultaneously separate and quantify glucuronic, lactic, and acetic acids. Standard solutions at 2 mg/mL were analyzed to validate retention times and resolution.

Applied Instrumentation

  • HPLC system equipped with Refractive Index (RI) detector
  • Column: Eurokat H, 10 µm particle size, 300 × 8 mm

Methodology

  • Eluent: 0.01 N sulfuric acid (isocratic)
  • Flow rate: 0.5 mL/min
  • Column temperature: 40 °C
  • Injection volume: 20 µL
  • Analytes: glucuronic acid, lactic acid, acetic acid (2 mg/mL each)

Main Results and Discussion

Baseline separation of all three acids was achieved under isocratic conditions. Each analyte produced a distinct peak with good symmetry and reproducible retention times. The refractive index detector provided sufficient sensitivity for quantitative analysis at the tested concentration levels.

Benefits and Practical Applications of the Method

  • High reproducibility and robustness for routine quality control
  • Simple isocratic elution reduces complexity and maintenance
  • Suitable for monitoring fermentation processes and metabolic studies

Future Trends and Potential Applications

  • Integration with mass spectrometric detection for enhanced sensitivity and specificity
  • Miniaturization and microflow HPLC formats for reduced solvent consumption
  • Real‐time process analytics and online monitoring in bioreactors

Conclusion

The described HPLC method VFD0135J offers a straightforward and reliable approach for the simultaneous determination of glucuronic, lactic, and acetic acids. Its simplicity and robustness make it well-suited for both research and industrial laboratories.

References

No literature references were provided in the original text.

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