Lucia Parráková, Cornelia A. Karg, S Hofer, Pablo Monfort‐Lanzas, Celina Wilgermein, Kevin Allmer, Sabine Scholl‐Bürgi, Anita Siller, Harald Schennach, Simon Geisler, Dietmar Fuchs, Thomas K. Felder, Johanna M. Gostner
High Resolution Image Download MS PowerPoint Slide Aromatic amino acids are precursors of neurotransmitters and immunomodulatory molecules, and their catabolism is dysregulated in various disorders associated with inflammation. This dysregulation often correlates with disease stage, symptom severity, comorbidities, quality of life, and cognitive performance, making its measurement valuable for research, diagnostics, and personalized monitoring. We developed a rapid, reliable, and cost-effective HPLC method for the simultaneous quantification of phenylalanine, tyrosine, tryptophan, and kynurenine in human serum and plasma. After protein precipitation, analytes were separated on a reversed-phase C18 column under isocratic conditions. Detection was performed based on intrinsic fluorescence for tryptophan, phenylalanine, and tyrosine and on UV absorption for kynurenine and the internal standard nitrotyrosine. The method showed linearity (R 2 > 0.99) over 0.31–20 μM for kynurenine, 1.56–200 μM for phenylalanine, 0.08–200 μM for tryptophan, and 0.78–200 μM tyrosine. Limits of detection were 0.01 μM for tryptophan,0.08 μM, 0.08 μM for tyrosine and kynurenine, and 0.39 μM for phenylalanine. Precision and accuracy were within 15%, and recovery rates ranged from 98 to 100%. Samples remained stable after processing and after three freeze–thaw cycles. Interlaboratory testing confirmed the reproducibility of the results. This validated method enables sensitive, accurate, and simultaneous quantification of key aromatic amino acids, providing a practical alternative to LC–MS/MS for routine diagnostics and biomarker studies.