Abstract

Analysis of amino acids by gas chromatography-mass spectrometry (GC–MS) requires at least one derivatization step to enable solubility in GC–MS-compatible water-immiscible organic solvents such as toluene, to make them volatile to introduce into the gas chromatograph and thermally stable enough for separation in the GC column and introduction into the ion-source, and finally to increase their ionization by increasing their electronegativity using F-rich reagents. In this work we investigated the long-term stability of the methyl esters pentafluoropropionic (Me-PFP) derivatives of 21 urinary amino acids prepared by a two-step derivatization procedure and extraction by toluene. In situ prepared trideuteromethyl ester pentafluoropropionic derivatives were used as internal standards. GC–MS analysis (injection of 1 µL aliquots and quantification by selected-ion monitoring of specific mass fragments) was performed on days 1, 2, 8, and 15. Measured peak areas and calculated peak area ratios were used to evaluate the stability of the derivatives of endogenous amino acids and their internal standards, as well as the precision and the accuracy of the method. All analyses were performed under routine conditions. Me-PFP derivatives of endogenous amino acids and their stable-isotope labelled analogs were stable in toluene for 14 days. The peak area values of the derivatives of most amino acids and their internal standards were slightly higher on days 8 and 15 compared to days 1 and 2, yet the peak area ratio values of endogenous amino acids to their internal standards did not change. Our study indicates that Me-PFP derivatives of amino acids from human urine samples can easily be prepared, are stable at least for 14 days in the extraction solvent toluene, and allow for precise and accurate quantitative measurements by GC–MS using in situ prepared deuterium-labelled methyl ester as internal standard.

Highlights

  • Amino acids are carboxylic acids and contain at least one primary or secondary amine group and additional functionalities such as a hydroxyl (OH) group (Scheme 1)

  • In previous work [7,8], we found that a two-step derivatization step (Scheme 2) is useful for the reliable simultaneous quantitative measurement of amino acids by gas chromatography-mass spectrometry (GC–MS) in different biological samples including plasma, serum and urine

  • The mean ratios of the peak area (PA) values of the urinary amino acids to the PA values of the respective internal standards measured in the seven urine samples are summarized in

Read more

Summary

Introduction

Amino acids are carboxylic acids and contain at least one primary or secondary amine group and additional functionalities such as a hydroxyl (OH) group (Scheme 1). Amino acids and many of their metabolites are generally not accessible to gas chromatography (GC)-based analysis because they are not volatile and are thermally labile. Their injection in the gas chromatograph would lead to decomposition in the usually hot injector port to release small gases most likely including CO2 , NH3 and H2 O. Native amino acids are not compatible with GC-based techniques such as gas chromatography-mass spectrometry (GC–MS). This trouble can be solved by chemical reactions of the carboxylic (COOH)

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call