Accurate determination of amino acids by quadruple isotope dilution-reverse phase liquid Chromatography-Tandem mass spectrometry after derivatization with 2-Naphthoyl chloride


ÖZTÜRK ER E., ERARPAT S., Bodur S., GÜNKARA Ö. T., ÖZBEK B., BAKIRDERE S.

JOURNAL OF CHROMATOGRAPHY A, cilt.1667, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1667
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1016/j.chroma.2022.462870
  • Dergi Adı: JOURNAL OF CHROMATOGRAPHY A
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, PASCAL, Analytical Abstracts, Aqualine, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, CAB Abstracts, Chemical Abstracts Core, Chimica, Compendex, EMBASE, Environment Index, Food Science & Technology Abstracts, MEDLINE, Pollution Abstracts, Veterinary Science Database
  • Anahtar Kelimeler: Amino acids, Derivatization, Human serum, Human urine, Isotope dilution, QUANTITATIVE-ANALYSIS, HUMAN SERUM, QUANTIFICATION, OPTIMIZATION, SINGLE
  • İstanbul Teknik Üniversitesi Adresli: Hayır

Özet

The determination of amino acids in biological samples is central to the diagnosis of inherited metabolic disorders and also gives significant information about the metabolisms in the cells and living body. The development of analytical method for reliable quantification of amino acids in biological samples is still challenging because of the polar nature of amino acids and complex nature of biological samples causing a high degree of interferences during analysis. In the present study, a pre-column derivatization method using 2-naphtoyl chloride combined with liquid chromatography-tandem mass spectrometry method was developed for the determination of 17 amino acids in human serum and urine matrices. Low detection limits were obtained in the range of 0.015 - 0.266 mu mol kg(-1) and acceptable recovery results were obtained in human serum and urine samples. Isotopically labelled (N-15 labelled) amino acids were spiked to standards and samples before derivatization to compensate for the analytical errors in the whole procedure. The combination of quadrupole isotope dilution strategy with the derivatization based reversed phase chromatography allowed to improve method accuracy and precision. (c) 2022 Elsevier B.V. All rights reserved.