Accurate quantitation of choline and ethanolamine plasmalogen molecular species in human plasma by liquid chromatography–tandem mass spectrometry

• Published in: Journal of pharmaceutical and biomedical analysis Vol. 134; pp. 77 - 85
• Main Authors: Otoki, Yurika, Kato, Shunji, Kimura, Fumiko, Furukawa, Katsutoshi, Yamashita, Shinji, Arai, Hiroyuki, Miyazawa, Teruo, Nakagawa, Kiyotaka
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 05.02.2017
• Subjects: Alzheimer Disease - blood; Alzheimer’s disease; Animals; Chromatography, Liquid - methods; Chromatography, Liquid - standards; Human plasma; Humans; Mass spectrometry; Phospholipid; Plasmalogen; Plasmalogens - blood; Rats; Sodium adduct; Tandem Mass Spectrometry - methods; Tandem Mass Spectrometry - standards; Human plasma; LLE; Phospholipid; MRM; SPE; DP; LC–MS/MS; MMSE; Pls; Sodium adduct; PE-Pls; LOD; CE; AD; Alzheimer’s disease; PUFA; EP; LOQ; CV; PC; PC-Pls; PE; Plasmalogen; CXP; PL; Mass spectrometry
• ISSN: 0731-7085; 1873-264X; 1873-264X
• DOI: 10.1016/j.jpba.2016.11.019

[Display omitted] •Novel accurate plasmalogen quantitation method by LC–MS/MS was reported.•In the presence of sodium, selective and sensitive detection was achieved.•This extraction method from human plasma was simple, accuracy and precise.•Enough separation by LC enables to avoiding matrix effects.•The method has been successfully applied to quantitate clinical samples. Concentration of both choline plasmalogen (PC-Pls) and ethanolamine Pls (PE-Pls) in human plasma/serum has been getting attention to, since certain patients including those with neurodegenerative disorders, have been reported to exhibit reduced levels of specific Pls species. However, despite using liquid chromatography–tandem mass spectrometry (LC–MS/MS), accurate quantitation of Pls is still difficult because of less product ion from PC-Pls and quantitative issues (e.g., extraction recoveries and matrix effects). The present study aimed to develop a method for accurate identification and quantitation of Pls molecular species using LC–MS/MS operated in the multiple reaction monitoring mode. The LC–MS/MS conditions in the presence of sodium, and the extraction method using methanol protein precipitation were optimized. Under the optimal condition, Pls was detected at femtomole levels. The recoveries of Pls from human plasma were nearly 100%, and matrix effects were not observed. The novel method enabled determination of each Pls species in human plasma at the concentrations of 0.5–13.6μM. Then the PC-Pls and PE-Pls species in the plasma of both healthy subjects and patients with Alzheimer’s disease were quantitated. The method developed herein represents a powerful tool for analyzing Pls, which may provide a better understanding of their physiological roles in vivo.