脂类学
色谱法
化学
代谢组学
亲水作用色谱法
代谢组
质谱法
样品制备
脑脊液
固相萃取
脂质体
萃取(化学)
高效液相色谱法
生物化学
生物
神经科学
作者
Kourosh Hooshmand,Jin Xu,Anja Hviid Simonsen,Asger Wretlind,Andressa de Zawadzki,Karolina Sulek,Steen Gregers Hasselbalch,Cristina Legido‐Quigley
标识
DOI:10.1007/s12035-023-03666-4
摘要
Abstract Cerebrospinal fluid (CSF) is a metabolically diverse biofluid and a key specimen for exploring biochemical changes in neurodegenerative diseases. Detecting lipid species in CSF using mass spectrometry (MS)-based techniques remains challenging because lipids are highly complex in structure, and their concentrations span over a broad dynamic range. This work aimed to develop a robust lipidomics and metabolomics method based on commonly used two-phase extraction systems from human CSF samples. Prioritizing lipid detection, biphasic extraction methods, Folch, Bligh and Dyer (B&D), Matyash, and acidified Folch and B&D (aFolch and aB&D) were compared using 150 μL of human CSF samples for the simultaneous extraction of lipids and metabolites with a wide range of polarity. Multiple chromatographical separation approaches, including reversed-phase liquid chromatography (RPLC), hydrophilic interaction liquid chromatography (HILIC), and gas chromatography (GC), were utilized to characterize human CSF metabolome. The aB&D method was found as the most reproducible technique (RSD < 15%) for lipid extraction. The aB&D and B&D yielded the highest peak intensities for targeted lipid internal standards and displayed superior extracting power for major endogenous lipid classes. A total of 674 unique metabolites with a wide polarity range were annotated in CSF using, combining RPLC-MS/MS lipidomics ( n = 219), HILIC-MS/MS ( n = 304), and GC-quadrupole time of flight (QTOF) MS ( n = 151). Overall, our findings show that the aB&D extraction method provided suitable lipid coverage, reproducibility, and extraction efficiency for global lipidomics profiling of human CSF samples. In combination with RPLC-MS/MS lipidomics, complementary screening approaches enabled a comprehensive metabolite signature that can be employed in an array of clinical studies. Graphical abstract
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