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High-throughput one-pot micro-volume chemical derivatization combined with targeted lipidomics for the analysis of oxylipins in cells

Journal 2026 · IF 5.1 · 发表于 2026 年 5 月 5 日
作者: Di Rao,Zongyuan Wu,Zuojian Qin,Xia Xiang,Yu Chen,Dan Wang,Xin Lv,Tang Tang,Hong Chen,Fang Wei
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摘要

Oxylipins, generated from polyunsaturated fatty acids (PUFAs), are essential for regulating fundamental physiological processes, such as tissue repair, immunity, and inflammation. However, their intracellular concentrations are inherently low, and many are rapidly transformed or degraded through enzymatic or non-enzymatic reactions, resulting in extremely short half-lives. The complex and time-consuming pretreatment, typically involving sequential cell lysis, solvent extraction, solid-phase clean-up, evaporation, and off-line chemical derivatization, undermines the accuracy of oxylipin analysis in cells. A high-throughput one-pot micro-volume chemical derivatization combined with targeted lipidomics analysis method was developed. Initially, cells were sorted into a 54-well micro sample tube array using flow cytometry. Then, a one-pot method was employed to simultaneously perform cell disruption, oxylipin extraction, and N, N‑diethyl-1,3-diaminopropane (DEPA) labeling. The derivatization of 54 cell samples was completed within 1 min at room temperature, enabling the entire pretreatment to be completed in 10 min. Finally, an ultra-high performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) was utilized for profiling oxylipins. A total of 14 oxylipins were identified in 1000 RAW 264.7 cell samples, and 8 distinct oxylipins were successfully detected in single-cell analysis including 12-HEPE, 15-HEPE, 12-HETE, PGD2, and PGE2. The proposed method exhibited high sensitivity, with concentration ranges of 0.03–2.98 nmol/L, excellent linearity (R² = 0.992–0.999), and a limit of detection as low as 0.2 pmol/L, demonstrating good accuracy and precision. This protocol eliminates solvent transfers, evaporation, and reconstitution through a one-step micro-volume reaction, drastically minimizing sample loss and oxidation risk. The entire workflow is completed in 10 min for 54 samples with -level sensitivity. Fully compatible with flow-sorted cells, automated liquid handling, and on-line MS, it delivers precise, reproducible oxylipin profiles from rare primary cells, clinical biopsies, or single cells, thereby opening new frontiers in single-cell lipidomics and precision medicine research.