Improvement of analysis throughput for LC/MS assay
Improvement of analysis throughput for LC/MS assay
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提高 LC/MS 测定的分析通量
DOI:
10.1007/s44211-022-00089-4
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发表时间:
2022
期刊:
影响因子:
--
通讯作者:
S. Ogawa
中科院分区:
文献类型:
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作者:
Takeru Sagae;Mariko Yokogawa;Ryoichi Sawazaki;Yuichiro Ishii;Nao Hosoda;Shin-ichi Hoshino;Shunsuke Imai;Ichio Shimada;Masanori Osawa;S. Ogawa
Analysis of compounds in various biological samples, including body fluids, tissues, cells, and even raw food material or food ingredients, may contribute our understanding of their biological activities, diagnosis for various diseases, new drug and novel biomarker discovery. Liquid chromatography (LC)/mass spectrometry (MS or MS/MS) is the most powerful and reliable methodology for the quantification of metabolites due to its selectivity and sensitivity, and broad coverage of many compounds. As is already widely known, chemical derivatization method often makes the detection ability of LC/MS more powerfully due to the desirable LC separation behavior and enhanced MS assay sensitivity of the derivatized metabolites [1–3]. Ohno et al. reported a development of novel proton affinitive derivatization reagent: 5-butylpicolinic acid and applied the reagent to the analysis of a trace amount of testosterone and dihydrotestosterone in saliva [4]. Furthermore, Nagatomo et al., applied the derivatization method to determination of short-chain fatty acids in feces samples by LC/MS/MS [5]. As shown in the above example, the use of derivatization as a sensitivity improvement method in LC/MS/MS analysis continues to be reported [6–8].On the other hand, LC/MS assays have been required improvements in analytical throughput. Because the LC/MS method requires a long measurement time for each analysis in exchange for the high reliability of the measured values by chromatographic separation. Thus, the derivatization might be also a hopeful approach to overcome this disadvantage. That is the multiplexing of some analytical samples in the single LC/MS run, which is achieved by derivatization of the multiple samples with the multiple reagents