Isomeric discrimination of kaempferol versus luteolin by online energy-resolved mass spectrometry.
10.19540/j.cnki.cjcmm.20210302.301
- Author:
Hui-Ting TANG
1
;
Jun JIANG
2
;
Yan CAO
1
;
Peng-Wei GUAN
1
;
Han LI
1
;
Yi-Jia ZHAO
1
;
Juan YU
3
;
Peng-Fei TU
1
;
Jun LI
1
;
Yue-Lin SONG
1
Author Information
1. Modern Research Center for Traditional Chinese Medicine,School of Chinese Materia Medica,Beijing University of Chinese Medicine Beijing 100029,China.
2. Shandong Institute for Food and Drug Control Ji'nan 250100,China.
3. Zhangzhou Pien Tze Huang Pharmaceutical Co.,Ltd. Zhangzhou 363000,China.
- Publication Type:Journal Article
- Keywords:
breakdown graph;
kaempferol;
luteolin;
online energy-resolved mass spectrometry
- MeSH:
Chromatography, Liquid;
Flavonoids;
Kaempferols;
Luteolin;
Tandem Mass Spectrometry
- From:
China Journal of Chinese Materia Medica
2021;46(14):3599-3604
- CountryChina
- Language:Chinese
-
Abstract:
Isomers are widely distributed in Chinese herbal medicines,and can be discriminated by energy-resolved mass spectrometry( ER-MS). However,ER-MS was performed through direct injection of reference compounds with syringe pump,which encountered a significant technical barrier for high-throughput and automated measurements. Herein,online ER-MS was conducted using LC-MS platform,and a pair of isomers,kaempferol vs luteolin,were employed as a case study to illustrate and assess the utility of online ER-MS for isomeric discrimination. High-resolution tandem mass spectrometry data of both flavonoids were acquired on LC-QE-Orbitrap-MS,and the fragmentation pathways responsible for the primary fragment ions were proposed. The primary signal in MS1 occurred at m/z 285( [M-H]-),and the primary signals of either compound generated by retro-Diels-Alder fragmentation were observed at m/z 151 and 133. The spectral information was subsequently transferred onto LC-Qtrap-MS platform to carry out online ER-MS. Two precursor-to-product ion transition candidates were constructed as m/z 285>151 and 285>133,and either afterward derived a set of pseudo-ion transitions( PITs) and so forth,exactly corresponding to a series of progressive collision energies( eg-5,-8,-11 e V,and so on). All PITs were typed into the monitoring list of multiple reaction monitoring program to generate the peak area datasets. Either dataset was normalized using the highest values in the set and imported into Graph Pad Prism software to plot the Gaus-sian-shaped curve that was termed as the break-down graph. The apex of the regressive curve was termed as optimal collision energy( OCE). The OCE values corresponding to m/z 285>151 were calculated as-29. 06 e V and-35. 71 e V for kaempferol and luteolin,respectively. In the case of m/z 285>133,the OCEs were yielded as-44. 15 e V for kaempferol and-49. 01 e V for luteolin. With re-ference to their chemical structures,the location of hydroxyl group was regarded to be responsible for the differences of either m/z 285>151 or 285>133 between the isomers,attributing to their different bond properties. Above all,online ER-MS offers an eligible tool for isomeric discrimination,and provides meaningful information for the accurate chemical composition characterization based on LC-MS,which is not limited to Chinese herbal medicines.
