Development of sensitive derivatization method for aldosterone in liquid chromatography-electrospray ionization tandem mass spectrometry of corticosteroids

被引:48
|
作者
Yamashita, Kouwa [1 ]
Okuyama, Mitsunobu [2 ]
Nakagawa, Risa [2 ]
Honma, Seijiro [2 ]
Satoh, Fumitoshi [3 ]
Morimoto, Ryo [3 ]
Ito, Sadayoshi [3 ]
Takahashi, Madoka [1 ]
Numazawa, Mitsuteru [1 ]
机构
[1] Tohoku Pharmaceut Univ, Fac Pharmaceut Sci, Aoba Ku, Sendai, Miyagi 9818558, Japan
[2] Teikoku Hormone Med Co Ltd, Takatsu Ku, Kanagawa 2138522, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Med, Div Nephrol Endocrinol & Vasc Med,Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
aldosterone; high-performance liquid chromatography; electrospray ionization tandem mass; spectrometry; picolinyl ester; derivatization;
D O I
10.1016/j.chroma.2008.05.034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly sensitive quantification method liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) was investigated in a positive mode using recently developed picolinyl derivatization. Aldosterone was smoothly and quantitatively converted to the ethyl ether-picolinyl derivative by treatment with HCI-ethanol followed by the esterification with picolinic acid in the presence of 2-methyl-6-nitrobenzoic anhydride and 4-dimethylaminopyridine. The positive ion-ESI mass spectrum of the ethyl ether-picolinyl derivative was characterized by an appearance of protonated molecule ([M+H](+)) as a base peak. The ethyl ether-picolinyl derivatization gave a successful result in a separation of alclosterone from corticosterone, dehydrocorticosterone and cortexolone, and also provided an approximately 10-fold higher ESI response in the positive-LC-ESI-MS/MS (selected reaction monitoring; SRM) when compared to that of underivatized molecule (negative mode). The limit of quantification of aldosterone by SRM using ethyl ether-picolinyl derivatization (m/z 494 -- m1z 448) was 1 pg/0.2 ml serum with accuracy and precision of 92.6% and 5.6%, respectively. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:114 / 121
页数:8
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