Simultaneous Determination of Twelve Tetrahydrocorticosteroid Glucuronides in Human Urine by Liquid Chromatography/Electrospray Ionization-Linear Ion Trap Mass Spectrometry

被引:26
作者
Ikegawa, Shigeo [1 ]
Hasegawa, Maki [1 ]
Okihara, Rika [1 ]
Shimidzu, Chikara [2 ]
Chiba, Hitoshi [3 ]
Iida, Takashi [4 ]
Mitamura, Kuniko [1 ]
机构
[1] Kinki Univ, Fac Pharmaceut Sci, Higashiosaka, Osaka 5778502, Japan
[2] Hokkaido Univ Hosp, Kita Ku, Sapporo, Hokkaido 0608648, Japan
[3] Hokkaido Univ, Fac Hlth Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[4] Nihon Univ, Dept Chem, Coll Humanities & Sci, Tokyo 1568550, Japan
基金
日本学术振兴会;
关键词
ENZYME-ASSISTED SYNTHESIS; APPARENT MINERALOCORTICOID EXCESS; PHASE-II METABOLITES; LC-MS-MS; 3-ALPHA; 5-ALPHA-TETRAHYDRO DERIVATIVES; CONJUGATED METABOLITES; CHEMICAL CONVERSION; CORTISOL; CORTICOSTEROIDS; STEROIDS;
D O I
10.1021/ac9018632
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A liquid chromatography/electrospray ionization (ESI)-mass spectrometry (MS) method for the direct determination of 12 tetrahydrocorticosteroid glucuronides in human urine has been developed. The analytes were Sand 21-monoglucuronides of tetrahydrocortisol, tetrahydrocortisone, tetrahydro-11-deoxycortisol, and their 5 alpha-stereoisomers. The mass spectrometric behaviors of these glucuronides in negative-ion ESI-MS/MS revealed the production of intense, structure-specific product ions within the same group of glucuronides. Regioisomeric glucuronides could be distinguished by collision-induced dissociation and tandem mass spectrometry. Using a linear ion trap instrument operating in the negative-ion mode and by monitoring the transition ions of [M - H](-) -> [M - H - CH(2)O](-) for 3-monoglucuronides and [M - H](-) -> [M - H - CH(2)OG](-) for 21-monoglucuronides, a sensitive and specific assay was developed. Initial steps in the assay were a simple solid-phase extraction and the addition of [9,12,12,21,21-d(5)]-tetrahydrocortisone-3-glucuronide (prepared by enzyme-assisted synthesis) as an internal standard. The method was applied to determine the 12 tetrahydrocoticosteroid glucuronides in urine from healthy subjects and from patients with excessive cortisol production. The method described here appears to be useful for clinical and biochemical studies.
引用
收藏
页码:10124 / 10135
页数:12
相关论文
共 47 条
[11]   Human uridine diphosphate-glucuronosyltransferase UGT2B7 conjugates mineralocorticoid and glucocorticoid metabolites [J].
Girard, C ;
Barbier, O ;
Veilleux, G ;
El-Alfy, M ;
Bélanger, A .
ENDOCRINOLOGY, 2003, 144 (06) :2659-2668
[12]   Isolation and characterization of the monkey UGT2B30 gene that encodes a uridine diphosphate-glucuronosyltransferase enzyme active on mineralocorticoid, glucocorticoid, androgen and oestrogen hormones [J].
Girard, C ;
Barbier, O ;
Turgeon, D ;
Bélanger, A .
BIOCHEMICAL JOURNAL, 2002, 365 :213-222
[13]   Development of a liquid chromatography-tandem mass spectrometry method for the determination of 23 endogenous steroids in small quantities of primate urine [J].
Hauser, Barbara ;
Deschner, Tobias ;
Boesch, Christophe .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2008, 862 (1-2) :100-112
[14]   Enzyme-assisted synthesis and structure characterization of glucuronide conjugates of eleven anabolic steroid metabolites [J].
Hintikka, Laura ;
Kuuranne, Tiia ;
Aitio, Olli ;
Thevis, Mario ;
Schaenzer, Wilhelm ;
Kostiainen, Risto .
STEROIDS, 2008, 73 (03) :257-265
[15]  
HOSODA H, 1983, CHEM PHARM BULL, V31, P4001
[16]  
HOSODA H, 1985, CHEM PHARM BULL, V33, P4281
[17]  
HOSODA H, 1990, CHEM PHARM BULL, V38, P1949
[18]  
HOSODA H, 1982, CHEM PHARM BULL, V30, P2110
[19]   Enzyme-assisted synthesis and characterization of glucuronide conjugates of neuroactive steroids [J].
Jantti, Sirkku E. ;
Kiriazis, Alexandros ;
Reinila, Ruut R. ;
Kostiainen, Risto K. ;
Ketola, Raimo A. .
STEROIDS, 2007, 72 (03) :287-296
[20]   The use of deuterium-labeled cortisol for in vivo evaluation of renal 11β-HSD activity in man:: urinary excretion of cortisol, cortisone and their A-ring reduced metabolites [J].
Kasuya, Y ;
Shibasaki, H ;
Furuta, T .
STEROIDS, 2000, 65 (02) :89-97