Liquid chromatography-tandem mass spectrometric method for determination of salivary 17α-hydroxyprogesterone:: A noninvasive tool for evaluating efficacy of hormone replacement therapy in congenital adrenal hyperplasia

被引:33
|
作者
Shibayama, Yujin [1 ]
Higashi, Tatsuya [1 ]
Shimada, Kazutake [1 ]
Kashimada, Ken-ichi [2 ]
Onishi, Toshikazu [2 ,3 ]
Ono, Makoto [2 ]
Miyai, Kentaro [2 ]
Mizutani, Shuki [2 ]
机构
[1] Kanazawa Univ, Grad Sch Nat Sci & Technol, Div Pharmaceut Sci, Kakuma, Kanazawa 9201192, Japan
[2] Tokyo Med & Dent Univ, Grad Sch Med, Dept Pediat & Dev Biol, Bunkyo Ku, Tokyo 1138519, Japan
[3] Kinki Cent Hosp, Itami, Hyogo 6648533, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2008年 / 867卷 / 01期
基金
日本学术振兴会;
关键词
17; alpha-hydroxyprogesterone; saliva; liquid chromatography-electrospray ionization-tandem mass spectrometry; derivatization; congenital adrenal hyperplasia; hormone replacement therapy;
D O I
10.1016/j.jchromb.2008.03.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive liquid chromatography-electrospray ionization-tandem mass spectrometric (LC-ESI-MS-MS) method for the quantification of 17 alpha-hydroxyprogesterone (17OHP) in human saliva has been developed and validated. The saliva was deproteinized with acetonitrile, purified using a Strata-X cartridge, derivatized with a highly proton-affinitive reagent, 2-hydrazinopyridine, and subjected to LC-MS-MS. Quantification was based on the selected reaction monitoring, and deuterated 17OHP was used as the internal standard. This method allowed the reproducible and accurate quantification of the salivary 17OHP using a 200-mu l sample, and the limit of quantitation was 5.0 pg/ml. The developed method was applied to clinical studies. A linear relationship was found to be positive (r(2) = 0.975) between the blood 17OHP level and the salivary 17OHP level measured using the proposed method. The result from the salivary 17OHP measurement in patients with congenital adrenal hyperplasia demonstrated that the proposed method is very useful for monitoring of the therapeutic efficacy during hormone replacement therapy. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 56
页数:8
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