SIMPLIFIED ASSAY FOR THE QUANTIFICATION OF 2,3-DINOR-6-KETO-PROSTAGLANDIN-F(1-ALPHA) BY GAS-CHROMATOGRAPHY MASS-SPECTROMETRY

被引:43
作者
DANIEL, VC
MINTON, TA
BROWN, NJ
NADEAU, JH
MORROW, JD
机构
[1] VANDERBILT UNIV, MED CTR, SCH MED, DEPT PHARMACOL, NASHVILLE, TN 37232 USA
[2] VANDERBILT UNIV, MED CTR, SCH MED, DEPT MED, NASHVILLE, TN 37232 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 1994年 / 653卷 / 02期
关键词
D O I
10.1016/0378-4347(93)E0432-P
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Endogenous prostacyclin production is best assessed by the measurement of its excreted metabolites, of which a major one is 2,3-dinor-6-ketoprostaglandin F1alpha (2,3-dinor-6-keto-PGF1alpha). Gas chromatographic-mass spectrometric (GC-MS) assays have been developed for this compound but are cumbersome and time-consuming. We now report a modified assay for the measurement of 2,3-dinor-6-keto-PGF1alpha employing GC-MS in which sample preparation time is markedly shortened by replacing a number of extraction steps with reversed-phase column extraction and by modifying derivatization procedures. Precision of the assay is +/- 5% and the accuracy is 98%. The lower limit of detection in urine is approximately 15 pg/mg creatinine. Normal urinary levels of this metabolite were found to be 141 +/- 54 pg/mg creatinine (mean +/- S.D.). Urinary excretion of 2,3-dinor-6-keto-PGF1alpha is markedly altered in situations associated with abnormalities of prostacyclin generation when quantified using this assay. Thus, this assay provides a sensitive and accurate method to assess endogenous prostacyclin production and to further explore the role of this compound in human health and disease.
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页码:117 / 122
页数:6
相关论文
共 20 条
[1]   IMPROVED DERIVATIVE OF 6-KETO-PROSTAGLANDIN-F1-ALPHA FOR GAS-CHROMATOGRAPHIC MASS-SPECTROMETRIC ANALYSIS [J].
BAZAN, AC ;
KNAPP, DR .
JOURNAL OF CHROMATOGRAPHY, 1982, 236 (01) :201-207
[2]   ARTERIAL-WALLS GENERATE FROM PROSTAGLANDIN ENDOPEROXIDES A SUBSTANCE (PROSTAGLANDIN-X) WHICH RELAXES STRIPS OF MESENTERIC AND CELIAC ARTERIES AND INHIBITS PLATELET-AGGREGATION [J].
BUNTING, S ;
GRYGLEWSKI, R ;
MONCADA, S ;
VANE, JR .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 1976, 12 (06) :897-913
[3]   MEASUREMENT OF RENAL AND NONRENAL EICOSANOID SYNTHESIS [J].
CATELLA, F ;
NOWAK, J ;
FITZGERALD, GA .
AMERICAN JOURNAL OF MEDICINE, 1986, 81 (2B) :23-29
[4]  
CATELLA F, 1990, METHOD ENZYMOL, V187, P42
[5]  
CHIABRANDO C, 1985, J CHROMATOGR, V495, P1
[6]   SUPPRESSION OF THROMBOXANE-A2 BUT NOT OF SYSTEMIC PROSTACYCLIN BY CONTROLLED-RELEASE ASPIRIN [J].
CLARKE, RJ ;
MAYO, G ;
PRICE, P ;
FITZGERALD, GA .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (16) :1137-1141
[7]   QUANTITATIVE ANALYSIS OF TWO DINOR URINARY METABOLITES OF PROSTAGLANDIN I2 [J].
FALARDEAU, P ;
OATES, JA ;
BRASH, AR .
ANALYTICAL BIOCHEMISTRY, 1981, 115 (02) :359-367
[8]   PLATELET ACTIVATION IN UNSTABLE CORONARY-DISEASE [J].
FITZGERALD, DJ ;
ROY, L ;
CATELLA, F ;
FITZGERALD, GA .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (16) :983-989
[9]   INCREASED PROSTACYCLIN BIOSYNTHESIS IN PATIENTS WITH SEVERE ATHEROSCLEROSIS AND PLATELET ACTIVATION [J].
FITZGERALD, GA ;
SMITH, B ;
PEDERSEN, AK ;
BRASH, AR .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (17) :1065-1068
[10]   EICOSANOID BIOSYNTHESIS IN HUMAN CARDIOVASCULAR-DISEASE [J].
FITZGERALD, GA ;
CATELLA, F ;
OATES, JA .
HUMAN PATHOLOGY, 1987, 18 (03) :248-252