RAPID AND SENSITIVE DETERMINATION OF CATECHOLAMINES AND THE METABOLITE 3-METHOXY-4-HYDROXYPHEN-ETHYLENEGLYCOL USING HPLC FOLLOWING NOVEL EXTRACTION PROCEDURES

Citation
E. Hollenbach et al., RAPID AND SENSITIVE DETERMINATION OF CATECHOLAMINES AND THE METABOLITE 3-METHOXY-4-HYDROXYPHEN-ETHYLENEGLYCOL USING HPLC FOLLOWING NOVEL EXTRACTION PROCEDURES, Life sciences (1973), 63(9), 1998, pp. 737-750
Citations number
45
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
Journal title
ISSN journal
00243205
Volume
63
Issue
9
Year of publication
1998
Pages
737 - 750
Database
ISI
SICI code
0024-3205(1998)63:9<737:RASDOC>2.0.ZU;2-X
Abstract
In the present study assays were improved for the determination of fre e catecholamines and 3-methoxy-4-hydroxyphenethyleneglycol (MHPG), the major metabolite of peripheral and central noradrenaline. The compoun ds were extracted by a fluid phase extraction: a diphenyl boric acid m ethod for the purification of catecholamines and an ethyl acetate extr action for MHPG were used, respectively. High-performance liquid chrom atography with electrochemical detection was employed for quantitative analysis. In previous studies, significant differences between plasma concentrations of these substances in normal volunteers and hospital patients were demonstrated. Therefore, we established valid reference values for a hospital population. Blood and urine samples of 59 patien ts without disorders and medication affecting catecholamine synthesis and metabolism or the activity of the sympatho-adrenal system were col lected and analyzed for free and total (free plus conjugated) MHPG, no radrenaline (NA), adrenaline (A) and dopamine (DA); total MHPG was ass ayed after enzymatic hydrolysis of conjugates. Our data clearly demons trate that these methods are sensitive, specific, rapid, and can easil y be standardized. The intra- and inter-assay precision were high (CV 2.6-5.3% and 4.3-6.9% for plasma, CV 3.8-4.9% and 5.1-8.2% for urine, respectively). For plasma, the mean concentrations +/- SD were determi ned to be 20.82+/-4.70 pmol/ml for free MHPG, 68.43+/-16.21 pmol/ml fo r total MHPG, 2.11+/-0.24 pmol/ml for NA and 0.31+/-0.08 pmol/ml for A . For 24h-urine the mean concentrations +/-SD were determined to be 0. 44+/-0.13 mmol/24h for free MHPG, 8.79+/-2.13 mmol/24h for total MHPG, 169.8+/-58.25 nmol/24h for NA, 62.19+/-21.79 nmol/24h for A and 757.2 +/-382.6 nmol/24h for DA. In summary, these novel and rapid methods ca n clearly be employed in a routine clinical setting.