Determination of ethyl-p-hydroxybenzoate in sow pancreatic juice by reversed-phase high-performance liquid chromatography

被引:9
作者
Di Giovannandrea, R
Diana, L
Fiori, M
Ferretti, E
Foglietta, G
Caronna, R
Severini, G
机构
[1] Ist Super Sanita, Biochim Clin Lab, I-00161 Rome, Italy
[2] Ist Super Sanita, Lab Med Vet, I-00161 Rome, Italy
[3] Univ La Sapienza, Cattedra Patol Chirurg 9, Rome, Italy
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 751卷 / 02期
关键词
ethyl-p-hydroxybenzoate;
D O I
10.1016/S0378-4347(00)00477-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a high-performance liquid chromatographic-UV-Vis-diode-array detection (HPLC-DAD) method for the determination of ethyl-p-hydroxybenzoate, a hydrolytic degradation product of the synthetic protease inhibitor, gabexate-mesilate erhyl-p-(6-guanidinohexanoyloxy) benzoate methanesulfonate (CM) (FOY) in sow pancreatic juice. Methyl-p-hydroxybenzoate (I) was used as the internal standard. The pancreatic juice was deproteinised by acetonitrile and the analytes were chromatographed on a reversed-phase C-18 LC column using the gradient elution method. The mobile phase consisted of a solution of 0.017 M orthophosphoric acid and another solution of acetonitrile-water (80:20, v/v). The wavelength of detection was 237 nm. The limit of quantification of the method was 0.20 muM at a 9:1 Signal-to-noise ratio. The overall intra- and inter-day accuracy (relative error, RE) ranged from 14.2 to 8.3% and from 13.3 to 9.8, respectively. The overall intra- and inter-day precision (relative standard deviation, RSD) ranged from 7.6 to 2.62% and from 6.7 to 3.1%, respectively. The method proved to be sensitive, specific, accurate and precise and was successfully used to determine the ethyl-p-hydroxybenzoate (II) in sow pancreatic juice. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:365 / 369
页数:5
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