Raman spectroscopy-based metabolomics for differentiating exposures to triazole fungicides using rat urine

被引:19
作者
Cherney, Daniel P.
Ekman, Drew R.
Dix, David J.
Collette, Timothy W. [1 ]
机构
[1] US EPA, Off Res & Dev, Natl Exposure Res Lab, Athens, GA 30605 USA
[2] US EPA, Off Res & Dev, Natl Ctr Computat Toxicol, Res Triangle Pk, NC 27711 USA
关键词
D O I
10.1021/ac070856n
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Normal Raman spectroscopy was evaluated as a metabolomic tool for assessing the impacts of exposure to environmental contaminants, using rat urine collected during the course of a toxicological study. Specifically, one of three triazole fungicides, myclobutanil, propiconazole, or triadimefon, was administered daily via oral gavage to male Sprague-Dawley rats at doses of 300, 300, or 175 mg/kg, respectively. Urine was collected from all three treatment groups and also from vehicle control rats on day six, following five consecutive days of exposure. Spectra were acquired with a CCD-based dispersive Raman spectrometer, using 785-nm diode laser excitation. To optimize the signal-to-noise ratio, urine samples were filtered through a stirred ultrafiltration cell with a 500 nominal molecular weight limit filter to remove large, unwanted urine components that can degrade the spectrum via fluorescence. However, a subsequent investigation suggested that suitable spectra can be obtained in a high-throughput fashion, with little or no Raman-specific sample preparation. For the sake of comparison, a parallel H-1 NMR-based metabolomic analysis was also conducted on the unfiltered samples. Results from multivariate data analysis demonstrated that the Raman method compares favorably with NMR in regard to the ability to differentiate responses from these three contaminants.
引用
收藏
页码:7324 / 7332
页数:9
相关论文
共 39 条
[1]   2-DIMENSIONAL SPECTROSCOPY - APPLICATION TO NUCLEAR MAGNETIC-RESONANCE [J].
AUE, WP ;
BARTHOLDI, E ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (05) :2229-2246
[2]   Metabolism of myclobutanil and triadimefon by human and rat cytochrome P450 enzymes and liver microsomes [J].
Barton, H. A. ;
Tang, J. ;
Sey, Y. M. ;
Stanko, J. P. ;
Murrell, R. N. ;
Rockett, J. C. ;
Dix, D. J. .
XENOBIOTICA, 2006, 36 (09) :793-806
[3]   NMR-based metabonomic studies on the biochemical effects of commonly used drug carrier vehicles in the rat [J].
Beckwith-Hall, BM ;
Holmes, E ;
Lindon, JC ;
Gounarides, J ;
Vickers, A ;
Shapiro, M ;
Nicholson, JK .
CHEMICAL RESEARCH IN TOXICOLOGY, 2002, 15 (09) :1136-1141
[4]   Multicomponent blood analysis by near-infrared Raman spectroscopy [J].
Berger, AJ ;
Koo, TW ;
Itzkan, I ;
Horowitz, G ;
Feld, MS .
APPLIED OPTICS, 1999, 38 (13) :2916-2926
[5]   An NMR-based metabonomic approach to the investigation of coelomic fluid biochemistry in earthworms under toxic stress [J].
Bundy, JG ;
Osborn, D ;
Weeks, JM ;
Lindon, JC ;
Nicholson, JK .
FEBS LETTERS, 2001, 500 (1-2) :31-35
[6]  
Clarke S, 2003, METABOLIC PROFILING: ITS ROLE IN BIOMARKER DISCOVERY AND GENE FUNCTION ANALYSIS, P95
[7]   Optimization of Raman spectroscopy for speciation of organics in water [J].
Collette, TW ;
Williams, TL ;
D'Angelo, JC .
APPLIED SPECTROSCOPY, 2001, 55 (06) :750-766
[8]   Effects of feeding and body weight loss on the 1H-NMR-based urine metabolic profiles of male Wistar Han rats:: implications for biomarker discovery [J].
Connor, SC ;
Wu, W ;
Sweatman, BC ;
Manini, J ;
Haselden, JN ;
Crowther, DJ ;
Waterfield, CJ .
BIOMARKERS, 2004, 9 (02) :156-179
[9]   Quantitative analysis of metabolites in urine using a highly precise, compact near-infrared Raman spectrometer [J].
Dou, X ;
Yamaguchi, Y ;
Yamamoto, H ;
Doi, S ;
Ozaki, Y .
VIBRATIONAL SPECTROSCOPY, 1996, 13 (01) :83-89
[10]  
Dou XM, 1997, BIOSPECTROSCOPY, V3, P113, DOI 10.1002/(SICI)1520-6343(1997)3:2<113::AID-BSPY4>3.0.CO