Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P00790 (PGA)
 2,475 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The purpose of this research was to determine mandelic, phenylglyoxylic, hippuric, o-, m- and p-methylhippuric acids, the six urinary metabolites of styrene, toluene and xylene by high performance liquid chromatography (HPLC). These metabolites were extracted in an acid medium, transferred into a basic solution and back extracted again using ethyl acetate, and the organic phase was evaporated to dryness under a compressed air flow at room temperature. The residue obtained was dissolved in 1 ml mobile phase solution of 0.01 M potassium orthophosphate in 0.3% acetic acid (adjusted to a pH of 2.5 with orthophosphoric acid):tetrahydrofuran:acetonitrile(87:5:8) and 100 microl was injected into a HPLC equipped with a 4.6 x 250 mm ODS3-C18 reversed phased column and ultraviolet (UV) detector at a wavelength of 254 nm. All metabolites were clearly separated within 21 minutes. The detection limits of the method were 1.1 ng/ml for PGA, 4.9 ng/ml for HA, 17.0 ng/ml for MA, 2.5 ng/ml for o-MHA, 1.7 ng/ml for p-MHA and 2.0 ng/ml for m-MHA. The percent recoveries of the six metabolites were 99.2-101.8% with percent coefficients of variation of less than 2%. The method was applied to the analysis of urine samples of twelve workers exposed to toluene, xylene and styrene in a paint factory. The 5-day post-shift urinary excretions of the six metabolites in these workers are presented. The metabolites were found at levels greater than the Biological Exposure Index (BEI) recommended by the American Conference of Governmental Industrial Hygienists (ACGIH).
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PMID:High performance liquid chromatography for determination of urinary metabolites of toluene, xylene and styrene and its application. 1906 9

A convenient and reliable gas chromatographic method was developed for the simultaneous determination of six aromatic acid metabolites of styrene and styrene-oxide in rat urine; i.e., benzoic (BA), phenylacetic (PAA), mandelic (MA), phenylglyoxylic (PGA), hippuric (HA) and phenylaceturic (PAUA) acids. The method involves a one-pot esterification-extraction procedure, performed directly on urine without prior treatment. Analyses were performed on a RTX-1701 capillary column and the recovered isopropyl esters derivatives were detected by flame ionization detection. The analytical method was validated for selectivity, linearity, detection and quantification limits, recovery and intra-day and inter-day precisions. Calibration curves showed linearity in the range of 8-800 mg/L, except for HA and PAUA (40-800 mg/L). Limits of detection were between 0.2 (PPA) and 7.0 (PAUA) mg/L. The intra-day precisions determined at three concentrations levels were less than 5% for BA, PAA, MA and PGA and 9% for HA and PAUA, respectively. The corresponding mean inter-day precisions for these two groups were 8 and 16%, respectively. The method was successfully applied to quantitatively analyze styrene, styrene-oxide, ethylbenzene and toluene metabolites in urine samples from rats exposed by inhalation to these compounds at levels close to the occupational threshold limit values. Provided that this method can be transposed to human urine, it could have applications as part of biological monitoring for workers exposed to styrene or related compounds.
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PMID:Simultaneous determination of aromatic acid metabolites of styrene and styrene-oxide in rat urine by gas chromatography-flame ionization detection. 2249 63

Volatile organic compounds (VOCs) are present in several working activities. This work is aimed at comparing oxidative stress and DNA damage biomarkers to specific VOCs in the occupational exposure of painters. Dose-response relationships between biomarkers of oxidative stress and of dose were studied. Unmetabolized VOCs and their urinary metabolites were analyzed. Urinary Methylhyppuric acids (MHIPPs, xylenes metabolite), Phenylglyoxylic and Mandelic acid (PGA, MA ethylbenzene metabolites), S-Benzylmercapturic acid (SBMA, toluene metabolite), and S-Phenylmercapturic acid (SPMA, benzene metabolite) were quantified at the end of work-shift. Oxidative stress was determined by: urinary excretion of 8-oxodGuo, 8-oxoGua and 8-oxoGuo and direct/oxidative DNA damage in blood by Fpg-Comet assay. Multivariate linear regression models were used to assess statistical significance of the association between dose and effect biomarkers. The regressions were studied with and without the effect of hOGG1 and XRCC1 gene polymorphisms. Statistically significant associations were found between MHIPPs and both 8-oxoGuo and oxidative DNA damage effect biomarkers measured with the Comet assay. Oxidative DNA damage results significantly associated with airborne xylenes and toluene, whilst 8-oxodGuo was significantly related to urinary xylenes and toluene. Direct DNA damage was significantly associated to SBMA. XRCC1 wild-type gene polymorphism was significantly associated with lower oxidative and total DNA damage with respect to heterozygous and mutant genotypes. The interpretation of the results requires some caution, as the different VOCs are all simultaneously present in the mixture and correlated among them.
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PMID:Direct and Oxidative DNA Damage in a Group of Painters Exposed to VOCs: Dose - Response Relationship. 3297 63