2003
DOI: 10.1016/j.jchromb.2003.08.009
|View full text |Cite
|
Sign up to set email alerts
|

Determination of the major mercapturic acids of 1,3-butadiene in human and rat urine using liquid chromatography with tandem mass spectrometry

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

4
57
3
2

Year Published

2005
2005
2015
2015

Publication Types

Select...
5
4

Relationship

1
8

Authors

Journals

citations
Cited by 64 publications
(66 citation statements)
references
References 11 publications
4
57
3
2
Order By: Relevance
“…Although numerous methods for the quantification of different MAs by LC-MS/MS have been reported in the recent past, the majority of those assays target a rather small set of up to six MAs [8,17,[20][21][22][24][25][26]. In addition, many of these methods lack the capability of quantifying MAs from environmental exposures in low levels.…”
Section: Discussionmentioning
confidence: 99%
“…Although numerous methods for the quantification of different MAs by LC-MS/MS have been reported in the recent past, the majority of those assays target a rather small set of up to six MAs [8,17,[20][21][22][24][25][26]. In addition, many of these methods lack the capability of quantifying MAs from environmental exposures in low levels.…”
Section: Discussionmentioning
confidence: 99%
“…Urban et al achieved excellent results in the detection of two mercapturic acids of 1,3-butadiene and several other mercapturic acids applying atmospheric pressure chemical ionisation (APCI) [32] with limits of detection (LOD) in the lower g/L range. We therefore tested the APCI-source and compared it to electrospray ionisation (ESI) on the API 2000.…”
Section: Mass Spectrometrymentioning
confidence: 99%
“…It is therefore difficult to retain these substances on traditional reversed phases (RP). In previous works chromatographic separation of mercapturic acids was predominantly achieved by using more polar RP-columns like "polar embedded" stationary phases or stationary phases with shorter chain lengths (C8-columns) [9,17,20,24,27,33]. Separation on these columns was mostly realized by using high amounts of aqueous mobile phase and a low amount of organic solvents.…”
Section: Chromatographymentioning
confidence: 99%
“…Metabolism of butadiene leads to the excretion of two mercapturic acids in urine: 3,4-dihydroxybutyl mercapturic acid (DHBMA) and monohydroxy-3-butenyl mercapturic acid (MHBMA), whereas the latter consists of two isomeric forms (see Fig. 1) [21][22][23][24][25]. In human urine DHBMA is usually found in higher concentrations than MHBMA [26,27].…”
Section: Introductionmentioning
confidence: 99%