1987
DOI: 10.3109/03602538708998298
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Metabolism and Disposition of Glycol Ethers

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Cited by 36 publications
(14 citation statements)
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“…These effects are associated with certain glycol ethers such as ethoxyethanol, ethoxymethanol, butoxyethanol or PGME-b. This can be explained by the fact that they are metabolised by alcohol dehydrogenase into the corresponding alkoxyacetic acid, the active metabolite [5,7]. In contrast, PGME-a and related glycol ethers that are not primary alcohols do not give rise to alkoxyacetic acid metabolites [7,9].…”
Section: Introductionmentioning
confidence: 96%
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“…These effects are associated with certain glycol ethers such as ethoxyethanol, ethoxymethanol, butoxyethanol or PGME-b. This can be explained by the fact that they are metabolised by alcohol dehydrogenase into the corresponding alkoxyacetic acid, the active metabolite [5,7]. In contrast, PGME-a and related glycol ethers that are not primary alcohols do not give rise to alkoxyacetic acid metabolites [7,9].…”
Section: Introductionmentioning
confidence: 96%
“…The studies on the metabolism of PGME-a in rats have shown that the majority (about 60%) of the absorbed dose of PGME-a is excreted in expired air as CO 2 , while about 20% of the dose is excreted in urine as 1,2-propanediol (about 4% of the total dose), as unchanged PGME (about 2% of the total dose) or in greater proportion as conjugated PGME (sulphate and glucuronide conjugates; about 15% of the total dose) [7,9,12].…”
Section: Introductionmentioning
confidence: 99%
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“…EAA was not included in the test set. The major route of metabolism of glycol ethers and derivatives is oxidation via the alcohol/aldehyde dehydrogenase pathway [21]. The fact that almost every glycol ether or glycol ether derivative tested negative in the ReProGlo assay (with the only exception of diethylene glycol mono-n-butyl ether, which shows unspecific results) suggests that ES cells lack the respective dehydrogenase activities.…”
Section: False Negativesmentioning
confidence: 99%
“…The toxicity of propylene glycol monomethyl ether-a (PGME-a, CAS number 107-98-2) and propylene glycol monomethyl ether-b (PGME-b, CAS number 1320-67 -8) and the way they are metabolised have been studied in rats by Miller et al [7,8,9,10]. These studies have shown that the majority (approximately 60%) of the absorbed dose of PGME-a is excreted in expired air as CO 2 , while approximately 20% of the dose is excreted in urine as 1, 2-propanediol, as unchanged PGME-a or in greater proportion as conjugated PGME-a (sulphate and glucuronide conjugates) [7,9,11].…”
Section: Introductionmentioning
confidence: 99%