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Toxicokinetics of captan and folpet biomarkers in dermally exposed volunteers

✍ Scribed by Aurélie Berthet; Michèle Bouchard; David Vernez


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
164 KB
Volume
32
Category
Article
ISSN
0260-437X

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✦ Synopsis


ABSTRACT

To better assess biomonitoring data in workers exposed to captan and folpet, the kinetics of ring metabolites [tetrahydrophthalimide (THPI), phthalimide (PI) and phthalic acid] were determined in urine and plasma of dermally exposed volunteers. A 10 mg kg^−1^ dose of each fungicide was applied on 80 cm^2^ of the forearm and left without occlusion or washing for 24 h. Blood samples were withdrawn at fixed time periods over the 72 h following application and complete urine voids were collected over 96 h post‐dosing, for metabolite analysis. In the hours following treatment, a progressive increase in plasma levels of THPI and PI was observed, with peak levels being reached at 24 h for THPI and 10 h for PI. The ensuing elimination phase appeared monophasic with a mean elimination half‐life (t~½~) of 24.7 and 29.7 h for THPI and PI, respectively. In urine, time courses PI and phthalic acid excretion rate rapidly evolved in parallel, and a mean elimination t~½~ of 28.8 and 29.6 h, respectively, was calculated from these curves. THPI was eliminated slightly faster, with a mean t~½~ of 18.7 h. Over the 96 h period post‐application, metabolites were almost completely excreted, and on average 0.02% of captan dose was recovered in urine as THPI while 1.8% of the folpet dose was excreted as phthalic acid and 0.002% as PI, suggesting a low dermal absorption fraction for both fungicides. This study showed the potential use of THPI, PI and phthalic acid as key biomarkers of exposure to captan and folpet. Copyright © 2011 John Wiley & Sons, Ltd.


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Toxicokinetics of captan and folpet biom
✍ Aurélie Berthet; Michèle Bouchard; Brigitta Danuser 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 214 KB

## ABSTRACT The time courses of key biomarkers of exposure to captan and folpet was assessed in accessible biological matrices of orally exposed volunteers. Ten volunteers ingested 1 mg kg^−1^ body weight of captan or folpet. Blood samples were withdrawn at fixed time periods over the 72 h followin