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Fate of the antifungal drug clotrimazole in agricultural soil
Author(s) -
Sabourin Lyne,
AlRajab Abdul Jabbar,
Chapman Ralph,
Lapen David R.,
Topp Edward
Publication year - 2011
Publication title -
environmental toxicology and chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.1
H-Index - 171
eISSN - 1552-8618
pISSN - 0730-7268
DOI - 10.1002/etc.432
Subject(s) - clotrimazole , loam , biosolids , soil water , chemistry , environmental chemistry , mineralization (soil science) , pesticide , agronomy , environmental science , antifungal , environmental engineering , biology , soil science , microbiology and biotechnology
Abstract Clotrimazole is a broad‐spectrum antimycotic drug used for the treatment of dermatological and gynecological infections; it is incompletely broken down during sewage treatment and could potentially reach agricultural land through the application of municipal biosolids or wastewater. In the absence of any environmental fate data, we evaluated the persistence and dissipation pathways of 3 H‐clotrimazole during laboratory incubations of agricultural soils. Clotrimazole was removed from a loam (time to dissipate 50% = 68 d), a sandy loam (time to dissipate 50% = 36 d), and a clay loam (time to dissipate 50% = 55 d), with formation of nonextractable residues being the major sink for 3 H. Their parent compound had no significant mineralization, as evidenced by the lack of formation of 3 H 2 O. Up to 15% of the applied radioactivity was recovered in the form of [ 3 H]‐(2‐chlorophenyl)diphenyl methanol. The rate of clotrimazole dissipation in the loam soil did not vary with moisture content, but it was slower at a lower temperature (number of days to dissipate 50% = 275.6 d at 4°C). Addition of municipal biosolids to the loam soil did not vary the clotrimazole dissipation rate. In summary, the present study has established that clotrimazole is dissipated in soil, at rates that varied with soil texture and temperature. Clotrimazole dissipation was accompanied by the formation of nonextractable residues and detectable extractable residues of the transformation product (2‐chlorophenyl)diphenyl methanol. Environ. Toxicol. Chem. 2011; 30:582–587. © 2010 SETAC