Bioconcentration of two basic pharmaceuticals, verapamil and clozapine, in fish
The present study examined the bioconcentration of 2 basic pharmaceuticals: verapamil (a calcium channel blocker) and clozapine (an antipsychotic compound) in 2 fresh water fishes, fathead minnow and channel catfish. In 4 separate bioconcentration factor (BCF) experiments (2 chemicals × 1 exposure c...
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Published in | Environmental toxicology and chemistry Vol. 35; no. 3; pp. 593 - 603 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Pergamon
01.03.2016
Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | The present study examined the bioconcentration of 2 basic pharmaceuticals: verapamil (a calcium channel blocker) and clozapine (an antipsychotic compound) in 2 fresh water fishes, fathead minnow and channel catfish. In 4 separate bioconcentration factor (BCF) experiments (2 chemicals × 1 exposure concentration × 2 fishes), fathead minnow and channel catfish were exposed to 190 μg/L and 419 μg/L of verapamil (500 μg/L nominal) or 28.5 μg/L and 40 μg/L of clozapine (50 μg/L nominal), respectively. Bioconcentration factor experiments with fathead consisted of 28 d uptake and 14 d depuration, whereas tests conducted on catfish involved a minimized test design, with 7 d each of uptake and depuration. Fish (n = 4–5) were sampled during exposure and depuration to collect different tissues: muscle, liver, gills, kidneys, heart (verapamil tests only), brain (clozapine tests only), and blood plasma (catfish tests only). Verapamil and clozapine concentrations in various tissues of fathead and catfish were analyzed using liquid chromatography–mass spectrometry. In general, higher accumulation rates of the test compounds were observed in tissues with higher perfusion rates. Accumulation was also high in tissues relevant to pharmacological targets in mammals (i.e. heart in verapamil test and brain in the clozapine test). Tissue‐specific BCFs (wet wt basis) for verapamil and clozapine ranged from 0.7 to 75 and from 31 to 1226, respectively. Tissue‐specific concentration data were used to examine tissue–blood partition coefficients. Environ Toxicol Chem 2016;35:593–603. © 2016 SETAC |
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Bibliography: | http://dx.doi.org/10.1002/etc.3244 ark:/67375/WNG-MK7F09RZ-T istex:5CDD54276BD577D6E4E90CC71FE62F3EE0BDDF0F ArticleID:ETC3244 Pfizer Global Research and Development ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0730-7268 1552-8618 |
DOI: | 10.1002/etc.3244 |