Limited bioconcentration of water-associated pharmaceutical active compounds through short-term exposure in signal crayfish (Pacifastacus leniusculus)

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Anna Koubová , Worrayanee Thammatorn , Antonín Kouba , Vladimír Žlábek , Bent Speksnijder , Daniel Cerveny , Oksana Golovko
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引用次数: 0

Abstract

Pharmaceutical active compounds (PhACs) increasingly appear as complex mixtures in aquatic ecosystems, yet their bioconcentration in non-target organisms is poorly understood. This study examined tissue-specific distribution of five PhACs – bicalutamide, amitriptyline, furosemide, daidzein and sertraline – in signal crayfish (Pacifastacus leniusculus) after 96-hour exposure and an equal depuration period. Crayfish were subjected to environmentally relevant and 10-fold elevated mixture concentrations. Water and tissues (haemolymph, hepatopancreas, muscle) were analysed using ultra-high performance liquid chromatography–tandem mass spectrometry. Despite verified water concentrations and stable conditions, none of the compounds were quantifiable in tissues, except trace sertraline near the detection limit in some controls. The lack of detectable residues indicates minimal bioconcentration, likely due to physicochemical properties (low log Kow), rapid metabolism and efficient excretion. Results underscore the need for longer exposures and metabolite-focused studies to better assess environmental fate, tissue kinetics and potential risks of PhAC mixtures in freshwater invertebrates.
信号小龙虾(Pacifastacus leniusculus)短期暴露对水相关药物活性化合物生物浓度的影响。
药物活性化合物(PhACs)越来越多地作为复杂的混合物出现在水生生态系统中,但它们在非靶生物中的生物浓度却知之甚少。本研究检测了信号小龙虾(Pacifastacus leniusculus)暴露96小时和同等净化时间后,五种PhACs(比卡鲁胺、阿米替林、速尿、大豆苷元和舍曲林)的组织特异性分布。小龙虾受到环境相关和10倍的混合物浓度升高。水和组织(血淋巴、肝胰腺、肌肉)采用超高高效液相色谱-串联质谱法进行分析。尽管验证了水的浓度和稳定的条件,但在组织中没有一种化合物是可量化的,除了在一些对照中接近检测限的痕量舍曲林。缺乏可检测的残留物表明最低的生物浓度,可能是由于物理化学性质(低log Kow),快速代谢和有效排泄。研究结果强调,需要进行更长时间的暴露和以代谢物为重点的研究,以更好地评估淡水无脊椎动物中PhAC混合物的环境命运、组织动力学和潜在风险。
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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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