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Compatibility Of Hydroxypropyl-β-cyclodextrin With Algal Toxicity Bioassays

机译:羟丙基-β-环糊精与藻类毒性生物测定的相容性

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Numerous reports have indicated that hydrophobic organic compound bioaccessibility in sediment and soil can be determined by extraction using aqueous hydroxypropyl-β-cyclodextrin (HPCD) solutions. This study establishes the compatibility of HPCD with Selenastrum capricomutum and assesses whether its presence influences the toxicity of reference toxicants. Algal growth inhibition (72 h) showed no significant (P> 0.05) difference at HPCD concentrations up to and including 20 mM. HPCD presence did not influence the toxicity of the inorganic reference toxicant (ZnSO_4), with IC50 values of 0.82 μM and 0.85 μM, in the presence and absence of HPCD (20 mM), respectively. However, HPCD presence (20 mM) reduced the toxicity of 2,4-dichlorophenol and the herbicides diuron and isoproturon. These reductions were attributed to inclusion complex formation between the toxicants and the HPCD cavity. Liberation of complexed toxicants, by sample manipulation prior to toxicity assessment, is proposed to provide a sensitive, high throughput, bioassay that reflects compound bioaccessibility.
机译:大量报告表明,可以通过使用羟丙基-β-环糊精(HPCD)水溶液萃取来确定沉积物和土壤中疏水性有机化合物的生物可及性。这项研究建立了HPCD与山羊齿硒的相容性,并评估其存在是否会影响参考毒物的毒性。藻类生长抑制作用(72小时)在HPCD浓度不超过20 mM(包括20 mM)时无显着差异(P> 0.05)。 HPCD的存在不影响无机参考毒物(ZnSO_4)的毒性,在存在和不存在HPCD(20 mM)的情况下,IC50值分别为0.82μM和0.85μM。但是,HPCD的存在(20 mM)降低了2,4-二氯苯酚和除草剂敌草隆和异丙隆的毒性。这些减少归因于毒物和HPCD腔之间形成了包合物。建议在毒性评估之前通过样品处理来释放复杂的有毒物质,以提供灵敏,高通量的生物测定方法,以反映化合物的生物可及性。

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