Department of Environmental Sciences, The University of Toledo, OH 43606, USA.
Arch Environ Contam Toxicol. 2010 Oct;59(3):343-51. doi: 10.1007/s00244-010-9500-y. Epub 2010 Mar 26.
Biosolids land application is an important pathway introducing pharmaceuticals into the environment. In this work, laboratory column and dissipation experiments were performed using soils of varying properties in order to study the fate and transport of pharmaceutical residues introduced by the land application of biosolids. For experimentation, five pharmaceutical compounds (carbamazepine, diphenhydramine, fluoxetine, diltiazem, and clindamycin) and two metabolites (carbamazepine-10,11-epoxide and norfluoxetine) commonly found in biosolids were selected. Leaching experiments indicate that the selected pharmaceuticals have low mobility in tested soils. However, small portions of the applied pharmaceuticals were recovered in the leachates, likely attributed to sorption to dissolved organic matter. Dissipation experiments show that carbamazepine, diphenhydramine, and fluoxetine were persistent in soils, whereas the dissipation of diltiazem and clindamycin was affected by redox conditions and soil properties.
生物固体土地应用是将药物引入环境的重要途径。在这项工作中,使用具有不同性质的土壤进行了实验室柱和消散实验,以研究通过生物固体土地应用引入的药物残留的归趋和迁移。在实验中,选择了五种药物化合物(卡马西平、苯海拉明、氟西汀、地尔硫卓和克林霉素)和两种代谢物(卡马西平-10,11-环氧化物和去甲氟西汀),这些物质通常存在于生物固体中。淋滤实验表明,所选药物在测试土壤中的迁移性较低。然而,在淋出液中回收了少量施加的药物,这可能归因于溶解有机质的吸附。消散实验表明,卡马西平、苯海拉明和氟西汀在土壤中具有持久性,而地尔硫卓和克林霉素的消散受氧化还原条件和土壤性质的影响。