长江重点江段枯水期药物及个人护理品(PPCPs)的空间分布特征及来源

药物及个人护理品(PPCPs)由于潜在的生态效应引起广泛关注,近年来在长江流域中也被普遍检出.本文研究了长江攀枝花、宜宾、泸州、重庆、涪陵、三峡、岳阳、武汉、九江和南京共计10个重点江段枯水期表层水中57种PPCPs及部分代谢产物的分布和来源,为长江流域的污染管控提供了科学支撑.结果表明,长江表层水中57种PPCPs均...     

Naproxen,ibuprofen, and diclofenac residues in river water,sediments and Eichhornia crassipes of Mbokodweni river in South Africa: An initial screening

In the last 5 years, naproxen, ibuprofen and diclofenac have been the subject of investigation in the South African water resources. In this study, their occurrence in river water, sediments and aquatic plants was investigated. The concentrations of compounds detected in river water and sediments varied from 0.59 to 2.3 µg L^?1 and 0.2 to 9.2?ng g^?1, respectively. The partitioning coefficients (L kg^?1) for naproxen, ibuprofen and diclofenac varied from one sampling location to the other in ranges of 3.36–4, 1.3–1.9 and 0.13–0.91, respectively. This indicates that the fate of these pharmaceuticals can be influenced by the surrounding conditions such as climate and presence of other water pollutants as well as differences in physicochemical parameters. In the aquatic plant species (Eichhornia crassipes), the concentrations of target compounds varied in different parts of the plant material (roots, stems and leaves). Naproxen was the most abundant in Eichhornia crassipes, with the maximum concentration of 12.0?ng g^?1 found in leaves. In this initial assessment, we found no rational trend for the concentrations detected in various parts of Eichhornia crassipes, however, it is speculated that these pharmaceuticals diffuse from water into the roots of the aquatic plants and get translocated into the stem and leaves. Overall, the occurrence of naproxen, ibuprofen and diclofenac in river water, sediments and Eichhornia crassipes was observed, which is an indication that Eichhornia crassipes has the ability to reduce water pollution through the uptake of pharmaceuticals through plant roots.     

Determination of veterinary pharmaceuticals in poultry litter and soil by methanol extraction and liquid chromatography-tandem mass spectrometry

Pharmaceuticals are emerging contaminants with potential risks to the environment and human health. A liquid chromatography-tandem mass spectrometry (LC-MS-MS) method was developed for determination of the antimicrobials virginiamycin, monensin, salinomycin, narasin and nicarbazin in poultry litter and soil. This method involves methanol extraction and clean-up of extracts through glass microfibre filters, introduction of the extracts and separation of compounds on a Zorbax Eclipse XDB C8 column, and compound detection in a Quattro Micro Micromass spectrometer. For litter samples, Method Detection Limits ranged from 0.1–0.6 μg Kg^{? 1}, while Limits of Quantitation (LOQs) were 2, 1, 0.4, 1 and 2 μg Kg^{? 1} for virginiamycin, monensin, salinomycin, narasin and nicarbazin, respectively. For soil samples calculated LOQs were 2, 3, 1, 1, and 1 μg Kg^{? 1} for virginiamycin, monensin, salinomycin, narasin and nicarbazin, respectively. Application of the LC-MS-MS method for detection of veterinary pharmaceuticals in litter collected from commercial poultry farms showed that compounds were present at concentrations ranging from 10–11,000 μg Kg^{? 1}.     

典型药物污染物的SPE-UPLC-MS-MS检测方法

采用固相萃取-高效液相色谱-串联质谱法(SPE-UPLC-MS-MS)测定自然水体中的10种典型药物污染。比较了2种萃取柱HLB和C18的富集效果,并对水样pH、萃取柱的淋洗溶剂及水样体积进行了优化。结果表明,采用HLB小柱进行富集净化,水样体积为500 mL,调节pH=3.0,95%甲醇洗脱,在0~200μg/L范围内10种药物的标准曲线线性关系良好(r≥0.999),方法检出限0.5~2.0 ng/L,精密度高(RSD10%),加标回收率为64.3%~100.7%。经过对太湖和某污水厂排水口水样的测试,表明该方法适用于自然水体药物的快速检测,同时大部分药物被检出,说明选择的10种目标药物及建立的检测方法对研究中国水体药物污染具有一定的参考价值。     

污水处理厂PPCPs的污染现状与去除技术

近年来,药品和个人护理品(PPCPs)作为一类新兴有机污染物在环境中被广泛报道.传统的污水处理厂处理工艺难以有效去除污水中的PPCPs,残留在污水处理厂出水中的PPCPs及其代谢物进入水环境会严重威胁人类健康和生态环境.介绍了PPCPs的类别、性质以及水环境中PPCPs的赋存水平及其潜在危害,提出风险熵法(RQ)是国内...     

Transport of oxytetracycline,chlortetracycline, and ivermectin in surface runoff from irrigated pasture

The transport of oxytetracycline, chlortetracycline, and ivermectin from manure was assessed via surface runoff on irrigated pasture. Surface runoff plots in the Sierra Foothills of Northern California were used to evaluate the effects of irrigation water application rates, pharmaceutical application conditions, vegetative cover, and vegetative filter strip length on the pharmaceutical discharge in surface runoff. Experiments were designed to permit the maximum potential transport of pharmaceuticals to surface runoff water, which included pre-irrigation to saturate soil, trimming grass where manure was applied, and laying a continuous manure strip perpendicular to the flow of water. However, due to high sorption of the pharmaceuticals to manure and soil, less than 0.1% of applied pharmaceuticals were detected in runoff water. Results demonstrated an increase of pharmaceutical transport in surface runoff with increased pharmaceutical concentration in manure, the concentration of pharmaceuticals in runoff water remained constant with increased irrigation flow rate, and no appreciable decrease in pharmaceutical runoff was produced with the vegetative filter strip length increased from 30.5 to 91.5 cm. Most of the applied pharmaceuticals were retained in the manure or within the upper 5 cm of soil directly beneath the manure application sites. As this study evaluated conditions for high transport potential, the data suggest that the risk for significant chlortetracycline, oxytetracycline, and ivermectin transport to surface water from cattle manure on irrigated pasture is low.     

城市污水处理厂出水中的药品和个人护理品

药品和个人护理品(PPCPs)是近年来受到环境界普遍关注、具有潜在生态风险的新型有机微污染物.城市污水处理厂(STPs)出水排放是PPCPs向环境迁移最重要的途径,而控制PPCPs随STPs出水排放则是控制PPCPs环境影响的关键.本文分类综述了抗生素、消炎止痛药物、精神类药物、β受体拮抗剂、环境雌激素、调血脂药物、合成麝香、其它类等PPCPs的药理与功能、分类、应用现状和生态毒性,重点总结了1998～2012年间全球STPs出水中频繁检出的典型PPCPs及其最高浓度,为开展STPs排放控制研究提供依据.最后,展望了本领域的未来研究方向与发展趋势.     

新型针状二氧化锰的制备、表征及其对土壤中有机物氧化性能研究

由化学法合成了一种新型类针状的二氧化锰(MnO2)材料,通过X射线衍射(XRD)、透射电镜(TEM)、比表面积测试(BET)、傅里叶转换红外光谱(FTIR)和X射线光电子能谱(XPS)等手段表征其结构特性,由MnO2对酚类有机物和医药类污染物的去除实验来评价其活性.结果表明,此材料为典型的δ-MnO2,其比表面积相对较大,为41m2·g-1,MnO2以MnO6八面体结构存在,Mn以MnO2形式存在.从MnO2对2-氯酚(2-CP)的去除及中间产物分析可知,MnO2对2-CP有较强的脱氯作用.另外,pH对2-CP的去除有较大影响.对酚类有机物和医药类污染物的去除实验考察发现,2,4-二氯酚(2,4-DCP)和2,4,6-三氯酚(2,4,6-TCP)的去除效率明显大于苯酚(Ph)和2-CP,而环丙沙星的去除与安替比林、布洛芬、苯妥英和苯海拉明相比更加容易,经过96h反应,去除率可达74%.     

Rapid resolution liquid chromatography-tandem mass spectrometry method for the determination of endocrine disrupting chemicals (EDCs), pharmaceuticals and personal care products (PPCPs) in wastewater irrigated soils

A multiresidue analytical method was developed for the determination of 9 endocrine disrupting chemicals (EDCs) and 19 pharmaceuticals and personal care products (PPCPs) including acidic and neutral pharmaceuticals in water and soil samples using rapid resolution liquid chromatography-tandem mass spectrometry (RRLC-MS/MS). Solid phase extraction (SPE), and ultrasonic extraction combined with silica gel purification were applied as pretreatment methods for water and soil samples, respectively. The extracts of the EDCs and PPCPs in water and soil samples were then analyzed by RRLC-MS/MS in electrospray ionization (ESI) mode in three independent runs. The chromatographic mobile phases consisted of Milli-Q water and acetonitrile for EDCs and neutral pharmaceuticals, and Milli-Q water containing 0.01 % acetic acid (v/v) and acetonitrile: methanol (1:1, v/v) for acidic pharmaceuticals at a flow rate of 0.3 mL/min. Most of the target compounds exhibited signal suppression due to matrix effects. Measures taken to reduce matrix effects included use of isotope-labeled internal standards, and application of matrix-match calibration curves in the RRLC-MS/MS analyses. The limits of quantitation ranged between 0.15 and 14.08 ng/L for water samples and between 0.06 and 10.64 ng/g for solid samples. The recoveries for the target analytes ranged from 62 to 208 % in water samples and 43 to 177 % in solid samples, with majority of the target compounds having recoveries ranging between 70–120 %. Precision, expressed as the relative standard deviation (RSD), was obtained less than 7.6 and 20.5 % for repeatability and reproducibility, respectively. The established method was successfully applied to the water and soil samples from four irrigated plots in Guangzhou. Six compounds namely bisphenol-A, 4-nonylphenol, triclosan, triclocarban, salicylic acid and clofibric acid were detected in the soils.     

Determination and occurrence of endocrine disrupting compounds,pharmaceuticals and personal care products in fish (Morone saxatilis)

Endocrine disrupting compounds (EDCs), pharmaceuticals and personal care products (PPCPs) have attracted much attention due to widespread contamination in aquatic environment. In this study, we determined 13 EDCs and PPCPs in fish blood, bile and muscle by using gas chromatography-mass spectrometry (GC-MS). The limits of quantitation (LOQ) were in the ranges of 0.23–2.54, 0.22–2.36 ng·mL⁻¹, and 0.24–2.57 ng·g⁻¹ dry weight (dw) for fish blood, bile and muscle, respectively. Recoveries of target compounds spiked into sample matrices and passed through the entire analytical procedure ranged from 65% to 95%, from 60% to 92% and from 62% to 91% for blood, bile and muscle, respectively. The methods were applied to the analysis of fish from a lake in California. Target compounds were relatively low in bile, and only bisphenol A (BPA) and diclofenac were measurable near the LOQ. Seven of 13 compounds were detected in blood, with total concentrations up to 39 ng·mL⁻¹. Only BPA was frequently found in muscle, with mean concentration of 7.26 ng·g⁻¹ dw. The estimated daily intake of BPA through fish consumption for U.S. resident was significantly lower than the tolerable daily intake recommended by the European Food Safety Authority. This study showed that the exposure to the bisphenol A from fish diet is unlikely to pose a health risk.