Pharmaceuticals And Personal Care Products In Water Research Articles

Pollution levels and ecological risks of PPCPs in water and sediment samples of Danjiangkou Reservoir.

The concentrations and distribution patterns of three typical pharmaceuticals and personal care products (PPCPs) in water and sediment samples obtained from Danjiangkou Reservoir during two seasonal sampling periods were studied to determine their impact on water quality. The temporal and spatial variations in concentrations measured were analyzed and related to ecological risks with data obtained during the mean-flow period (in June) and the dry period (in November). We found a high detection rate of ketoprofen (KTP) in water samples from Danjiangkou Reservoir; the concentrations ranged from not detected (ND) to 46.80ng/L with the highest values measured in the Hanku tributary samples followed by the samples collected in the main body of Danjiangkou Reservoir. The KTP concentrations in the Danku tributary samples were the lowest measured in this study. In addition, the concentrations of KTP in the Shending River, Sihe River, Jianghe River, Guanshan River, and Jianhe River water samples were relatively high in the mean-flow period. The water sample detection rates and concentrations of triclosan (TCS) and triclocarban (TCC) were low in both the mean-flow period and the dry period. All three kinds of PPCPs were detected in the sediment samples with the concentrations of KTP, TCS, and TCC ranging from 0.76 to 7.89μg/kg, 0.01 to 0.59μg/kg, and 0.01 to 11.36μg/kg, respectively. Overall, the concentrations of the three measured PPCPs in the water and sediment samples were all relatively low compared to results reported in the recent literature. The dry period concentrations of PPCPs in the water samples were lower than the concentrations measured in the mean-flow period. However, dry period concentrations were higher in the sediment samples compared to those in the mean-flow period samples. Our interpretation of the spatial and temporal patterns of PPCPs in Danjiangkou Reservoir suggests that these compounds were likely mainly derived from wastewater discharge in the upper reaches of the reservoir. The risk quotient (RQ) method was used for an ecological risk assessment of the detected PPCPs in this study. We found that TCS in water and sediment posed medium ecological risks to algae at different times of the year. In view of the extreme importance of water safety in Danjiangkou Reservoir, the ecological risks of PPCPs require additional attention.

Determination of 145 pharmaceuticals and personal care products in eleven categories in water by ultra-high performance liquid chromatography-triple quadrupole mass spectrometry

Pharmaceuticals and personal care products (PPCPs) are emerging contaminants frequently detected in aquatic environments at trace levels. These chemicals have diverse structures and physicochemical properties and includes pharmaceuticals like antibiotics, antihypertensive drugs, antiviral drugs, and psychotropic drugs that are widely used in large quantities worldwide. Considering the large number of pharmaceuticals currently in usage, it is crucial to establish a priority list of PPCPs that should be monitored and/or treated first. An accurate understanding of the occurrence and levels of PPCPs in aquatic environments is essential for providing objective materials for monitoring these emerging contaminants. Therefore, accurate, efficient, sensitive, and high-throughput screening techniques need to be established for determining and quantifying PPCPs. This study developed a method for the determination of 145 PPCPs (grouped into eleven categories: antibiotics, antihypertensive drugs, antidiabetic drugs, antiviral drugs, β-receptor agonists, nitroimidazoles, H2 receptor antagonists, psychotropic drugs, hypolipidemic drugs, non-steroidal anti-inflammatory drugs, and others) in water. The method was based on large volume direct injection without sample enrichment and cleanup and used ultra-high performance liquid chromatography-triple quadrupole mass spectrometry (UHPLC-MS/MS). Water samples were collected and filtered through a 0.22-μm regenerated cellulose (RC) filter membrane. Subsequently, Na2EDTA was added to the samples to adjust their pH to 6.0-8.0. Internal standards were mixed with the solutions, and because of the addition of Na2EDTA, the interference of metal ions could be eliminated in the determination of compounds, especially for tetracycline and quinolone antibiotics. Among the six filter membranes tested in this study (PES, PFTE-Q, PFTE, MCE, GHP, and RC), RC filter membranes were screened for water sample filtration. The UHPLC-MS/MS parameters were optimized by comparing the results of various mobile phases, as well as by establishing the best instrumental conditions. The 145 PPCPs were separated using an Phenomenex Kinetex C18 column (50 mm×3 mm, 2.6 μm) via gradient elution. The mobile phases were 0.1% (v/v) formic acid aqueous solution containing 5 mmol/L ammonium formate and acetonitrile for positive ion modes, 5 mmol/L aqueous solutions of ammonium formate and acetonitrile for negative ion modes. The samples were quantified using the scheduled multiple reaction monitoring (scheduled-MRM) mode with electrospray ionization in positive and negative ion modes. A standard internal calibration procedure was used to calculate contents of sample. The established method was systematically verified, and it demonstrated a good linear relationship. The average recoveries of the 145 PPCPs at the three spiked levels were in the range of 80.4%-128% with relative standard deviations (RSDs, n=6) of 0.6%-15.6%. The method detection limits (MDLs) ranged from 0.015 to 5.515 ng/L. Finally, the optimization method was applied to analyze the 145 PPCPs in 11 surface water samples and 6 drinking water samples. Overall, 93 (64%) out of the 145 analytes were detected. The total contents of the PPCPs in surface water samples ranged from 276.9 to 2705.7 ng/L. The detection frequencies of antidiabetic, antiviral, and psychotropic drugs were 100%. The total contents of the PPCPs in drinking water samples ranged from 140.5 to 211.5 ng/L, and antibiotics, antidiabetic drugs, and antiviral drugs comprised the largest proportion of analytes (by mass concentration) in drinking water samples. Our method exhibited high analytical speed and high sensitivity. It is thus suitable for the trace analysis and determination of the 145 PPCPs in environmental water and showed improved detection efficiency for PPCPs in water, indicating that it has a high potential for practical applications. This study can extend technical support for further pollution-level analysis of PPCPs in water and provide an objective basis for environmental management.

Occurrence and distribution of PPCPs in water from two largest urban lakes of China: First perspective from DGT in-situ measurement

Pharmaceutical and personal care products (PPCPs) are an important group of emerging contaminants that may threaten organisms at trace concentrations. However, research on the occurrence of PPCPs in urban lakes in China is still scarce. In this study, 15 PPCPs in the Tangxun Lake and the Donghu Lake were collected using the diffusive gradients in thin-films (DGT) technique and analyzed by high performance liquid chromatography tandem-mass spectrometry (HPLC-MS/MS). Thirteen of the 15 targeted PPCPs were detected in the Tangxun Lake, and all PPCPs were detected in the Donghu Lake, with total concentrations ranging from 160 to 730 ng/L (average: 401 ng/L) and 187 to 1933 ng/L (average: 653 ng/L), respectively. Bisphenol A (BPA) was the dominant PPCP, followed by disinfectants in both lakes. The total concentrations of PPCPs in the Donghu Lake were higher than those in the Tangxun Lake. The spatial distribution characteristics of PPCPs in the two lakes were different, with higher total concentrations in the eastern part than in the western part of the Tangxun Lake spatially and higher in the north-western part than in the south-eastern part of the Donghu Lake. The results of the risk assessment showed that BPA and estrone posed high risks to the aquatic environment (RQ ≥ 1), while triclosan and estriol presented a medium risk (0.1 ≤ RQ < 1) in some sites. This study was the first attempt to apply DGT for providing vital data on the evaluation of the ecological risk of PPCPs in the two largest lakes in China, and attention should be paid to the long-term ecological effects caused by the occurrence of PPCPs in lakes.

Effects of Long-Term Exposure of Pharmaceuticals and Personal Care Products on Algogenic Organic Matter Characteristics

Algal organic matter (AOM) released from microalgae has high potential effects for water treatment. In response to the complex problem of algal-laden water treatment, this study investigated the characteristics of AOM of Microcystis aeruginosa under long-term exposure to pharmaceuticals and personal care products (PPCPs). The results indicated that algae under low carbamazepine (&lt;10 µg/L), high naproxen (&gt;10 µg/L), and/or diclofenac at any concentration treatment promoted the release of total organic matter, whereas they were inhibited at high carbamazepine and low naproxen exposure. Macromolecular organics of AOM were inhibited when algae were subjected to long-term exposure to carbamazepine at any concentration (0.25–1000 µg/L), and the higher the carbamazepine concentration was, the more seriously macromolecular organics were inhibited. For naproxen and diclofenac treatment, macro- and medium-molecular-weight organics were promoted under high concentration treatment (&gt;1 µg/L), yet they were inhibited under low concentration &lt;10 µg/L. The fluorescent organics of AOM were also changed by fluorescence excitation-emission matrices-parallel factor analysis, with the fluorescent intensity of humic-like and protein-like substances inhabited under carbamazepine of any concentration, whereas they were promoted under high naproxen treatment (&gt;10 µg/L). This research had significant effects on algal-laden water treatment containing various PPCPs concentrations as well as the risk assessment of PPCPs in water.

Elucidating the charge redistribution in bimetallic metal–organic frameworks: High-electron-density reactive center for removal of organic micropollutants in water

For the elimination of pharmaceutical and personal care products (PPCPs) from water, various methods and materials have been designed, while the removal effect of PPCPs is still mediocre due to the limitation of trace concentration. Therefore, constructing high-electron-density reactive centers (HRCs) for effective processing is urgent due to the potential threat to human health posed by PPCPs in water. Herein, a bimetallic metal–organic framework (BMOF-Ti/Zr6%) was synthesized by a solvothermal method with enhanced adsorption and photocatalytic capacity to address the issue. The Zr doping in metal clusters elevated the adsorption capacity of 2,2′,4,4′-tetrehydroxybenzophenone (BP-2) on BMOF-Ti/Zr6% to 4032 μmol/g, and the photocatalytic rate was more than 6 times higher than that of the pristine metal–organic framework. The enhanced adsorption and photodegradation of PPCPs on BMOFs was ascribed to the charge redistribution between Ti and Zr inducing the formation of HRCs. The electrons accumulated on HRCs altered the adsorption performance of metal sites and facilitated the generation of reactive oxygen species, which was further confirmed by theoretical calculations and indirectly validated by the interface behaviors of dissolved organic matter (DOM). Moreover, the possible reaction pathway of BP-2 degradation was explored. In addition, the BMOF-Ti/Zr6% retained more than 90% of initial adsorption capacity in photocatalytic regeneration experiments, demonstrating the potential for application in natural water matrix. These findings reinforce the understanding of charge behaviors in bimetallic materials and contribute to understand the impact of DOM in water remediation processes.

Molecular Oxygen Activation by Citric Acid Boosted Pyrite–Photo–Fenton Process for Degradation of PPCPs in Water

Pyrite has been used in photo-Fenton reactions for the degradation of pollutants, but the application of photo-Fenton processes with extra H2O2 in real water/wastewater treatment has still been limited by the economic cost of H2O2 and artificial light sources. Herein, citric acid (CA) and simulated/natural sunlight are used to develop a pyrite-based photo-Fenton system (pyrite-CA-light) in situ generating H2O2 through the enhanced activation of molecular oxygen. The degradation of pharmaceuticals and personal care products (PPCPs), especially acetaminophen (APAP) as the main target pollutant, in the pyrite-CA-light system was investigated. The effects of influencing factors such as various organic acids, APAP concentration, pH, pyrite dosage, CA concentration and co-existing anions (HCO3-, Cl-, NO3-, SO42- and H2PO4-) were examined. At a pyrite dosage of 0.1 g L-1, CA concentration of 0.6 mM and an initial pH of 6.0, the degradation efficiency of APAP (30 μM) was 99.1% within 30 min under the irradiation of xenon lamp (70 W, λ ≥ 350 nm). Almost the same high efficiency of APAP degradation (93.9%) in the system was achieved under natural sunlight irradiation (ca. 650 W m-2). The scavenging experiments revealed that the dominant active species for degrading APAP was hydroxyl radical (HO•). Moreover, a quantitative structural-activity relationship (QSAR) model for pseudo-first-order rate constants (kobs) was established with a high significance (R2 = 0.932, p = 0.001) by using three descriptors: octanol-water partition coefficient (logKow), dissociation constant (pKa) and highest occupied molecular orbital (HOMO). This work provides an innovative strategy of the photo-Fenton process for the degradation of PPCPs using natural minerals and ordinary carboxylic acid under sunlight.

Interaction between graphene oxide and acetaminophen in water under simulated sunlight: Implications for environmental photochemistry of PPCPs

In recent years, graphene oxide (GO) as a new carbon material has been widely investigated as adsorbent and catalyst. However, effects of GO on the micro-pollutants such as pharmaceuticals and personal care products (PPCPs) under sunlight remains unclear. In this study, the degradation of PPCPs in a simulated sunlight-GO photocatalytic system was systematically investigated. Specifically, GO rapidly degrade 95% of acetaminophen (APAP) within 10 min under simulated sunlight irradiation (λ ≥ 350 nm). The influencing factors such as APAP concentration, pH, GO dosage, water matrixes (Cl−, NO3−, HCO3−, SO42−, Ca2+, Fe3+and fulvic acid) were investigated. At a GO dosage of 100 mg L−1 and an initial pH of 7, the APAP (5 μM) photodegradation kinetic constant kobs was calculated to be 0.4547 min−1. In practical applications, the GO photocatalysis system still degrade over 90% APAP within 60 min in real surface water. The electron spin resonance and radical scavenging experiments revealed that the dominated active species for degrading APAP was photogenerated holes (h+), while other mechanisms (1O2 and O2•−/HO2•) played a minor role. Furthermore, the photochemical transformation of some other typical PPCPs were comparatively studied to reveal the relationship between degradation kinetics and molecular structure. Based on descriptive variables including molar refractive index parameter, octanol-water partition coefficient, dissociation constant and dipole moment, a quantitative structural-activity relationship (QSAR) model for predicting pseudo-first-order rate constants was established with a high significance (R2 = 0.996, p < 0.05). This study helps to understand the interaction between GO and PPCPs and its effects on the photochemical transformation of PPCPs in water.

A multifunctional chitosan composite aerogel for PPCPs adsorption

Pharmaceuticals and personal care products (PPCPs) are gaining attention due to their persistence in the environment. Therefore, the development of novel adsorbents to remove them is strongly anticipated. In this study, an improved dual ice-template assembly method had been used for the preparation of ZIF-67/QGO/SB-CS aerogel through ZIF-67, benzoquinone-modified graphene oxide (QGO), and sulfobetaine-modified chitosan (SB-CS) for the adsorption and removal of PPCPs in water. We reported for the first time that the chitosan composite aerogel has antifouling, bacterial filtration and oil-water separation abilities with excellent PPCPs adsorption performance and reusable, which would be a viable option for long-lasting adsorbents for PPCPs in water.

Contamination, transport, and ecological risks of pharmaceuticals and personal care products in a large irrigation region

Pharmaceuticals and personal care products (PPCPs) have attracted widespread attention owing to their extensive use and potential adverse effects on human and ecosystem health. There is a lack of information regarding the occurrence and environmental fate of PPCPs in large agricultural irrigation areas in China. In this study, we conducted a comprehensive survey on 30 PPCPs in water from Hetao Irrigation District, one of the three largest irrigation areas in China. The ΣPPCP-concentrations ranged 82.13–1409.24 ng/L in August and 40.53–887.20 ng/L in November, with caffeine (CAF), norfloxacin (NOR), erythromycin (ERY), sulfamethoxazole (SMX) and ofloxacin (OFL) being the predominant compositions. Spatially, the average ΣPPCP concentrations increased from irrigation to drainage water, and then decreased in Wuliangsuhai Lake. Less PPCP mass loading (55.05 kg/y) migrated from Wuliangsuhai Lake to Yellow River than that from the Yellow River to Hetao Irrigation District (425.88 kg/y), indicating that Wuliangsuhai Lake plays an important role in improving water quality. An ecological risk assessment showed that it is worthwhile to consider the presence of CAF, ERY, NOR, and OFL in natural surface water and to control their potential risks.

Pharmaceuticals and personal care products (PPCPs) in water, sediment and freshwater mollusks of the Dongting Lake downstream the Three Gorges Dam.

Pharmaceuticals and personal care products (PPCPs) are a group of emerging anthropogenic pollutants. Here we investigated the occurrence and concentrations of 35 typical PPCPs in water, sediment, and freshwater mollusks (Hyriopsis cumingii, Unio douglasiae, Sinanodonta woodiana, Lamprotula leai and Corbicula fluminea) of the Dongting Lake downstream of the Three Gorges Dam. As results, 33 PPCPs were detected in water and sediment of the lake. Ketoprofen (not detected (ND)-292.8ng/L, mean 91.1ng/L) and roxithromycin (13.7-141.9ng/L, mean 30.4ng/L) were the primary PPCPs measured in lake water, while ibuprofen (ND-105.0ng/g, mean 30.0ng/g) and ketoprofen (ND-142.9ng/g, mean 27.6ng/g) were dominant in the sediment. Distinct seasonal difference in PPCP compositions was observed in both water and sediment of the Dongting Lake, potentially associated with the water-level fluctuations driven by the Three Gorges Dam operations. Ketoprofen and ibuprofen were also frequently detected in the soft tissues of freshwater mollusks, with concentrations of 42.5-1206.6 and 44.9-992.7ng/g, respectively. Significant species-specific accumulation characteristics of PPCPs in mollusks were observed, with the highest total contents being reported for Corbicula fluminea (3.18±1.13μg/g). Moreover, gonads of mollusks were identified as the target organ to accumulate these compounds. Correlation analysis further revealed the strong associations of PPCP concentrations in mollusks with those in water and sediment, suggesting the importance of controlling dissolved and sedimentary bioavailability of PPCPs for ecological risk management in this freshwater lake ecosystems.

Multimedia Distribution Characteristics and Risk Assessment of 22 PPCPs in the Water Environment of Qingpu District, Yangtze River Delta Demonstration Area

In this study, 50 surface water and sediment samples were collected from 25 sampling points in Qingpu District (including Taipu River basin, Jinze Reservoir, and Qingxi country park) in the Yangtze River Delta integration demonstration area, and 22 pharmaceuticals and personal care products (PPCPs) in the samples were analyzed using high-performance liquid chromatography tandem mass spectrometry (HPLC/MS-MS). The distribution characteristics, sources, and influencing factors of targeted PPCPs in the study area were studied in detail. The ecological and health risks of the target PPCPs were evaluated using the quotients method. The results showed that a total of 19 PPCPs were detected in the surface water and sediment samples from 25 sampling points in Qingpu District, with total concentrations ranging from 0.06 to 178.67 ng·L-1 and 0.07 to 37.68 ng·g-1, respectively. The average value of sulfachloropyridazine (SCP) in the surface water was the highest with a concentration of 129.54 ng·L-1, whereas the average value of sulfamethoxazole (SMX) in the sediment was the highest with a concentration of 70.62 ng·g-1. The spatial distribution of the total amount of PPCPs showed a trend of Qingxi country park > Jinze Reservoir > Taipu River basin. Principal component analysis showed that the main sources of pollution were animal antibiotics used in aquaculture and the discharge of domestic sewage. There was a significant correlation between lg Koc and lg Kd (P<0.05), indicating that the organic carbon plays an important role in the distribution of the target PPCPs in water and sediments. The ecological risk assessment results revealed that the fungicides (TCC and TCS) in the surface waters showed a moderate risk to aquatic organisms of different trophic levels. The Qingxi country park and Jinze Reservoir were the regions with the highest ecological risks of PPCPs in surface water and sediment. The health risk entropy (HQ) of people of all age groups exposed through drinking was less than 1; however, with the continuous emission and accumulation of PPCPs, the pollution control of PPCPs in the environment still requires further attention.

CQDs/biochar from reed straw modified Z-scheme MgIn2S4/BiOCl with enhanced visible-light photocatalytic performance for carbamazepine degradation in water

The application of environmental-friendly and sustainable green materials in constructing photocatalysts to degrade pharmaceuticals and personal care products (PPCPs) attracts more attention. Herein, biochar (BC) or biomass carbon quantum dots (CQDs) were used to modify MgIn2S4/BiOCl (MB) heterojunction photocatalyst with Z-scheme structure, and improved the photocatalytic degradation performance for carbamazepine (CBZ) in the aqueous solution. Both BC and CQDs could form electron transfer interface with MB heterojunction, resulting in the photodegradation rate of MgIn2S4/BiOCl/CQDs (MBC, 96.43%) and MgIn2S4/BiOCl/BC (MBB, 88.09%) to CBZ within 120 min visible-light irradiation, which were significantly higher than that of MB (65.84%). Moreover, photoelectrochemical and photoluminescence tests verified that CQDs could act as a bridge for storing and transferring electrons in the entire Z-scheme system. Thence, compared with MBB, MBC could produce more •OH and •O2− under the visible light, which was indicated by the results of radical quenching experiments and electron paramagnetic resonance. Interestingly, under the natural sunlight, the photocatalytic performance of MBC to CBZ was even better than under laboratory conditions. In addition, the TOC removal efficiencies of MBB and MBC could reach 85.09% and 93.79% respectively, and ECOSAR program was utilized to further evaluate the eco-toxicity of CBZ and the intermediates towards fish, daphnid, and green algae, indicating that the photocatalytic process involving MBB and MBC showed outstanding toxicity reduction performance. Finally, compared with other composites, MBB and MBC showed higher photocatalytic performance and lower energy consumption, which would provide a green strategy for biochar materials in the photocatalytic treatment of PPCPs in water.

Janus particles with pH switchable properties for high-efficiency adsorption of PPCPs in water

Pharmaceuticals and personal care products (PPCPs) are emerging pollutants and have received increasing attention in recent years. The regeneration of conventional adsorption materials used to remove PPCPs involves the desorption of secondary organic pollution, which is harmful and problematic. In this work, the impact of pH-responsive magnetic Janus particle catalysts on PPCPs’ performance of high-efficiency adsorption and degradation was studied. Magnetic core-shell Fe3O4@SiO2 nanoparticles were prepared via the STÖBER method. Polylactic acid (PLA) was grafted using a template method, and the polymerization of pH-responsive monomer 2-(diethylamino)ethyl methacrylate (DEAEMA) was initiated to obtain the pH-responsive magnetic Janus particles (Janus-Fe-P). SEM (scanning electron microscopy), particle size analysis, TEM (transmission electron microscopy), and N2 adsorption-desorption tests were used to characterize the morphology, magnetic property, and pH-responsive performance of the Janus-F-P. The Janus-F-P was used in the adsorptions of two kinds of representative PPCPs, i.e., hydrophilic (antipyrine) and hydrophobic (tiamulin), under neutral conditions. Commercially available NORIT CN activated carbon was used for comparison, and the adsorption results showed that the adsorption efficiency of Janus particles was higher than that of activated carbon. Therefore, Janus-F-P could be used to efficiently catalyze the degradation of adsorbed PPCPs in the Fenton/hydroxylamine system. The removal rate of PPCPs was above 85 % after repeated use (5 times).

Pharmaceutical and Personal Care Products in Different Matrices: Occurrence, Pathways, and Treatment Processes

The procedures for analyzing pharmaceuticals and personal care products (PPCPs) are typically tedious and expensive and thus, it is necessary to synthesize all available information from previously conducted research. An extensive collection of PPCP data from the published literature was compiled to determine the occurrence, pathways, and the effectiveness of current treatment technologies for the removal of PPCPs in water and wastewater. Approximately 90% of the compiled published papers originated from Asia, Europe, and the North American regions. The incomplete removal of PPCPs in different water and wastewater treatment processes was widely reported, thus resulting in the occurrence of PPCP compounds in various environmental compartments. Caffeine, carbamazepine, diclofenac, ibuprofen, triclosan, and triclocarban were among the most commonly reported compounds detected in water and solid matrices. Trace concentrations of PPCPs were also detected on plants and animal tissues, indicating the bioaccumulative properties of some PPCP compounds. A significant lack of studies regarding the presence of PPCPs in animal and plant samples was identified in the review. Furthermore, there were still knowledge gaps on the ecotoxicity, sub-lethal effects, and effective treatment processes for PPCPs. The knowledge gaps identified in this study can be used to devise a more effective research paradigm and guidelines for PPCP management.

Distribution Characteristics and Risk Assessment of PPCPs in Surface Water and Aquatic Organisms in Chaoshan Coastal Area along the South China Sea

To investigate the occurrence, distribution, and potential risks of pharmaceuticals and personal care products (PPCPs) in the South costal area of China, a total of 20 PPCPs in water and aquatic organisms (fish, crab, and shellfish), obtained from 7 coastal rivers of the Chaoshan area, were determined using solid-phase extraction (SPE) and high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS). The results showed that up to 16 to 18 kinds of PPCPs could be detected in the rivers and aquatic organisms of the Chaoshan area, and the concentrations of PPCPs in the rivers and organisms ranged from 0.30-2223 ng ·L-1 to 0.143-80.3 ng ·g-1, respectively, with a high detection rate for many pollutants. Significant differences were observed in the samples of water and organisms. The total concentration of PPCPs in the rivers of the Chaoshan area was in the order of Huanggang River > Lianjiang River > Huangjiang River > Longjiang River > Luohe River > Rongjiang River > Hanjiang River, with the dominance of sulfamethoxazole (SMX) and caffeine (CAF). The total concentrations of PPCPs in the aquatic organisms from the Huanggang River, Hanjiang River, Lianjiang River, and Luohe River were higher than the concentrations of PPCPs in the aquatic organisms from the Longjiang River and Rongjiang River, with a dominance of trimethoprim (TMP), SMX, and CAF. The total concentration of PPCPs in fish was significantly higher than that in crab and shellfish. The results of bioconcentration factor (BCF) showed that a variety of PPCPs were accumulated in the organisms from the Chaoshan rivers; among them, the BCF value in fish was higher, which was more likely to bioaccumulate than crabs and shellfish. The ecological risks in terms of risk quotient (RQ) for 12 typical PPCPs were assessed in the Chaoshan area. It was discovered that the risk for fleas and algae was significantly higher than that for fish. The RQ values of SMX, erythromycin (ERY), and sulfadiazine (SDZ) were all greater than 1, which posed potential ecological risks for algae in the Huanggang River and Lianjiang Rivers and for fleas in the Huangjiang River.

A Review of Recently Developed LC-MS/MS Methods for the Analysis of Pharmaceuticals and Personal Care Products in Water.

Pharmaceuticals and personal care products (PPCPs) are present in the environment in trace concentrations. These compounds may cause health hazards to human beings and animals. The concerns related to their existence has led to development of a number of sensitive, accurate, and robust analytical methods. This article aims to review the recently developed chromatography-MS-based methods for the analysis of PPCPs in varied aqueous matrices and also presents a brief overview of the current status of PPCPs in the Indian aquatic environment. It demonstrates existing and recent trends in sampling, sample preparation techniques, and instrumentation methods for estimation of PPCPs in water. Solid-phase extraction is found to be the most commonly used sample preparation technique, and LC-tandem MS (MS/MS; with electrospray ionization) is the most extensively used instrumentation technique for the analysis of PPCPs. The analytical methods reviewed here provide a detailed overview of the procedures for detection and quantification of PPCPs in water. These methods are useful for monitoring these compounds in environmental matrices and facilitate risk assessment studies. This paper reviews the analytical methods for estimation of PPCPs in aquatic environmental matrices and presents their comprehensive evaluation.

Pharmaceuticals and personal care products in water, sediments, aquatic organisms, and fish feeds in the Pearl River Delta: Occurrence, distribution, potential sources, and health risk assessment

This study investigated the occurrence, distribution, and potential sources of 34 pharmaceuticals and personal care products (PPCPs) in water, sediments, aquatic organisms (fish and shellfish), and fish feeds from the mariculture areas of the Pearl River Delta (PRD). The health risk presented by this class of compounds was also assessed in relation to their intake via seafood consumption. Of the 34 PPCPs, a total of 9, 21, 14, and 28 PPCPs were detected in water, sediments, fish feeds, and aquatic organisms, respectively. Trimethoprim, norfloxacin, ofloxacin, and spectinomycin were detected in all matrices. The levels of PPCPs in water and sediment samples were relatively low. Spectinomycin, paracetamol, ciprofloxacin, norfloxacin, and ibuprofen were the most frequently detected PPCPs in feeds. Ibuprofen and ketoprofen were widely detected in aquatic organisms, with average concentrations of 562 and 267 ng/g wet weight, respectively. The residual levels of PPCPs in shellfish such as ME (mussel, Mytilus edulis) and OS (oyster, Ostrea gigas) were significantly higher (p < 0.05) than those in other species including CA (topmouth culter, Culter alburnus) and EO (orbfish, Ephippus orbis). Correlation analysis indicated that the medicated feeds were a potential source of PPCPs in the mariculture areas of the PRD, but other anthropogenic sources should not be ignored. Based on maximum residue limits and acceptable daily intake, the health risks presented to humans via seafood consumption are negligible. However, as multiple antibiotics were frequently detected in the mariculture environment, aquatic organisms, and feeds, the induction and dissemination of antimicrobial resistance associated with antibiotic usage in aquaculture would be of great concern. It is necessary to establish a centralized management system and control the use of veterinary drugs in mariculture to protect the aquaculture environment and ensure the safety of seafood.

High-throughput screening and quantitative analysis method of 112 pharmaceutical and personal care products in water based on ultra-high performance liquid chromatography with high-resolution mass spectrometry

An effective method based on ultra-high performance liquid chromatography-triple quadrupole/electrostatic field orbitrap mass spectrometry (UHPLC-Q-Orbitrap MS) was developed for high-throughput screening and quantitative analysis of 112 pharmaceutical and personal care products (PPCPs) in water. The water samples were separately extracted under alkaline and acidic conditions and cleaned on an SPE column (Cleanert PEP-2). The sample was separated and detected by UHPLC-Q-Orbitrap MS, and the data were collected in full MS scan/date dependent MS2 mode. All the 112 PPCPs in water were qualitatively screened and quantified on the basis of the peak area of the precursor ion. The PPCPs showed a good linear response in the mass concentration range of three orders of magnitude (r2 ≥ 0.9901), and the limits of quantification were between 0.002 μg/L and 0.8 μg/L. The recoveries of 60.1%-129.5% were achieved at different spiked levels of 0.2, 0.4, and 0.8 μg/L, and the RSDs were 1.1%-17.8% (n=6). Moreover, the method was used to screen the PPCPs in water samples acquired from seven regions of Dalian city (China), and 16 PPCPs were identified and quantified. Therefore, this simple method with high sensitivity and wide screening range can be applied to water quality management and environmental risk monitoring.

Beyond the conventional life cycle inventory in wastewater treatment plants

The conventional approach for the environmental assessment of wastewater treatment plants (WWTPs) is typically based on the removal efficiency of organic load and nutrients as well as the quantification of energy and chemicals consumption. Current wastewater treatment research entails the monitoring of direct emissions of greenhouse gases (GHG) and emerging pollutants such as pharmaceutical and personal care products (PPCPs), which have been rarely considered in the environmental assessment of a wastewater treatment facility by life cycle assessment (LCA) methodology. As a result of that, the real environmental impacts of a WWTP may be underestimated.In this study, two WWTPs located in different climatic regions (Atlantic and Mediterranean) of Spain were evaluated in extensive sampling campaigns that included not only conventional water quality parameters but also direct GHG emissions and PPCPs in water and sludge lines. Regarding the GHG monitoring campaign, on-site measurements of methane (CH4) and nitrous oxide (N2O) were performed and emission factors were calculated for both WWTPs. GHG direct emissions accounted for 62% of the total global warming potential (GWP), much more relevant than indirect CO2 emissions associated with electricity use.Regarding PPCPs, 19 compounds were measured in the main streams: influent, effluent and sludge, to perform the evaluation of the toxicity impact categories. Although the presence of heavy metals in the effluent and the sludge as well as the toxicity linked to the electricity production may shade the toxicity impacts linked to PPCPs in some impact categories, the latter showed a notable influence on freshwater ecotoxicity potential (FETP). For this impact category, the removal of PPCPs within the wastewater treatment was remarkably important and arose as an environmental benefit in comparison with the non-treatment scenario.

Multi-residue analytical methods for the determination of pesticides and PPCPs in water by LC-MS/MS: a review

Abstract Residues of pesticides, pharmaceutical and personal care products (PPCPs) are contaminants of world-wide concern. Consequently, there is a growing need to develop reliable analytical methods, which enable rapid, sensitive and selective determination of these pollutants in environmental samples, at trace levels. In this paper, a review of the liquid chromatography-tandem mass spectrometry (LC-MS/MS) based methods for the determination of pesticides and PPCPs in the environment is presented. Advanced aspects of current LC-MS/MS methodology, including sample preparation and matrix effects, are discussed.