Pharmaceuticals And Personal Care Products Research Articles

Optimization and reusability of photocatalytic g-C3N4/W-TiO2/PVDF membranes for degradation of sulfamethazine.

Pharmaceuticals and personal care products (PPCPs) are prevalent emerging pollutants in the aquatic environment. The photocatalysis process has proven high efficiency in degrading PPCPs; however, the fate and repercussions of photocatalyst residuals are a major concern. To avoid that, we developed a composite from graphitic carbon nitride/tungsten doped with titanium dioxide (g-C3N4/W-TiO2) and loaded it on polyvinylidene fluoride (PVDF) membranes by the phase-inversion method. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and other different analyses implied the successful synthesis of g-C3N4/W-TiO2 composite and coating on PVDF membranes. A Box-Behnken design (BBD) was used to optimize the operational parameters, including pH, g-C3N4 ratio in the composite, and initial SMZ concentration by the response surface methodology (RSM). The highest SMZ degradation percentage was 98.60% after 240min of irradiation. Liquid chromatography with tandem mass spectrometry (LC-MS/MS) along with suspect screening was used to identify the intermediate transformation products and propose the SMZ degradation pathway. The loss in membrane activity after five cycles of photocatalytic degradation was about 18%. According to the current study, the photocatalytic membrane g-C3N4/W-TiO2/PVDF is promising for removing sulfonamide antibiotics from wastewater.

Indirect photodegradation of pharmaceutical and personal care products in dissolved black carbon solution: The role of microheterogeneous distribution of hydroxyl radical and sorption

Dissolved black carbon (DBC) with a hyperconjugated structure is ubiquitous in nature, and plays a crucial role in the migration and transformation of environmental contaminants due to its prominent properties of accepting electrons and sorption. However, little is known about the DBC-induced phototransformation of pharmaceutical and personal care products (PPCPs) in natural waters. Herein, the photodegradation kinetics of PPCPs were investigated in DBC solution under simulated solar irradiation and compared with those in Suwannee River natural organic matter (SRNOM) solution. The decay rates for the positively charged PPCPs (mean 1.484 ± 0.041 h-1) were significantly higher than those for the negatively charged PPCPs (mean 0.014 ± 0.002 h-1) in DBC solution due to the charge interaction. Moreover, the decay rates for the positively charged PPCPs in DBC solution were approximately 3–16 times of those in SRNOM solution due to the discrepant sorption and ability to produce bonded HO•. Finally, a microheterogeneous photodegradation mechanism of HO•-labile PPCPs in DBC solution involving the sorption and subsequent reaction with bonded HO• in the DBC microphase was proposed, which was verified using isopropanol and isopropamide as selective HO• scavengers. This work will provide useful insights into the photochemistry of DBC and also the DBC-involved phototransformation of PPCPs in aquatic environments.

Effects of DOM and cations on the diffusion migration of PPCPs through ion exchange membranes

The transportation of pharmaceuticals and personal care products (PPCPs) in ion-exchange membranes was worrying, especially in complex substrates. Dissolved organic matter (DOM), the complexation of PPCPs and the membrane pollution formed by DOM were often confused in the existing studies. This paper investigated the diffusive migration patterns of three kinds of (PPCPs) through ion exchange membranes (IEMs) in complex substrates. Triclosan (TCS) exhibited the most probability of migration. Without considering the interference of environmental factors, more than 90 % of TCS was adsorbed by IEMs. The migration of sulfadiazine sodium (SD) and carbamazepine (CBZ) was less than 5 %. The DOM and cations altered the interaction of PPCPs and IEMs. DOM fouling on IEMs converted the direct strong binding of TCS to IEMs to indirect weak binding, and increased the transmembrane migration of TCS consequently. The presence of cations (Ca2+ and Mg2+) increased the inorganic binding of TCS to IEMs, and also promoted the transmembrane migration of TCS. However, coexisting of Mg2+ and humic acid (HA) decreased TCS migration through anion exchange membrane (AM), but increased TCS migration through cation exchange membrane (CM) due to the increasing of solution potential. The research provided a theoretical basis for exploring the safety of product solutions in IEMs systems.

Effluents from septic systems and impact on groundwater contamination: a systematic review.

Globally, 2.2 billion people rely on groundwater for their water supply, and 2.8 billion use onsite sanitation systems for their sanitation needs. Groundwater contamination from septic systems is a critical public health concern, linked with diseases related to water sanitation and hygiene. Despite the severe impacts of septic systems on groundwater quality, comprehensive global studies remain limited. This study conducted a systematic review of articles published between 2012 and 2023 on topics related to septic systems and groundwater contamination, and 82 peer-reviewed articles met the inclusion criteria. The review identified key contaminants, including E.coli, nitrate, Enterococcus spp., total coliform, ammonium, phosphate, chlorides, and pharmaceuticals. Research on microbial indicators is more prevalent in Africa, while research on nutrients is common in North America. Research on organic contaminants including polyfluoroalkyl substances (PFAS), pharmaceuticals, and personal care products (PCPPs) is limited, particularly in low-and middle-income countries. Critical factors contributing to groundwater contamination include soil, hydrogeological conditions, climate, septic system maintenance and functioning, and septic density. The goal of this study was to comprehensively assess the extent of groundwater contamination resulting from septic system effluents by identifying the major contaminants typically found in affected groundwater sources and exploring the factors contributing to contamination. Identifying the major contaminants and factors related to groundwater contamination from septic systems is crucial for developing effective management strategies to protect groundwater sources.

Simultaneous degradation of pharmaceuticals and personal care products in hospital wastewater using ozone under ultraviolet irradiation

The discharge of Pharmaceuticals and personal care products (PPCPs) from industries and hospitals are responsible for the contamination of water body with slow or non-degradable toxic compounds. The removal of these contaminants required advanced treatment process because of unable to treat by conventional wastewater treatment process. In this study, the degradation of PPCP compounds, including caffeine (CAF), atenolol (ATL), carbamazepine (CBZ), sulfamethoxazole (SMX), trimethoprim (TMP), and acetaminophen (ACT) was evaluated under exposure to 1.0 and 1.5 mg/L dissolved ozone (O3), both with and without ultraviolet (UV) irradiation (254 nm). Using liquid chromatography with tandem mass spectrometry, we determined that the removal efficiency for the targeted contaminants exceeded 95 % within just 20 min of exposure to both 1.0 and 1.5 mg/L O3. However, when treated with UV light alone, the removal efficiency was limited at 3 %–11 %. A combination treatment involving dissolved 1.5 mg/L O3 and UV light led to over 97 % removal within 7 min. This outcome was attributed to hydroxylation reactions, aromatic ring opening, oxidation, and mineralization facilitated by the HO and peroxide generated through the photolysis of O3. The degradation rate of PPCP compounds followed pseudo-first-order kinetics and showed a decrease in the presence of humic acid and hospital wastewater further decreased it. Moreover, O3/UV treatment generated lower-weight degradation products. The toxicity analysis revealed that these transformation products exhibited environmental benignity and minimal health risks which O3/UV treatment potentially minimizes the presence of harmful byproducts. These findings provide a foundation for developing combined hybrid systems for PPCP containing wastewater, containing membrane filtration with ozonation system.

Effect, Fate and Remediation of Pharmaceuticals and Personal Care Products (PPCPs) during Anaerobic Sludge Treatment: A Review.

Biomass energy recovery from sewage sludge through anaerobic treatment is vital for environmental sustainability and a circular economy. However, large amounts of pharmaceutical and personal care products (PPCPs) remain in sludge, and their interactions with microbes and enzymes would affect resource recovery. This article reviews the effects and mechanisms of PPCPs on anaerobic sludge treatment. Most PPCPs posed adverse impacts on methane production, while certain low-toxicity PPCPs could stimulate volatile fatty acids and biohydrogen accumulation. Changes in the microbial community structure and functional enzyme bioactivities were also summarized with PPCPs exposure. Notably, PPCPs such as carbamazepine could bind with the active sites of the enzyme and induce microbial stress responses. The fate of various PPCPs during anaerobic sludge treatment indicated that PPCPs featuring electron-donating groups (e.g., ·-NH2 and ·-OH), hydrophilicity, and low molecular weight were more susceptible to microbial utilization. Key biodegrading enzymes (e.g., cytochrome P450 and amidase) were crucial for PPCP degradation, although several PPCPs remain refractory to biotransformation. Therefore, remediation technologies including physical pretreatment, chemicals, bioaugmentation, and their combinations for enhancing PPCPs degradation were outlined. Among these strategies, advanced oxidation processes and combined strategies effectively removed complex and refractory PPCPs mainly by generating free radicals, providing recommendations for improving sludge detoxification.

Microalgae to remove pharmaceutical and personal care products (PPCPs) from wastewater

Substances used for medicinal, cosmetic, hygiene, and health care objectives are included in the category of pharmaceuticals and personal care products (PPCPs). They are a major source of public concern because of their ubiquitous manufacturing, usage, and careless disposal of expired products into the environment. Many PPCPs, including antibiotics, analgesics, endocrine disruptors, and microbial/disinfecting agents, are commonly detected in freshwater systems, groundwater, and wastewater treatment effluents in amounts ranging from nanograms per liter to milligrams per milliliter. Additionally, these compounds frequently show persistence and accumulate in biological tissue, eventually finding their way into crops, vegetables, and drinking water supplies. Because many PPCPs are known to have the ability to upset ecosystems and/or provide health hazards, they are categorized as “emerging contaminants.” The research on the occurrence, fate, and possible health and environmental hazards related to PPCPs in both aquatic and terrestrial habitats is thoroughly reviewed in this work. It also covers reported cases of danger or health concerns in humans, although a full assessment may not be possible given the limitations of the data at hand. This review aims to provide a comprehensive and well-focused overview of the current understanding of bioremediation strategies for the removal of pharmaceuticals and personal care products (PPCPs), with an emphasis on the application of macroalgae, microalgae, and aquatic macrophytes. It examines the physicochemical properties of PPCPs and their potential risks to environmental and human health. Additionally, the review explores the potential and challenges associated with the broader application of biotechnologies employing algae and aquatic macrophytes. This includes research efforts to correlate the operational parameters of these biotechnologies with the primary mechanisms responsible for PPCP removal. In conclusion, algae and macrophytes present promising, eco-friendly solutions for wastewater treatment, significantly contributing to the mitigation of PPCP contamination.

Boosted electrochemical reduction detoxification and oxidation of clofibric acid by polymerized ionic liquid functionalized cathode: Parameter optimization and degradation mechanisms

The application of electrocatalytic degradation technology in the treatment of pharmaceuticals and personal care products (PPCPs) has attracted widespread attention currently. Through structure and properties characterization of catalysts we found that more uniformly distributed metal particles and excellent thermal stability were obtained by modification with poly(1-vinyl-3-butylimidazole hexafluorophosphate) ([(PV)BIM]PF6) on graphene to anchor the metal CoNi nanoparticles (CoNi/PILs-rGO). For assessing its application potential, the CoNi/PILs-rGO cathode in combination with Ti/RuO2/IrO2 anode to set up an experimental reaction system for the electrocatalytic degradation of clofibric acid (CA) simulated wastewater. Reactor settings for experimentation are optimized, and intermediates, alterations in toxicity during degradation, and active species are detected. The results of the single-factor experiment showed that the average removal rate of CA by the cathodic compartment was 97.18 % when the conditions were optimal. Two possible pathways of degradation are deduced from the CA intermediates, one is the C-Cl bond breaking in electrochemical reduction, and the other is that the C-O bond is directly broken by anodic reactive oxygen. Toxicity tests have shown that the anode produces some by-products that are more hazardous than the original chemical, while the cathode produces a dechlorination process that is ultimately more detoxifying.

Geographical and environmental factors in pharmaceuticals and personal care products removal from drinking water plants

Pharmaceuticals and personal care products (PPCPs) are unintentionally released into the environment from treated and untreated wastewater, agricultural runoff, and stormwater, and enter drinking water treatment plants (DWTPs). However, very little is known about the occurrence of PPCPs and their removal effectiveness during the drinking water treatment processes (conventional or advanced treatment) in multiple DWTPs, especially within the same geographical area. To address this important knowledge gap, source and finished drinking water samples were collected monthly from May to September in 2018 and 2019 from four DWTPs in Northern Ohio, USA. The total and individual PPCP concentrations varied among DWTPs and sampling dates in both source and finished water. Despite the site and time differences, caffeine and 17-beta-estradiol were detected at a frequency of 100% in all four DWTPs on all dates, while acetaminophen, estrone and nicotine consistently were not detected. Significant correlations were identified between the source water PPCPs and some environmental variables, such as dissolved organic carbon (DOC), temperature and pH. The PPCP removal efficiency from finished water samples varied depending on DWTP (61.2–84.2%), sampling month (28.3–89.7%), and different PPCP compounds (31.2% and 99.3%). Overall, this study demonstrated that PPCPs were consistently present in low concentrations (ng/L) in the freshwater systems; conventional treatment methods could only partially mitigate PPCP contaminants, while advanced techniques, such as UV-peroxide treatment, provided better removal efficiencies. PPCP removal also depended on the season, with summer demonstrating the highest removal in all four treatment plants.

Exposure to microplastics contaminated with pharmaceuticals and personal care products: Histological effects on Ucides cordatus

Pharmaceuticals and personal care products (PPCPs) are known to interact with microplastics (MPs) in aquatic environments, with substances such as the antimicrobial triclosan (TCS) and the synthetic hormone 17α-ethinylestradiol (EE2) being prevalent. These persistent contaminants are linked to toxic effects in aquatic organisms. This study aimed to investigate histological and morphometric changes in the gills of Ucides cordatus exposed to microplastics alone and microplastics contaminated with PPCPs. The experimental design included four treatment groups: 1) control (C), 2) virgin microplastics (MP), 3) microplastics fortified with triclosan (MPT), and 4) microplastics fortified with 17α-ethinylestradiol (MPE), with exposure durations of 3 or 7 days. Significant differences were observed in the histopathological indices for treatments with PPCP-fortified microplastics at 3 days (MPT and MPE) and 7 days (MPT). Notable pathologies included necrosis, fibrosis, and circulatory disorders. Exposure duration was significantly associated with morphometric changes, including secondary lamellar width in MPT and secondary lamellar length in MPE. These findings indicate that exposure to microplastics contaminated with PPCPs may impair the osmoregulatory and respiratory functions of Ucides cordatus.

Pharmaceuticals and personal care products contamination in the rivers of Chennai city during the COVID-19 pandemic.

Pharmaceuticals and personal care products (PPCPs) monitoring in surface water is crucial to address the escalating threat of antimicrobial resistance and safeguard public health. This study aimed to investigate the occurrence of 21 different PPCPs, including wastewater chemical markers, antibiotics, and parabens in the surface water of Chennai city using Ultra Performance Liquid Chromatography-Triple Quadrupole Mass Spectrometry (UPLC-MS/MS) analysis. It is noteworthy that chemical markers viz., carbamazepine (CBZ) and caffeine (CAF) were detected in all the sites and contributed to more than 95% of the total PPCPs load indicating a significant intrusion of wastewater. Among the antibiotics, fluoroquinolones were dominant in this study. Interestingly, a significant and strong correlation was seen between fluoroquinolones, CBZ and CAF (R2 = 0.880-0.928, p < 0.05), suggesting similarities in their sources. More than 50% of the sites exhibited a risk for antimicrobial resistance (RQAMR) withRQAMR > 1 for ciprofloxacin, indicating a significantpublic health concern. The ecotoxicological risk assessment of PPCPs showed no risk to any organisms, except for triclosan, which posed a risk to fish and daphnids at one sitenear an open drain in Buckingham canal.

Effect of Soil-pH, temperature and moisture content on sorption dynamics of Metformin and Erythromycin.

The rising soil-groundwater quality issues due to pharmaceuticals and personal care products (PPCPs) have spurred significant concern. To understand the sorption characteristics of metformin (MTN) and erythromycin (ETM) in sandy and sandy loam soils with varying organic matter and particle composition, sorption kinetics (single and competitive), isotherms, and thermodynamics were studied. The effects of pH and soil moisture content (SMC) were also investigated at environmentally relevant concentrations. The equilibrium time of MTN and ETM sorption by the three soils in a competitive solute system was about 4 h, and the sorption process was in line with a pseudo-second-order model. The rate-determining step in the process involved both intraparticle diffusion and liquid film diffusion mechanisms for the two PPCPs. The highest pollutant uptake occurred in soils with higher organic matter, driven by enhanced H-bonding, electrostatic interactions, and π-π and n-π interactions facilitated by the organic matter. The equilibrium data in the three soils was well described by the Freundlich model and confirmed favourable adsorption (1/nf = 1.01 - 1.90). The sorption coefficient (Kd) on the three soils ranged from 2.1 to 332 L/kg for MTN and from 6.25 to 845 L/kg for ETM. The adsorption process was feasible at 293 K and 303 K (ΔG° = - 0.16 to -10.24 kJ/mol), physical and exothermic in nature (ΔH° = -75.21 to -10.30 kJ/mol) for both the contaminants. Observed alterations in Qe with pH confirmed the participation of electrostatic interactions. A low SMC favoured both MTN and ETM sorption onto the sandy soil. Overall, ETM exhibits higher expected sorption, whereas MTN has a greater tendency for migration in the soils and is thus liable to contaminate the groundwater. The study accentuates novel insights into the transport and fate of MTN and ETM in soil-groundwater systems at environmentally relevant concentrations.

Pharmaceutical and personal care products in recycled water for edible crop irrigation: Understanding the occurrence, crop uptake, and water quantity effects

Global water scarcity poses a great challenge to agriculture productivity. Recycled water offers a promising alternative for agricultural irrigation, yet residual pharmaceutical and personal care products (PPCPs) in recycled water can transfer to edible crops during irrigation, and adversely affect food safety. Furthermore, irrigation water quantity can influence the accumulation of PPCPs in edible crops. This study comprehensively investigates the use of recycled water for agricultural irrigation by critically reviewing three key components: PPCPs occurrence in recycled water, their accumulation in edible crops, and the impact of water quantity on PPCPs accumulation. Literature analysis showed that PPCPs were present from 130 to 1400 ng/L in secondary effluent and 25–400 ng/L in tertiary effluent, with sulfamethoxazole being the most prevalent in both effluents. PPCPs uptake and accumulation varied between leafy and fruity vegetables, with diclofenac accumulating highest in leafy vegetables and fluoxetine in fruity vegetables. Furthermore, the water requirement of leafy and fruity crops vary throughout the growing season. In leafy vegetables, PPCPs accumulation in leaves is influenced by transpiration rate, with reduced accumulation occurring under limited water availability due to slower transpiration. In fruity vegetables, osmotic adjustment drives the water transport in fruits, leading to increased PPCPs accumulation under limited water conditions. This study contributes insights into PPCPs occurrence, accumulation, and irrigation water quantity, aiding in the development of effective strategies for recycled water use in agriculture.

Differentiated adsorption of acetaminophen and diclofenac via alkyl chain-modified quaternized SBA-15: Insights from molecular simulation

The increasing presence of pharmaceuticals and personal care products (PPCPs) in aquatic systems pose significant environmental concerns. This study addresses this issue by synthesizing quaternized mesoporous SBA-15 (QSBA) with varied alkyl chain lengths of C1QSBA, C8QSBA, and C18QSBA. QSBA utilizes dual mechanisms: hydrophobic interactions via the alkyl chain and electrostatic attraction/ion exchange via the ammonium group. Diclofenac (DCF) and acetaminophen (ACT) were selected as target PPCPs due to their contrasting dissociation properties and hydrophobicity, which are the main characteristics of PPCPs. The adsorption of DCF and ACT revealed that longer alkyl chains enhanced the adsorption capacity of ACT through hydrophobic interactions, whereas dissociated DCF (DCF–) adsorption was superior owing to its high hydrophobicity (log Kow = 4.5) and electrostatic attraction. pH levels between 6 and 8 resulted in a high affinity for DCF–. Notably, among the three alkyl chains, only C18QSBA exhibited the most effective adsorption for DCF–. These PPCPs adsorption trends were confirmed through molecular simulations of adsorption under conditions in which competing ions coexisted. The molecular simulations show that while DCF– has lower adsorption energy than Cl−, OH−, and H3O+ ions in QSBA, enhancing its adsorption under various pH conditions. Conversely, ACT exhibits a higher adsorption energy, which reduces its adsorption efficiency. This suggests the potential application of QSBA with long alkyl chains in the treatment of highly hydrophobic and negatively charged PPCPs. Furthermore, this study emphasizes the importance of simulating adsorption under competing ion conditions.

Drug Use Patterns in Wastewater and Socioeconomic and Demographic Indicators

Measuring drug use behaviors in individuals and across large communities presents substantial challenges, often complicated by socioeconomic and demographic variables. To detect spatial and temporal changes in community drug use by analyzing concentrations of analytes in influent wastewater and exploring their associations with area-based socioeconomic and sociodemographic metrics like the area deprivation index (ADI) and rural-urban commuting area (RUCA) codes. This longitudinal, cross-sectional wastewater study was performed from May 2022 to April 2023 and included biweekly influent wastewater samples of 39 analytes from 8 sampling locations across 6 wastewater treatment plants in southern Nevada. Statistical analyses were conducted in December 2023. It was hypothesized that wastewater monitoring of pharmaceuticals and personal care products (PPCPs) and high-risk substances (HRSs) could reveal true spatial and temporal drug use patterns in near-real time. Data collection of samples for PPCPs and HRSs was performed using mass spectrometry. Both ADI and RUCA scores were utilized to characterize neighborhood contexts in the analysis. The false discovery rate (FDR) method was utilized to correct for multiple comparisons (PFDR). Over the 12-month wastewater monitoring period, 208 samples for PPCPs and HRSs were collected, and analysis revealed an increase in the consumption of HRSs and the seasonal variation in PPCP use in southern Nevada. There was a significant increase in levels of stimulant-associated analytes, such as cocaine (β = 9.17 × 10-4; SE = 1.29 × 10-4; PFDR = 1.40 × 10-10), and opioids or their metabolites, notably norfentanyl (β = 1.48 × 10-4; SE = 1.88 × 10-4; PFDR = 1.66 × 10-12). In contrast, DEET, an active ingredient in mosquito and tick repellents, demonstrated a seasonal use pattern (β = -4.85 × 10-4; SE = 2.09 × 10-4; PFDR = 4.87 × 10-2). Wastewater from more disadvantaged or rural neighborhoods, as assessed through ADI and RUCA scores, was more likely to show a significant positive correlation with HRSs, such as cocaine (β = 0.075; SE = 0.038; P = .05) and norfentanyl (β = 0.004; SE = 0.001; P = 1.64 × 10-5). These findings suggest that wastewater monitoring of PPCPs and HRSs offers a complementary method to existing public health tools, providing timely data for tracking substance use behaviors and use of PPCPs at a population level.

Simultaneous removal of nutrients and pharmaceuticals and personal care products using two-stage woodchip bioreactor-biochar treatment systems

The co-occurrence of nutrients and pharmaceuticals and personal care products (PPCPs) in sewage effluent can degrade water quality of the receiving watersheds. This study investigated the simultaneous removal of excess nutrients and PPCP contaminants by developing a novel woodchip bioreactor and biochar (B2) treatment system. The result revealed that woodchip bioreactors could effectively remove nitrate via a denitrification process and adsorb some PPCPs. Biochar as a secondary treatment system significantly reduced the concentrations of PPCPs and dissolved reactive phosphorus (DRP) (p < 0.05), compared to the woodchip bioreactor. The removal efficiencies of all targeted contaminants by the B2 system were evaluated using various hydraulic retention times (HRTs) and biochar types (pelletized versus granular biochar). Longer HRTs and smaller biochar particles (granular biochar) could enhance the removal efficiencies of targeted contaminants. Average contaminant removals were 77.25 % for nitrate-N, 99.03 % for DRP, 69.51 % for ibuprofen, 73.65 % for naproxen, 91.09 % for sitagliptin, and 96.96 % for estrone, with woodchip bioreactor HRTs of 12 ± 1.4 h and granular biochar HRTs of 2.1 ± 0.1 h. Notably, the second-stage biochar systems effectively mitigated by-products leaching from woodchip bioreactors. The presence of PPCPs in the woodchip bioreactors enriched certain species, such as Methylophilus (69.6 %), while inhibiting other microorganisms and reducing microbial community diversity. Furthermore, a scaled-up B2 system was analyzed and assessed, indicating that the proposed engineering treatment system could provide decades of service in real-world applications. Overall, this study suggests that the B2 system has promising applications for addressing emerging and conventional contaminants.

Pharmaceuticals and personal care products and heavy metals in the Ganga River, India: Distribution, ecological and human health risk assessment

In the present study, pharmaceuticals and personal care products (PPCPs), endocrine disrupting compounds (EDCs), and heavy metals (HMs), were measured in water and sediment of the Ganga River during summer and winter seasons for two consecutive years. Additionally, this study estimated the ecological and human health risks associated with PPCPs, EDCs, and HMs. HMs detected in the range of not detected (n.d.) to 23.59 μg/L and 0.01–391.44 μg/g in water and sediment samples, respectively. All studied HMs were within the permissible limits, except for As in water, and Cr and Ni in sediment. The geo-accumulation index (Igeo) indicated that Cr (0.71–5.98) and Pb (0.90–3.90) had high Igeo compared to other metals in sediment samples. Pb showed the highest ecological risk, followed by Cd, Co, Ni, Cu, Cr, As, and Zn. The maximum potential ecological risk index was observed at site G8. The hazard index (HI) value for water (0.08–0.89) and sediment (0.02–0.29) intake by adults remained within the acceptable limits, except at sites G8 (1.27) and G9 (1.34) for water intake. However, for children, the HI value was above the acceptable limit for water intake at sites G4 to G13 and for sediment at site G8. Among the studied compounds, metformin, triclosan, triclocarban, diclofenac, and methylparaben were the most abundant compounds present in the Ganga River. PPCPs and EDCs detected in the range of n.d. to 5850.04 ng/L and n.d. to 1080.41 ng/g in water and sediment samples, respectively. The environmental risk assessment identifies the maximum ecological risk in water exhibited by triclocarban followed by 17α-ethinylestradiol (EE2), diclofenac, and triclosan, while in sediment, the maximum ecological risk exhibited by triclocarban, followed by EE2, 17 β-estradiol (E2), triclosan, and diclofenac. However, none of the compounds showed human health risk, except for EE2, E2, and atenolol.

Estimation of suspected estrogenic transformation products generated during preservative butylparaben chlorination using a simplified effect-based analysis approach

Estrogenic transformation products (TPs) generated after water chlorination can be considered as an environmental and health concern, since they can retain and even increase the estrogenicity of the parent compound, thus posing possible risks to drinking water safety. Identification of the estrogenic TPs generated from estrogenic precursor during water chlorination is important. Herein, butylparaben (BuP), which was widely used as preservative in food, pharmaceuticals and personal care products (PPCPs), was selected for research. A simplified effect-based analysis (EDA) approach was applied for the identification of estrogenic TPs generated during BuP chlorination. Despite the removal of BuP corresponds to the decrease of estrogenicity in chlorinated samples, an significant increase of estrogenicity was observed (at T = 30 min, presented an estrogenicity equivalent to 17β-estradiol). Chemical analysis of the estrogenic chlorinated samples that have been previously subjected to biological analysis (in vitro assays), in combination with the principal component analysis (PCA) evaluation, followed by validating the estrogenic potency of most relevant estrogenic TPs through an in silico approach (molecular dynamics simulations), identified that the halogenated TP3 (3,5-Dichloro-butylparaben) increased by 62.5 % and 61.8 % of the estrogenic activity of the parent compound in samples chlorinated with 30 min and 1 h, respectively being classified as a potentially estrogenic activity driver after BuP chlorination. This study provides a scientific basis for the more comprehensive assessment of the environmental and health risk associated with BuP chlorination, highlighting the necessity of identifying the unknown estrogenic TPs generateded from estrogenic precursors chlorination.

Characteristics and functional bacteria of an efficient benzocaine-mineralizing bacterial consortium

The extensive use of pharmaceutical and personal care products (PPCPs) has led to widespread residual pollution, which increases the risk of the development of drug resistance in pathogenic microorganisms. Benzocaine is a PPCP that is widely used medical anesthesia and in sunscreen. Microorganisms are essential for the degradation of residual PPCPs. However, no studies have reported the microbial degradation of benzocaine. In this study, through continuous enrichment of the initial consortium HJ1, the highly efficient benzocaine-degrading consortium HJ7 was obtained, HJ7 exhibited a degradation rate that was 1.92 times greater than that of HJ1. Methyl 4-aminobenzoate and 4-aminobenzoic acid were identified as major intermediate products during benzocaine biodegradation by consortium HJ1 or HJ7. Methylobacillus (57.8 % ± 0.9 %) and Pseudomonas (22.1 % ± 0.7 %), which are thought to harbor essential species for benzocaine degradation, were significantly enriched in consortium HJ7. Two benzocaine-degrading strains, Pseudomonas sp. A8 and Microbacterium sp. A741, and one methyl 4-aminobenzoate-degrading strain, Achromobacter sp. A5, were isolated from consortium HJ7, and they synergistically mineralized benzocaine. These findings not only provide new insights into the biotransformation of benzocaine but also provide strain resources for the bioremediation of residual benzocaine in the environment.

Heterogeneous Photocatalytic Degradation of Selected Pharmaceuticals and Personal Care Products (PPCPs) Using Tungsten Doped TiO2: Effect of the Tungsten Precursors and Solvents.

Pharmaceuticals and personal care products (PPCPs) which include antibiotics such as tetracycline (TC) and ciprofloxacin (CIP), etc., have attracted increasing attention worldwide due to their potential threat to the aquatic environment and human health. In this work, a facile sol-gel method was developed to prepare tungsten-doped TiO2 with tunable W5+/W6+ ratio for the removal of PPCPs. The influence of solvents in the synthesis of the three different tungsten precursors doped TiO2 is also taken into account. WCl6, ammonium metatungstate (AMT), and Na2WO4●2H2O not only acted as the tungsten precursors but also controlled the tungsten ratio. The photocatalyst prepared by WCl6 as the tungsten precursor and ethanol as the solvent showed the highest photodegradation performance for ciprofloxacin (CIP) and tetracycline (TC), and the photodegradation performance for tetracycline (TC) was 2.3, 2.8, and 7.8 times that of AMT, Na2WO4●2H2O as the tungsten precursors and pristine TiO2, respectively. These results were attributed to the influence of the tungsten precursors and solvents on the W5+/W6+ ratio, sample crystallinity and surface properties. This study provides an effective method for the design of tungsten-doped TiO2 with tunable W5+/W6+ ratio, which has a profound impact on future studies in the field of photocatalytic degradation of PPCPs using an environmentally friendly approach.