Pharmaceuticals And Personal Care Products Research Articles

Parabens and triclosan in red swamp crayfish (Procambarus clarkii) from China: Concentrations, tissue distribution and related human dietary intake risk

Parabens (PBs) and triclosan (TCS) are commonly found in pharmaceuticals and personal care products (PPCPs). As a result, they have been extensively found in the environment, particularly in aquaculture operations. Red swamp crayfish (Procambarus clarkii) consumption has significantly risen in China. Nevertheless, the levels of PBs and TCS in this species and the associated risk to human dietary intake remain undisclosed. This study assessed the amounts of five PBs, i.e., methyl-paraben (MeP), ethyl-paraben (EtP), propyl-paraben (PrP), butyl-paraben (BuP) and benzyl-paraben (BzP), as well as TCS in crayfish taken from five provinces of the middle-lower Yangtze River. MeP, PrP and TCS showed the highest detection rates (hepatopancreas: 46–86 %; muscle: 63–77 %) since they are commonly used in PPCPs. Significantly higher levels of ∑5PBs (median: 3.69 ng/g) and TCS (median: 7.27 ng/g) were significantly found in the hepatopancreas compared to the muscle (median: 0.39 ng/g for ∑5PBs and 0.16 ng/g for TCS) (p < 0.05), indicating bioaccumulation of these chemicals in the hepatopancreas. The estimated daily intake values of ∑5PBs and TCS calculated from the median concentrations of crayfish were 6.44–7.94 ng/kg bw/day and 11.4–14.0 ng/kg bw/day, respectively. Although no health risk was predicted from consuming crayfish (HQ <1), consumption of the hepatopancreas is not recommended.

Azadirachta indica leaf extract based green-synthesized ZnO nanoparticles coated on spent tea waste activated carbon for pharmaceuticals and personal care products removal

Pharmaceuticals and personal care products (PPCPs) are emerging contaminants in aqueous systems, posing threat to both human health and environment. In prior research, predominant focus has been on examining various adsorbents for removing PPCPs from single-pollutant systems. However, no study has delved into simultaneous adsorption of PPCPs multi-pollutant mixture. This study evaluates performance of Azadirachta indica leaf extract-based green-synthesized ZnO nanoparticles coated on spent tea waste activated carbon (ZTAC) for removing sulfadiazine (SZN) and acetaminophen (ACN). Adsorption investigations were conducted in single-component (ACN/SZN) and binary-component (ACN + SZN) systems. The synthesized ZTAC was characterized using SEM, XRD, FTIR, EDX, porosimetry and pHpzc analysis. The study examines impact of time (1–60 min), dose (0.2–4 g/L), pH (2–12) and PPCPs concentration (1–100 mg/L) on ACN and SZN removal. Various kinetic and isotherm models were employed to elucidate mechanisms involved in sorption of PPCPs. Furthermore, synergistic and antagonistic aspects of sorption process in multi-component system were investigated. ZTAC, characterized by its crystalline nature and surface area of 980.85 m2/g, exhibited maximum adsorption capacity of 47.39 mg/g for ACN and 34.01 mg/g for SZN under optimal conditions of 15 min, 3 g/L and pH 7. Langmuir isotherm and pseudo-second-order kinetic model best-fitted the experimental data indicating chemisorption mechanism. Removal of ACN and SZN on ZTAC demonstrated synergistic nature, signifying cooperative adsorption. Overall, valorization of ZTAC offers effective and efficient adsorbent for elimination of PPCPs from wastewater.

Edge state engineering of nitrogen/phosphorus co-doped graphene nanoribbons towards electron-transfer-based peroxydisulfate activation

The electron transfer-based nonradical advanced oxidation processes (AOPs) exhibit great potential for degrading organic pollutants. However, achieving efficient electron transfer-based nonradical AOPs remains challenging. In this study, we developed the edge-rich and nitrogen/phosphorus (N/P) co-doped graphene nanoribbons by unfolding the multi-walled carbon nanotubes (MWCNTs). The catalysts with the edge-rich structure are capable of efficiently activating the peroxydisulfate (PDS) towards the degradation of carbamazepine (CBZ), a representative pharmaceutical and personal care products (PPCPs). Through adjusting the N/P ratio, the N/P co-doped graphene nanoribbons presented the optimal degradation kinetic constant of 0.452 min−1, compared with 0.0611 min−1 for the intact MWCNTs. Electrochemical characterizations, in situ Raman, galvanic oxidation tests, and quenching experiments confirmed that the N/P co-doped graphene nanoribbons followed an electron transfer-dominated nonradical pathway for pollutant degradation. Density functional theory (DFT) demonstrated that the exposed N/P co-doped edges at the boundary of graphene nanoribbons could elongated OO bond of PDS in facilitating PDS activation. This study provides a new approach to develop the nonradical AOPs-based techniques.

Comprehensive viewpoint on ionic liquids applications in sustainable pharmaceutical technology (experiments, simulations, and managerial insights)

Ionic liquids (ILs) have many applications, one of which is their use in the pharmaceutical and medical industries. In the pharmaceutical industry, there are many obstacles and challenges to the synthesis of solid crystal active pharmaceutical ingredients (APIs), and ILs can be used to solve these obstacles. Combining APIs with ILs (API-ILs) improves some of their properties, such as solubility, permeability, biological activity, and drug delivery, and how to improve these properties has been examined in this review. Also, ILs are used as catalysts in synthesizing drugs due to their unique properties, which are directly in some reactions and indirectly in others. In the last part, the removal of pharmaceuticals and personal care products (PPCPs) from sewage and underground water, which threatens the health of humans and animals, is investigated. This removal is done using ILs, and it is very important. Molecular Dynamic modeling demonstrated that the behavior of the ILs with different applications can be predicted. Likewise, by applying thermodynamic and Monte Carlo simulations, IL production programming can be done with the highest efficiency. Finally, the development of Monod modeling can be useful due to designing a sustainable system for recycling IL-based pharmaceutical wastewater as a sample of the circular economy.

For the occurrence of PPCPs from source to tap: A novel approach modified in terms of sample preservation and SPE cartridge to monitor PPCPs in our water supply

BackgroundThe ongoing infusion of pharmaceutical and personal care products (PPCPs) into ecosystems sustains a perpetual life cycle and leads to multi-generational exposures. Limited understanding of their environmental impact and their intrinsic ability to induce physiological effect in humans, even at low doses, pose great risks to human health. Few scholarly works have conducted systematic research into the occurrence of PPCPs within potable water systems. Concurrently, the associated monitoring techniques have not been comprehensively examined with regards to the specific nature of drinking water, namely whether the significant presence of disinfectants may influence the detection of PPCPs. ResultsA modified approach in terms of detailed investigation of sample preservation and optimization of an in-lab fabricated solid phase extraction (SPE) cartridge filled with DVB-VP and PS-DVB sorbent was proposed. Favorable methodological parameters were achieved, with correlation coefficients spanning from 0.9866 to 0.9998. The LODs of the PPCPs fluctuated from 0.001 to 2 μg L−1, while the LOQs varied from 0.002 to 5 μg L−1. The analysis of spiked samples disclosed a methodological precision of 2.31–9.86 % and a recovery of 52.4–119 %. We utilized the established method for analyzing 14 water samples of three categories (source water, finished water and tap water) from five centralized water supply plants. A total of 24 categories encompassing 72 PPCPs were detected, with the concentrations of PPCPs manifested a marked decrease from source water to finished water and finally to tap water. SignificanceOur research meticulously examined the enhancement and purification effects of widely used commercial SPE cartridges and suggested the use of in-lab fabricated SPE cartridges packed with DVB-VP and PS-DVB adsorbents. We also conducted a systematic evaluation of the need to incorporate ascorbic acid and sodium thiosulfate as preservatives for PPCP measurement, in consideration of the unique characteristics of drinking water matrices, specifically, the significant concentration levels of disinfectants. Furthermore, the proposed method was effectively employed to study the presence of PPCPs in source water, finished water, and tap water collected from centralized water supply plants.

Combined effects of pH and dissolved organic matter on the availability of pharmaceuticals and personal care products in aqueous environment

The interaction between pharmaceuticals and personal care products (PPCPs) with dissolved organic matter (DOM) can alter their bioavailability and toxicity. Nevertheless, little is known about how pH and DOM work together to affect the availability of PPCPs. This study investigated the impact of pH and DOM on the availability of seven PPCPs, namely Carbamazepine, Estrone, Bisphenol A, Testosterone Propionate, Triclocarban, 4-tert-Octylphenol and 4-n-Nonylphenol, using negligible depletion solid-phase microextraction (nd-SPME). The uptake kinetics of PPCPs by the nd-SPME fibers increased proportionally with DOM concentrations, likely due to enhanced diffusive conductivity in the unstirred water layer. At neutral pH, the partitioning coefficients of PPCPs for Humic Acid (log KDOC 3.87–5.25) were marginally higher than those for Fulvic Acid (log KDOC 3.64–5.11). Also, the log KDOC values correlated linearly with the log DOW (pH 7.0) values of PPCPs, indicating a predominant role for hydrophobic interactions in the binding of DOM and PPCPs. Additionally, specific interactions like hydrogen bonding, π-π, and electrostatic interactions occur for certain compounds, influenced by the polarity and spatial conformation of the compounds. For these ionizable PPCPs, the log DDOC values exhibit a strong dependence on pH due to the dual influence of pH on both DOM and PPCPs. The log DDOC values rose from pH 1.0 to 3.0, peaked at pH 5.0 to 9.0, and then (sharply) declined from 11.0 to 13.0. The reasons are that in strong acidic circumstances, the coiled and compressed shape of DOM inhibits the hydrophobic interaction, whereas in strong alkaline conditions, significant electrostatic repulsion reduces the sorption. This study reveals that the effects of DOM on the bioavailability of PPCPs are dependent on both pH and the specific compound involved.

One-step solvent thermal synthesis of 3D networked MOF composites for preparation of anultrasensitive chemosensor for hydroquinone and catechol.

Pharmaceuticals and personal care products (PPCPs) have a significant impact on the environment and human health, due to their sometimestoxic and carcinogenic characteristics. Therefore, an innovative chemosensor was constructed for ultrasensitive determinationof two typical PCCPs (hydroquinone (HQ) and catechol (CC)) in several minutes. The homemade chemosensor (UiO-67@GO/MWCNTs) consisted of MOF(UiO-67), graphene oxide (GO), and multi-walled carbon nanotubes (MWCNTs) composites; it was a networked, structurally sparse, porosity-rich, homogeneous octahedral composite, and had ultra-high electrical conductivity, which provided lots of active adsorption sites, promote charge transfer, and enrich lots of molecules to be measured in a few minutes. The prepared electrochemical sensor showed good long-term stability, applicability, reproducibility, and immunity to interference for the determination of HQ and CC, with a wide linear range of response of 5.0 ~ 940µM for both HQ and CC, and a low limit of detection with satisfactory recoveries. In addition, a new strategy of using MOF composites as the basis for electrochemical determination of organic small molecules was established, and a new platform was constructed for the quantitative determination of organic small molecules in various environmental samples.

Occurrence, distribution, and ecological risk assessment of pharmaceuticals and personal care products in the surface water of Lipu River, China

Pharmaceuticals and Personal Care Products (PPCPs) are inadvertently released into the aquatic environment, causing detrimental effects on aquatic ecosystem. There is an urgent need of an in-deep investigation on contamination information of PPCPs in aquatic environment as well as the ecological risks to the aquatic ecosystem. This study was carried out in Lipu River basin, China, to investigate the distribution pattern and ecological risks of PPCPs. Results showed that PPCPs pollution is ubiquitous, 29 out of 30 targeted PPCPs were detected in Lipu River. Fourteen PPCPs were detected with a frequency of 100% in all water samples, and ten PPCPs were detected with a frequency of more than 80%. The cumulated PPCPs concentrations ranged from 33.30 ng/L to 99.60 ng/L, with a median value of 47.20 ng/L in Lipu River. CAF, FQ, NF, and LMLX were the predominant PPCPs in study area. CAF showed high ecological risk, five and seven individual PPCP showed medium and low ecological risk to algae.

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.

The fate of pharmaceuticals and personal care products (PPCPs) in sewer sediments:Adsorption triggering resistance gene proliferation

In recent years, large quantities of pharmaceuticals and personal care products (PPCPs) have been discharged into sewers, while the mechanisms of PPCPs enrichment in sewer sediments have rarely been revealed. In this study, three PPCPs (tetracycline, sulfamethoxazole, and triclocarban) were added consecutively over a 90-day experimental period to reveal the mechanisms of PPCPs enrichment and the transmission of resistance genes in sewer sediments. The results showed that tetracycline (TC) and triclocarban (TCC) have higher adsorption concentration in sediments compared to sulfamethoxazole (SMX). The absolute abundance of Tets and suls genes increased in sediments under PPCPs pressure. The increase in secretion of extracellular polymeric substances (EPS) and the loosening of the structure exposed a large number of hydrophobic functional groups, which promoted the adsorption of PPCPs. The absolute abundance of antibiotic resistance genes (ARGs), EPS and the content of PPCPs in sediments exhibited significant correlations. The enrichment of PPCPs in sediments was attributed to the accumulation of EPS, which led to the proliferation of ARGs. These findings contributed to further understanding of the fate of PPCPs in sewer sediments and opened a new perspective for consideration of controlling the proliferation of resistance genes.

Enhanced properties of a positive-charged nanofiltration membrane containing quaternarized chitosan through second interfacial polymerization for the removal of salts and pharmaceuticals.

Nanofiltration (NF) membrane technology has been widely used in the removal of salts and trace organic pollutants, such as pharmaceuticals and personal care products (PPCPs), due to its superiority. A positive-charged composite NF membrane with an active skin layer was prepared by polyethyleneimine (PEI), trimethyl benzene chloride, and quaternate chitosan (HTCC) through second interfacial polymerization on the polyethersulfone ultrafiltration membrane. The physicochemical properties of the nanocomposite membrane were investigated using surface morphology, hydrophilicity, surface charge, and molecular weight cut-off (MWCO). The influence of the concentration and reaction time of PEI and HTCC was documented. The optimized membrane had a MWCO of about 481 Da and possessed a pure water permeability of 25.37 L·m-2·h-1·MPa-1. The results also exhibited salt rejection ability as MgCl2 > CaCl2 > MgSO4 > Na2SO4 > NaCl > KCl, showing a positive charge on the fabricated membrane. In addition, the membrane had higher rejection to atenolol, carbamazepine, amlodipine, and ibuprofen at 89.46, 86.02, 90.12, and 77.21%, respectively. Moreover, the anti-fouling performance and stability of the NF membrane were also improved.

Exploring organic and inorganic contaminant histories in sediment cores across the anthropocene: Accounting for site/area dependent factors

Sedimentary records help chronologically identify anthropogenic contamination in environmental systems. This study analysed dated sediment cores from L’Albufera Lake (Valencia, Spain), to assess the occurrence of heavy metals (HMs), polycyclic aromatic hydrocarbons (PAHs), perfluoroalkyl substances (PFASs), organophosphorus flame retardants (OPFRs), pesticides and pharmaceuticals and personal care products (PPCPs). The results evidence the continuing vertical presence of all types of contaminants in this location. The sediment age was difficult to establish. However, the presence of shells together with an historical estimation and the knowledge of sedimentary rates could help. HMs contents are higher in the upper layer reflecting the most recent increase of the industrial and agricultural practices in the area since the middle 20th century. Higher availability index of these HMs in the upper sediment layers is associated with point and diffuse contamination sources in the area. PAHs and OPFRs were homogeneous distributed through the sediments with few exceptions such as phenanthrene in the North and fluoranthene in the South. Perfluorooctanoic acid (PFOA) and perfluorooctanesulfonate (PFOS) were detected throughout the sediment core while short-chain PFASs (except perfluoropentanoic acid (PFPeA)) were detected only in the top layer. Pesticides and PPCPs showed appreciable down-core mobility. The vertical concentration profiles of organic contaminants did not exhibit a clear trend with depth, then, it is difficult to develop a direct relationship between sediment age and contaminant concentrations, and to elucidate the historical trend of contamination based on dated sediment core. Consequently, linking contaminant occurrence in sediments directly to their historical use is somewhat speculative at least in the conditions of L’Albufera Lake.

Anaerobic co-metabolic biodegradation of pharmaceuticals and personal care products driven by glycerol fermentation

Anaerobic digestion in two sequential phases, acidogenesis and methanogenesis, has been shown to be beneficial for enhancing the biomethane generation from wastewater. In this work, the application of glycerol (GOH) as a fermentation co-substrate during the wastewater treatment was evaluated on the biodegradation of different pharmaceuticals and personal care products (PPCPs). GOH co-digestion during acidogenesis led to a significant increase in the biodegradation of acetaminophen (from 78 to 89%), ciprofloxacin (from 25 to 46%), naproxen (from 73 to 86%), diclofenac (from 36 to 48%), ibuprofen (from 65 to 88%), metoprolol (from 45 to 59%), methylparaben (from 64 to 78%) and propylparaben (from 68 to 74%). The heterotrophic co-metabolism of PPCPs driven by glycerol was confirmed by the biodegradation kinetics, in which kbio (biodegradation kinetics constant) values increased from 0.18 – 2.11 to 0.27 – 3.60 L g-1-VSS d-1, for the operational phases without and with GOH, respectively. The assessment of metabolic pathways in each phase revealed that the prevalence of aromatic compounds degradation, metabolism of xenobiotics by cytochrome P450, and benzoate degradation routes during acidogenesis are key factors for the enzymatic mechanisms linked to the PPCPs co-metabolism. The phase separation of anaerobic digestion was effective in the PPCPs biodegradation, and the co-fermentation of glycerol provided an increase in the generation potential of biomethane in the system (energetic potential of 5.0 and 6.3 kJ g-1-CODremoved, without and with GOH, respectively). This study showed evidence that glycerol co-fermentation can exert a synergistic effect on the PPCPs removal during anaerobic digestion mediated by heterotrophic co-metabolism.

Phytoremediation of pharmaceuticals and personal care products using the constructed wetland

Pharmaceuticals and personal care products (PPCPs) are ubiquitously found pseudo-persistent group of emerging contaminants that causes ecotoxicity even at nano-concentrations. Due to their persistence and bio-accumulative behavior, long-term exposure to these pollutants increases the risk of severe health disorders in humans and poses ecological risks to aquatic life. Sedimentation, membrane filtration, advanced oxidation, activated sludge, and membrane bioreactors are a few of the treatment processes with treatment efficiency ranging from 50 to 95%, but they have limitations such as high investment, towering operating costs, use of chemicals, membrane fouling issues etc. Constructed wetlands (CW) are promising low cost, nature-based solutions having potential of PPCPs removal by simultaneous action of physical, chemical and biological processes. Herein, substrate material, plants and microbes play crucial roles in eliminating PPCPs. Phytoremediation of PPCPs occurs via plant uptake, translocation and degradation. Plants like Canna indica and Phragmites australis have shown ~70–90% antibiotics removal efficiency. Biofilm formation and colonization of microbes lead to the microbial degradation of micro-pollutants apart from the synergistic effect of the plant-endophytic relationship. This bacterial property could be used in CWs for bioremediation of water and wastewaters, as substrates provide substratum for microbial adherence and biofilm formation. Quorum sensing (QS) is a density-based cell-communication system where bacterial cells send signals among themselves during biofilm formation. In this respect, QS-assisted biodegradation via augmentation of engineered bacteria with genes to enhance QS can be a novel approach for the degradation of organic pollutants in CWs with microbial richness.

Ratiometric fluorescent probes based on carbon dots and europium for rapid detection of tetracycline

Tetracycline (TC) is a typical emerging pharmaceuticals and personal care products (PPCPs) pollutants in the environment. However, TC residues cause severe effects on human health. It is crucial to exploit simple, rapid and sensitive methods to detect TC in water samples. A ratiometric fluorescent probes (CDs-Eu3+) is constructed using carbon dots (CDs) and europium ions (Eu3+) for the visual detection of tetracycline (TC). Under 390 nm excitation, CDs-Eu3+ shows a strong yellow fluorescence at 545 nm and a weak red fluorescence at 619 nm, respectively. In the presence of TC, the fluorescence intensity at 545 nm decreased while the fluorescence intensity at 619 nm increased, which attributed to the internal filtering effect (IFE) and “antenna effect”, respectively. Sensing performance of CDs-Eu3+ probes is further evaluated with respect to various conditions, including salt concentration, Eu3+ concentration, pH, and reaction time. Results reveal that the proposed ratiometric fluorescent probes exhibits a specific recognition ability toward TC. An excellent linear relationship is observed between the fluorescence intensity ratio (F619/F545) and TC concentrations (1⁓100 μM), with a low detection limit (LOD) of 31 nM. The solution (CDs-Eu3+-TC) color gradually changes from yellow to red after adding TC. The probes are successfully applied to determine TC in water with recoveries of 85.43⁓97.53%. Finally, a fluorescent test strip is prepared and used for rapid visual semi-quantitative TC detection.

Using the fish plasma model to evaluate potential effects of pharmaceuticals in effluent from a large urban wastewater treatment plant

Several pharmaceuticals and personal care products (PPCPs) were evaluated using the fish plasma model (FPM) for juvenile Chinook salmon exposed to effluent from a large urban wastewater treatment plant. The FPM compares fish plasma concentrations to therapeutic values determined in human plasma as an indication of potential adverse effects. We used human Cmax values, which are the maximum plasma concentration for a minimum therapeutic dose. Observed and predicted plasma concentrations from juvenile Chinook salmon exposed to a dilution series of whole wastewater effluent were compared to 1%Cmax values to determine Response Ratios (RR) ([plasma]/1%Cmax) for assessment of possible adverse effects. Several PPCPs were found to approach or exceed an RR of 1, indicating potential effects in fish. We also predicted plasma concentrations from measured water concentrations and determined that several of the values were close to or below the analytical reporting limit (RL) indicating potential plasma concentrations for a large number of PPCPs that were below detection. Additionally, the 1%Cmax was less than the RL for several analytes, which could impede predictions of possible effect concentrations. A comparison of observed and predicted plasma concentrations found that observed values were frequently much higher than values predicted with water concentrations, especially for low log10Dow compounds. The observed versus predicted values using the human volume of distribution (Vd), were generally much closer in agreement. These data appear to support the selection of whole-body concentrations to predict plasma values, which relies more on estimating simple partitioning within the fish instead of uptake via water. Overall, these observations highlight the frequently underestimated predicted plasma concentrations and potential to cause adverse effects in fish. Using measured plasma concentrations or predicted values from whole-body concentrations along with improved prediction models and reductions in analytical detection limits will foster more accurate risk assessments of pharmaceutical exposure for fish.

Mechanistic insight into efficient PPCPs removal on waste biological activated carbon for low-carbon emission reutilization

Over 3.9 × 107 t/a of biological activated carbon (BAC) waste was generated from Chinese drinking water treatment plants. Traditional disposal methods, such as thermal regeneration and incineration, contributed significantly to high energy consumption and CO2 emissions. To tackle this issue, a low-carbon-emitting reutilization approach was proposed to reutilize waste BAC used for eight years (BAC-8Y) to efficiently remove pharmaceuticals and personal care products (PPCPs) from wastewater. The long-term operation of a BAC-8Y column demonstrated excellent removal efficiencies of tetracycline hydrochloride (TC, >98%) and diclofenac sodium (DS, >90%) with the original concentrations of 2–5 mg/L in the artificially prepared wastewater. Even for the real sewage with the addition of 2 mg/L DS/TC, BAC-8Y could also achieve >99 % removal efficiency for both within 40 days. The results of the adsorption control test using thimerosal to inhibit microbial activity showed that adsorption contributed 94.94% of the TC removal by BAC-8Y, while the DS removal benefitted from the combined effect of adsorption (69.10%) and biodegradation (30.90%). Microbial analysis revealed that Acidobacteriota and Dadabacteria was the dominant phyla, while norank_f__Blastocatellaceae and norank_f__Oxalobacteraceae was the key genera. Moreover, compared to traditional methods, the carbon emission from reutilizing 1 t waste BAC in this study was negligible (4.18 kgCO2), which was mainly from transportation. This was also aligned with China's carbon peaking and carbon neutrality goals.

A quantitative method of PPCPs in DOM-PPCPs coexisting system by differential spectroscopy

Pharmaceuticals and personal care products (PPCPs) were widely present in the water environment, posing a threat to both the ecological environment and human health. Dissolved organic matter (DOM) was ubiquitous in aquatic system and could form strong complexes with PPCPs, thereby interfering with accurate quantification. This paper proposed a novel method that utilized ultraviolet differential spectroscopy to accurately quantify PPCPs in DOM-PPCPs coexisting systems. A linear regression equation was established between UV–vis absorbance change (ΔA) at the characteristic peaks of specific PPCP and its concentration, resulting in the creation of a standard curve. The coefficient of determination (R2) of the linear regression equations established by four DOM (humic acid, fulvic acid, bovine serum albumin and sodium alginate) and the given PPCPs were consistently above 92 %. Moreover, real water samples were collected for the purpose of conducting a standard recovery experiment. The recovery rates of three types of PPCPs (carbamazepine, sodium sulfadiazine and triclosan) ranged from 90 % to 120 %, suggesting the feasibility of quantifying PPCPs in the DOM-PPCPs coexisting system using this method. The method proposed for quantifying PPCPs in DOM-PPCPs coexisting systems using UV differential spectroscopy introduced a new approach to quantifying PPCPs.

Investigating pharmaceuticals and personal care products in Musi River: A exploratory study in Hyderabad, India

This study investigated the presence of 46 pharmaceuticals and personal care products (PPCPs), including antibiotics, anti-inflammatory, antifungal, surfactant, antidepressants, and anticonvulsants, in wastewater samples collected from 11 sites along the Musi River in Hyderabad, India. These samples were obtained from diverse points along the river, representing urban, industrial, and hospital-related sources. This strategic selection ensures a comprehensive assessment of water quality, covering areas of varying population density and industrial activity. The samples were extracted for PPCPs using solid-phase extraction and quantified using ultra-performance liquid chromatography-tandem mass spectrometry in multiple reaction mode. Of the 46, 16 target analytes were detected at concentrations ranging from 0.01 ± 0.001 μg/L (for fluoxetine) to 19.295 ± 4.16 μg/L (for ciprofloxacin). An ecological risk assessment was conducted in terms of risk quotient (RQ) for acute and chronic effects for three trophic levels of aquatic organisms (algae, fish, and invertebrates) for each detected contaminant at every site. In the case of acute toxicity, high RQ values (>>1) were obtained for the antibiotics, naproxen, diclofenac, caffeine, fluconazole, propyl paraben, fluoxetine, and benzalkonium chloride C-12. In the case of chronic toxicity, high RQ values (>>1) were estimated for some of the commonly used PPCPs. This study aimed to investigate the contamination levels of PPCPs in various wastewater discharge points along the Musi River in Hyderabad, a densely populated urban center with a population density of up to 45,000/sq km. Additionally, the research conducted an ecotoxicological risk assessment to evaluate the risk posed by these pollutants to three trophic levels (algae, fish, and invertebrates) using RQ analysis. Notably, this study represents the first attempt to conduct such an assessment in this region, providing valuable insights into environmental health and pollution management.

Construction of bismuth based MOF for efficient removal of sodium diclofenac via adsorption and photocatalysis

The mass production and widespread use of Pharmaceuticals and Personal Care Products (PPCPs) have posed a serious threat to the water environment and public health. In this work, a green metal-based Metal Organic Framework (MOF) Bi-NH2-BDC was prepared and characterized, and the adsorption characteristics of Bi-NH2-BDC were investigated with typical PPCPs—diclofenac sodium (DCF). It was found that DCF mainly covered the adsorbent surface as a single molecular layer, the adsorption reaction was a spontaneous, entropy-increasing exothermic process and the adsorption mechanisms between Bi-NH2-BDC and DCF were hydrogen bonding, π-π interactions and electrostatic interactions. In addition, Bi-NH2-BDC also had considerable photocatalytic properties, and its application in adsorbent desorption treatment effectively solved the problem of secondary pollution, achieving a green and sustainable adsorption desorption cycle.