Concentrations In Drinking Water Research Articles

Risk assessment for perfluorooctanoic acid (PFOA) in air, blood serum and water: mortality from liver and kidney disease

BackgroundCancer and non-cancer associations have been observed with PFAS (perfluoroalkyl and polyfluoroalkyl) substances in the general population, in populations from locally contaminated environments and in exposed workers.MethodsA quantitative risk assessment...

Low levels of per- and polyfluoroalkyl substances (PFAS) detected in drinking water in Norway, but elevated concentrations found near known sources

Per- and polyfluoroalkyl substances (PFAS) are ubiquitous contaminants which are also found in drinking water. Concentration levels in drinking water vary widely and range from a very low contribution to total daily exposure for humans to being the major source of uptake of PFAS. PFAS concentrations in Norwegian drinking water has been rarely reported. We investigated concentrations of 31 PFAS in 164 water samples, representing both source water (i.e., before drinking water treatment) and finished drinking water. Samples were taken from 18 different water bodies across Norway. The 17 waterworks involved supply drinking water to 41 % of the Norwegian population. Only four of the waterworks utilised treatment involving activated carbon which was able to significantly reduce PFAS from the source water. Samples of source water from waterworks not employing activated carbon in treatment were therefore considered to represent drinking water with regards to PFAS (142 samples). All samples from one of the water bodies exceeded the environmental quality standard (EQS) for perfluorooctane sulfonic acid (PFOS) according to the water framework directive (0.65 ng/L). No concentrations exceeded the sum of (20) PFAS (100 ng/L) specified in the EU directive 2020/2184 for drinking water. Several EU countries have issued lower guidelines for the sum of the four PFAS that the European Food Safety Authority (EFSA) has established as the tolerable weekly intake (TWI) for PFOS, perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorohexane sulfonic acid (PFHxS). Denmark and Sweden have guidelines specifying 2 and 4 ng/L for the sum of these PFAS. Only one of the 142 drinking water samples exceeded the Danish TWI and contained a sum of 6.6 ng/L PFAS. A population exposure model, for individuals drinking water from the investigated sources, showed that only 0.5 % of the population was receiving PFAS concentrations above the Danish limit of 2 ng/L.

Simultaneous removal of fluoride and arsenic from drinking groundwater using limestones from Bajío Guanajuatense, Mexico

Numerous groundwater wells in Mexico exceed the maximum allowable fluoride (F−) and arsenic (As) drinking water concentration requirements, posing an environmental and health risk to the population that relies solely on these wells for drinking water sources. Since encouraging results have been obtained utilizing native limestones to remove some toxic elements from contaminated water, the ability of the limestone rock outcrop to the south of the Sierra de Guanajuato in Mexico to remove As and F− from groundwater was assessed. A sampling campaign was conducted in the study area, focusing on wells exhibiting elevated concentrations of arsenic (As) and fluoride (F−) in compliance with international standards. This water was employed in the treatment experiment involving limestone rocks. The rock sampling process involved a reconnaissance campaign covering the study area and outcrop points of limestone rocks. Representative limestone samples were collected and subsequently subjected to mineralogical and geochemical characterization. Using rock samples, synthetic water, and groundwater from contaminated wells in the region, batch experiments were conducted to evaluate the As and F− removal capacity of limestone. The batch testing consisted of water–rock interactions at various times with different samples of limestone rocks, grain sizes, and water containing distinct concentrations of both elements, artificial and groundwater extracted close to the limestones outcrop. The results indicate that the rock with the highest calcium carbonate (CaCO3) content and the smallest grain size (< 0.05 mm) removes the highest concentrations of both As and F−, with As removal being superior. The removal mechanisms were studied using scanning electron microscopy with energy-dispersive spectroscopy (SEM–EDS) images, saturation index calculations, and Eh–pH diagrams,. Fluoride precipitation was favored when the pH of the solution was slightly acidic, whereas sorption was favored when the pH was higher. The results obtained are encouraging for the removal of high levels of As, and to a lesser extent for F−; consequently, the use of regional limestone rocks could be a viable option for improving the water quality ingested by rural inhabitants in the study area. Calcium carbonate (CaCO3) concentration can be used to identify limestone rocks with the potential to effectively remove As and F− in other locations.

Determination of radon concentration in bottled drinking water of Dhaka City

ABSTRACT Among all natural radiation sources, exposure to radon (222Rn) is considered as the most hazardous to human health. Recognizing the significance of water in preserving a healthy life style, assessing the 222Rn activity in drinking water is crucial. The 222Rn activity concentration was measured in 20 different branded bottled drinking waters purchased from Dhaka city using both alpha and gamma-ray spectrometry systems. Activity concentrations of 222Rn in bottled water obtained via RAD7 detector varied from 0.1 ± 0.02 Bq/L to 0.42 ± 0.01 Bq/L with an average value of 0.26 ± 0.02, while the value varied from 0.12 ± 0.01 Bq/L to 0.52 ± 0.31 Bq/L with an average value of 0.29 ± 0.09 by HPGe detector. The obtained results show lower concentrations when compared with other studies around the world as well as the US-EPA reference level of 11.1 Bq l−1 or 300 pCi l−1. The total annual effective dose calculated for different age groups and internal organ doses were found below the action level recommended by WHO (0.1 mSv y−1) and ICRP (3–10 mSv y−1), due to 222Rn, 3H and 40K in drinking water. Based on the obtained radon concentration and concomitant dose values, this study suggested negligible health hazards due to the consumption of bottled drinking water in Bangladesh. The results of this study could serve as a reference data for future studies in the area and beyond.

Efficient detection of Sn2+ by 4-aminobenzenesulfonamide based Schiff base chemosensor

A novel Schiff base colorimetric and fluorometric chemosensor N-((E)-2-hydroxy-3-methoxybenzylidene)-4-(((Z)-2-hydroxy-3-methoxybenzylidene)amino)benzenesulfonamide (SOV), has been designed, synthesized and characterized by using spectroscopic techniques. The chemosensor SOV showed selective and sensitive colorimetric sensing ability for Sn2+ metal ion in THF: H2O (9:1, v/v) solvent mixture exhibited colorless to light yellow changes. When Sn2+ ion was added, it showed a considerable fluorescence enhancement, because photoinduced electron transfer (PET) has been blocked. More importantly that spectroscopic studies showed SOV to be a fast-responding, low detection limit (3.034 × 10−9M), which are much lower than the WHO-approved drinking water concentration and a good binding constant (2.81 × 103M−1). Furthermore, it was discovered that the EDTA in chemosensor SOV made it to function as a reversible fluorescence probe towards the Sn2+ ions. A metal coordination, PET, as well as an internal charge transfer (ICT) process might be interpreted as the detecting mechanism based on physicochemical and analytical techniques such as 1H NMR spectra, FT-IR, Elemental analysis, ESI-mass spectrometry, Job’s plot, and DFT studies. Fluorescence imaging experiments of Sn2+ in living MCF 7 cells demonstrated its value of practical applications in biological systems.

Prediction of human health risk and disability-adjusted life years induced by heavy metals exposure through drinking water in Fars Province, Iran

Exposure to heavy metals in contaminated drinking water is strongly correlated with various cancers, highlighting the burden of disease. This study aimed to assess the non-carcinogenic and carcinogenic risks associated with exposure to heavy metals (As, Pb, Cd, and Cr) in drinking water of Fars province and evaluate the attributed burden of disease. Non-carcinogenic risk assessment was performed using the hazard quotient (HQ) method, while the carcinogenic risk assessment utilized the excess lifetime cancer risk approach. The burden of disease was evaluated in terms of years of life lost, years lived with disability, and disability-adjusted life years (DALY) for three specific cancers: skin, lung, and kidney cancer. The average drinking water concentrations of arsenic (As), cadmium (Cd), chromium (Cr) and lead (Pb) were determined to be 0.72, 0.4, 1.10 and 0.72 μg/L, respectively. The total average HQ of heavy metals in drinking water in the study area were 0.127, 0.0047, 0.0009 and 0.0069, respectively. The average ILCRs of heavy metal in the entire country were in the following order: 1.15 × 10−5 for As, 2.22 × 10−7 for Cd and 3.41 × 10−7 for Cr. The results also indicated that among the various counties analyzed, Fasa experiences the greatest burden of disease in terms of DALYs, with a value of 87.56, specifically attributed to cancers caused by exposure to arsenic. Generally, it can be said that the burden of disease is a critical aspect of public health that requires comprehensive understanding and effective intervention.

Prenatal exposure to nitrosatable drugs and timing of puberty in sons and daughters: A nationwide cohort study.

N-nitroso compounds (NOCs) can be formed by endogenous reactions between nitrosatable drugs and nitrite. Animal studies have found that several NOCs are teratogenic, and epidemiological studies report associations between prenatal exposure to nitrosatable drugs and adverse birth outcomes. It is unknown whether prenatal exposure to nitrosatable drugs is harmful to the child's reproductive health, including pubertal development. We investigated whether prenatal exposure to nitrosatable drugs was associated with timing of puberty and whether nitrate, nitrite and antioxidant intake modified any association. The population-based Danish National Birth Cohort (DNBC) Puberty Cohort, which includes 15,819 children, was used to investigate the association between prenatal exposure to nitrosatable drugs and timing of puberty. Around gestational week 11 and gestational week 18, mothers provided information about drug use during pregnancy. The children's self-reported information on onset of pubertal milestones was collected every six months from 11 years of age and throughout puberty. To investigate potential effect modification by nitrite, nitrate and antioxidant intake, information on these factors was obtained from a food frequency questionnaire completed by the mothers in gestational week 25, and information on nitrate concentration in maternal drinking water at her residential address was obtained from monitoring data from public waterworks. Data were analysed using a multivariable regression model for interval-censored data estimating difference in months in timing of puberty between exposure groups. A total of 2,715 children were prenatally exposed to nitrosatable drugs. We did not find an association between prenatal exposure to nitrosatable drugs and timing of puberty. This finding was supported by null-findings in the following sub-analyses investigating: 1. subtypes of nitrosatable drugs (secondary and tertiary amines and amides), 2. dose-dependency (duration of drug intake), 3. effect modification by maternal intake of nitrate, nitrite, and antioxidants. 4. confounding by indication. Prenatal exposure to nitrosatable drugs was not associated with timing of puberty. Nitrosatable drugs are commonly used drugs in pregnancy, and further research is needed to allow firm conclusions on the potential effect of prenatal exposure to nitrosatable drugs on the child's reproductive health.

Removal of disinfection byproducts through integrated adsorption and reductive degradation in a membrane-less electrochemical system

Proper control/removal of disinfection byproducts (DBPs) is important to drinking water safety and human health. In this study, a membrane-less electrochemical system was developed and investigated to remove DPBs through integrated adsorption and reduction by granular activated carbon (GAC)-based cathode. Representative DPBs including trihalomethanes and haloacetonitriles at drinking water concentrations were used for removal experiments. The proposed system achieved >70% removal of most DBPs in a batch mode. The comparison with control tests under either open circuit or hydrolysis demonstrated the advantages of electrochemical treatment, which not only realized higher DPBs removal but also extended GAC cathode lifetime. Such advantages were further demonstrated with continuous treatment. High dechlorination and debromination efficiencies were obtained in both batch (82.2 and 94.3%) and continuous (79.3 and 87.6%) reactors. DBPs removal was mainly contributed by the electrochemical reduction and adsorption by the GAC-based cathode, while anode showed little oxidizing effect on DBPs and halide ions. Dehalogenated products of chloroform and dichloroacetonitrile were identified with toxicity reduction. The energy consumption of the continuously operated system was estimated to be 0.28 to 0.16 kWh m−3. The proposed system has potential applications for wastewater reuse or further purification of drinking water.

Tritium concentration in bottled drinking water and internal dose assessment

Tritium concentration in bottled drinking water and internal dose assessment

Nanoprecipitated CoPi enhanced photoelectrochemical water oxidation toward sensitive and selective Co2+ detection

The detection of heavy metal ions Co2+ is of great significance to the environment and human health. Herein, a simple, highly selective and sensitive photoelectrochemical detection strategy for Co2+ was developed based on the enhanced activity by nanoprecipitated CoPi on the Au nanoparticle decorated BiVO4 electrode. The new photoelectrochemical sensor has a low detection limit of 0.03 μΜ and wide detection range of 0.1–10, and 10–6000 μΜ, with a high selectivity over other metal ions. The Co2+ concentration in tap water and commercial drinking water has also been successfully determined with the proposed method. Scanning electrochemical microscopy technique was employed to characterize the photocatalytic performance and heterogenous electron transfer rate of electrodes in situ, further revealing the photoelectrochemical sensing mechanism. Besides determining Co2+ concentration, this approach of enhanced catalytic activity by nanoprecipitation can be further extended to develop a variety of electrochemical, photoelectrochemical and optical sensing platforms for many other hazardous ions and biological molecules.

A comparative study of underground water arsenic contamination and suffering of people in Flood Plain with Deltaic reason of Bangladesh

The people were drinking arsenic-contaminated underground water in Bangladesh. We had analyzed 33,092 hand tube-well water samples, collected from all four geomorphological areas (i.e., from all 64 districts) in Bangladesh and found arsenic in 60 districts that were above the WHO recommended value in drinking water (10 μg/L) and in 50 districts that were above maximum permissible limit, 50 μg/L. In this paper, I have reported the magnitude of arsenic contamination in the tubewell water samples that were collected from two districts of Bangladesh, one from Flood Plain, named Chandpur, and another one from Deltaic region, named Madaripur. It describes the analytical report of arsenic concentrations in underground drinking water and biological samples, and people suffering from arsenic toxicity in these two districts. In the Madaripur district, 19.62% of the total tubewell water samples (n=2,309) contained arsenic concentrations that were below WHO recommended value (10 μg/L) and safe to drink, and 80.38% and 59.59% of the tubewells contained levels arsenic that were above 10 μg/L and 50 μg/L, respectively. In Chandpur district (n=1,165 tubewell water samples), these values are 4.12, 95.88, and 92.79%, respectively. Of the samples in Madaripur, the percentage of water samples with arsenic are 26.94, 12.68, 3.29. 0.91, and 0.22% in the ranges 100-299, 300-499, 500-699, 700-1,000, and above 1,000 μg As/L, respectively. In Chandpur district, these values are 57.86, 25.15, 4.81, 1.80, and 0.43%, respectively.

Azithromycin induces read-through of the nonsense Apc allele and prevents intestinal tumorigenesis in C3B6F1 ApcMin/+ mice

Therapeutic strategies that promote read-through of a mutant gene have proved effective for certain non-neoplastic diseases. However, the efficacy of this approach is unproven regarding neoplastic diseases with germline nonsense mutations, including familial adenomatous polyposis. Here we examined the cancer-preventive efficacy of the macrolide antibiotic azithromycin, with a reported read-through effect, on intestinal tumorigenesis in C3B6F1 ApcMin/+ mice harboring a nonsense Apc mutation resulting in a truncated Apc protein. Mice were given drinking water lacking azithromycin or containing 0.0125–0.2 mg/mL azithromycin from 3 weeks of age. The small intestine and cecum were analyzed for pathological changes and alterations of intestinal flora. Azithromycin suppressed the number of tumors and the proportion of adenocarcinomas, with the most effective drinking-water concentration being 0.0125 mg/mL. Furthermore, azithromycin recovered the cellular level of full-length Apc, resulting in downregulation of β-catenin and cyclin D1. Conversely, the effect of azithromycin on the diversity of the intestinal microbiota depended on the drinking-water concentration. These results suggest that the balance between azithromycin-mediate read-through of mutant Apc mRNA and antibacterial effects influences intestinal tumorigenesis. Thus, azithromycin is a potential anticancer agent for familial adenomatous polyposis patients harboring nonsense mutations.

Estimation of Serum PFOA Concentrations from Drinking and Non-Drinking Water Exposures.

Estimation of Serum PFOA Concentrations from Drinking and Non-Drinking Water Exposures.

Spatio-temporal trends in livestock exposure to per- and polyfluoroalkyl substances (PFAS) inform risk assessment and management measures

The migration of per- and polyfluoroalkyl substances (PFAS) onto agricultural properties has resulted in the accumulation of PFAS in livestock. The environmental determinants of PFAS accumulation in livestock from the grazing environment are poorly understood, resulting in limited capacity to manage livestock exposure and subsequent transfer of PFAS through the food chain. Analytical- (n = 978 samples of soil, water, pasture, and serum matrices), farm management/practice- and livestock physiology data were collated and interrogated from environmental PFAS investigations across ten farms, from four agro-ecological regions of Victoria (Australia). Statistical analysis identified perfluorooctane sulfonate (PFOS) and perfluorohexane sulfonate (PFHxS) as key analytes of concern for livestock bioaccumulation. PFOS and PFHxS concentrations in livestock drinking water were positively correlated with serum concentrations while other intake pathways (pasture and soil) had weaker correlations. Seasonal trends in PFAS body burden (serum concentrations) were identified and suggested to be linked to seasonal grazing behaviours and physiological water requirements. The data showed for the first time that livestock exposure to PFAS is dynamic and with relatively short elimination half-lives, there is opportunity for exposure management. Meat from cattle, grazed on PFAS impacted sites, may exceed health-based guideline values for PFAS, especially for markets with low limits (like the European Commission Maximum Limits or EC MLs). This study found that sites with mean livestock drinking water concentrations as low as 0.003 μg PFOS/L may exceed the EC ML for PFOS in cattle meat. Risk assessment can be used to prioritise site cleanup and development of management plans to reduce PFAS body burden by considering timing of stock rotation and/or supplementation of primary exposure sources.

Toxicity Studies of Sodium Metavanadate and Vanadyl Sulfate Administered in Drinking Water to Sprague Dawley (Hsd:Sprague Dawley SD) Rats and B6C3F1/N Mice.

Oral human exposure to vanadium may occur due to its presence in food and drinking water and its use in dietary supplements. The most prevalent oxidation states of vanadium in food and drinking water have been characterized as tetravalent and pentavalent. Vanadyl sulfate and sodium metavanadate were selected as representative tetravalent (V4+) and pentavalent (V5+) test articles for these studies, respectively. To assess the potential for oral toxicity of vanadium compounds with differing oxidation states under similar test conditions, the 3-month National Toxicology Program (NTP) toxicity studies of sodium metavanadate and vanadyl sulfate in male and female Sprague Dawley (Hsd:Sprague Dawley SD) rats (including perinatal exposure) and in B6C3F1/N mice. Drinking water concentrations for sodium metavanadate (0, 31.3, 62.5, 125, 250, and 500 mg/L) and vanadyl sulfate (0, 21.0, 41.9, 83.8, 168, and 335 mg/L) were selected on the basis of previously published 14-day drinking water studies conducted as part of the NTP vanadium research program. (Abstract Abridged).

Estimating historical exposure to perfluoroalkyl acids in Security, Fountain, and Widefield Colorado: use of water-infrastructure blending and toxicokinetic models.

Drinking water can be a major source of poly- and perfluoroalkyl substance (PFAS) exposure for humans. The lack of historic data on PFAS drinking-water concentrations and consumption patterns are a limiting factor for developing estimates of past exposure. Here, in contribution to a community-scale PFAS health effects study near fire training facilities that contaminated a local aquifer with PFASs, we present a novel water-infrastructure, mass-balance mixing model coupled to a non-steady state, single-compartment toxicokinetic model that used Monte Carlo simulations to estimate the start of PFAS exposure in drinking water for individuals within three PFAS-impacted communities in El Paso County, Colorado. Our modeling focused on perfluorohexane sulfonic acid (PFHxS) because median serum PFHxS concentrations in a sample of local residents (n = 213) were twelve times the median observed in the U.S. National Health and Nutrition Examination Survey (2015-2016). Modeling results for study participants were grouped according to their community of residence, revealing a median start of exposure for the town of Fountain of 1998 (25-75% interquartile range [IQR], 1992 to 2010), 2006 (IQR 1995 to 2012) for Security, and 2009 (IQR 1996-2012) for Widefield. Based on the towns' locations relative to an identified hydraulically upgradient PFAS source, the modeled exposure sequencing does not completely align with this conceptual flow model, implying the presence of an additional PFAS source for the groundwater between Widefield and Fountain.

Iodine Concentration in Brazilian Drinking Water and Its Possible Contribution to Iodine Intake for Different Physiological Groups.

The objective is to analyze the concentration of iodine in Brazilian drinking water and its possible contribution to iodine intake for different groups. Water samples collected from primary healthcare units in eight locations distributed across all five macroregions of Brazil were analyzed. The quantification of iodine in the water samples was done by spectrophotometry (leuco crystal violet method). To classify the degree of iodine concentration, the recommendation of the Ministry of Health (China) was followed since Brazil lacks a classification standard. To verify the possible contribution of drinking water to iodine intake for different groups, the recommended water intake for each group according to the United States Institute of Medicine (2004) was considered. The percentage of iodine in drinking water and its contribution to iodine intake for different physiological groups were calculated based on the estimated average requirement (EAR) of iodine. A descriptive statistical analysis was performed using SPSS version 21.0 and Statistical Analysis Systems (SAS) version 9.2. Significant differences were found between the maximum and minimum concentrations of iodine in water samples from the same location. In Pinhais (south region), the difference was 44.32 μg· L-1; in Viçosa (southeast region), it was 27.86 μg·L-1; in Rondonópolis (midwest region), it was 12.66 μg·L-1; in São Luís (northeast region), it was 11.82 μg·L-1; in Brasilian Federal District (midwest region), it was 10.98 μg·L-1; in Macaé (southeast region), it was 10.14 μg· L-1; in Palmas (north region), it was 4.22 μg·L-1; and in Vitória (southeast region), it was 1.69 μg·L-1. The maximum concentrations of iodine found in the drinking water of Pinhais and Viçosa can contribute more than 70.0% and 50.0%, respectively, to daily iodine intake for all groups. Monitoring the concentration of iodine in drinking water from different locations in each city or Federal District is a preventive measure against inadequate iodine intake and possible adverse changes in population health.

Glyphosate-based herbicide (GBH) causes damage in embryo-larval stages of zebrafish (Danio rerio)

Glyphosate-Based Herbicides (GBH) show risks to the environment and also to aquatic organisms, such as fish. The present work aimed to evaluate the effects of GBH and Pure Glyphosate (PG) exposure on Danio rerio embryos at drinking water concentrations. Zebrafish embryos were exposed to 250, 500, and 1000 μg L−1 of Roundup Original DI® and pure glyphosate for 96 h. Glyphosate concentration in water, parameters physicochemical water, survival, hatching rate, heart rate, malformations, behavior, and biomarkers were evaluated. We verified that at 6 h post-fertilization (hpf), animals exposed to GBH 500 showed decreased survival as compared to the control. The hatching rate increased in all groups exposed to GBH at 48 hpf as compared to the control group. The embryos exposed did not present changes in the spontaneous movement and touch response. Exposed groups to GBH demonstrated a higher number of malformations in fish embryos as compared to the control. Most malformations were: pericardial edema, yolk sac edema, body malformations, and curvature of the spine. In heart rate, bradycardia occurred in groups exposed, as predicted due to cardiac abnormalities. As biochemical endpoints, we observed a decrease in Glutathione S-transferase (GBH 250, GBH 500 and PG 250) and Acetylcholinesterase (GBH 250 and PG 250) activity. No differences were found between the groups in the concentration of protein, Total Antioxidant Capacity Against Peroxyl Radicals, Lipid peroxidation, Reactive Oxygen Species, Non-protein thiols, and Catalase. In conclusion, the damage in all evaluated stages of development was aggravated by survival and malformations. Therefore, the large-scale use of GBHs, coupled with the permissiveness of its presence could be the cause damage to the aquatic environment affecting the embryonic development of non-target organisms.

Nationwide geospatial analysis of county racial and ethnic composition and public drinking water arsenic and uranium

There is no safe level of exposure to inorganic arsenic or uranium, yet recent studies identified sociodemographic and regional inequalities in concentrations of these frequently detected contaminants in public water systems across the US. We analyze the county-level association between racial/ethnic composition and public water arsenic and uranium concentrations from 2000–2011 using geospatial models. We find that higher proportions of Hispanic/Latino and American Indian/Alaskan Native residents are associated with significantly higher arsenic and uranium concentrations. These associations differ in magnitude and direction across regions; higher proportions of non-Hispanic Black residents are associated with higher arsenic and uranium in regions where concentrations of these contaminants are high. The findings from this nationwide geospatial analysis identifying racial/ethnic inequalities in arsenic and uranium concentrations in public drinking water across the US can advance environmental justice initiatives by informing regulatory action and financial and technical support to protect communities of color.

Bayesian Estimation of Human Population Toxicokinetics of PFOA, PFOS, PFHxS, and PFNA from Studies of Contaminated Drinking Water.

Setting health-protective standards for poly- and perfluoroalkyl substances (PFAS) exposure requires estimates of their population toxicokinetics, but existing studies have reported widely varying PFAS half-lives (T½) and volumes of distribution (Vd). We combined data from multiple studies to develop harmonized estimates of T½ and Vd, along with their interindividual variability, for four PFAS commonly found in drinking water: perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), perfluorononanoic acid (PFNA), and perfluorohexane sulfonate (PFHxS). We identified published data on PFAS concentrations in human serum with corresponding drinking water measurements, separated into training and testing data sets. We fit training data sets to a one-compartment model incorporating interindividual variability, time-dependent drinking water concentrations, and background exposures. Use of a hierarchical Bayesian approach allowed us to incorporate informative priors at the population level, as well as at the study level. We compared posterior predictions to testing data sets to evaluate model performance. Posterior median (95% CI) estimates of T½ (in years) for the population geometric mean were 3.14 (2.69, 3.73) for PFOA, 3.36 (2.52, 4.42) for PFOS, 2.35 (1.65, 3.16) for PFNA, and 8.30 (5.38, 13.5) for PFHxS, all of which were within the range of previously published values. The extensive individual-level data for PFOA allowed accurate estimation of population variability, with a population geometric standard deviation of 1.57 (95% CI: 1.42, 1.73); data from other PFAS were also consistent with this degree of population variability. Vd estimates ranged from 0.19 to across the four PFAS, which tended to be slightly higher than previously published estimates. These results have direct application in both risk assessment (quantitative interspecies extrapolation and uncertainty factors for interindividual variability) and risk communication (interpretation of monitoring data). In addition, this study provides a rigorous methodology for further refinement with additional data, as well as application to other PFAS. https://doi.org/10.1289/EHP10103.