Fact-checked by Grok 2 weeks ago

Chronic toxicity

Chronic toxicity refers to the adverse effects resulting from repeated or prolonged exposure to a substance over an extended period, often at relatively low doses that do not produce immediate symptoms. These effects can impact human health or ecological systems, involving cumulative damage to organs, tissues, or populations, and may manifest months or years after initial exposure, contrasting sharply with acute toxicity, which arises from a single high-dose or short-term exposure causing rapid onset of symptoms.^[1]^[2]^[3] In toxicology, chronic toxicity is evaluated through long-term studies in mammalian species, such as rodents, lasting a significant portion of the animal's lifespan—often 12 months or more—and in non-mammalian organisms like fish and invertebrates, to identify sublethal outcomes like reduced growth, reproductive impairment, histopathological changes, behavioral alterations, and increased cancer risk.^[4]^[5] Such studies are essential for establishing safe exposure guidelines, including the reference dose (RfD) for human health, calculated by dividing the no-observed-adverse-effect level (NOAEL) from chronic data by uncertainty factors to account for interspecies and intraspecies variability, as well as predicted no-effect concentration (PNEC) for environmental protection.^[6]^[7] Chronic toxicity poses risks in occupational, environmental, and consumer settings for humans, and in ecosystems through ongoing low-level exposures to chemicals, heavy metals, or pollutants, potentially leading to irreversible conditions. Notable examples include long-term arsenic exposure causing skin, lung, and bladder cancers, as well as liver and kidney damage in humans, chronic cadmium inhalation linked to emphysema, chronic obstructive pulmonary disease, and renal dysfunction, and effects on aquatic organisms such as reduced reproduction in fish from endocrine-disrupting chemicals.^[8]^[9]^[10]^[11] Regulatory frameworks, such as those from the EPA, OSHA, and international bodies like the OECD, use chronic toxicity data to classify substances under categories like Specific Target Organ Toxicity—Repeated Exposure (STOT-RE) and to derive environmental quality standards, guiding hazard communication, permissible exposure limits, and ecological risk assessments.^[2]^[12]

Core Concepts

Definition

Chronic toxicity is defined as the adverse health effects that occur in living organisms due to prolonged or repeated exposure to low concentrations of a toxic substance, with symptoms developing gradually over an extended period, typically spanning weeks, months, or even the organism's lifetime.^[13]^[14] Unlike acute toxicity, which manifests rapidly following high-dose, short-term exposure, chronic toxicity arises from sublethal doses that accumulate over time, often targeting multiple physiological systems.^[3] Key characteristics of chronic toxicity include the progressive accumulation of damage, leading to subtle yet persistent alterations in biological functions, such as impaired organ performance and systemic dysfunction.^[15] These effects commonly encompass disruptions in reproductive and developmental processes, where low-level exposures can compromise fertility, fetal growth, or offspring viability.^[16] Additionally, chronic exposure may induce behavioral modifications, including changes in locomotion, response to stimuli, or social interactions, serving as early indicators of neurotoxicity.^[17] The concept of chronic toxicity was formalized in the mid-20th century amid growing concerns in toxicology, particularly through post-World War II investigations into synthetic pesticides like DDT, which highlighted long-term ecological and human health risks from persistent environmental contaminants.^[18] This era marked a shift from acute poisoning studies to evaluating cumulative, delayed-onset effects, driven by observations of widespread pesticide residues in food chains and wildlife.^[19] Representative chronic endpoints include carcinogenicity, where prolonged exposure promotes tumor formation; mutagenicity, involving DNA alterations that may be heritable; teratogenicity, resulting in structural birth defects; and endocrine disruption, which interferes with hormone regulation and can lead to metabolic or reproductive disorders.^[20]^[21] These outcomes underscore the importance of chronic toxicity assessments in regulatory frameworks for chemical safety.^[22]

Distinction from Acute Toxicity

Acute toxicity refers to adverse effects resulting from a single high-dose exposure to a substance, with rapid onset typically occurring within hours to days and often manifesting as lethality or severe impairment.^[13] A common metric for assessing acute toxicity is the LD50, or median lethal dose, which quantifies the dose required to kill 50% of a test population in a short observation period, usually 24 to 96 hours.^[23] These effects are evaluated through short-term tests focusing on endpoints like mortality or immobility at relatively high concentrations.^[3] In contrast, chronic toxicity arises from prolonged or repeated low-level exposures, typically over weeks to months or a significant portion of the organism's lifespan, leading to sublethal effects such as growth inhibition, reproductive impairment, or developmental abnormalities rather than immediate death.^[24] While acute exposures last less than 96 hours and do not span a substantial part of the organism's life, chronic exposures extend through critical life stages, like full life cycles in aquatic organisms, using subthreshold doses that accumulate over time.^[13]^[3] Dose-response relationships further highlight these differences: acute toxicity curves are often steep and sigmoidal, reflecting rapid, high-dose responses with minimal thresholds for lethal outcomes, whereas chronic curves exhibit more gradual slopes, clear thresholds, and no-observed-adverse-effect concentrations (NOAEC) due to adaptive responses and cumulative low-dose impacts.^[25] Regulatory frameworks, such as those from the U.S. Environmental Protection Agency (EPA), recognize chronic effects as occurring at concentrations generally below 10% of acute lethal levels, informing extrapolation via acute-to-chronic ratios (ACRs) that account for this disparity in sensitivity.^[26]

Mechanisms of Chronic Effects

Chronic toxicity arises from prolonged, low-level exposure to toxicants, where bioaccumulation and biomagnification play central roles in amplifying harm over time. Bioaccumulation occurs when organisms absorb toxins faster than they eliminate them, leading to buildup in tissues such as fat, liver, and gonads; for instance, per- and polyfluoroalkyl substances (PFAS) like PFOS exhibit high bioconcentration factors (BCF > 2000 L/kg) in aquatic species, resulting in persistent internal doses that disrupt physiological functions.^[27] Biomagnification further exacerbates this by increasing toxin concentrations up the food chain, with biomagnification factors (BMF) exceeding 1 for long-chain PFAS in ecosystems like Antarctic food webs, where predators accumulate levels 3–10 times higher than prey, culminating in chronic effects such as reproductive impairment and developmental anomalies.^[27] Heavy metals like mercury exemplify this process, accumulating in fish muscle and biomagnifying in piscivorous birds and mammals, leading to neurological deficits from sustained exposure.^[28] At the cellular and molecular levels, chronic toxicity induces a cascade of disruptions beginning with oxidative stress, where reactive oxygen species (ROS) generated from toxin metabolism overwhelm antioxidant defenses, damaging lipids, proteins, and nucleic acids.^[29] This oxidative damage manifests as DNA lesions, such as 8-oxo-2′-deoxyguanosine (8-oxodG), which promotes mutagenesis through base mispairing (e.g., G:C to T:A transversions) and genomic instability, a hallmark of long-term carcinogenesis and neurodegeneration.^[29] Enzyme inhibition compounds these effects; for example, toxins can impair base excision repair (BER) enzymes like OGG1, reducing the removal of oxidized bases and perpetuating cellular dysfunction.^[29] Epigenetic alterations, including global DNA hypomethylation and histone modifications, arise from ROS interference with enzymes like TET proteins, which regulate DNA demethylation; this leads to aberrant gene expression, accelerated cellular senescence, and heightened susceptibility to age-related diseases like Alzheimer's.^[30] Organ-specific effects emerge from the targeted accumulation and metabolism of toxins in vulnerable tissues during chronic exposure. Hepatotoxicity, common in the liver due to its role in detoxification, involves persistent inflammation and steatosis from toxins like acetaminophen or industrial solvents overwhelming metabolic pathways, progressing to fibrosis and cirrhosis over months to years.^[31] Neurotoxicity targets the nervous system, where accumulated metals such as manganese or aluminum induce mitochondrial dysfunction and ROS-mediated neuronal damage, resulting in dopaminergic neuron loss and symptoms akin to Parkinson's disease.^[32] In both cases, these effects stem from disrupted neurotransmitter regulation and protein aggregation, underscoring the tissue-specific vulnerabilities amplified by bioaccumulation.^[33] At the population level, chronic toxicity manifests through sublethal impairments that alter demographic rates and ecosystem dynamics. Reduced fecundity, such as a 10% reduction in reproductive parameters from chronic toxicant exposure, lowers population growth rates (λ) in species like Chinook salmon, shifting stable age distributions and increasing extinction risk under environmental stressors.^[34] These individual-level effects propagate to communities, where toxin-induced immune suppression and growth inhibition in key species disrupt trophic interactions, leading to altered biodiversity and simplified ecosystem structures, as observed in aquatic systems contaminated by persistent pollutants.^[34]

Testing Protocols

General Testing Approaches

Chronic toxicity testing employs both in vivo and in vitro approaches to evaluate the long-term effects of substances on biological systems. In vivo testing utilizes whole organisms, such as rodents subjected to lifetime or near-lifetime exposures, to assess systemic impacts including organ function and overall health under realistic physiological conditions.^[35] In contrast, in vitro testing relies on cell-based assays or isolated tissues for initial screening, offering rapid identification of potential hazards like cytotoxicity or genotoxicity without involving live animals, though it may not fully capture organism-level interactions.^[36] These methods complement each other, with in vitro serving as a preliminary filter to prioritize compounds for more resource-intensive in vivo studies.^[37] Exposure regimes in chronic toxicity assessments typically involve prolonged, low-dose administrations to mimic environmental or occupational scenarios, contrasting with acute high-dose exposures. Continuous exposure maintains steady substance levels, often through daily oral gavage, diet, or inhalation in mammalian models, while pulsed or intermittent regimes simulate variable real-world contact, such as periodic dermal applications.^[38] Test durations vary by organism and regulatory guidelines: for rodents, exposures often span 12 months or 70-90% of the lifespan to detect cumulative effects, whereas shorter protocols, like 21 days for certain invertebrates, focus on key life stages such as growth and maturation.^[1] Full life-cycle tests, encompassing development from embryo to reproduction, provide comprehensive insights into generational impacts across species.^[39] Key endpoints in chronic toxicity evaluations include survival rates, growth metrics like body weight gain, and reproductive outcomes such as fecundity or offspring viability, which indicate sublethal effects over time.^[40] Histopathological examinations reveal tissue damage in organs like the liver or kidneys, while biochemical markers, including elevated enzyme levels (e.g., alanine aminotransferase for liver stress), signal early molecular disruptions.^[35] These measurements, collected periodically throughout the study, enable detection of delayed or progressive toxicities not evident in shorter assays.^[41] Ethical considerations in chronic toxicity testing adhere to the 3Rs principle—replacement, reduction, and refinement—introduced by Russell and Burch in 1959 to minimize animal suffering.^[42] Replacement promotes non-animal alternatives like in vitro models where feasible; reduction optimizes study designs to use fewer animals while maintaining statistical power; and refinement improves procedures to lessen pain, such as through humane endpoints that allow early termination of moribund subjects.^[43] This framework, now integral to international guidelines, balances scientific needs with welfare standards in long-term studies.^[44]

Aquatic-Specific Tests

Aquatic-specific tests for chronic toxicity evaluate the long-term effects of chemicals on key organisms in freshwater and marine environments, focusing on sublethal endpoints such as growth, reproduction, and development to assess ecological risks.^[45] These standardized protocols, developed by organizations like the OECD and EPA, target primary producers, invertebrates, and fish, which represent foundational trophic levels in aquatic ecosystems.^[46] Unlike general approaches, these tests incorporate water quality parameters like pH, temperature, and dissolved oxygen to mimic natural conditions, ensuring relevance to environmental exposure scenarios.^[47] For primary producers, the OECD Test No. 201 (Freshwater Alga and Cyanobacteria, Growth Inhibition Test) is widely used to measure chronic effects on algal populations.^[45] This 72-hour assay exposes unicellular algae, such as Pseudokirchneriella subcapitata, to the test substance under static or semi-static conditions, quantifying inhibition of growth rate and biomass yield over multiple cell divisions, which serves as a proxy for chronic population-level impacts.^[48] The test is particularly valuable for detecting effects on photosynthesis and cell proliferation in poorly soluble or volatile compounds.^[49] Invertebrate tests emphasize reproduction and survival, with the OECD Test No. 211 (Daphnia magna Reproduction Test) as a core method.^[50] Young female Daphnia magna (≤24 hours old) are exposed for 21 days in semi-static or flow-through systems, monitoring the number of living offspring produced, parent survival, and body length to identify reproductive impairments.^[51] Similarly, the EPA OPPTS 850.1300 (Daphnid Chronic Toxicity Test) uses Daphnia magna or D. pulex over 21 days, assessing immobilization, fecundity, and optional growth metrics to evaluate hazard potential.^[46] Fish early-life stage tests address developmental and growth effects, exemplified by OECD Test No. 210.^[52] Embryos and larvae of species like the fathead minnow (Pimephales promelas) or zebrafish (Danio rerio) are continuously exposed from fertilization until 28-90 days post-hatch (species-dependent) in flow-through or semi-static setups, with endpoints including hatching success, survival, larval growth (weight and length), and teratogenic abnormalities.^[47] The EPA OCSPP 850.1400 mirrors this, applying 28-90 day exposures to early stages of fish like rainbow trout (Oncorhynchus mykiss) to detect sublethal chronic impacts.^[53] Exposure systems in these tests vary to maintain consistent chemical concentrations, with static systems suitable for stable, non-volatile substances where solutions are not renewed, and flow-through systems preferred for prolonged tests involving degradable or adsorbing compounds to ensure steady-state exposure.^[54] Flow-through designs, which continuously renew test media at rates of 3-12 volumes per day, minimize accumulation of metabolites or depletion of the test substance, enhancing the reliability of chronic effect measurements.^[55] For chemicals suspected of endocrine disruption, multi-generational tests extend beyond single-generation assessments to capture transgenerational effects. The OECD Test No. 240 (Medaka Extended One Generation Reproduction Test) and EPA OCSPP 890.2200 expose Japanese medaka (Oryzias latipes) from embryonic stages through the F1 generation (up to 12-16 weeks), evaluating reproduction, gonadal development, and offspring viability across parental (F0) and filial (F1) generations to detect hormonal interference.^[56]^[57] These protocols incorporate histopathology and steroid hormone analyses to link observed effects to endocrine pathways.^[58]

Data Interpretation

Statistical Endpoints (NOEC/LOEC)

In chronic toxicity assessments, statistical endpoints such as the No Observed Effect Concentration (NOEC) and Lowest Observed Effect Concentration (LOEC) provide threshold values for identifying concentrations at which adverse effects begin to appear in test organisms. The NOEC represents the highest tested concentration that shows no statistically significant adverse effect compared to the control group, typically determined using a significance level of p < 0.05.^[59] Conversely, the LOEC is the lowest tested concentration exhibiting a statistically significant adverse effect relative to the control.^[59] These endpoints are derived from data generated in standardized chronic exposure tests, focusing on sublethal responses rather than immediate lethality. The calculation of NOEC and LOEC relies on hypothesis testing to compare treatment groups against controls, often applied to endpoints such as reproduction rates, growth, or survival in organisms like Daphnia magna.^[60] Parametric approaches, including analysis of variance (ANOVA) followed by multiple comparison tests like Dunnett's procedure, assess differences assuming normality and homogeneity of variance.^[59] For trend detection in monotonic dose-response data, step-down procedures such as Williams' test are employed, sequentially evaluating concentrations from highest to lowest while adjusting for multiple comparisons to identify the NOEC.^[59] Simpler t-tests may be used for pairwise comparisons in cases with fewer concentrations, though they lack the power of trend-based methods for ordered data.^[3] Despite their utility, NOEC and LOEC determinations face limitations rooted in statistical and methodological assumptions. The selection of endpoints introduces subjectivity, as choices like reproduction rate over growth can influence outcomes based on the researcher's focus and test design.^[59] Additionally, parametric tests like ANOVA assume data normality and equal variances, which are frequently violated in ecotoxicity datasets due to biological variability, potentially leading to unreliable results without transformations or non-parametric alternatives.^[60]

Derived Toxicity Metrics (MATC/CV)

Derived toxicity metrics provide continuous estimates of safe chronic exposure levels by extrapolating from discrete statistical endpoints like the no observed effect concentration (NOEC) and lowest observed effect concentration (LOEC), enabling more precise application in regulatory contexts.^[61] The Maximum Acceptable Toxicant Concentration (MATC) represents the highest concentration of a substance that does not cause adverse effects on aquatic organisms over their full life cycle, serving as a key estimate for chronic safe levels in single-species tests. It is calculated as the geometric mean of the NOEC and LOEC from chronic toxicity bioassays, using the formula:

\text{MATC} = \sqrt{\text{NOEC} \times \text{LOEC}}

This approach, which bridges the gap between observed thresholds, was introduced by the U.S. Environmental Protection Agency (EPA) in the 1970s as part of early efforts to develop aquatic life criteria under the Clean Water Act, building on chronic bioassay data to protect sensitive life stages like reproduction and growth.^[61]^[62]^[63] The Chronic Value (CV), in contrast, addresses community-level protection by deriving a protective concentration from species sensitivity distributions (SSDs), which statistically model the variation in chronic toxicity across multiple species. In EPA methodologies, the CV is typically the 5th percentile (HC₅) of an SSD constructed from final chronic values (geometric means of NOEC and LOEC for each species), ensuring that only 5% of species are potentially affected and safeguarding ecosystem diversity.^[64] These metrics find practical application in environmental regulation, particularly for setting effluent discharge limits under the National Pollutant Discharge Elimination System (NPDES) and evaluating pesticide safety during registration. For instance, MATC values from standardized chronic tests on fish and invertebrates inform restrictions on pesticide use near water bodies, ensuring residues do not exceed levels harmful to non-target aquatic life over long-term exposures.^[65]

Risk Assessment Ratios (PEC/PNEC, ACR/AF)

In environmental risk assessment for chemicals, the Predicted Environmental Concentration (PEC) represents the estimated exposure level of a substance in a specific environmental compartment, such as surface water, derived from models incorporating emission sources, usage patterns, and dispersal processes like dilution in wastewater treatment or atmospheric deposition.^[66] For instance, PEC for surface water (PEC_SW) is often calculated using default parameters such as a penetration factor of 0.01 for human medicinal products and a dilution factor of 10 in receiving waters.^[66] The Predicted No-Effect Concentration (PNEC) is the threshold concentration below which adverse effects on populations or ecosystems are not expected, typically derived by dividing a chronic toxicity endpoint—such as the no-observed-effect concentration (NOEC) or EC10—from laboratory studies by an assessment factor (AF) to account for uncertainties like inter- and intraspecies variability. Under REACH guidelines, AF values for aquatic PNEC derivation from chronic data vary with data availability: an AF of 10 applies when chronic NOECs are available from at least three species representing different trophic levels (e.g., algae, Daphnia, and fish); an AF of 50 for two chronic NOECs from different trophic levels; and an AF of 100 for a single chronic NOEC from one species. These factors ensure extrapolation from controlled lab conditions to real-world ecosystems, with lower AFs (e.g., 1–5) possible for extensive, high-quality datasets covering multiple taxa.^[67] The risk characterization ratio, or risk quotient, is calculated as PEC divided by PNEC; a value less than 1 indicates negligible risk, while a value greater than or equal to 1 signals potential concern requiring further refinement or mitigation measures.^[66] This deterministic approach integrates modeled exposure with protective effect thresholds, often applied in regulatory frameworks like the EU's REACH for prioritizing substances in probabilistic assessments. When chronic toxicity data are limited, the Acute-to-Chronic Ratio (ACR) facilitates extrapolation by dividing a chronic NOEC by an acute toxicity measure like the LC50, yielding a factor typically ranging from 10 to 100 across industrial chemicals and pesticides.^[68] For example, median ACR values are approximately 9.9 for aquatic species, with the 90th percentile at 58.5, supporting an default ACR of 100 to protect over 90% of cases in risk assessments.^[68] Assessment factors (AFs) for data gaps, such as using acute data to estimate chronic PNEC, commonly apply a value of 100 for single-species acute tests, increasing to 1000 without any chronic information, thereby embedding ACR-like extrapolations into broader uncertainty adjustments.

Influencing Factors

Chemical Properties

Chemical properties of toxicants play a pivotal role in determining the extent and nature of chronic toxicity by influencing their environmental fate, exposure duration, and bioavailability to organisms. Persistence, defined as resistance to degradation, is a key factor; substances with a half-life exceeding 60 days in aquatic environments remain available for prolonged exposure, thereby elevating chronic risks compared to rapidly degrading compounds.^[69] For instance, persistent organic pollutants like polychlorinated biphenyls (PCBs) exhibit half-lives in sediment often surpassing 180 days, leading to sustained low-level exposures that accumulate over time.^[70] Bioaccumulation potential is strongly linked to lipophilicity, quantified by the octanol-water partition coefficient (log Kow). Compounds with log Kow values greater than 3 are considered lipophilic and prone to bioaccumulation in fatty tissues, increasing chronic toxicity risks through biomagnification in food chains.^[71] PCBs exemplify this, with log Kow ranging from 5.6 to 8.3, facilitating their uptake and retention in organisms and resulting in long-term health effects such as endocrine disruption.^[72] Speciation and reactivity further modulate chronic toxicity, particularly for metals, where the form of the ion dictates uptake efficiency. Free metal ions or labile complexes often exhibit higher bioavailability and toxicity than inert species, as they can cross biological membranes more readily; for example, free copper ions (Cu²⁺) in neutral pH waters exhibit high bioavailability and gill uptake in aquatic organisms during extended exposures, while formation of hydroxy complexes can reduce free ion concentrations and thereby lower toxicity.^[73]^[74] This speciation-dependent reactivity can prolong toxic effects by altering dissolution and interaction rates in chronic scenarios.^[75] Environmental pH influences solubility and ionization, thereby affecting bioavailability in chronic toxicity assessments. Ionized forms of weak acids or bases predominate at pH values distant from their pKa, reducing lipid solubility and membrane permeability, which can lower chronic uptake rates; conversely, at pH near pKa, the unionized fraction increases, potentially heightening long-term exposure risks for ionizable organics.^[76] For metals like cadmium, acidic conditions (pH <6) enhance solubility and free ion concentrations, amplifying bioavailability over chronic exposure periods.^[77]

Biological Variables

Biological variables play a critical role in determining the outcomes of chronic toxicity, as they influence how organisms respond to prolonged exposure to toxicants. Species sensitivity varies significantly across taxa due to differences in physiological and ecological traits. For instance, in chronic toxicity assessments of organic compounds, fish often exhibit greater vulnerability than certain invertebrates, with data indicating that fish are slightly more sensitive overall in chronic endpoints compared to invertebrates.^[78] This differential sensitivity arises from variations in toxicokinetic processes, such as uptake and elimination rates, and toxicodynamic responses, including receptor interactions and repair mechanisms.^[79] Life stage effects further modulate chronic toxicity, with juveniles typically showing heightened susceptibility owing to their elevated metabolic rates and immature physiological systems. Higher metabolic demands in early life stages increase the rate of toxicant absorption and distribution, while underdeveloped detoxification organs, such as the liver and kidneys, limit the capacity for biotransformation and excretion. For example, in aquatic organisms, fish larvae display reduced tolerance to metals and organics due to incomplete gill development and lower levels of protective enzymes like cytochrome P450, making prolonged exposures more detrimental during these phases.^[80] This stage-specific vulnerability underscores the importance of using early life stage tests in chronic toxicity evaluations to capture sensitive periods.^[60] Genetic variability introduces additional complexity, particularly through polymorphisms in genes encoding detoxification enzymes such as the cytochrome P450 (CYP450) family. These genetic variations can alter enzyme activity, affecting the metabolism of environmental toxicants and leading to interindividual differences in chronic toxicity outcomes. For instance, polymorphisms in CYP1A1 and CYP2D6 have been linked to increased risk of pathological conditions, including endocrine disruption and neurological disorders, under chronic exposure to organochlorine pesticides, as variant alleles impair xenobiotic breakdown via the aryl hydrocarbon receptor pathway.^[81] Such genetic factors highlight the need for considering population-level diversity in toxicity assessments to avoid underestimating risks in susceptible subgroups.^[82] Ecosystem interactions amplify chronic toxicity through processes like food chain transfer, where bioaccumulation and biomagnification lead to elevated contaminant levels in higher trophic levels. Persistent organic pollutants, for example, accumulate in primary producers and herbivores before transferring to predators, resulting in chronic exposure that exceeds direct environmental concentrations and causes sublethal effects like reproductive impairment in top consumers. This trophic magnification is particularly pronounced in aquatic food webs, where lipid-rich organisms facilitate the upward transfer of hydrophobic toxicants, thereby intensifying long-term ecological impacts.^[83] Understanding these interactions is essential for predicting population-level consequences beyond individual organism responses.^[84]

Challenges and Limitations

Methodological Issues

Chronic toxicity tests often require extended durations, typically spanning 6 to 12 months or longer, to capture sublethal effects from prolonged exposure, which demands substantial resources including specialized facilities for maintaining stable environmental conditions and large numbers of test organisms. These studies can cost thousands of dollars per test, for example, ranging from $1,160 to $1,394 for specific aquatic chronic assays, due to the need for continuous monitoring, multiple dose groups, and post-exposure observations.^[85] The resource-intensive nature of these protocols limits their scalability and accessibility, particularly for smaller research entities. A significant challenge in chronic toxicity testing lies in the subjectivity of defining adverse effects, as subtle changes such as behavioral alterations or early histological modifications may not clearly indicate impairment without contextual interpretation.^[86] For instance, distinguishing treatment-related exacerbation from spontaneous age-related lesions, like chronic progressive nephropathy in rodents, requires case-by-case judgment based on severity, incidence, and historical data, often leading to inconsistencies in endpoint classification.^[86] This ambiguity complicates the establishment of no-observed-adverse-effect levels (NOAELs) and underscores the need for standardized criteria to reduce interpretive variability. Advancements in in vitro methods, particularly organ-on-a-chip (OOC) models developed post-2010, offer promising alternatives for simulating chronic toxicity by replicating physiological conditions over extended periods while minimizing animal use.^[87] Liver-on-a-chip systems, for example, have enabled 30-day cultures of hepatocyte spheroids to assess chronic hepatotoxicity, providing human-relevant data that traditional animal models often fail to predict accurately.^[87] Similarly, multi-organ chips integrating liver and kidney functions have modeled drug metabolism and cumulative toxicity interactions, such as those from aristolochic acid, over weeks, promoting ethical reductions in vertebrate testing.^[87] These microfluidic platforms enhance predictive power for long-term effects but require further validation against in vivo outcomes to gain regulatory acceptance. Standardization gaps in chronic toxicity testing arise from inter-laboratory variability in protocols and data quality, which can compromise reproducibility and reliability of results.^[88] The introduction of Good Laboratory Practice (GLP) regulations in the late 1970s, prompted by revelations of data integrity issues in toxicology studies during the mid-1970s, established mandatory quality systems for test facility management, personnel training, and record-keeping to address these inconsistencies. GLP compliance, now internationally harmonized through organizations like the OECD, ensures that chronic studies meet rigorous standards, though challenges persist in adapting these to emerging in vitro technologies.^[89]

Variability in Results

Chronic toxicity assessments often exhibit significant variability due to differences in inter-laboratory reproducibility, where coefficients of variation (CV) for no observed effect concentrations (NOEC) in growth or reproduction endpoints can reach up to 57% across 75% of participating labs in standardized tests.^[90] This inter-lab variation arises from subtle differences in test conditions, organism sourcing, and analytical techniques, leading to NOEC values that may differ by factors of 2-10 between facilities, even when following identical protocols.^[90] Such discrepancies underscore the need for robust quality control measures, though they persist as a fundamental challenge in data reliability. Environmental confounders further contribute to variability by modulating toxicity outcomes in ways not fully captured by controlled lab settings. For example, temperature shifts can alter chemical uptake and organism physiology, with rising temperatures generally increasing sensitivity to contaminants like chlorpyrifos in freshwater fish, where toxicity escalates as temperatures approach species-specific thermal limits (e.g., from 20°C to 30°C).^[91] In broader reviews, temperature elevations have been shown to enhance metal toxicity in 80% of analyzed studies on aquatic biota, potentially amplifying sensitivity by 10-50% depending on the contaminant and species, though effects can be species-specific or even inverse under certain conditions.^[92] These interactions highlight how climate-driven changes, such as projected 2°C global warming, may unpredictably heighten chronic risks in natural ecosystems compared to static test environments. Mixture effects introduce additional variability, as single-substance chronic tests overlook interactions among co-occurring pollutants prevalent in real-world aquatic settings. For the great pond snail Lymnaea stagnalis, binary metal mixtures (e.g., Cd/Ni or Cu/Zn) showed that combined toxicity exceeded that of the most toxic single metal in approximately half of the cases in 14-day growth tests, complicating extrapolation from isolated compound data.^[93] This underscores the limitations of current assessments in addressing multi-pollutant scenarios. Evolving challenges from emerging contaminants like microplastics and nanomaterials exacerbate variability in chronic toxicity evaluations, particularly in post-2015 research. These particles complicate assessments due to their tendency to form eco-coronas that alter bioavailability and facilitate trophic transfer, yet studies often rely on short exposure durations that fail to mimic lifelong chronic accumulation in aquatic food webs.^[94] Nanomaterials pose additional hurdles through inconsistent standardization in toxicity protocols, leading to variable results on bioaccumulation and sublethal effects like oxidative stress in fish and invertebrates, with gaps in understanding organ-specific transfer and long-term degradation dynamics.^[94] Overall, these factors contribute to high uncertainty, as evidenced by inter-study CVs exceeding 100% for nanomaterial endpoints in recent reviews.^[94]

Regulatory Applications

Role in Environmental Guidelines

Chronic toxicity data play a pivotal role in establishing environmental quality standards under the European Union's Water Framework Directive (2000/60/EC), which aims to protect aquatic ecosystems from priority substances. For instance, the chronic predicted no-effect concentration (PNEC) for cadmium in surface waters with low hardness (<40 mg CaCO₃/L) is set at 0.08 µg/L, derived from species sensitivity distributions (SSDs) using geometric mean no-observed-effect concentrations (NOECs) from long-term toxicity tests on aquatic organisms such as Daphnia magna and various fish species.^[95] This value incorporates a safety factor to account for extrapolation uncertainties, ensuring protection against bioaccumulation and sublethal effects in sensitive invertebrate and algal communities.^[95] In the United States, the Environmental Protection Agency (EPA) integrates chronic toxicity metrics into national water quality criteria for protecting freshwater aquatic life. The chronic criterion for total ammonia nitrogen (TAN) is 1.9 mg/L at pH 7.0 and 20°C, primarily based on genus mean chronic values (GMCVs) from effect concentrations (EC20) in sensitivity distributions, with alignment to maximum acceptable toxicant concentrations (MATCs) from early life-stage tests on sensitive species like unionid mussels (Lampsilis spp.) and rainbow trout.^[96] This standard reflects updated data emphasizing reproductive and growth impairments in invertebrates, superseding earlier criteria to better safeguard biodiversity in ammonia-impacted waters.^[96] Globally, the World Health Organization (WHO) incorporates chronic toxicity endpoints into drinking water guidelines to prevent adverse effects from pesticide contamination, often drawing on ecological data for source water protection. For atrazine, the guideline value is 100 µg/L, established using a no-observed-adverse-effect level (NOAEL) from chronic mammalian studies but informed by aquatic chronic NOECs to assess broader environmental persistence and trophic transfer risks.^[97] This approach ensures that guideline derivation considers long-term exposure thresholds from toxicity tests on algae, invertebrates, and fish, mitigating potential endocrine disruption in water sources.^[97] Since the early 2000s, the incorporation of SSDs has advanced chronic toxicity applications in environmental guidelines worldwide, enabling probabilistic derivations of protective concentrations like the hazardous concentration for 5% of species (HC5). In the EU Water Framework Directive, SSDs have been routinely applied since its 2000 adoption to set environmental quality standards for priority pollutants, using chronic NOEC datasets from at least 10 taxonomic groups to enhance ecosystem-level predictions over deterministic methods. Similar integrations in guidelines from Australia and Canada since the mid-2000s have refined chronic benchmarks, prioritizing multi-species chronic data to address variability in sensitivity and support sustainable water management.^[98]

Integration with Broader Risk Assessments

Chronic toxicity data play a pivotal role in human health risk assessments by informing the derivation of reference doses (RfD), which represent chronic oral exposure levels estimated to be without appreciable risk of adverse effects over a lifetime. These RfDs are often derived from animal studies extrapolating to human endpoints, incorporating uncertainty factors for interspecies and intraspecies variability. For instance, the U.S. Environmental Protection Agency (EPA) established an oral RfD for benzene of 4 × 10^{-3} mg/kg-day based on hematological effects observed in exposed populations, adjusted from benchmark dose modeling of human data but informed by supporting animal toxicity studies. This integration ensures that chronic toxicity endpoints, such as reproductive or developmental effects from long-term animal exposures, underpin safe exposure guidelines for environmental contaminants in food, water, and air. In ecological risk assessments, chronic toxicity metrics are integrated into tiered frameworks that combine hazard identification with probabilistic exposure modeling to evaluate population-level impacts on non-target species. Initial screening tiers use conservative chronic no-observed-adverse-effect concentrations (NOAECs) from standardized tests, while higher tiers incorporate site-specific exposure models, such as fugacity or multimedia fate models, to refine risk quotients (e.g., predicted environmental concentration divided by chronic toxicity threshold). This approach, as outlined in EPA guidelines, allows for iterative refinement, where chronic data on sensitive species like fish or invertebrates inform probabilistic risk characterizations, reducing false positives in complex ecosystems. For example, tiered assessments for pesticides evaluate chronic reproductive toxicity in birds alongside modeled dietary exposures to prioritize mitigation. Occupational health frameworks leverage chronic toxicity data to set recommended exposure limits (RELs) for inhalation hazards, focusing on preventing long-term effects like respiratory sensitization or carcinogenicity in workers. The National Institute for Occupational Safety and Health (NIOSH) derives RELs from chronic animal inhalation studies, applying safety margins to protect against cumulative exposures. A representative case is formaldehyde, for which NIOSH recommends a REL of 0.016 ppm as an 8- or 10-hour time-weighted average, based on nasal squamous cell metaplasia observed in rodent chronic exposure studies.^[99] These limits integrate chronic endpoints into workplace monitoring and engineering controls, ensuring alignment with broader industrial hygiene practices. Emerging integrations employ quantitative structure-activity relationship (QSAR) models, increasingly powered by artificial intelligence (AI), to predict chronic toxicity endpoints without extensive animal testing, enhancing efficiency in regulatory screening. Since 2020, AI-driven QSAR approaches, such as transformer-based neural networks, have achieved high accuracy in forecasting chronic aquatic and mammalian toxicity from molecular structures alone, validated against large datasets like ToxCast. For instance, these models predict no-observed-effect levels for developmental toxicity by learning patterns from chemical descriptors, supporting read-across strategies in chemical registration processes.^[100] This AI integration facilitates proactive risk assessment for data-poor substances, complementing traditional chronic studies while adhering to principles of the 3Rs (replacement, reduction, refinement).

References

[1]
40 CFR 798.3260 -- Chronic toxicity. - eCFR
The objective of a chronic toxicity study is to determine the effects of a substance in a mammalian species following prolonged and repeated exposure.
[2]
[PDF] Hazard Classification Guidance for Manufacturers, Importers ... - OSHA
... Chronic Toxicity. Adverse effects resulting from repeated doses or exposures to a substance over a relatively prolonged period of time. Decomposition ...<|separator|>
[3]
[PDF] Using Toxicity Tests in Ecological Risk Assessment - EPA
Chronic toxicity tests generally are longer-term tests that measure the effects of exposure to relatively lower, less toxic concentrations.
[4]
Health Effects Test Guidelines OPPTS 870.4100 Chronic Toxicity
The objective of a chronic toxicity study is to determine the effects of a substance in a mammalian species following prolonged and repeated exposure.
[5]
Assessment of Toxicity - Science and Judgment in Risk ... - NCBI - NIH
This chapter discusses the methods used to evaluate the toxicity of a substance for the purpose of health risk assessment.<|control11|><|separator|>
[6]
Health and Ecological Hazards Caused by Hazardous Substances
Dec 4, 2024 · In some cases, hazardous substances may irritate the skin or eyes, make it difficult to breathe, cause headaches and nausea, result in other ...
[7]
Health Effects of Chronic Arsenic Exposure - PMC - NIH
Arsenic has been confirmed as a human carcinogen that can induce skin, lung, and bladder cancer. There are also reports of its significant association to liver ...
[8]
What Diseases Are Associated with Chronic Exposure to Cadmium?
Most studies have associated chronic occupational exposure to cadmium fumes and dusts with increased risk of chronic obstructive lung disease and emphysema.
[9]
[PDF] Appendix A. Glossary of Useful Terms - EPA
Chronic Toxicity – Adverse effects on any living organism in which symptoms develop slowly over a period of time (often the life time of the organism) or ...
[10]
[PDF] Module One Introduction to Toxicology
It relies on the concept that a dose, or a time of exposure (to a chemical, drug, or toxic substance), will cause an effect (response) on the exposed organism.
[11]
Toxicity, mechanism and health effects of some heavy metals - PMC
Long-term exposure can lead to the formation of skin lesions, internal cancers, neurological problems, pulmonary disease, peripheral vascular disease, ...
[12]
[PDF] Guidelines for Developmental Toxicity Risk Assessment
Exposure to agents affecting development can result in any one or more of the following manifestations of developmental toxicity: death, structural abnormality, ...
[13]
The Scope and Promise of Behavioral Toxicology - NCBI - NIH
Behavioral toxicology first emerged as an alternative to traditional markers of toxicity such as tissue damage and as a potential reservoir of more sensitive ...
[14]
Review Persistent pollutants: A brief history of the discovery of the ...
Here we will review the research literature beginning in the Depression and World War II era that led to the growing recognition of chlorinated hydrocarbons as ...
[15]
https://pmc.ncbi.nlm.nih.gov/articles/PMC4427717/
[16]
Mutagenicity assessment downstream of oil and gas produced water ...
Numerous studies have shown that both acute and chronic toxicity (e.g. endocrine disruption, mutagenicity, etc.) are elevated in surface water downstream of ...
[17]
Research Progress of the Endocrine-Disrupting Effects of ...
Jun 28, 2022 · It is the major objective of this paper to summarize the reported potential endocrine-disrupting effects of the identified DBPs in the view of adverse outcome ...
[18]
Reference Dose (RfD): Description and Use in Health Risk ... - EPA
Mar 15, 1993 · This characteristic distinguishes systemic endpoints from carcinogenic and mutagenic endpoints, which are often treated as nonthreshold ...
[19]
A Review of the LD50 and Its Current Role in Hazard Communication
Dec 21, 2020 · Figure 1 displays LD50 values from least toxic (sucrose) to most toxic (TCDD) for acute oral toxicity in rats to substances of varying acute ...
[20]
40 CFR 132.2 -- Definitions. - eCFR
Chronic toxicity is concurrent and delayed adverse effect(s) that occurs only as a result of a chronic exposure. Connecting channels of the Great Lakes are the ...
[21]
A Mechanism-based QSTR Model for Acute to Chronic Toxicity ...
Jul 20, 2017 · Figure 1 shows the comparisons of the dose-response curves for the acute and chronic toxicity. In particular, the antibiotics at low ...
[22]
[PDF] EPA Regions 8, 9 and 10
The long-term average for chronic toxicity (LTAc) and the long-term average for acute toxicity. (LTAa,c) in the effluent discharge are calculated using the ...
[23]
Bioaccumulation, Biodistribution, Toxicology and Biomonitoring of ...
Jun 11, 2021 · Toxicological study of PFOS/PFOA to zebrafish ... Acute and chronic toxicity of short chained perfluoroalkyl substances to Daphnia magna.
[24]
Bioaccumulation and biomagnification of heavy metals in marine ...
Nov 27, 2023 · Environmental chemistry and ecotoxicology of hazardous heavy metals: environmental persistence, toxicity, and bioaccumulation. J. Chem. 2019 ...
[25]
Cellular and Molecular Mechanisms of Oxidative DNA Damage and ...
DNA is continuously exposed to endogenous and exogenous factors that induce oxidative modifications leading to mutations and genomic instability.
[26]
Epigenetics and Oxidative Stress in Aging - PMC - NIH
Jul 20, 2017 · We give a comprehensive overview on how the combination of different epigenetic alterations and oxidative stress affects the process of aging.
[27]
Toxic Hepatitis (Liver Toxicity): Symptoms, Causes & Treatments
Toxic hepatitis, or liver toxicity, is liver swelling from contact with, breathing or swallowing a toxin. Over time, inflammation causes permanent liver ...Missing: neurotoxicity | Show results with:neurotoxicity
[28]
Manganese Neurotoxicity: A Comprehensive Review of ...
Apr 4, 2025 · Oxidative stress is one of the most implicated mechanisms of Mn-induced neurotoxicity. Mn accumulation in the brain can lead to damage in the ...
[29]
Molecular mechanisms of aluminum neurotoxicity: Update on ... - PMC
The underlying mechanisms of Al(III) neurotoxicity were shown to involve oxidative and endoplasmic reticulum stress, mitochondrial dysfunction, inflammation, ...<|separator|>
[30]
Relating results of chronic toxicity responses to population‐level ...
Nov 5, 2009 · Compounds affecting various toxicity endpoints, such as growth, fecundity, behavior, or immune function, alter different demographic traits and ...
[31]
Test No. 452: Chronic Toxicity Studies - OECD
The duration of the exposure period should be 12 months. The study report should include: measurements (weighing) and regular detailed observations ( ...
[32]
Understanding In Vitro and In Vivo Toxicology Testing for Chemicals
Feb 11, 2018 · In vitro tests are done outside living organisms, using isolated tissues, while in vivo tests are done in living organisms, like rats or ...Missing: chronic | Show results with:chronic
[33]
Chronic Toxicity Study - an overview | ScienceDirect Topics
Toxicity Studies. In vivo animal toxicology studies and in vitro studies are conducted to determine a drug's short- and long-term functional and morphologic ...
[34]
[PDF] Test No. 452: Chronic Toxicity Studies (EN) - OECD
Jun 25, 2018 · Changes in gait, posture and response to handling as well as the presence of clonic or tonic movements, stereotypies. (e.g., excessive grooming, ...Missing: behavioral | Show results with:behavioral
[35]
Redbook 2000: IV.B.1. General Guidelines for Toxicity Studies - FDA
Oct 26, 2017 · The test substance used in toxicity studies should be the same substance that the petitioner/notifier intends to market. A single lot of test ...
[36]
http://www.chemsafetypro.com/Topics/CRA/Understanding_In_Vitro_and_In_Vivo_Toxicology_Testing_for_Chemicals.html
[37]
Exploring Greater Flexibility for Chronic Toxicity Study Designs ... - NIH
May 31, 2024 · Chronic repeated-dose toxicity studies are required to support long-term, late-stage clinical trials and often vary widely in species selection, ...
[38]
Animal Use Alternatives (3Rs) | National Agricultural Library - USDA
Drs. William Russell and Rex Burch first described the 3Rs in 1959 in their book, "The Principles of Humane Experimental Technique". Russell and Burch advocated ...
[39]
The 3Rs - NC3Rs
The principles of the 3Rs (Replacement, Reduction and Refinement) were developed over 50 years ago providing a framework for performing more humane animal ...What are the 3Rs? · Definitions of the 3Rs · Replacement
[40]
Russell and Burch's 3Rs Then and Now: The Need for Clarity in ...
Central to Russell and Burch's definitions of the 3Rs are 2 concepts first used by the Principles: inhumanity and its opposite, humanity. Humanity, as Russell ...
[41]
Freshwater Alga and Cyanobacteria, Growth Inhibition Test - OECD
The purpose of this test is to determine the effects of a substance on the growth of freshwater microalgae and/or cyanobacteria.
[42]
[PDF] Ecological Effects Test Guidelines OPPTS 850.1300 Daphnid ...
Chronic toxicity test means a method used to determine the concentra- tion of a substance in water that produces an adverse effect on a test orga- nism over an ...
[43]
[PDF] Test Guideline No. 210 Fish, Early-life Stage Toxicity Test - OECD
Tests with the early-life stages of fish are intended to define the lethal and sub lethal effects of chemicals on the stages and species tested.
[44]
[PDF] Test No. 201: Freshwater Alga and Cyanobacteria, Growth Inhibition ...
Jul 28, 2011 · Water quality – Guidelines for algal growth inhibition tests with poorly soluble materials, volatile compounds, metals and waster water. (3).
[45]
Biological test method: growth inhibition test using a freshwater alga
Mar 22, 2023 · Chronic toxicity implies long-term effects that are related to changes in metabolism, growth, reproduction, or ability to survive. In this ...
[46]
Test No. 211: Daphnia magna Reproduction Test - OECD
The test method described in this Test Guideline assesses the effect of chemicals on the reproductive output of Daphnia magna Straus.
[47]
[PDF] Test Guideline No. 211 Daphnia magna reproduction test - OECD
Oct 2, 2012 · The Daphnia magna reproduction test assesses the effect of chemicals on the reproductive output of young female Daphnia over 21 days, measuring ...
[48]
Test No. 210: Fish, Early-life Stage Toxicity Test | OECD
The test method described in this Test Guideline, is intended to define the lethal and sub-lethal effects of chemicals on the early life stages of the species ...
[49]
Ecological Effects Test Guidelines OCSPP 850.1400: Fish Early Life ...
OECD Guidelines for Testing of Chemicals, Guideline 210, Fish Early Life-Stage Toxicity Test. (13) U.S. EPA, 1972. Recommended Bioassay Procedure for ...
[50]
https://www.oecd.org/en/publications/2012/10/test-no-211-daphnia-magna-reproduction-test_g1g24069.html
[51]
[PDF] Methods for Measuring the Acute Toxicity of Effluents and Receiving ...
... in a static, recirculated, or flow-through systems. Flow-through systems require large volumes of water and may not be feasible in some laboratories. 3.3 ...
[52]
[PDF] Test Guideline No. 240 Medaka Extended One Generation ... - OECD
Jul 4, 2023 · 1. The Medaka Extended One Generation Reproduction Test (MEOGRT) describes a comprehensive test based on fish exposed over multiple generations ...
[53]
Medaka Extended One Generation Reproduction Test (MEOGRT)
This document provides guidance for conducting the test, and is also used by EPA, the public and the companies that are subject to data submission requirements.
[54]
Final Test Guidelines; Endocrine Disruptor Screening Program Test ...
Aug 25, 2015 · EPA is announcing the availability of three final test guidelines: Medaka Extended One-generation Reproduction Test (MEOGRT), OCSPP Test ...Missing: aquatic | Show results with:aquatic<|control11|><|separator|>
[55]
[PDF] Report of the OECD Workshop on Statistical Analysis of Aquatic ...
The stated aim of this Guideline is to enable LOECs and NOECs to be determined. No consideration is given to EC50 estimation, although acute end-points may ...
[56]
[PDF] Short-term Methods for Estimating the Chronic Toxicity of Effluents ...
... CHRONIC TOXICITY. 2.1 INTRODUCTION. 2.1.1 The objective of aquatic toxicity tests with effluents or pure compounds is to estimate the "safe" or "no effect ...
[57]
[PDF] Statistical and Biological Interpretation of Test Endpoints Relative to ...
The MATC is a point estimate set as the geometric mean of the NOEC and the. LOEC. • We report NOEC, LOEC, and MATC values for our tests. We also report.Missing: formula | Show results with:formula
[58]
[PDF] QUALITY CRITERIA FOR WATER
To the Reader: Thousands of fine scientists throughout the country have contributed directly or indirectly to this publication on. "Quality Criteria for ...
[59]
[PDF] Ecological Effects Test Guidelines OPPTS 850.1350 Mysid Chronic ...
The following definitions also apply to this guideline: Chronic toxicity test is a method used to determine the concentration of a substance that produces an ...
[60]
[PDF] Water Quality Standards Academy Aquatic Life Criteria
Mar 24, 2021 · Species Sensitivity Distribution (SSD). 0.0. 0.1. 0.2. 0.3. 0.4. 0.5. 0.6 ... Chronic Value = 26.8 µg/L. (NOEC = 15; LOEC = 30). Concentration ...
[61]
Data Requirements for Pesticide Registration | US EPA
Mar 24, 2025 · These data requirements apply to anyone or any company that registers pesticides under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
[62]
[PDF] guideline-environmental-risk-assessment-medicinal-products ...
Aug 22, 2024 · To determine a potential risk to the surface water compartment, the PECSW (as calculated in Phase I) is compared to the PNECSW. This PNEC is ...
[63]
[PDF] Environmental Hazard Assessment of Substances - ECETOC
Where chronic toxicity data are available, the PNEC may be derived by dividing the lowest no-observed-effect concentration (NOEC) by 5, whereas the NOEC ...
[64]
Evaluation of acute-to-chronic ratios of fish and Daphnia to predict ...
May 12, 2016 · The result suggests that an acute-to-chronic extrapolation factor of 100 is protective for more than 90 % of the chemicals.
[65]
Safer Choice Standard and Criteria | US EPA
Limitations on persistent, bioaccumulative and toxic chemicals: Acceptable chemicals must not be persistent (half-life >60 days), bioaccumulative (BCF/BAF = ...
[66]
[PDF] Technical Report No. 90 Persistence of Chemicals in the Environment
Half-life >60 days in marine water or >40 days in. Half-life >60 days in ... or a half-life in marine sediment > 180 days are considered to be persistent.
[67]
CLP, 4.1.2., Classification criteria for substances - REACH Online
Using a cut-off value of log Kow ≥ 4 is intended to identify only those substances with a real potential to bioconcentrate. While this represents a potential to ...
[68]
Global occurrence, bioaccumulation factors and toxic effects of ...
Polychlorinated biphenyls (PCBs) tend to accumulate in adipose tissue and induce toxicity due to their high lipophilicity and persistence.
[69]
Speciation in Metal Toxicity and Metal-Based Therapeutics - PMC
Apr 28, 2015 · Metallic elements, ions and compounds produce varying degrees of toxicity in organisms with which they come into contact. Metal speciation ...
[70]
Improving and testing geochemical speciation predictions of metal ...
As metal bio-uptake, biological responses and toxicity are dependent on metal speciation, it is desirable to be able to measure and predict the free ion ...Missing: chronic | Show results with:chronic
[71]
Optimal choice of pH for toxicity and bioaccumulation studies of ...
Aug 5, 2011 · It is recognized that the pH of exposure solutions can influence the toxicity and bioaccumulation of ionizing compounds.Data Collection · Acids: Toxicity · Cell Model
[72]
pH-Dependent Bioavailability, Speciation, and Phytotoxicity of ...
Apr 27, 2018 · The aim of this study was to investigate plant growth as well as W and nutrient uptake depending on soil chemical properties such as soil pH and texture.
[73]
[PDF] Aquatic Hazard Assessment II - ECETOC
practical point of view, adoption of an acute to chronic ratio of 100 (as explained in the footnote to Table 39) would seem to be quite safe for 95% of ...
[74]
Species Sensitivity to Toxic Substances: Evolution, Ecology and ...
We review current knowledge on how toxicokinetic, toxicodynamic, physiological, and ecological traits contribute to differences in sensitivity.
[75]
Why are Early Life Stages of Aquatic Organisms more Sensitive to ...
Jan 23, 2013 · The choice of early life stages has been based on the premise that they are the most susceptible to toxicants.
[76]
CYP polymorphisms and pathological conditions related to chronic ...
May 26, 2017 · The association between genetic variations in the cytochrome P450 (CYP) family genes and pathological conditions related to long-term ...
[77]
Genetic Polymorphism and Toxicology—With Emphasis on ...
Individual susceptibility to environmental, chemical, and drug toxicity is to some extent determined by polymorphism in drug-metabolizing enzymes.Abstract · GENETIC POLYMORPHISM... · IMPORTANT EXAMPLES OF...
[78]
Biological Traits and the Transfer of Persistent Organic Pollutants ...
Oct 24, 2019 · We investigate transfer pathways of polychlorinated biphenyls, polybrominated diphenyl ethers, and organochlorine through a river food web.
[79]
Trophic transfer and biomagnification potential of environmental ...
Jan 1, 2024 · This article discusses the essences on the determination, potential and plausible factors of trophic transfer and biomagnification of environmental contaminants
[80]
[PDF] Attachment 4. Summary of Aquatic Toxicity Test Costs
Chronic Methods. Blank. Blank. Blank. EPA Method 1000.0 - Pimephales promelas. 2. $1,338 to $1,394. $1,366. EPA Method 1001.0 - Pimephales promelas. 4. $1,160 ...
[81]
Characterizing “Adversity” of Pathology Findings in Nonclinical ...
Apr 21, 2016 · The integrated toxicology report should consider adversity at the study level as a basis for setting both the no observed adverse effect level ( ...
[82]
Drug Toxicity Evaluation Based on Organ-on-a-Chip Technology
Abstract. Organ-on-a-chip academic research is in its blossom. Drug toxicity evaluation is a promising area in which organ-on-a-chip technology can apply.
[83]
Recent organ-on-a-chip advances toward drug toxicity testing - Deng
Oct 25, 2018 · In this review, we introduce some recent advances in novel organ-on-a-chip systems that primarily target drug toxicity testing.
[84]
History of FDA good laboratory practices - ResearchGate
Aug 6, 2025 · GLP guidelines were established in response to the discovery of problems with quality and data integrity in several toxicology studies in the ...
[85]
https://www.waterboards.ca.gov/water_issues/programs/state_implementation_policy/docs/attachment_4_summary_aquatic_toxicity_test_costs.pdf
[86]
[PDF] Understanding and Accounting for Method Variability in Whole ...
For the NOEC of growth or reproduction endpoints in chronic toxicity tests, 75 percent of laboratories have a CV no more than 0.43 to 0.57, depending on the ...
[87]
Interactions between water temperature and contaminant toxicity to ...
Jun 1, 2015 · On the one hand, chronic exposure to common contaminants may reduce the upper thermal tolerance of fish by as much as 5.9 °C 4, increasing the ...
[88]
Effect of a temperature rise on metal toxicity for the aquatic biota
In 80% of the studies analyzed, a temperature rise was responsible for increasing the toxicity of metals for the aquatic organisms.
[89]
Chronic Toxicity of Binary Mixtures of Six Metals (Ag, Cd, Cu, Ni, Pb ...
Apr 15, 2018 · The present study aims at addressing the data gap on metal mixture chronic toxicity to aquatic organisms. Chronic toxicity of binary mixtures ...<|separator|>
[90]
Toxicological review of micro- and nano-plastics in aquatic ...
Jun 15, 2024 · This review provides a detailed report of the transmission and dangers of MNPs in aquatic ecosystems, environmental behavior, and interactions within aquatic ...
[91]
[PDF] Cadmium and its Compounds - CIRCABC
Jul 31, 2005 · ... PNEC is considered: ≈ 0.08 – 0.25 µg/l). This is illustrated by the ... µg Cd /l limit value of the drinking water directive. But as ...
[92]
[PDF] Aquatic Life Ambient Water Quality Criteria for Ammonia - EPA
At an example pH of 7 and temperature of 20°C, the 2013 acute criterion magnitude is 17 mg TAN/L and the chronic criterion magnitude is 1.9 mg TAN/L. At pH ...
[93]
[PDF] Atrazine and Its Metabolites in Drinking-water
This WHO document is a background document for developing guidelines on atrazine and its metabolites in drinking water.
[94]
[PDF] Estimating toxicity thresholds for aquatic ecological communities ...
Species sensitivity distributions are generally derived using data from single-species toxicity tests. The species used in these tests are often from a ...
[95]
NIOSH Pocket Guide to Chemical Hazards - Formaldehyde - CDC
Ca [20 ppm] See: 50000. Exposure Limits. NIOSH REL. Ca TWA 0.016 ppm C 0.1 ppm [15-minute] See Appendix A. OSHA PEL. [1910.1048] TWA 0.75 ppm ST 2 ppm.
[96]
Transformers enable accurate prediction of acute and chronic ...
Mar 6, 2024 · We present a AI-based model for predicting chemical toxicity. The model uses transformers to capture toxicity-specific features directly from the chemical ...