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Developmental toxicity information


Developmental toxicity is any developmental malformation that is caused by the toxicity of a chemical or pathogen. It is the structural or functional alteration, reversible or irreversible, which interferes with homeostasis, normal growth, differentiation, development or behavior. Developmental toxicity is caused by environmental insult, which includes drugs, alcohol, diet, toxic chemicals, and physical factors.

More factors causing developmental toxicity are radiation, infections (e.g. rubella), maternal metabolic imbalances (e.g. alcoholism, diabetes, folic acid deficiency), drugs (e.g. anticancer drugs, tetracyclines, many hormones, thalidomide), and environmental chemicals (e.g. mercury, lead, dioxins, PBDEs, HBCD, tobacco smoke).In addition, it is the study of adverse effects on the development of the organism that can result from exposure to toxic agents before conception, during fetal development, or even following birth.

The first few weeks of embryogenesis in humans. Beginning at the fertilized egg, ending with the closing of the neural tube. The embryogenesis is the most crucial time for the action of any teratogenic substances resulting in birth defects.

Certain pathogens are also included since the toxins they secrete are known to cause adverse effects on the development of the organism when the mother or fetus is infected. The term  developmental toxicity has widely replaced the early term for the study of primarily structural congenital abnormalities, teratology, to enable inclusion of a more diverse spectrum of congenital disorders. The substances that cause developmental toxicity from embryonic stage to birth are called teratogens. The effect of the developmental toxicants depends on the type of substance, dose, duration, and time of the exposure. The first few weeks of embryogenesis in humans is more susceptible to these agents.

The embryogenesis is the most crucial time for the action of any teratogenic substances to result in birth defects. Once fertilization has taken place, the toxicants in the environment can pass through the mother to the developing embryo or fetus across the placental barrier. The fetus is at greatest risk during the first 14th to 60th day of the pregnancy when the major organs are being formed. However, depending on the type of toxicant and amount of exposure, a fetus can be exposed to toxicants at any time during pregnancy, but have different effects. For example, exposure to a particular toxicant at one time in the pregnancy may result in organ damage and at another time in the pregnancy could cause death of the fetus and miscarriage.

There are a number of chemicals, biological agents (such as bacteria and viruses), and physical agents (such as radiation) used in a variety of workplaces that are known to cause developmental disorders. Developmental disorders can include a wide range of physical abnormalities, such as bone or organ deformities, or behavioral and learning problems, such as an intellectual disability. Exposures to some chemicals during pregnancy can lead to the development of cancer later in life, called transgenerational carcinogens. Exposure to toxicants during the second and third trimesters of a pregnancy can lead to slow fetal growth and result in low birth weight.

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Developmental toxicity

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development or behavior. Developmental toxicity is caused by environmental insult, which includes drugs, alcohol, diet, toxic chemicals, and physical factors...

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Piperonyl butoxide

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identify: Dermal toxicity Eye irritation Inhalation toxicity Oral toxicity Skin irritation Skin sensitization PBO has a low acute toxicity by oral, inhalation...

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Reproductive toxicity

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fertility as well as causing developmental toxicity in the offspring. Lowered effective fertility related to reproductive toxicity relates to both male and...

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Toxicology

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substance causes cancer and to examine other forms of toxicity. Factors that influence chemical toxicity: Dosage Both large single exposures (acute) and continuous...

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Chlormequat

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670 mg/kg. Exposure to high levels of chlormequat has been linked to developmental toxicity in animal models. Chlormequat has not previously been registered...

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Globally Harmonized System of Classification and Labelling of Chemicals

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organ toxicity hazard class are assigned to one of three hazard categories. Substances and mixtures of the repeated exposure target organ toxicity hazard...

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In vitro

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of in vitro toxicity data and physiologically based kinetic modeling to predict dose–response curves for in vivo developmental toxicity of glycol ethers...

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Conium maculatum

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Forsyth, Carol S.; Frank, Anthony A. (July 1993). "Evaluation of developmental toxicity of coniine to rats and rabbits". Teratology. 48 (1): 59–64. doi:10...

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ISO 10993

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requirements Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity Part 4: Selection of tests for interactions with blood Part 5: Tests for...

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Nivalenol

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males and females are not provided yet. Acute toxicity of nivalenol induces bone marrow toxicity and toxicity of lymphoid organs. Long-term exposure may...

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Prallethrin

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prallethrin indicate moderate acute toxicity via the oral and inhalation routes of administration (Category II) and low acute toxicity via the dermal route (Categories...

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In vitro toxicology

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In vitro toxicity testing is the scientific analysis of the toxic effects of chemical substances on cultured bacteria or mammalian cells. In vitro (literally...

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Teratology

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disorders that lack structural malformations. The related term developmental toxicity includes all manifestations of abnormal development that are caused...

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Birth defect

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2020 were that 19% of the 1065 chemicals yielded a prediction of developmental toxicity. Probably, the most well-known teratogenic drug is thalidomide....

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Sunset yellow FCF

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: 465  Sunset yellow FCF has no carcinogenicity, genotoxicity, or developmental toxicity in the amounts at which it is used.: 465  It has been claimed since...

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Food additive

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subchronic (at least 90 data) and chronic toxicity and carcinogenity; reproductive and developmental toxicity. Recent work has demonstrated that certain...

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Nickel

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carbonyl [Ni(CO)4] is an extremely toxic gas. The toxicity of metal carbonyls is a function of both the toxicity of the metal and the off-gassing of...

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Perfluorooctanoic acid

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Durda J (April 2019). "Perfluorohexanoic acid toxicity, part II: Application of human health toxicity value for risk characterization". Regulatory Toxicology...

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Salicylic acid

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cosmetic products demonstrates no evidence of a health risk from developmental toxicity". Regulatory Toxicology and Pharmacology. 94: 245–251. doi:10.1016/j...

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Polychlorinated dibenzodioxins

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toxicity, are given a toxicity rating from 0 to 1, where TCDD = 1 (see Dioxins and dioxin-like compounds). This toxicity rating is called the Toxic Equivalence...

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Methemoglobinemia

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an update on methemoglobinemia occurrence and reproductive and developmental toxicity". Regulatory Toxicology and Pharmacology. 23 (1 Pt 1): 35–43. doi:10...

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Ponceau 4R

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carcinogenicity, genotoxicity, neurotoxicity, or reproductive and developmental toxicity at the permitted dietary exposures; the European acceptable daily...

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Hydroxycarbamide

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constipation, mucositis, anorexia, stomatitis, bone marrow toxicity (dose-limiting toxicity; may take 7–21 days to recover after the drug has been discontinued)...

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Herbal Essences

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(August 2004). "Developmental toxicity evaluation of butylparaben in Sprague-Dawley rats". Birth Defects Research Part B: Developmental and Reproductive...

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Rabbit

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Carney, Edward W (2000). "The rabbit as a model for reproductive and developmental toxicity studies". Reproductive Toxicology. 14 (6): 477–493. doi:10...

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Difluoromethane

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the bronzing of leaves. Difluoromethane shows slight maternal and developmental toxicity at concentrations of approximately 50,000 ppm in rats, but not in...

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Perfluorooctanesulfonic acid

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PMID 11999053. Lau C, Butenhoff JL, Rogers JM (July 2004). "The developmental toxicity of perfluoroalkyl acids and their derivatives". Toxicol. Appl. Pharmacol...

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