National Toxicology Program

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National Toxicology Program
Logo National Toxicology Program.svg
Agency overview
Formed1978
Agency executive
  • Dr. Richard Woychik, Director, NIEHS & NTP
Parent agency United States Department of Health and Human Services, National Institute of Environmental Health Sciences
Child agencies
  • Office of the Report on Carcinogens
  • Interagency Center for the Evaluation of Alternative Toxicological Methods
Website ntp.niehs.nih.gov

The National Toxicology Program (NTP) is an inter-agency program run by the United States Department of Health and Human Services to coordinate, evaluate, and report on toxicology within public agencies. [1]

Contents

The National Toxicology Program is headquartered at the National Institute of Environmental Health Sciences (NIEHS). The NIEHS Director, currently Richard Woychik, also concurrently serves as NTP Director. [1]

History

The program was established in 1978 by Joseph A. Califano Jr., then the United States Secretary of Health, Education, and Welfare (today known as the Secretary of Health and Human Services). The program arose from congressional concerns about the health effects of chemical agents in the environment. In October 1981, Secretary Richard S. Schwiker granted permanent status to the program. [2]

Interagency Center for the Evaluation of Alternative Toxicological Methods

The NTP Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM) supports the development and evaluation of new, revised, and alternative methods for chemical safety testing. Alternative methods are methods for safety testing of chemicals and chemical products that use fewer or no animals or that minimize or prevent animal pain and distress. NICEATM is directed by Dr. Warren Casey, PhD, DABT.[ citation needed ]

The NIH Revitalization Act of 1993 [3] directed NIEHS to establish criteria for the validation and regulatory acceptance of alternative test methods and a process for their subsequent implementation. This led to the establishment of the Interagency Coordinating Committee on the Validation of Alternative Methods via the ICCVAM Authorization Act of 2000, [4] which stated that ICCVAM would exist as a permanent interagency committee of NIEHS under NICEATM.[ citation needed ]

In addition to supporting ICCVAM, NICEATM activities include:

NICEATM publishes results of its analyses of alternative test methods and approaches in the peer-reviewed literature and presents at meetings of the Society of Toxicology and the World Congress on Alternatives and Animal Use in the Life Sciences.[ citation needed ]

Office of the Report on Carcinogens

The United States federgovernment's NIEHS National Toxicology Program's Office of the Report on Carcinogens is responsible for publishing a Report On Carcinogens, first issued in 1980. [5]

The latest edition is the 15th Report, issued in 2021. [6] The 14th Report, published in 2016, contains "248 listings of agents, substances, mixtures, and exposure circumstances that are known or reasonably anticipated to cause cancer in humans." This edition added seven newly reviewed listings, of which the only synthetic chemical was trichloroethylene. [7]

Related Research Articles

The Draize test is an acute toxicity test devised in 1944 by Food and Drug Administration (FDA) toxicologists John H. Draize and Jacob M. Spines. Initially used for testing cosmetics, the procedure involves applying 0.5 mL or 0.5 g of a test substance to the eye or skin of a restrained, conscious animal, and then leaving it for set amount of time before rinsing it out and recording its effects. The animals are observed for up to 14 days for signs of erythema and edema in the skin test, and redness, swelling, discharge, ulceration, hemorrhaging, cloudiness, or blindness in the tested eye. The test subject is commonly an albino rabbit, though other species are used too, including dogs. The animals are euthanized after testing if the test renders irreversible damage to the eye or skin. Animals may be re-used for testing purposes if the product tested causes no permanent damage. Animals are typically reused after a "wash out" period during which all traces of the tested product are allowed to disperse from the test site.

<span class="mw-page-title-main">Ethyl carbamate</span> Chemical compound

Ethyl carbamate (also called urethane) is an organic compound with the formula CH3CH2OC(O)NH2. It is an ester of carbamic acid and a white solid. Despite its name, it is not a component of polyurethanes. Because it is a carcinogen, it is rarely used, but naturally forms in low quantities in many types of fermented foods and drinks.

The National Institute of Environmental Health Sciences (NIEHS) conducts research into the effects of the environment on human disease, as one of the 27 institutes and centers of the National Institutes of Health (NIH). It is located in the Research Triangle Park in North Carolina, and is the only primary division of the NIH located outside of the Washington metropolitan area.

<span class="mw-page-title-main">Nitrofurazone</span> Chemical compound

Nitrofurazone is an antimicrobial organic compound belonging to the nitrofuran class. It is most commonly used as a topical antibiotic ointment. It is effective against gram-positive bacteria, gram-negative bacteria, and can be used in the treatment of trypanosomiasis. Its use in medicine has become less frequent, as safer and more effective products have become available. Nitrofurazone is listed under California Prop 65, and has demonstrated clear evidence to be mutagenic and carcinogenic during animal studies, and has been discontinued for human use in the USA. The substance is pale yellow and crystalline. It was once widely used as an antibiotic for livestock.

Toxicogenomics is a subdiscipline of pharmacology that deals with the collection, interpretation, and storage of information about gene and protein activity within a particular cell or tissue of an organism in response to exposure to toxic substances. Toxicogenomics combines toxicology with genomics or other high-throughput molecular profiling technologies such as transcriptomics, proteomics and metabolomics. Toxicogenomics endeavors to elucidate the molecular mechanisms evolved in the expression of toxicity, and to derive molecular expression patterns that predict toxicity or the genetic susceptibility to it.

<span class="mw-page-title-main">David Rall</span> American physician

David Platt Rall was a cancer specialist and a leader in environmental health studies, whose work in environmental health helped turn it into a scientific discipline. Rall also advanced public health and prevention. He directed the National Institute of Environmental Health Sciences from 1971 to 1990, year in which he retired. His work on toxicology and carcinogenesis was recognized by his appointment as the first director of the National Toxicology Program in 1978. He held the rank of Assistant Surgeon General in the United States Public Health Service. He also chaired the World Health Organization's Program on Chemical Safety.

<span class="mw-page-title-main">Dimethylamine</span> Chemical compound

Dimethylamine is an organic compound with the formula (CH3)2NH. This secondary amine is a colorless, flammable gas with an ammonia-like odor. Dimethylamine is commonly encountered commercially as a solution in water at concentrations up to around 40%. An estimated 270,000 tons were produced in 2005.

<span class="mw-page-title-main">Retinyl palmitate</span> Vitamin A chemical compound

Retinyl palmitate, or vitamin A palmitate, is the ester of retinol (vitamin A) and palmitic acid, with formula C36H60O2. It is the most abundant form of vitamin A storage in animals.

<span class="mw-page-title-main">Benzyl butyl phthalate</span> Chemical compound

Benzyl butyl phthalate (BBP) is an organic compound historically used a plasticizer, but which has now been largely phased out due to health concerns. It is a phthalate ester of containing benzyl alcohol, and n-butanol tail groups. Like most phthalates, BBP is non-volatile and remains liquid over a wide range of temperatures. It was mostly used as a plasticizer for PVC, but was also a common plasticizer for PVCA and PVB.

<span class="mw-page-title-main">Nickel(II) oxide</span> Chemical compound

Nickel(II) oxide is the chemical compound with the formula NiO. It is the principal oxide of nickel. It is classified as a basic metal oxide. Several million kilograms are produced annually of varying quality, mainly as an intermediate in the production of nickel alloys. The mineralogical form of NiO, bunsenite, is very rare. Other nickel oxides have been claimed, for example: Nickel(III) oxide(Ni
2
O
3
) and NiO
2
, but they have yet to be proven by X-ray crystallography in bulk. Nickel(III) oxide nanoparticles have recently (2015) been characterized using powder X-ray diffraction and electron microscopy.

<span class="mw-page-title-main">Nickel(II) sulfate</span> Chemical compound

Nickel(II) sulfate, or just nickel sulfate, usually refers to the inorganic compound with the formula NiSO4(H2O)6. This highly soluble blue green coloured salt is a common source of the Ni2+ ion for electroplating.

<span class="mw-page-title-main">Alternatives to animal testing</span> Test methods that avoid the use of animals

Alternatives to animal testing are the development and implementation of test methods that avoid the use of live animals.

The National Toxicology Program (NTP) and the National Institute of Environmental Health Sciences (NIEHS) established the NTP Center for the Evaluation of Risks to Human Reproduction in 1998 as an environmental health resource to the public and regulatory and health agencies. The Center provides evaluations of the potential for adverse effects on reproduction and development caused by chemicals to which humans might be exposed.

<span class="mw-page-title-main">Formaldehyde releaser</span> Chemical compound used as a preservative that slowly releases formaldehyde.

A formaldehyde releaser, formaldehyde donor or formaldehyde-releasing preservative is a chemical compound that slowly releases formaldehyde. Formaldehyde-releasers are added to prevent microbial growth and extend shelf life. The intent of these compounds is that they release formaldehyde at levels that suppress microbial growth but sufficiently low to not threaten humans. The use of these chemicals in cosmetics has elicited controversy.

<span class="mw-page-title-main">Calcium chromate</span> Chemical compound

Calcium chromate is an inorganic compound with the formula CaCrO4, i.e. the chromate salt of calcium. It is a bright yellow solid which is normally found in the dihydrate form CaCrO4·2H2O. A very rare anhydrous mineral form exists in nature, which is known as chromatite.

The Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM) coordinates U.S. federal government evaluation of new, revised, and alternative test methods. Alternative methods are methods for safety testing of chemicals and chemical products that use fewer or no animals or that minimize or prevent animal pain and distress.

<span class="mw-page-title-main">Diepoxybutane</span> Chemical compound

Diepoxybutane is an epoxide which is a colorless liquid at room temperature. It is therefore highly reactive, more than other ethers. An epoxide is a cyclic ether that contains a three atom ring that comes close to an equilateral triangle. The primary structure of an epoxide contains two carbon atoms and a hydrocarbon attached to an oxygen atom. It polymerizes in the presence of catalysts or when heated. It’s hydrophilic, very flammable and easily ignited by heat or sparks.

The New England Anti-Vivisection Society (NEAVS) is a national, registered 501(c)(3) nonprofit organization "dedicated to ending the use of animals in research, testing, and science education" and replacing them with "modern alternatives that are ethically, humanely, and scientifically superior."

<span class="mw-page-title-main">Linda Birnbaum</span> American toxicologist

Linda Silber Birnbaum is an American toxicologist, microbiologist and the former director of the National Institute for Environmental Health Sciences, as well as the National Toxicology Program, positions she held from January 18, 2009 until October 3, 2019. She also serves as an adjunct professor at the University of North Carolina at Chapel Hill School of Public Health and as a member of the editorial board of Environment International.

<span class="mw-page-title-main">Glycidamide</span> Chemical compound

Glycidamide is an organic compound with the formula H2NC(O)C2H3O. It is a colorless oil. Structurally, it contains adjacent amides and epoxide functional groups. It is a bioactive, potentially toxic or even carcinogenic metabolite of acrylonitrile and acrylamide. It is a chiral molecule.

References

  1. 1 2 "Office of the National Toxicology Program". NIEHS. December 13, 2010. Archived from the original on December 20, 2010. Retrieved January 15, 2011.
  2. "History of the NTP - National Toxicology Program". National Toxicology Program. Archived from the original on October 16, 2010. Retrieved January 15, 2011.
  3. NIH Revitalization Act of 1993 (P.L. 103-43, codified at 42 U.S.C. 285l-1 and 42 U.S.C. 283e)
  4. ICCVAM Authorization Act of 2000 (P.L. 106-545, codified at 42 U.S.C. 285l-3)
  5. 1st Report on Carcinogens. 1980.
  6. 15th Report on Carcinogens. 2021.
  7. "14th Report on Carcinogens". National Toxicology Program. Retrieved February 17, 2021.