Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Toxicity tests health

The health effects of sorbic acid and sorbates have been reviewed (165—167). The extremely low toxicity of sorbic acid enhances its desirabiHty as a food preservative. The oral LD q for sorbic acid in rats is 7—10 g/kg body weight compared to 5 g/kg for sodium chloride (165—169). In subacute and chronic toxicity tests in rats, 5% sorbic acid in the diet results in no abnormal effects after 90 days or lifetime feeding studies. A level of 10% in rat diets results in a slight enlargement of the Hver, kidneys, and thyroid gland (170). This same dietary level fed to mice also resulted in an increase in Hver and kidney weight... [Pg.287]

Because of the concern over hnman health hazards associated with PCDDs, many toxicity tests have been performed on rodents. Some toxicity data are given for 2,3,7,8-TCDD as follows ... [Pg.158]

There is a continuing interest in the development of biomarker assays for use in environmental risk assessment. As discussed elsewhere (Section 16.6), there are both scientific and ethical reasons for seeking to introduce in vitro assays into protocols for the regulatory testing of chemicals. Animal welfare organizations would like to see the replacement of toxicity tests by more animal-friendly alternatives for all types of risk assessment—whether for environmental risks or for human health. [Pg.314]

McCrary JE, Heagler MG. 1997. The use of a simultaneous multiple species acute toxicity test to compare the relative sensitivities of aquatic organisms to mercury. J Environ Sci Health Part A Environ Sci Eng Toxic Hazardous Substance Control 32 73-81. [Pg.180]

Data for PCP and terrestrial wildlife are incomplete and — in view of the large interspecies variations in sensitivity — need to be collected. Research is needed on reproductive effects in animals following inhalation exposure to PCP additional acute and intermediate toxicity testing chronic duration exposure studies on cancer induction, genotoxicity, and immunotoxicity and the development of alternate biomarkers of PCP exposure and antidotes (WHO 1987 USPHS 1994). Until the results of these studies become available, it seems reasonable to apply to wildlife the same levels recommended for human health protection. [Pg.1223]

EPA, U.S. Environmental Protection Agency, Prenatal Developmental Toxicity Study, Health Effects Test Guidelines, OPPTS 870.3700, EPA 712-C-98-207,1998a. http //www. epa.gov/opptsfrs/OPPTS Harmonized/870 Health Effects Test Guidelines/Series/870-6300.pdf... [Pg.339]

Toxicology and environmental health studies often lack a firm foundation of baseline data, and the NASGLP is a perfect starting point for a baseline data survey. During the field component of the survey, the crews collected two composite samples. One represented the top 5 cm of the soil directly below the litter layer (which will include a lot of the airborne components if they are present), and a second came from the 0-30-cm interval, independent of which soil horizon this may represent. Within this interval (the active layer), most of the interactions between biota and the non-living soil components take place, and thus is the important interval for this type if study. Environment Canada s Biological Methods Division selected one of the northern New Brunswick sites to collect a bulk sample in an attempt to create reference sites across Canada for standardized toxicity test methods. [Pg.187]

Category A lists three types of studies for human health effects basic acute toxicity tests, a 28-day animal study (referred to in other discussions as a "sub-chronic" test), and a series of two (or more) screening tests for mutagenicity and carcinogenicity. [Pg.62]

In the pharmaceutical industry, acute toxicity testing has uses other than for product safety determinations. First, as in other industries, acute toxicity determinations are part of industrial hygiene or occupational health environmental impact assessments (Deichmann and Gerarde, 1969). These requirements demand testing not only for finished products but frequently of intermediates as well. These issues and requirements, however, are discussed in Chapter 2 and are not directly addressed here. [Pg.130]

Festing, M.W. (1979). Properties of inbreed strains and outbreed stocks, with special reference to toxicity testing, J Toxicol Environ Health 5 53-68. [Pg.331]

Federal agencies such as the FDA and EPA require a battery of toxicity tests in laboratory animals to determine an additive s or a pesticide s potential for causing adverse health effects, such as cancer, birth defects, and adverse effects on the nervous system or other organs. Tests are conducted for both short-term (acute) and long-term (chronic) toxicity. For chronic effects other than cancer, laboratory animals are exposed to different doses to determine the level at which no adverse effects occur. This level is divided by an uncertainty or safety factor (usually 100) to account for the uncertainty of extrapolating from laboratory animals to humans and for individual human differences in... [Pg.49]

Influence of the Photopolymer Plate to the health Acute toxic tests with mouses show that the exposed Photopolymer Plate has no toxidity at all and even the unexposed Photopolymer Plate has only a very weak toxidity therefore, there are no bad influences to the health and the Photopolymer Plate can be handled safely. [Pg.279]

A manufacturer seeks approval from the FDA for the marketing of a new non-caloric sweetening agent. The manufacturer has conducted extensive animal toxicity testing on this new food additive, and has also provided to the FDA information about the chemical s use rates in foods and the expected rate of intake consumers might experience. Is it possible to predict whether the new additive will pose a health risk to consumers if it were to be approved for use in food ... [Pg.203]

In summary, probably due to the complex experimental work involved, bioaccumulation and chronic toxicity tests are scarce [40, 58] however, these studies are very important for a better knowledge of the effects on human health. [Pg.231]

APHA. Toxicity Testing with Phytoplancton. Standard Methods for the Examination of Water and Wastewater, 17th Ed. American Pubhc Health Association Washington, DC, 1989. [Pg.57]

Toxicology. 2. Toxicity testing. 3. Health risk assessment. 4. Environmental risk assessment. I. [Pg.426]

In their note, they also commented extensively on the deficiencies of a voluntary system. Grosset and Linstead concluded their note with a plea to set on foot, with or without further enquiry, the preparation of a comprehensive statute dealing with drugs and medicines that will bring the whole field, including the supervision of toxicity testing and clinical trials, under the responsibility of the Health Ministers advised by a central body of experts. ... [Pg.469]

Svirbely JL Toxicity tests of decaborane for laboratory animals. I. Acute toxicity studies. Arch Ind Health 11 132-137, 1955... [Pg.204]

Tansy MF, Werley M, Landin W Subacute inhalation toxicity testing with iodoform vapor. Toxicol Environ Health 8 59-70, 1981... [Pg.404]

Parchment, R.E. (1998) Alternative testing systems for evaluating noncarcinogenic, hematologic toxicity. Environmental Health Perspectives, 106 (Suppl. 2), 541-547. [Pg.437]

The reader is also referred to the OECD Guidance Document No. 43 on Reproductive Toxicity Testing and Assessment (13), which will form the basis for the methodological points discussed below. More information can also be found in the IPGS paper on principles for evaluating health risks to reproduction associated with exposure to chemicals (14) as well as in an overview paper by Buschmann (15). [Pg.41]

OECD (2008) Environment, Health and Safety Publications Series on Testing and Assessment, No. 43. Guidance Document on Reproductive Toxicity Testing and Assessment. Environment Directorate, Organisation for Economic Co-operation and Development. http //www.oecd.org/ officialdocuments/ displaydocumentpdficote=env/jm/mono%2 8 2008%29168tdoclanguage=en. Accessed 12 Feb 2012... [Pg.56]


See other pages where Toxicity tests health is mentioned: [Pg.289]    [Pg.37]    [Pg.458]    [Pg.255]    [Pg.122]    [Pg.178]    [Pg.47]    [Pg.211]    [Pg.176]    [Pg.199]    [Pg.406]    [Pg.392]    [Pg.31]    [Pg.146]    [Pg.153]    [Pg.357]    [Pg.491]    [Pg.516]    [Pg.75]    [Pg.301]    [Pg.342]    [Pg.356]    [Pg.30]    [Pg.43]    [Pg.59]    [Pg.195]    [Pg.228]    [Pg.183]   
See also in sourсe #XX -- [ Pg.13 , Pg.14 , Pg.15 , Pg.16 , Pg.17 , Pg.18 , Pg.19 , Pg.20 , Pg.21 ]




SEARCH



Toxic Toxicity test

Toxicity test

© 2024 chempedia.info