1975
DOI: 10.1289/ehp.751095
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Studies on the evaluation of the toxicity of various salts of lead, manganese, platinum, and palladium.

Abstract: Preliminary studies have been conducted on various parameters in order to assess the possible and relative toxicities of a number of metallic salts. Upon oral administration in lethal-dose experiments, two soluble Pt4+ salts were more toxic than the other salts tested. Following intraperitoneal injection in lethal-dose experiments, PbC1, was less toxic than several of the soluble or partially soluble salts of Pt'+, Pd2+, and Mn'+. An intake of a total of approximately 250 mg of Pt4+ per rat in the drinking flu… Show more

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Cited by 59 publications
(10 citation statements)
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“…Toxicity of metal catalyst salts toward rats via ingestion is taken from MSDS and literature sources. Similar to the method previously mentioned, LD 50 values for salts are chosen to being the most unfavorable.…”
Section: Methodsmentioning
confidence: 99%
“…Toxicity of metal catalyst salts toward rats via ingestion is taken from MSDS and literature sources. Similar to the method previously mentioned, LD 50 values for salts are chosen to being the most unfavorable.…”
Section: Methodsmentioning
confidence: 99%
“…(424) The fractional absorption of palladium, administered as the chloride, from the gastrointestinal tract of adult rats is <5 Â 10 À3 (Moore et al, 1974(Moore et al, , 1975b. Acute toxicity data from experiments on rats indicate that the fractional absorption of palladium administered as PdO or PdSO 4 is even smaller than that of the chloride (Holbrook et al, 1975).…”
Section: Ingestionmentioning
confidence: 99%
“…(589) Information regarding the detection limit for routine individual measurement is not available. , 1981), a fractional absorption value of 0.01 was recommended for all chemical forms of platinum based on the animal studies by Moore et al (1975) and Holbrook et al (1975). This value was also adopted in Publication 68 (ICRP, 1994a).…”
Section: Individual Monitoringmentioning
confidence: 99%
“…In animals, the lack of Mn can result in impaired insulin production, alterations in lipoprotein metabolism, impaired oxidant defense system, and perturbations in growth factor metabolism (for review see Keen et al, 1999). When rats are treated orally with high doses of Mn salts, retention of excess concentrations of Mn are not detectable after 14 days in any tissue suggesting that the rate of accumulation and overall toxicity of Mn is rather low (Holbrook et al, 1975). In line with that assumption, confirmed cases of Mn toxicosis in humans are currently restricted to cases of exposure to high levels of airborne Mn, and to cases in which Mn excretory pathways are malfunctioning (Keen et al, 1999).…”
Section: Hepatic Manganese Contentmentioning
confidence: 99%