Lethal doses

Va2o-64, ALC (approx lethal concentration) Va2o-67, LC q. Va2o-64, -52, -88, ALD (approx lethal dose) Va2o-67, LD. See text for chemical names and stmctures. 

In laboratory tests, appHcation of DMAC to the skin of pregnant rats has caused fetal deaths when the dosages were close to the lethal dose level for the mother. Embryonal malformations have been observed at dose levels 20% of the lethal dose and higher. However, when male and female rats were exposed to mean DMAC concentrations of 31,101, and 291 ppm for 6 h per day over several weeks, no reproductive effects were observed (6). 

The lethal dose for 50% of the test animals, expressed ia terms of g of material per kg of body weight. 

Toxicity. The lethal dose of Mgp2 to guinea pigs by ingestion is 1000 mg/kg (17). 

Toxicology and Handling. The lethal dose by ingestion in guinea pigs is 150 mg/kg body weight (13). The TLV for KHF2 is 2.5 mg /m ... 

Table 11 summarizes values for the median lethal dose (LD q) for several species. In case of massive exposure, convulsions must be controlled, and glucose, fluid balance, and uriaary output must be maintained. Medical surveillance requires checking for damage to the Hver, the organ that apparently sustains initial damage, and monitoring for changes ia the blood profile. 

Most iron salts and compounds may be safely handled following common safe laboratory practices. Some compounds are irritants. A more serious threat is ingestion of massive quantities of iron salts which results in diarrhea, hemorrhage, fiver damage, heart damage, and shock. A lethal dose is 200 250 mg/kg of body weight. The majority of the victims of iron poisoning are children under five years of age. 

Table 8. Acute Lethal Doses of Lanthanide Chlorides for Mice...

The lowest dose reported to have caused death (lethal dose low). 

Value is LD q = lethal dose low, ie, lowest dose of a substance iatroduced by any route other than inhalation, adrninistered over any given period of time ia a single or divided dosage that has been reported to have caused death in the test organism. 

Environmental Impact of Ambient Ozone. Ozone can be toxic to plants, animals, and fish. The lethal dose, LD q, for albino mice is 3.8 ppmv for a 4-h exposure (156) the 96-h LC q for striped bass, channel catfish, and rainbow trout is 80, 30, and 9.3 ppb, respectively. Small, natural, and anthropogenic atmospheric ozone concentrations can increase the weathering and aging of materials such as plastics, paint, textiles, and mbber. For example, mbber is degraded by reaction of ozone with carbon—carbon double bonds of the mbber polymer, requiring the addition of aromatic amines as ozone scavengers (see Antioxidants Antiozonants). An ozone decomposing polymer (noXon) has been developed that destroys ozone in air or water (157). 

Chinese Herbal Medicines. Many traditional Chinese medicines have been screened for radioprotective activity in experimental animals. In one study of more than a thousand Chinese herbs, a number of agents increased the survival rate of dogs exposed to a lethal dose of y-rays by 30—40%, and some symptoms of radiation injury were ameHorated. These effects are potentially related to stimulation of the hemopoietic and immune systems (130). Extracts of five Chinese dmg plants, as weU as aspirin, effectively protected mice exposed to 7.5—8.0 Gy (750—800 rad) of y-radiation, and increased survival rates by 8—50% (131). Several Chinese traditional medicines, adininistered ip before or after irradiation, protected against Hpid peroxidation in a variety of mouse tissues, including BM, Hver, and spleen, as weU as in mouse Hver microsomal suspensions irradiated in vitro (132). 

The monoalkyl derivatives in salt form appear to have low toxicity. The monomethyl sulfate sodium salt has an approximate oral lethal dose greater than 5000 mg/kg of body weight for rats (129). Monododecyl sulfate sodium salt is widely marketed as a detergent and shampoo ingredient (oral LD q 1268 mg/kg for rats) (126). Both dimethyl sulfate and monomethyl sulfate occur in the environment in coal fly-ash and in airborne particulate matter (130). 

Tb allium, which does not occur naturaHy in normal tissue, is not essential to mammals but does accumulate in the human body. Levels as low as 0.5 mg/100 g of tissue suggest thallium intoxication. Based on industrial experience, 0.10 mg /m of thallium in air is considered safe for a 40-h work week (37). The lethal dose for humans is not definitely known, but 1 g of absorbed thallium is considered sufficient to kHl an adult and 10 mg/kg body weight has been fatal to children. In severe cases of poisoning, death does not occur earlier than 8—10 d but most frequently in 10—12 d. Tb allium excretion is slow and prolonged. For example, tb allium is present in the feces 35 d after exposure and persists in the urine for up to three months. 

Acute toxicity studies are often dominated by consideration of lethaUty, including calculation of the median lethal dose. By routes other than inhalation, this is expressed as the LD q with 95% confidence limits. For inhalation experiments, it is convenient to calculate the atmospheric concentration of test material producing a 50% mortaUty over a specified period of time, usually 4 h ie, the 4-h LC q. It is desirable to know the nature, time to onset, dose—related severity, and reversibiUty of sublethal toxic effects. 

The more soluble forms of barium such as the carbonate, chloride, acetate, sulfide, oxide, and nitrate, tend to be more acutely toxic (50). Mean lethal doses for ingested barium chloride were 300—500 mg/kg in rats and 7—29 mg/kg in mice (47). 

The threshold of a toxic dose in adult humans is about 0.2—0.5 g Ba the lethal dose in untreated cases is 3—4 g Ba, LD q about 66 mg/kg (47). The fatal dose of barium chloride for humans is reported to be between 0.8 and 0.9 g (0.55—0.60 g of Ba) (50). However, for most of the acid-soluble salts of barium, doses greater than 1 g have been tolerated (51). Lethal doses are summarized in Table 5. Dusts of barium oxide are considered potential dermal and nasal irritants (52). 

Table 5. Acute Lethal Doses of Soluble Barium Compounds ...

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