Subcutaneous toxicity

Hoechst. 1966a. Alpha-thiodan Acute oral and subcutaneous toxicity to the mouse. Hoechst Aktiengesellschaft, Frankfurt, Germany. Doc A14023. [unpublished study]... 

Subcutaneous Toxicity. This route has been popular for investigational studies of various types, particularly to assess the effect of therapy given by other routes. Times to onset of signs are usually within minutes, and effects are similar to those seen by the i.v. route. However, as is well known with other chemicals dosed by the s.c. route, absorption may be erratic depending on the tissue stratum into which the injection is given. 

Health and Safety Factors. The following toxicities have been reported for cyanoacetic acid oral LD q (rat) 1500 mg/kg subcutaneous LD q (rabbit), 1900 mg/kg and subcutaneous LD q (frog) 1300 mg/kg (29). Eor ethyl cyanoacetate the following toxicities have been reported interperitoneal LD q (mice), 750 mg/kg subcutaneous LD q (rabbits), 1500 mg/kg and subcutaneous LD q (frogs), 4000 mg/kg. 

The only reported toxicity data on zinc fluoride in the NIOSH RTECS file is a LD q of 280 mg/kg for subcutaneous adniinistration in frogs. 

Barium peroxide is a strong oxidizer and can cause fire when in contact with combustible materials. It is a powerful irritant to skin, eyes, and mucous membranes (2). Consequendy, it is also toxic via the subcutaneous route protective clothing should be worn during handling. The LD q value (mouse, oral) is 50 mg/kg (2). 

In Vivo Effects of Florfenicol. Comparative acute toxicities of florfenicol, chloramphenicol, and thiamphenicol in mice ate given in Table 6. As can be seen, florfenicol is similar to thiamphenicol in acute toxicity by oral and subcutaneous (sc) adininistration, but is comparable to chloramphenicol by intraperitoneal (ip) and intravenous (iv) routes. Semm levels in mice following either a single or subcutaneous dose of 200 mg/kg of amphenicol have... 

Toxicity. No mortahty in laboratory animals was induced in percutaneous doses up to 3.8 g/kg body weight (19,20). Subcutaneous adininistration of sulfolane gives LD q values for rats, mice, and rabbits of 1.606, 1.360, and 1.900—3.500 g/kg body weight, respectively (21). LD q values... 

The relative toxicities of thallium compounds depend on their solubHities and valence states. Soluble univalent thallium compounds, eg, thaHous sulfate, acetate, and carbonate, are especiaHy toxic. They are rapidly and completely absorbed from the gastrointestinal tract, skin peritoneal cavity, and sites of subcutaneous and intramuscular injection. Tb allium is also rapidly absorbed from the mucous membranes of the respiratory tract, mouth, and lungs foHowing inhalation of soluble thallium salts. Insoluble compounds, eg, thaHous sulfide and iodide, are poorly absorbed by any route and are less toxic. 

In order to induce a toxic effect, local or systemic, the causative material must first come into contact with an exposed body surface these are the routes of exposure. In normal circumstances, and depending on the nature of the material, the practical routes of exposure are by swallowing, inhalation, and skin and eye contact. In addition, and for therapeutic purposes, it may be necessary to consider intramuscular, intravenous, and subcutaneous injections as routes of adininistration. 

Newer bleomycins such as peplomycin and especially liblomycin, are more resistant to bleomycin hydrolase. This results in less lung toxicity but more bone marrow toxicity, and allows for a different spectmm of antitumor action. Bleomycin is inactive orally it is given intravenously, intramuscularly, subcutaneously, or directiy into a cavity such as the pleural cavity. The majority of dmg is excreted unchanged in the urine. 

Melarsonyl potassium (Mel W, Trimelarsen) [13355-00-5] is a thioarsenite closely related to melarsoprol, and it also has been used for the treatment of trypanosomiasis (172). However, it appears to be more toxic and less effective than melarsoprol. The only advantage of melarsonyl potassium is that it is water-soluble and can be adrninistered intramuscularly or subcutaneously. This property is useful when the intravenous route caimot be employed. 

Effects in Animals. The LD ia rats for all light chlorophenols, irrespective of the administration route, ties between 130 and 4000 mg/kg body weight. The toxicity of these compounds ia order of increasing strength is tetrachlorophenols > monochloropheno1 s > dichlorophenols > trichlorophenols when the chlorophenol is administered either orally or by subcutaneous iajection. 

The water solubiUty of glutaric acid fosters its toxicity. Glutaric acid is a known nephrotoxin. Renal failure has been documented ia rabbits adruinistered sodium glutarate subcutaneously (124). Dibasic ester (Du Pont), which contains primarily dimethyl glutarate, has low acute toxicity by inhalation and by ingestion, and is moderately toxic via dermal absorption. The acid is both a dermal and ocular irritant of humans. The ester is a severe skin irritant and may cause a rash ia humans (120). 

Pharmacology. Lycorine was first examined by Morishima wl found it relatively non-toxic to mammals. Given per os or subcutaneous, to the dog or cat, it causes, in small doses, salivation and in large dos vomiting and diarrhoea. It has no special effect on the blood pressure death seems to be due to a generalised collapse. Post mortem —hyper m and ecchymoses in the stomach, intestine, pulmonary pleura and end... 

Of the other Strychnos alkaloids vomicine has been investigated by Ruickoldt, who finds that in mice and rabbits it causes clonic convulsions, due to stimulation above the level of the anterior corpore quad-ragemina. Convulsions can be elicited after intravenous, but not after subcutaneous, injections. The toxicity is low twelve times the convulsive dose does not cause death. No special action is exerted on blood... 

Thiamin has a very low toxicity (oral LD5o of thiaminchloride hydrochloride in mice 3-15 g/kg body weight). The vitamin is used therapeutically to cure polyneuropathy, beri-beii (clinically manifest thiamin deficiency), and Wernicke-Korsakoff Syndrome ( Wernicke encephalopathy and Korsakoff psychosis). In mild polyneuropathy, 10-20 mg/d water-soluble or 5-10 mg/d lipid-soluble thiamin are given orally. In more severe cases, 20-50 mg/d water-soluble or 10-20 mg/d lipid-soluble thiamin are administered orally. Patients suffering from beri-beri or from early stages of Wernicke-Korsakoff Syndrome receive 50-100 mg of thiamin two times a day for several days subcutaneously or intravenously until symptoms are alleviated. Afterwards, the vitamin is administered orally for several weeks. 

Toxicity. MEDINA is apparently non-toxic to rabbit penile mucosa its cumulative effect on abraded and intact rabbit skin is slightly greater than Tetryl no damage was observed to rabbit cornea and there was no evidence of sensitization by subcutaneous injection in guinea pigs. It was concluded that its toxicity is similar to that of Tetryl (Ref 11, p 138)... 

The toxicity of IPN is evaluated by Ref 6 as follows (a) When inhaled as a vapor or adsorbed thru the skin, IPN acts as a vasodilator and produces a headache in the same manner as other organic nitrates (b) When injected subcutaneously into rats at the rate of 4cc/kg body wt, it was concluded that the max allowable concn is lOOppm and (c) When rats were exposed to different concn levels of IPN in air the following resulted ... 

Alkyl olefinsulfonates (AOS) are essentially nontoxic with reported LD50 values in mice of 3000 mg/kg (oral), 1660 mg/kg (subcutaneous), 170 mg/kg (intraperitoneal), and 90 mg/kg (intravenous). The toxic signs seen at the higher doses included reduced voluntary activity, diarrhea, anemia, dyspnea, and respiratory collapse. Clonic convulsion followed by respiratory collapse was seen in mice given the material intravenously [147,148]. 

OCDD. Signs of maternal toxicity were not observed in rats given 100 or 500 mg/kg/day OCDD. Examination of the fetuses did not reveal changes in fetal body measurements, incidence of fetal resorptions, or incidence of any fetal anomaly among litters or the fetal population. At 500 mg/kg/day, the incidence of subcutaneous edema was significantly increased among the fetal population (23/100 compared with 8/156 in controls) but not among litters (9/18 compared with 6/28 in controls). 

Although the initially reported tissue compatibility tests for subcutaneous implants of poly(BPA-iminocarbonate) were encouraging (41,42), it is doubtful whether this polymer will pass more stringent biocompatibility tests. In correspondence with the properties of most synthetic phenols, BPA is a known irritant and most recent results indicate that BPA is cytotoxic toward chick embryo fibroblasts in vitro (43). Thus, initial results indicate that poly(BPA-iminocarbonate) is a polymer with highly promising material properties, whose ultimate applicability as a biomaterial is questionable due to the possible toxicity of its monomeric building blocks. 

Earlier studies by Wiles et al. (5) in which palytoxin was administered by various routes showed that this material was extremely toxic to rabbits, dogs, and monkeys. The effect of route of administration on toxicity varies in that intravenous (iv), intramuscular (im), and subcutaneous (sc) toxicity is high, yet intrarectal (ir) or oral (po) palytoxin is relatively ineffective. It was also observed that palytoxin... 

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