Effects of piroxicam on tissue distribution of sulfadimidine in West African Dwarf male and female goats.

Cases of Stevens-Johnson syndrome have been increasingly reported in Nigeria by individuals who consumed meat products of animals especially goats injected sulfonamides. Hence, tissue distribution and residues of intramuscular sulfadimidine were studied in West African Dwarf (WAD) goats. Twenty goats divided into two groups of 10 each (five males; five females) weighing 10.4 ± 1.63 kg were administered intramuscular sulfadimidine (100 mg/kg body weight), and the second group was coadministered 5 mg/kg of piroxicam via right and left thigh muscle, respectively. Samples of the liver, kidney, spleen, heart, lung, intestine, brain, and skeletal muscle were collected into sterile cellophane bags. Two untreated goats were killed and used for preparation of tissue standards. The tissue samples were stored frozen for analysis. High concentration of sulfadimidine residues was found in all the tissues of goats administered sulfadimidine as well as tissues of goats coadministered sulfadimidine/piroxicam for up to 30 days postdrug administration. Generally, residues of sulfadimidine were observed to be significantly higher than the acceptable limit (0.1 ppm). Hence, consumption of meats from WAD goats administered sulfadimidine may pose very high risk of Stevens-Johnson syndrome in sensitive humans. As such consumption of such meats should be avoided.

Acute toxicity studies of potassium permanganate in Swiss albino mice.

Acute toxicity study of potassium permanganate was carried out in Swiss albino mice. Potassium permanganate was administered at dose rate of 0.0, 500, 1000, 1500, 2000, 2500, 3000 and 3500mg/kg body weight to groups 1, 2, 3, 4, 5, 6, 7 and 8, ten per group for LD50 determination. The dead animals were posted for gross lesions. A predetermined dose of 160mg/kg of the chemical was administered to experimental group of 12 mice, whereas control group of 12 mice received 16ml/kg body weight of distilled water for a period of 7 days. Grower's marsh and water were provided ad libitum. The animals were weighed daily before administration of potassium permanganate. On the eighth day 1ml of blood sample was collected from both control and experimental mice for haematology and plasma biochemistry into ethylene diamine tetraacetic acid bottles. The median lethal dose (LD50) was estimated at 1449.7mg/kg body weight. There was no significant difference between the mean weight of control and experimental group. Haematological and biochemical parameters of both control and experimental groups did not increase significantly though there was a significant (P < 0.05) decrease in chloride ion level in plasma. Toxicity signs observed are rapid and shallow respiration, rough hair coat, dullness, diarrhoea, bloat, gastroenteritis, congestion of liver, paleness of lungs and hypochloraemia.