Biomarkers for Testing Toxicity and Monitoring Exposure to Xenobiotics

2019 ◽  
pp. 1165-1174 ◽  
Author(s):  
Jorge Estévez ◽  
Eugenio Vilanova ◽  
Miguel A. Sogorb
Keyword(s):  
Chemosphere ◽  
1981 ◽  
Vol 10 (10) ◽  
pp. 1123-1126 ◽  
Author(s):  
S. Galassi ◽  
M. Vighi

1987 ◽  
Vol 70 (6) ◽  
pp. 1049-1055 ◽  
Author(s):  
Dan B Prelusky ◽  
Robert M G Hamilton ◽  
Brian C Foster ◽  
Locksley H Trenholm ◽  
Brian K Thompson

Abstract The optimization of a simple, sensitive procedure using a chick embryotoxicity screening test (CHEST) bioassay for detection of toxic compounds is presented. Dosing protocols of eggs, using several mycotoxins (aflatoxin B„ deoxynivalenol, T-2 toxin) and appropriate controls, were evaluated for embryonic sensitivity, overall practicality of the procedure, and consistency of results. It was found that both type of carrier solvent and volume injected could significantly affect overall embryonic mortality. The chick embryo was most sensitive to the effects of toxins and solvents after 1 or 2 days of incubation; a rapid decrease in response was observed as the age of the embryo at dosing increased. Following administration of the toxins just below the shell membrane by way of a small hole (<0.5 mm diameter) punched in the shell, a good dose-response (°/o mortality) could be obtained regardless of the site of injection (except directly into the yolk), although dosing via the air sac position resulted in a slightly better statistical outcome. Although some variations in calculated LD50 values were found among repeated assays, statistical analyses showed that the differences were not due to dosing protocol but to the variations in embryo sensitivities among batches of eggs. Thus, if standard reference toxins for comparison are run concurrently, the CHEST assay can prove to be a very satisfactory model, as well as having considerable flexibility to be adapted to the needs and resources of many laboratories.


2004 ◽  
Vol 148 (1-2) ◽  
pp. 91-94 ◽  
Author(s):  
Mauro Vairano ◽  
Grazia Graziani ◽  
Lucio Tentori ◽  
Giuseppe Tringali ◽  
Pierluigi Navarra ◽  
...  

1918 ◽  
Vol 27 (5) ◽  
pp. 635-646 ◽  
Author(s):  
Herbert D. Taylor ◽  
J. Harold Austin

1. The substances injected intraperitoneally into mice and guinea pigs arranged in the order of their decreasing toxicity are: eucalyptol and brilliant green; mercurophen; mercuric chloride and chloramine-T; dichloramine-T and proflavine; hychlorite, Dakin's hypochlorite, Javelle water, and magnesium hypochlorite; iodine and phenol. 2. Now that Dakin's bland solvent, chlorcosane, is available as a vehicle for dichloramine-T, eucalyptol should probably be discarded for this purpose because of its much greater toxicity. 3. Inasmuch as experienced surgeons do not approve of the injection of solutions of iodine and phenol into closed cavities, it would seem advisable not to use any of the antiseptics here discussed in this manner inasmuch as all exhibit a greater toxicity for mice and guinea pigs than the two chemicals first named. 4. The method of testing toxicity of antiseptics by subcutaneous injection is not satisfactory because exudation and subsequent sloughing reduce the rate of absorption and make uncertain the amount finally absorbed.


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