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Setting Guidelines for Residues by Regulatory Authorities

Bound residues of tetracyclines may occur in bones of slaughtered animals for months after treatment. Theoretically, these could reach the food chain via contaminated (mechanically deboned) meat or meat and bonemeal. The accumulation of tetracyclines in tissues is illustrated by the findings of Toutain and Raynaud for oxytetracycline in calves (Table 2.8). Concentrations of oxytetracycline were relatively high in liver and kidney compared to the extrapolated zero-time concentration for serum (4.2 mg/1). The time required for residues to deplete to 0.1 mg/1 in serum was 143 hr, considerably shorter than the time required for residues to deplete to 0.1 mg/kg in liver and kidney, but similar to the depletion time for muscle. The data nicely illustrate the importance of tissue elimination half-life in determining decrease to the 0.1 mg/kg concentration despite an almost three-fold higher initial concentration [Pg.81]

18 and 0.06, respectively. Other tetracyclines, including tigecycline, recommended for human but not veterinary use. [Pg.81]

All advanced and several emerging economies have well-established, legally binding procedures for evaluating applications for marketing authorizations (MAs) for veterinary medicinal products (VMPs). The principal bodies and their legal status are indicated in Table 2.9. In the case of the EU of 27 member states, as well as the supranational [Pg.81]

TABLE 2.8 Oxytetracycline Residues in Calves after Intramuscular Administration of a Long-Acting Formulation  [Pg.81]

Tissue So (mg/kg) Tissue Serum Ratio at Zero Time fi/2p (h) Delay to Depletion to 0.1 mg/kg (h) [Pg.81]


See other pages where Setting Guidelines for Residues by Regulatory Authorities is mentioned: [Pg.81]    [Pg.81]   


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