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1.
J Am Assoc Lab Anim Sci ; 52(5): 553-9, 2013 Sep.
Article in English | MEDLINE | ID: mdl-24041210

ABSTRACT

We found that carprofen and meloxicam under 3 environmental conditions (ambient dark, ambient light, and 4 °C) remained stable for at least 7 d. We then evaluated the oral pharmacokinetics of meloxicam (20 mg/kg) and carprofen (10 mg/kg) in male C57BL/6 mice after oral gavage or administration in the drinking water. Mice did not drink meloxicam-medicated water but readily consumed carprofen-medicated water, consuming an average of 14.19 mL carprofen-medicated water per 100 g body weight daily; mice drank more during the dark phase than during the light phase. Plasma analyzed by HPLC (meloxicam) and tandem mass spectrometry (carprofen) revealed that the peak meloxicam and carprofen concentrations were 16.7 and 20.3 µg/mL and occurred at 4 and 2 h after oral gavage, respectively. Similar blood levels were achieved after 12 h access to the carprofen-medicated water bottle. At 24 h after oral gavage, the drugs were not detectable in plasma. Meloxicam plasma AUC, elimination half-life, apparent volume of distribution, and apparent oral clearance were 160.4 mg/L × h, 7.4 h, 0.36 L/kg, and 0.125 mL/h × kg, respectively. Carprofen plasma AUC, elimination half-life, apparent volume of distribution, and apparent oral clearance were 160.8 mg/L × h, 7.4 h, 0.42 L/kg, and 0.062 mL/h × kg, respectively. No gross or microscopic evidence of toxicity was seen in any mouse. Our findings indicate that carprofen can be administered in drinking water to mice and that medicated water bottles should be placed 12 to 24 h prior to painful procedures.


Subject(s)
Acute Pain/drug therapy , Anti-Inflammatory Agents, Non-Steroidal/pharmacokinetics , Carbazoles/pharmacokinetics , Thiazines/pharmacokinetics , Thiazoles/pharmacokinetics , Water/chemistry , Administration, Oral , Animals , Anti-Inflammatory Agents, Non-Steroidal/blood , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Carbazoles/blood , Carbazoles/chemistry , Chromatography, High Pressure Liquid , Drinking Behavior , Drug Stability , Half-Life , Male , Meloxicam , Mice , Mice, Inbred C57BL , Thiazines/blood , Thiazines/chemistry , Thiazoles/blood , Thiazoles/chemistry
2.
Can Vet J ; 48(1): 69-75, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17310625

ABSTRACT

Twenty-eight research dogs were enrolled to determine the prevalence of salmonellae shedding after consumption of 1 Salmonella-contaminated commercial raw food diet meal. Sixteen dogs were exposed to Salmonella-contaminated commercial raw food diets and 12 to Salmonella-free commercial raw food diets. Seven of the exposed dogs shed salmonellae 1-7 days after consumption of Salmonella-contaminated raw food diets. None of the dogs fed Salmonella-free diets shed salmonellae. No clinical signs were observed in either group. Five of the 7 dogs shed the same serotypes as those recovered from food samples used for feeding. Results showed the same serotypes and antimicrobial resistance pattern in 2 of the 7 shedders. Dogs fed Salmonella-contaminated raw food diets can shed salmonellae and may, therefore, be a source of environmental contamination potentially leading to human or animal illness.


Subject(s)
Animal Feed/microbiology , Dog Diseases/microbiology , Feces/microbiology , Food Contamination , Public Health , Salmonella Infections, Animal/microbiology , Animals , Colony Count, Microbial/veterinary , Dog Diseases/transmission , Dogs , Female , Food Contamination/analysis , Male , Risk Factors , Salmonella/isolation & purification , Salmonella Infections, Animal/transmission , Zoonoses
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