Pharmacokinetics of acetaminophen after intravenous and oral administration in fasted and fed Labrador Retriever dogs

被引:11
作者
Sartini, Irene [1 ]
Lebkowska-Wieruszewska, Beata [2 ]
Lisowski, Andrzej [3 ]
Poapolathep, Amnart [4 ]
Cuniberti, Barbara [5 ]
Giorgi, Mario [1 ,6 ]
机构
[1] Univ Sassari, Dept Vet Med, Sassari, Italy
[2] Univ Life Sci, Dept Pharmacol Toxicol & Environm Protect, Lublin, Poland
[3] Univ Life Sci, Inst Anim Breeding & Biodivers Conservat, Lublin, Poland
[4] Kasetsart Univ, Fac Vet Med, Dept Pharmacol, Bangkok, Thailand
[5] North West Vet Specialists, Runcorn, Cheshire, England
[6] Univ Pisa, Dept Vet Sci, Pisa, San Piero A Gra, Italy
关键词
acetaminophen; dog; fasted; fed; HPLC-UV; BIOAVAILABILITY; PARACETAMOL; METABOLITES; ACID;
D O I
10.1111/jvp.12893
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acetaminophen (paracetamol) is used in dogs to manage fever and mild pain. The aim of this study was to assess the pharmacokinetics of acetaminophen in both fed and fasted Labrador Retrievers after a single intravenous and oral administration (20 mg/kg). Six healthy dogs underwent three treatments in a randomized block study (a,n = 2; b,n = 2; c,n = 2). In phase one, group a received acetaminophen intravenously, group b and c orally after being fasted and fed, respectively. In phase two and three, groups were swapped, and the experiment was repeated. At the end of the trial, each dog received the same treatment. Acetaminophen plasma concentrations were detected using a validated HPLC-UV method. The pharmacokinetic analysis was performed using a noncompartmental model. Clearance, volume at steady state and half-life of acetaminophen in Labrador Retrievers were 0.42 L/kg hr, 0.87 L/kg and 1.35 hr, respectively. No significant statistical differences were found between fasted and fed dogs regarding maximum plasma concentration, time at maximum concentration and bioavailability as measured by the AUC. Feeding does not significantly affect the acetaminophen oral pharmacokinetics.
引用
收藏
页码:28 / 35
页数:8
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