Putecova Kristina, Nedbalcova Katerina, Bartejsova Iva, Zouharova Monika, Matiaskova Katarina, Jeklova Edita, Viskova Michaela, Zouzelkova Petra, Jerabek Martin, Stastny Kamil
Veterinary Research Institute, Brno, Czech Republic.
Tekro spol. s r.o., Prague, Czech Republic.
Vet Med (Praha). 2021 May 31;66(6):248-256. doi: 10.17221/190/2020-VETMED. eCollection 2021 Jun.
A rapid, simple and highly efficient analytical method for the targeted determination of trimethoprim and sulfamethoxazole in serum samples has been developed and used to measure the pharmacokinetic curve of these medicinal substances after administration to chicken broilers. The pharmacokinetics properties of trimethoprim and sulfamethoxazole were investigated in clinically healthy broiler chickens after the single oral administration of the commercial preparation Methoxasol (Eurovet Animal Health, B.V., The Netherlands) at a dose of 0.275 ml/kg b.w. After a single dose drug administration, the chickens were sacrificed by decapitation under general anaesthesia by Isoflurin 1 000 mg/g (Vetpharma AH, Spain) and the blood was collected at precisely defined intervals: 15, 30, 45, 60, 90, 120, 180, 360 and 720 min after the administration. The serum concentrations of amoxicillin were determined using Q Exactive tandem mass spectrometer (Thermo Fisher Scientific, USA) in conjunction with liquid chromatography. The detected pharmacokinetic parameters of trimethoprim after the oral administration were C = 2.1 ± 1.0 μg/ml; T = 1.5 h; t = 0.88 h; k 0.009 3 ± 0.001 1 1/h; AUC = 2.901 ± 1.4 μg.h/ml; AUC = 2.907 ± 1.5 μg.h/ml; V 2.632 l/kg; Cl = 2.7 l/h. The pharmacokinetic parameters of sulfamethoxazole after the oral administration were C = 47.1 ± 15.3 μg/ml; T = 1 h; t = 1.92 h; k = 0.004 6 ± 0.000 3 1/h; AUC = 89.676 ± 26.9 μg.h/ml; AUC = 94.612 ± 28.4 μg.h/ml; V = 0.584 l/kg; Cl = 0.21 l/h. To the best of our knowledge, this is the first pharmacokinetic study of the combination of sulfamethoxazole and trimethoprim in broiler chickens.
已开发出一种快速、简单且高效的分析方法,用于靶向测定血清样本中的甲氧苄啶和磺胺甲恶唑,并用于测量这些药物物质在给肉鸡给药后的药代动力学曲线。在临床健康的肉鸡单次口服商业制剂Methoxasol(荷兰Eurovet Animal Health公司),剂量为0.275 ml/kg体重后,研究了甲氧苄啶和磺胺甲恶唑的药代动力学特性。单次给药后,在异氟醚1000 mg/g(西班牙Vetpharma AH公司)全身麻醉下通过断头处死鸡,并在精确确定的时间间隔采集血液:给药后15、30、45、60、90、120、180、360和720分钟。使用Q Exactive串联质谱仪(美国赛默飞世尔科技公司)结合液相色谱法测定阿莫西林的血清浓度。口服给药后检测到的甲氧苄啶药代动力学参数为:C = 2.1±1.0 μg/ml;T = 1.5小时;t = 0.88小时;k = 0.009 3±0.001 1 1/小时;AUC = 2.901±1.4 μg·h/ml;AUC = 2.907±1.5 μg·h/ml;V = 2.632 l/kg;Cl = 2.7 l/小时。口服给药后磺胺甲恶唑的药代动力学参数为:C = 47.1±15.3 μg/ml;T = 1小时;t = 1.92小时;k = 0.004 6±0.000 3 1/小时;AUC = 89.676±26.9 μg·h/ml;AUC = 94.612±28.4 μg·h/ml;V = 0.584 l/kg;Cl = 0.21 l/小时。据我们所知;这是首次对肉鸡中磺胺甲恶唑和甲氧苄啶组合进行的药代动力学研究。