Clinical Veterinary Medicine Division Equine Research Institute, Japan Racing Association, Shimotsuke, Japan.
Drug Analysis Department, Laboratory of Racing Chemistry, Utsunomiya, Japan.
Equine Vet J. 2021 Nov;53(6):1239-1249. doi: 10.1111/evj.13406. Epub 2021 Jan 21.
First-generation cephalosporins have good activity against gram-positive bacteria and are extensively used in horses. There are few reports of pharmacokinetics and pharmacodynamics (PK/PD) analysis of cephalosporins in horses.
To optimise the dosages of the two first-generation cephalosporins cephalothin (CET) and cefazolin (CEZ) in horses using PK/PD concepts.
Experimental study with single administration.
Drug plasma concentrations following a single intravenous (i.v.) administration of 22 mg/kg bodyweight (bwt) CET in 12 horses and of 10 mg/kg bwt CEZ in six horses were measured using LC-MS/MS. Data were modelled using a nonlinear mixed effect modelling followed by Monte Carlo simulations. Minimum inhibitory concentrations (MICs) against Streptococcus zooepidemicus and Staphylococcus aureus isolated from horses were determined by the microbroth dilution method.
The percentages of CET and CEZ binding to serum proteins were 19.9% ± 8.4% and 15.2% ± 8.5% respectively. For both CET and CEZ, the MIC against S. zooepidemicus was 0.12 mg/L and against S. aureus was 0.5 mg/L. For CET, to achieve a probability of target attainment (PTA) of 90% for a PK/PD target of a free serum plasma concentration exceeding the MIC for 40% of the dosing interval, an empirical CET dosage regimen of 22 mg/kg bwt q8h and 22 mg/kg bwt q4h i.v. administration were required for S. zooepidemicus and S. aureus respectively. For CEZ, the corresponding dosage regimens were 10 mg/kg bwt q12h and 10 mg/kg bwt q8h.
Small sample size only in healthy horses.
For CET, more frequent administration than that currently recommended (22 mg/kg bwt q6-12h) is required to empirically control S. aureus infection in horses. For CEZ, less frequent administration compared to the dosage regimen currently proposed (10-22 mg/kg bwt q6h) could control S. zooepidemicus and S. aureus infections in horses.
第一代头孢菌素对革兰阳性菌具有良好的活性,在马中广泛使用。关于头孢菌素在马中的药代动力学和药效学(PK/PD)分析的报道很少。
使用 PK/PD 概念优化两种第一代头孢菌素头孢噻吩(CET)和头孢唑林(CEZ)在马中的剂量。
单次给药的实验研究。
12 匹马单次静脉注射(i.v.)22mg/kg 体重(bwt)CET 和 6 匹马单次静脉注射 10mg/kg bwt CEZ 后,采用 LC-MS/MS 测定药物血浆浓度。采用非线性混合效应模型进行数据建模,然后进行蒙特卡罗模拟。使用微量肉汤稀释法测定马源分离的马疱疹病毒和金黄色葡萄球菌的最小抑菌浓度(MIC)。
CET 和 CEZ 与血清蛋白的结合率分别为 19.9%±8.4%和 15.2%±8.5%。CET 和 CEZ 对马疱疹病毒的 MIC 均为 0.12mg/L,对金黄色葡萄球菌的 MIC 均为 0.5mg/L。对于 CET,为了实现 PK/PD 目标,即游离血清血浆浓度超过 MIC 的 40%给药间隔的概率(PTA)为 90%,对于马疱疹病毒和金黄色葡萄球菌,分别需要 22mg/kg bwt q8h 和 22mg/kg bwt q4h 的经验性 CET 剂量方案。对于 CEZ,相应的剂量方案分别为 10mg/kg bwt q12h 和 10mg/kg bwt q8h。
仅在健康马中进行了小样本量研究。
对于 CET,需要比目前推荐的更频繁的给药(22mg/kg bwt q6-12h),以经验性控制马的金黄色葡萄球菌感染。与目前建议的剂量方案(10-22mg/kg bwt q6h)相比,CEZ 给药频率更低,可控制马疱疹病毒和金黄色葡萄球菌感染。