Watson A D, Emslie D R, Martin I C, Egerton J R
J Vet Pharmacol Ther. 1986 Jun;9(2):140-9. doi: 10.1111/j.1365-2885.1986.tb00023.x.
Six penicillin preparations were administered to six dogs of various types, both when the dogs were fasted and when fed a standard meal immediately before dosing. The preparations used were: amoxycillin tablets and drops, ampicillin tablets, penicillin V tablets, phenethicillin tablets and cloxacillin capsules. A Latin square design was employed with ampicillin and the two amoxycillin preparations, while three separate cross-over studies were done with penicillin V, phenethicillin and cloxacillin. Dose rates used were 50 mg/kg for cloxacillin, and 10 mg/kg for the others. A microbiological method was used to assay penicillin in blood samples taken at intervals after dosing. Values for peak plasma drug concentration (Cmax), the time at which it occurred (Tmax), and area under the curve (AUC) were obtained for each curve of drug concentration plotted against time. In fasted dogs, ampicillin showed poorer systemic availability than did amoxycillin, with Cmax and AUC values of less than half those of amoxycillin. The solid and liquid preparations of amoxycillin had similar bioavailability. Ingesta adversely affected the systemic availability of antibiotic from all preparations tested. With ampicillin and both amoxycillin preparations, there were reduced Cmax and AUC and prolonged Tmax, indicating slowed and diminished absorption. Feeding did not alter Tmax with the other drugs, but reduced the Cmax of penicillin V, phenethicillin and cloxacillin and the AUC of cloxacillin. It is suggested that, if minimal impairment of bioavailability by ingesta is desired, then the penicillins commonly administered by mouth (amoxycillin, ampicillin, penicillin V, phenethicillin, cloxacillin) should be given to dogs that are fasting.
给6只不同类型的狗分别服用6种青霉素制剂,给药时狗处于禁食状态以及在给药前立即喂食标准餐两种情况下都进行了给药。所用制剂为:阿莫西林片和滴剂、氨苄西林片、青霉素V片、非奈西林片和氯唑西林胶囊。氨苄西林以及两种阿莫西林制剂采用拉丁方设计,而青霉素V、非奈西林和氯唑西林则进行了三项单独的交叉研究。所用剂量率为氯唑西林50mg/kg,其他制剂为10mg/kg。采用微生物学方法测定给药后不同时间采集的血样中的青霉素含量。针对每条药物浓度随时间变化的曲线,得出了血浆药物峰浓度(Cmax)、其出现的时间(Tmax)以及曲线下面积(AUC)的值。在禁食的狗中,氨苄西林的全身可用性比阿莫西林差,其Cmax和AUC值不到阿莫西林的一半。阿莫西林的固体和液体制剂具有相似的生物利用度。摄入食物对所有受试制剂的抗生素全身可用性都有不利影响。对于氨苄西林和两种阿莫西林制剂,Cmax和AUC降低,Tmax延长,表明吸收减慢且减少。喂食对其他药物的Tmax没有影响,但降低了青霉素V、非奈西林和氯唑西林的Cmax以及氯唑西林的AUC。建议,如果希望摄入食物对生物利用度的影响最小,那么通常口服的青霉素(阿莫西林、氨苄西林、青霉素V、非奈西林、氯唑西林)应该给禁食的狗服用。