Ensink J M, Barneveld A, Klein W R, van Miert A S, Vulto A G
Department of General and Large Animal Surgery, Faculty of Veterinary Medicine, Utrecht University.
Vet Q. 1994 May;16 Suppl 2:S113-6.
The plasma disposition of ampicillin after intravenous administration at a dose rate of 15 mg/kg was studied in six healthy, 1-month-old foals. The oral bioavailability of pivampicillin was determined in the same foals at four ages, ranging from 11 days to 4 months. Pivampicillin was administered orally at a dose rate of 19.9 mg/kg, which is equivalent on a molecular basis to 15 mg/kg ampicillin. Ampicillin concentrations in plasma were determined up to 12 hours after administration. After intravenous administration, the mean distribution and elimination half-lives of ampicillin were 0.121 and 0.624 h, respectively. The volume of distribution (Vss) appeared to be 0.334 l/kg. Orally administered pivampicillin was rapidly absorbed in all age groups, producing mean peak plasma concentrations of 3.83 to 5.69 micrograms/ml 1 h after administration. The mean bioavailability of pivampicillin in the different age groups ranged from 39.4 to 52.9%. There was no statistically significant difference in peak plasma concentration or bioavailability between the age groups. It is concluded that pivampicillin at a dose rate of 19.9 mg/kg orally gives satisfactory plasma concentrations in foals of all ages.
对6匹1月龄健康小马驹静脉注射剂量率为15mg/kg的氨苄西林后的血浆处置情况进行了研究。在同一批小马驹4个不同年龄阶段(11天至4个月)测定了匹氨西林的口服生物利用度。匹氨西林以19.9mg/kg的剂量率口服给药,在分子基础上相当于15mg/kg氨苄西林。给药后12小时内测定血浆中的氨苄西林浓度。静脉给药后,氨苄西林的平均分布半衰期和消除半衰期分别为0.121小时和0.624小时。分布容积(Vss)似乎为0.334l/kg。口服给药的匹氨西林在所有年龄组中均迅速吸收,给药后1小时血浆平均峰值浓度为3.83至5.69微克/毫升。不同年龄组中匹氨西林的平均生物利用度范围为39.4%至52.9%。各年龄组之间的血浆峰值浓度或生物利用度无统计学显著差异。得出结论,剂量率为19.9mg/kg口服的匹氨西林在所有年龄的小马驹中均能产生令人满意的血浆浓度。