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Pharmacokinetics and relative bioavailability of an oral amoxicillin-apramycin combination in pigs.


ABSTRACT: A new compound granular premix of amoxicillin (20% w/w dry mass)/apramycin (5% w/w dry mass) was developed, and its pharmacokinetics and relative bioavailability were determined in pigs following oral administration following a cross-over study design. The pharmacokinetic parameters of amoxicillin (t1/2? = 6.43 ± 4.85h, Cmax = 3.2 ± 1.35 ?g·mL-1, Tmax = 1.92 ± 0.58, AUCINF = 8.98 ± 2.11 h·?g·mL-1) and apramycin (t1/2? = 8.67±4.4h, Cmax = 0.23 ± 0.12 ?g·mL-1, Tmax = 2.25 ± 0.82 h, AUCINF = 12.37 ± 8.64h·?g·mL-1) when administered as the amoxicillin-apramycin granular premix did not significantly differ from those for the single-ingredient powder form of each component. The relative bioavailability of amoxicillin following oral administration of the amoxicillin-apramycin granular premix was 22.62% when compared to the intramuscular administration of commercial amoxicillin sodium-powder. This is the first report of a new amoxicillin-apramycin combination which has a potential veterinary application the for prevention and treatment digestive tract infections in pigs.

SUBMITTER: Dai C 

PROVIDER: S-EPMC5398684 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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Pharmacokinetics and relative bioavailability of an oral amoxicillin-apramycin combination in pigs.

Dai Chongshan C   Zhao Tingting T   Yang Xing X   Xiao Xilong X   Velkov Tony T   Tang Shusheng S  

PloS one 20170420 4


A new compound granular premix of amoxicillin (20% w/w dry mass)/apramycin (5% w/w dry mass) was developed, and its pharmacokinetics and relative bioavailability were determined in pigs following oral administration following a cross-over study design. The pharmacokinetic parameters of amoxicillin (t1/2λ = 6.43 ± 4.85h, Cmax = 3.2 ± 1.35 μg·mL-1, Tmax = 1.92 ± 0.58, AUCINF = 8.98 ± 2.11 h·μg·mL-1) and apramycin (t1/2λ = 8.67±4.4h, Cmax = 0.23 ± 0.12 μg·mL-1, Tmax = 2.25 ± 0.82 h, AUCINF = 12.37  ...[more]

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