Relative oral bioavailability of microgranulated amoxicillin in pigs.

A new microgranulated formulation of amoxicillin trihydrate for in-feed medication was developed using a lipogelled matrix. Its relative bioavailability was compared with powdered drug in pigs and an assessment was made to determine whether therapeutic concentrations were achieved. Microgranules containing 10% (MICR10) and 30% (MICR30) amoxicillin and free amoxicillin trihydrate powder (reference, AMX) were administered at dosages of 50 mg of amoxicillin/kg b.w. using a three-way-crossover design. Amoxicillin analysis in serum was performed by a sensitive high performance liquid chromatography (HPLC) method with fluorometric detection, using an extraction procedure already described for edible tissues of fish and adapted and validated for pig serum. The oral bioavailability of both microgranulated formulations was higher than that of the reference formulation [relative bioavailability (F): 153.9 +/- 58.2% for MICR10; 126.2 +/- 70.5% for MICR30] and the area under the concentration-time curve (AUC) values of MICR10 and AMX formulations were significantly different (P < 0.05). Differences between the mean maximum concentration (Cmax), time of Cmax (tmax) and mean residence time (MRT) of the drug formulations were not significant. Microgranulated amoxicillin is suitable for in-feed administration to pigs and, because of its higher oral bioavailability compared with the powdered compound, it may be more effective for the treatment of susceptible infections.

[1]  A. Grahnén,et al.  Nonlinearity of amoxicillin absorption kinetics in human , 2006, European Journal of Clinical Pharmacology.

[2]  P. Collier,et al.  The application of statistical moment theory to the evaluation ofin vivo dissolution time and absorption time , 1980, Journal of Pharmacokinetics and Biopharmaceutics.

[3]  G. Amidon,et al.  The effect of amiloride on the in vivo effective permeability of amoxicillin in human jejunum: experience from a regional perfusion technique. , 2002, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[4]  Y. Kataoka,et al.  A 10-year survey of antimicrobial susceptibility of streptococcus suis isolates from swine in Japan. , 2000, The Journal of veterinary medical science.

[5]  C. Friis,et al.  Bioavailability of amoxycillin in pigs. , 1998, Journal of veterinary pharmacology and therapeutics.

[6]  C. Friis,et al.  Water medication of a swine herd with amoxycillin. , 1998, Journal of veterinary pharmacology and therapeutics.

[7]  C. Friis,et al.  Penetration of amoxycillin into the respiratory tract tissues and secretions in pigs. , 1998, Research in veterinary science.

[8]  J. Nielsen,et al.  Penetration of amoxycillin to the respiratory tract tissues and secretions in Actinobacillus pleuropneumoniae infected pigs. , 1998, Research in veterinary science.

[9]  J. Freeman,et al.  Determination of amoxicillin in catfish and salmon tissues by liquid chromatography with precolumn formaldehyde derivatization. , 1996, Journal of AOAC International.

[10]  J. Peris,et al.  Low bioavailability of amoxicillin in rats as a consequence of presystemic degradation in the intestine , 1994, Antimicrobial Agents and Chemotherapy.

[11]  F. Torres-Molina,et al.  Nonlinearities in amoxycillin pharmacokinetics II. Absorption studies in the rat , 1992, Biopharmaceutics & drug disposition.

[12]  Claude Carbón,et al.  Reappraisal of amoxycillin absorption kinetics. , 1991, The Journal of antimicrobial chemotherapy.

[13]  Claude Carbón,et al.  Nifedipine enhances amoxicillin absorption kinetics and bioavailability in humans. , 1990, The Journal of pharmacology and experimental therapeutics.

[14]  A. Pijpers,et al.  In vitro activity of five tetracyclines and some other antimicrobial agents against four porcine respiratory tract pathogens. , 1989, Journal of veterinary pharmacology and therapeutics.

[15]  J. Egerton,et al.  Effect of ingesta on systemic availability of penicillins administered orally in dogs. , 1986, Journal of veterinary pharmacology and therapeutics.

[16]  J. Wagner,et al.  KINETIC ANALYSIS OF BLOOD LEVELS AND URINARY EXCRETION IN THE ABSORPTIVE PHASE AFTER SINGLE DOSES OF DRUG. , 1964, Journal of pharmaceutical sciences.