Pharmacokinetics of amoxicillin administered in drinking water to recently weaned 3- to 4-week-old pigs with diarrhea experimentally induced by Escherichia coli O149:F4

Gerda M. Jensen Department of Veterinary Pathobiology, The Royal Veterinary and Agricultural University, Ridebanevej 9, DK-1870 Frederiksberg C, Denmark.

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Jens Lykkesfeldt Department of Veterinary Pathobiology, The Royal Veterinary and Agricultural University, Ridebanevej 9, DK-1870 Frederiksberg C, Denmark.

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Kai Frydendahl Danish Institute for Food and Veterinary Research, Bülowsvej 27, DK-1790 Copenhagen V, Denmark.

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Kristian Møller Danish Institute for Food and Veterinary Research, Bülowsvej 27, DK-1790 Copenhagen V, Denmark.

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Ove Svendsen Department of Veterinary Pathobiology, The Royal Veterinary and Agricultural University, Ridebanevej 9, DK-1870 Frederiksberg C, Denmark.

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Abstract

Objective—To measure effects of Escherichia coli O149:F4–induced diarrhea on water consumption and pharmacokinetics of amoxicillin after administration in drinking water.

Animals—24 recently weaned 24- to 28-day-old crossbred pigs.

Procedure—10 pigs were inoculated with E coli O149:F4; all 10 pigs subsequently developed diarrhea. Pigs were medicated by administration of amoxicillin in the drinking water (0.75 mg/mL) for a 4-hour period on 2 consecutive days. Fourteen age-matched noninfected healthy pigs (control group) were medicated in a similar manner. Blood samples were obtained from both groups daily, and plasma concentrations of amoxicillin were analyzed by use of high-performance liquid chromatography.

Results—Diarrhea reduced the area under the plasma concentration-versus-time curve (AUC) and maximum plasma concentration (Cmax) of amoxicillin on the first day of medication by 56% and 63%, respectively. The AUC of amoxicillin on the second day of medication for diarrheic pigs did not differ significantly from that of control pigs on the first day of medication.

Conclusions and Clinical RelevanceE coli–induced diarrhea reduced the AUC of amoxicillin and time that plasma concentration of amoxicillin was > 0.025 μg/mL and, hence, less likely to have a therapeutic effect on the first day of administration in drinking water. On the assumption that plasma concentrations may indirectly reflect concentrations at the site of infection, analysis of our results suggests that higher doses of amoxicillin may be appropriate for administration in drinking water during a 4-hour period on the first day that pigs have diarrhea attributable to E coli O149:F4.

Abstract

Objective—To measure effects of Escherichia coli O149:F4–induced diarrhea on water consumption and pharmacokinetics of amoxicillin after administration in drinking water.

Animals—24 recently weaned 24- to 28-day-old crossbred pigs.

Procedure—10 pigs were inoculated with E coli O149:F4; all 10 pigs subsequently developed diarrhea. Pigs were medicated by administration of amoxicillin in the drinking water (0.75 mg/mL) for a 4-hour period on 2 consecutive days. Fourteen age-matched noninfected healthy pigs (control group) were medicated in a similar manner. Blood samples were obtained from both groups daily, and plasma concentrations of amoxicillin were analyzed by use of high-performance liquid chromatography.

Results—Diarrhea reduced the area under the plasma concentration-versus-time curve (AUC) and maximum plasma concentration (Cmax) of amoxicillin on the first day of medication by 56% and 63%, respectively. The AUC of amoxicillin on the second day of medication for diarrheic pigs did not differ significantly from that of control pigs on the first day of medication.

Conclusions and Clinical RelevanceE coli–induced diarrhea reduced the AUC of amoxicillin and time that plasma concentration of amoxicillin was > 0.025 μg/mL and, hence, less likely to have a therapeutic effect on the first day of administration in drinking water. On the assumption that plasma concentrations may indirectly reflect concentrations at the site of infection, analysis of our results suggests that higher doses of amoxicillin may be appropriate for administration in drinking water during a 4-hour period on the first day that pigs have diarrhea attributable to E coli O149:F4.

Contributor Notes

Dr. Frydendahl's present address is Chr. Hansen A/S, Culture QC Avedoere, Jernholmen 1-27, DK-2650 Hvidovre, Denmark.

Supported by the Danish Research Training Council, Danish Institute of Agricultural Sciences, Danish Institute for Food and Veterinary Research, and The Royal Veterinary and Agricultural University of Copenhagen.

The authors thank Jytte Nielsen, Lisbeth Hansen, Zaineb Alhilli, Jonas Michelsen, and Henning Rasmussen for technical assistance.

Dr. Svendsen.
  • 1

    Frydendahl K. Prevalence of serogroups and virulence genes in Escherichia coli associated with postweaning diarrhea and edema disease in pigs and a comparison of diagnostic approaches. Vet Microbiol 2002; 85: 169182.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 2

    Nagy B, Casey TA, Moon HW. Phenotype and genotype of Escherichia coli isolated from pigs with postweaning diarrhea in Hungary. J Clin Microbiol 1990; 28: 651653.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 3

    Hathorne WT, Keefe TJ. Amoxicillin as an antimicrobial agent in the control of colibacillosis in swine. Vet Med Small Anim Clin 1977; 72(suppl): 780783.

    • Search Google Scholar
    • Export Citation
  • 4

    Yeoman GH. Microbiology and bioavailability of amoxicillin. Vet Med Small Anim Clin 1977; 72(suppl): 720743.

  • 5

    Tsuji A, Nakashima E, Hamano S, et al. Physicochemical properties of amphoteric beta-lactam antibiotics I: stability, solubility, and dissolution behavior of amino penicillins as a function of pH. J Pharmacol Sci 1978; 67: 10591066.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 6

    Bigelow JA, Houpt TR. Feeding and drinking patterns in young pigs. Physiol Behav 1988; 43: 99109.

  • 7

    Brooks PH, Russell SJ, Carpenter JL. Water intake of weaned piglets from three to seven weeks old. Vet Rec 1984; 115: 513515.

  • 8

    Simonsen HB. Behaviour and distribution of fattening pigs in the multi-activity pen. Appl Anim Behav Sci 1990; 27: 311324.

  • 9

    Kenworthy R, Mitchell IDG. Escherichia coli infection of gnotobiotic pigs: significance of enterotoxin and endotoxin in the clinical state. J Comp Pathol 1976; 86: 275284.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10

    Jensen GM, Lykkesfeldt J, Frydendahl K, et al. Pharmacokinetics of amoxicillin after oral administration in recently weaned piglets with experimentally induced Escherichia coli O149:F4 diarrhea. Am J Vet Res 2004; 65: 992995.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11

    Argenzio RA. Pathophysiology of neonatal diarrhea. AgriPract 1984; 5: 2532.

  • 12

    Sjoevall J, Alván G, Aakerlund JE, et al. Dose-dependent absorption of amoxicillin in patients with an ileostomy. Eur J Clin Pharmacol 1992; 43: 277281.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 13

    Westphal JF, Jehl F, Brogaard JM, et al. Amoxicillin intestinal absorption reduction by amiloride: possible role of the Na(+)-H+ exchanger. Clin Pharmacol Ther 1995; 57: 257264.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14

    Marier JF, Beaudry F, Ducharme MP, et al. A pharmacokinetic study of amoxicillin in febrile beagle dogs following repeated administrations of endotoxin. J Vet Pharmacol Ther 2001; 24: 379383.

    • Search Google Scholar
    • Export Citation
  • 15

    Bucklin SE, Fujihara Y, Leeson MC, et al. Differential antibiotic-induced release of endotoxin from gram-negative bacteria. Eur J Clin Microbiol Infect Dis 1994; 13: 4351.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 16

    Crosby HA, Bion JF, Penn CW, et al. Antibiotic-induced release of endotoxin from bacteria in vitro. J Med Microbiol 1994; 40: 2330.

  • 17

    Sellwood R, Gibbons RA, Jones GW, et al. adhesion of enteropathogenic Escherichia coli to pig intestinal brush borders: the existence of two pig phenotypes. J Med Microbiol 1975; 8: 405411.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 18

    Frydendahl K, Imberechts H, Lehmann S. Automated 5′ nuclease assay for detection of virulence factors in porcine Escherichia coli. Mol Cell Probes 2001; 15: 151160.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19

    Franklin MA, Francis DB, Baker D, et al. A PCR-based method of detection and differentiation of K88+ adhesive Escherichia coli. J Vet Diagn Invest 1996; 8: 460463.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 20

    Grauballe PC, Vestergaard BF, Meyling A, et al. Optimized enzyme-linked immunosorbent assay for detection of human and bovine rotavirus in stools: comparison with electron-microscopy, immunoelectro-osmophoresis, and fluorescent antibody techniques. J Med Virol 1981; 7: 2940.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 21

    Henriksen SA, Aagaard K. A simple flotation and McMaster method [Danish]. Nord Vet Med 1976; 28: 392397.

  • 22

    Miyazaki K, Ohtani K, Sunada K, et al. Determination of ampicillin, amoxicillin, cephalexin, and cephradine in plasma by high-performance liquid chromatography using fluorometric detection. J Chromatogr 1983; 276: 478482.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23

    Agersø H, Friis C. Bioavailability of amoxicillin in pigs. J Vet Pharmacol Ther 1998; 21: 4146.

  • 24

    Gibaldi M, Perrier D. Pharmacokinetics. 2nd ed. New York: Marcel Dekker Inc, 1982; 1494.

  • 25

    Shant J, Ghosh S, Bhattacharyya S, et al. The alteration in signal transduction parameters induced by the excretory-secretory product from Giardia lamblia. Parasitology 2004; 129: 421430.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26

    Craft JC, Holt EA, Tan SH. Malabsorption of oral antibiotics in humans and rats with giardiasis. Pediatr Infect Dis J 1987; 6: 832836.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 27

    Alcalde AI, Barcina Y, Ilundain A, et al. Effect of amoxicillin on galactose transport across rat small intestine. Drug Nutr Interact 1987; 5: 7179.

    • Search Google Scholar
    • Export Citation
  • 28

    Balsbaugh RK, Curtis SE, Meyer RC. Body weight, total body water and hematocrit in diarrheic piglets. J Anim Sci 1986; 62: 307314.

  • 29

    Letendre L, Scott M, Dobson G, et al. Evaluating barriers to bioavailability in vivo: validation of a technique for separately assessing gastrointestinal absorption and hepatic extraction. Pharm Res 2004; 8: 14571462.

    • Search Google Scholar
    • Export Citation
  • 30

    Craig WA. Pharmacokinetic/pharmacodynamic parameters: rationale for antibacterial dosing of mice and men. Clin Infect Dis 1998; 26: 112.

  • 31

    Lindecrona RH, Friis C, Jensen NE. The pharmacodynamic effect of amoxicillin and danofloxacin against Actinobacillus pleuropneumoniae in an in-vitro pharmacodynamic model. Res Vet Sci 1999; 67: 9397.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 32

    Lindecrona RH, Friis C, Aarestrup FM. The pharmacodynamic effect of amoxicillin and danofloxacin against Salmonella typhimurium in an in-vitro pharmacodynamic model. Res Vet Sci 2000; 68: 261264.

    • Crossref
    • Search Google Scholar
    • Export Citation

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