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Journal of veterinary pharmacology and therapeutics2007; 30(2); 109-115; doi: 10.1111/j.1365-2885.2007.00833.x

Pulmonary disposition of erythromycin, azithromycin, and clarithromycin in foals.

Abstract: The objectives of the present study were to determine and compare the pulmonary disposition of azithromycin, clarithromycin, and erythromycin in foals. A single dose (10 mg/kg) of azithromycin, clarithromycin, or erythromycin was administered intragastrically to six healthy 1- to 3-month-old foals using an orthogonal design. Activity of the drugs was measured in serum, pulmonary epithelial lining fluid (PELF), and bronchoalveolar lavage (BAL) cells by use of a microbiologic assay. Peak drug activity in PELF was significantly higher in foals treated with clarithromycin (48.96+/-13.26 microg/mL) than in foals treated with azithromycin (10.00+/-7.46 microg/mL). Quantifiable erythromycin activity in PELF was only found in two of six foals. Peak drug activity in BAL cells was not significantly different between azithromycin (49.92+/-26.94 microg/mL) and clarithromycin (74.20+/-45.80 microg/mL) but activity for both drugs was significantly higher than that of erythromycin (1.02+/-1.11 microg/mL). Terminal half-life of azithromycin in serum (25.7+/-15.4 h), PELF (34.8+/-30.9 h), and BAL cells (54.4+/-17.5 h) was significantly longer than that of both clarithromycin and erythromycin. Peak azithromycin and clarithromycin activity was significantly higher in BAL cells, followed by PELF, and serum. In contrast, peak erythromycin activity in BAL cells was not significantly different from that of serum.
Publication Date: 2007-03-14 PubMed ID: 17348895DOI: 10.1111/j.1365-2885.2007.00833.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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The research investigates and compares the pulmonary disposition, essentially how it is distributed and behaves within the lungs, of three different drugs (azithromycin, clarithromycin, and erythromycin) in foals. Among the three, azithromycin was found to stay in the system the longest, while clarithromycin showed the highest concentration in the pulmonary epithelial lining fluid (PELF). Erythromycin, however, had the lowest activity in both PELF and bronchoalveolar lavage (BAL) cells.

Objective of Research

  • The study aimed to understand and compare how azithromycin, clarithromycin, and erythromycin, when given intragastrically, interact with the pulmonary system in foals (young horses).

Methodology

  • A single dose of 10 mg/kg of either azithromycin, clarithromycin, or erythromycin was administered intragastrically to six healthy young foals.
  • The activity of these drugs was then measured in the serum, pulmonary epithelial lining fluid (PELF), and bronchoalveolar lavage (BAL) cells using a microbiologic assay.

Results

  • Clarithromycin resulted in the highest peak drug activity in the PELF among the three drugs.
  • Azithromycin, on the other hand, had a longer terminal half-life (the time required for the concentration of the drug to reduce by half) in the serum, PELF, and BAL cells. This indicates that azithromycin stayed in the system the longest.
  • Erythromycin was significantly less active in both PELF and BAL cells compared to the other two drugs.

Conclusions

  • Of the three antibiotics, clarithromycin had the highest concentration in PELF, implying that it may be most effective in dealing with pulmonary infections in this fluid.
  • Azithromycin stayed in the system the longest of the three, meaning it may continue working for a more extended period.
  • Erythromycin had the least activity in both PELF and BAL cells, indicating it might be less effective in treating pulmonary conditions in the examined species.

Cite This Article

APA
Suarez-Mier G, Giguère S, Lee EA. (2007). Pulmonary disposition of erythromycin, azithromycin, and clarithromycin in foals. J Vet Pharmacol Ther, 30(2), 109-115. https://doi.org/10.1111/j.1365-2885.2007.00833.x

Publication

ISSN: 0140-7783
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 30
Issue: 2
Pages: 109-115

Researcher Affiliations

Suarez-Mier, G
  • Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.
Giguère, S
    Lee, E A

      MeSH Terms

      • Administration, Oral
      • Animals
      • Animals, Newborn
      • Anti-Bacterial Agents / administration & dosage
      • Anti-Bacterial Agents / blood
      • Anti-Bacterial Agents / pharmacokinetics
      • Azithromycin / administration & dosage
      • Azithromycin / blood
      • Azithromycin / pharmacokinetics
      • Bronchoalveolar Lavage / veterinary
      • Clarithromycin / administration & dosage
      • Clarithromycin / blood
      • Clarithromycin / pharmacokinetics
      • Erythromycin / administration & dosage
      • Erythromycin / blood
      • Erythromycin / pharmacokinetics
      • Female
      • Horses / metabolism
      • Lung / metabolism
      • Male

      Citations

      This article has been cited 5 times.
      1. Zúñiga MP, Badillo E, Abalos P, Valencia ED, Marín P, Escudero E, Galecio JS. Antimicrobial susceptibility of Rhodococcus equi strains isolated from foals in Chile.. World J Microbiol Biotechnol 2023 Jun 22;39(9):231.
        doi: 10.1007/s11274-023-03677-2pubmed: 37347336google scholar: lookup
      2. Wang J, Zhou X, Elazab ST, Park SC, Hsu WH. Should Airway Interstitial Fluid Be Used to Evaluate the Pharmacokinetics of Macrolide Antibiotics for Dose Regimen Determination in Respiratory Infection?. Antibiotics (Basel) 2023 Apr 3;12(4).
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      3. Huang A, Mao F, Huang L, Xie S, Pan Y, Qu W, Cheng G, Liu Z, Yuan Z, Peng D, Hao H. PK-PD Modeling and Optimal Dosing Regimen of Acetylkitasamycin against Streptococcus suis in Piglets.. Antibiotics (Basel) 2022 Feb 21;11(2).
        doi: 10.3390/antibiotics11020283pubmed: 35203885google scholar: lookup
      4. Acosta EP, Grigsby PL, Larson KB, James AM, Long MC, Duffy LB, Waites KB, Novy MJ. Transplacental transfer of Azithromycin and its use for eradicating intra-amniotic ureaplasma infection in a primate model.. J Infect Dis 2014 Mar;209(6):898-904.
        doi: 10.1093/infdis/jit578pubmed: 24179112google scholar: lookup
      5. Rodvold KA, George JM, Yoo L. Penetration of anti-infective agents into pulmonary epithelial lining fluid: focus on antibacterial agents.. Clin Pharmacokinet 2011 Oct;50(10):637-64.