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Veterinary parasitology2010; 170(1-2); 112-119; doi: 10.1016/j.vetpar.2010.01.038

Plasma disposition and fecal elimination of doramectin after oral or intramuscular administration in horses.

Abstract: A study was done to compare plasma disposition kinetics and the fecal elimination profile of doramectin (DRM) after oral or intramuscular (IM) administration in horses. Ten clinically healthy horses, 328-502 kg body weight (bw), were assigned to 2 experimental groups of 5 horses each. Group 1 was treated with an oral dose of 0.2 mg DRM/kg bw, while Group 2 was treated with 0.2 mg DRM/kg bw by IM route. Blood and fecal samples were collected at different times between 0.5h and 60 days post-treatment. After plasma and fecal drug extraction and derivatization, samples were analysed by high performance liquid chromatography (HPLC). A non-compartmental kinetic analysis was performed. Results were expressed as mean+/-standard deviation and were compared using Mann-Whitney U-test. The parent molecule was detected in plasma between 30 min and either 30 (oral) or 60 (IM) days post-treatment. Peak plasma concentrations (C(max)) of 51.6+/-22.2 and 33.3+/-10.5 ng/mL were obtained after oral administration and IM route, respectively. Differences between administration route were not statistically significant (P=0.42). The value for the area under the concentration-time curve (AUC) was 178.6+/-53.7 and 393.6+/-66.6 ng day/mL for Group 1 and Group 2, respectively. These differences were significant (P<0.0079). The averages for mean residence time (MRT) values were 7.7+/-0.9 and 13.2+/-4.5 days for oral and IM treated groups, respectively. In horses treated using the oral route, the peak fecal concentration (F C max) was 2295+/-593 ng/g observed at 1.9+/-0.5 days after oral treatment. Whereas, for those treated by IM route, the F C max was lower (162+/-26 ng/g) (P<0.0079) and it was observed at 5.6+/-2.9 days. The results of this study showed that the administration route affects plasma disposition kinetics, bioavailability and fecal elimination of DRM.
Publication Date: 2010-02-04 PubMed ID: 20197212DOI: 10.1016/j.vetpar.2010.01.038Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper discusses a study where scientists analyzed how doramectin, a medication often used to treat parasites in animals, behaves in a horse’s body when given orally or through an injection.

Study Design and Participants

  • Ten healthy horses were the subjects of this study and were divided into two equal groups.
  • Each horse received a specific dose of doramectin, based on its body weight.
  • Group 1 were given the drug orally, whereas Group 2 received it via intramuscular injection.

Data Collection

  • Blood and fecal samples were collected over a 60-day period post-treatment.
  • Dynamic changes in doramectin concentration were measured using high-performance liquid chromatography (HPLC).
  • A non-compartmental kinetic analysis was done to understand the drug’s behavior in the horse’s body.

Findings

  • The detection period of doramectin in the horse’s system differs depending on the mode of administration. After oral administration, it was detected for up to 30 days, while after intramuscular administration, it stayed up to 60 days.
  • The peak plasma concentrations did not significantly differ between oral and intramuscular administration routes. However, the area under the concentration-time curve (AUC), which reflects the drug’s exposure, was significantly greater for the group that received doramectin via injection.
  • The mean residence time (MRT), or the average time doramectin stayed in the body, was longer for the horses who received the drug through injection.
  • The peak fecal concentration is significantly higher in horses treated orally than in those treated with an injection.

Conclusion

  • The mode of doramectin administration impacts its plasma disposition kinetics, bioavailability, and fecal elimination. This result means that how the drug interacts with the horse’s body varies depending on whether the drug is given orally or injected directly into the muscle.

Cite This Article

APA
Pérez R, Godoy C, Palma C, Muñoz L, Arboix M, Alvinerie M. (2010). Plasma disposition and fecal elimination of doramectin after oral or intramuscular administration in horses. Vet Parasitol, 170(1-2), 112-119. https://doi.org/10.1016/j.vetpar.2010.01.038

Publication

ISSN: 1873-2550
NlmUniqueID: 7602745
Country: Netherlands
Language: English
Volume: 170
Issue: 1-2
Pages: 112-119

Researcher Affiliations

Pérez, R
  • Facultad de Medicina Veterinaria, Universidad de Concepción, Chillán, Chile. rubperez@udec.cl
Godoy, C
    Palma, C
      Muñoz, L
        Arboix, M
          Alvinerie, M

            MeSH Terms

            • Administration, Oral
            • Animals
            • Anthelmintics / administration & dosage
            • Anthelmintics / blood
            • Anthelmintics / pharmacokinetics
            • Area Under Curve
            • Feces / chemistry
            • Feces / parasitology
            • Female
            • Half-Life
            • Horses / metabolism
            • Horses / parasitology
            • Injections, Intramuscular / veterinary
            • Ivermectin / administration & dosage
            • Ivermectin / analogs & derivatives
            • Ivermectin / blood
            • Ivermectin / pharmacokinetics
            • Male
            • Parasite Egg Count / veterinary

            Citations

            This article has been cited 2 times.
            1. Lumaret JP, Errouissi F, Floate K, Römbke J, Wardhaugh K. A review on the toxicity and non-target effects of macrocyclic lactones in terrestrial and aquatic environments. Curr Pharm Biotechnol 2012 May;13(6):1004-60.
              doi: 10.2174/138920112800399257pubmed: 22039795google scholar: lookup
            2. Buono F, Veneziano V, Veronesi F, Molento MB. Horse and donkey parasitology: differences and analogies for a correct diagnostic and management of major helminth infections. Parasitology 2023 Oct;150(12):1119-1138.
              doi: 10.1017/S0031182023000525pubmed: 37221816google scholar: lookup