# Pharmacokinetic analysis and steady-state predictions of different preparations of metronidazole administered per rectum in adult horses

**Authors:** Jenni R E Auvinen, Janice E Kritchevsky, Jennifer M Reinhart, Alexandria E Gochenauer, Amber S Jannasch, Yu Han-Hallett

PMC · DOI: 10.1093/jvimsj/aalaf032 · Journal of Veterinary Internal Medicine · 2026-01-21

## TL;DR

This study compares how well different rectal forms of metronidazole work in horses, finding that higher doses may be needed for effectiveness.

## Contribution

The study evaluates the pharmacokinetics of rectal metronidazole preparations in horses, a topic not previously reported.

## Key findings

- Rectal metronidazole preparations showed low bioavailability compared to nasogastric administration.
- A 4-fold higher rectal dose in water achieved therapeutic levels in horses.
- Nasogastric and intravenous routes are more reliable for metronidazole administration in horses.

## Abstract

Manipulation of forms of rectally administered metronidazole to improve bioavailability in horses has not been reported.

Evaluate the pharmacokinetics of 3 rectal metronidazole preparations compared to nasogastric (NG) administration.

Seven healthy horses.

Phase 1A was a randomized, 3-way crossover, single-dose pharmacokinetic study, and Phases 1B and 2 were non-randomized, single-dose follow-up studies. Metronidazole (20 mg/kg) was administered NG and rectally in water (RW20), as a rectal gel (RG), and in dimethyl sulfoxide (DMSO). Metronidazole (80 mg/kg) was also administered rectally in water (RW80) to 3 horses. Plasma concentrations were measured using liquid chromatography/tandem mass spectrometry. Pharmacokinetic variables were calculated, and predicted steady-state area under the curve (AUC0-24,ss) to minimum inhibitory concentration ratio was used as a pharmacodynamic target.

Bioavailabilities for RW20 (33.7%), RG (2.49%), and DMSO (12.0%) were low relative to NG administration. When administered at a dosage of 20 mg/kg, only NG every 8 h was predicted to achieve the pharmacodynamic target in all horses. Administered rectally in water, the metronidazole maximum concentration increased from 3.11 +/− 0.63 μg/mL to 4.19 +/− 1.04 μg/mL when the dose was increased to 80 mg/kg. The RW80 predicted AUC0-24,ss for every 8 h administration was above target for all 3 horses.

With the tested preparations, rectal administration of metronidazole at a standard dosage of 20 mg/kg yielded subtherapeutic plasma concentrations. Administering a 4-fold higher dose rectally in water might overcome these limitations. Oral and intravenous routes remain the preferred methods for administering metronidazole in horses.

## Linked entities

- **Chemicals:** metronidazole (PubChem CID 4173), dimethyl sulfoxide (PubChem CID 679)

## Full-text entities

- **Diseases:** bacterial infections (MESH:D001424), MRT (MESH:D000377), ileus (MESH:D045823), pleuropneumonia (MESH:D011001), anaerobic infections (MESH:D007239), gastrointestinal disease (MESH:D005767), bacteremia (MESH:D016470), peritonitis (MESH:D010538), colitis (MESH:D003092), toxicity (MESH:D064420), lethargy (MESH:D053609), proctitis (MESH:D011349), diarrhea (MESH:D003967), colic (MESH:D003085), inflammation (MESH:D007249), rectal irritation (MESH:D012002), asthma (MESH:D001249)
- **Chemicals:** methyl tert-butyl ether (MESH:C043243), DMSO (MESH:D004121), (d4) metronidazole (-), PCCA (MESH:C075943), flunixin meglumine (MESH:C014558), water (MESH:D014867), methanol (MESH:D000432), ammonium formate (MESH:C030544), EDTA (MESH:D004492), acetonitrile (MESH:C032159), nitroimidazole (MESH:D009593), Metronidazole (MESH:D008795)
- **Species:** Equus caballus (domestic horse, species) [taxon 9796], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** RW80 — Mus musculus (Mouse), Embryonic stem cell (CVCL_6442)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12881942/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881942/full.md

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Source: https://tomesphere.com/paper/PMC12881942