Distribution of orally administered trimethoprim and sulfadiazine into noninfected subcutaneous tissue chambers in adult ponies.
Abstract: The distribution of trimethoprim (TMP) and sulfadiazine (SDZ) into subcutaneously implanted noninfected tissue chambers was studied in healthy adult ponies. Six ponies were given an oral TMP/SDZ paste formulation at a dose of 5 mg/kg TMP and 25 mg/kg SDZ at 12 h intervals for 2 days in order to reach steady-state concentrations. Plasma concentrations and tissue chamber fluid (TCF) concentrations of both drugs were measured at regular intervals during a period commencing 24 h after the last oral administration. The peak concentration of TMP (mean +/- SD) was 2.92 +/- 0.86 microg/mL for plasma and 1.09 +/- 0.25 microg/mL for TCF. For SDZ, the mean peak concentration was 40.20 +/- 14.74 microg/mL for plasma and 23.48 +/- 5.84 microg/mL for TCF. TMP peak concentrations in plasma were reached at 3.17 +/- 03.48 h and those in TCF at 7.33 +/- 03.72 h. SDZ peak concentrations in plasma were reached at 1.83 +/- 02.04 h and those in TCF at 8.00 +/- 03.10 h. Concentrations of TMP and SDZ in TCF remained above the generally accepted breakpoint for susceptibility (0.5/9.5 for the TMP/SDZ combination) for 12 h. Therefore, in ponies oral administration of TMP/SDZ at a dose rate of 30 mg/kg given twice daily in the form of a paste should be appropriate for effective treatment of infections caused by susceptible bacteria.
Publication Date: 2002-09-06 PubMed ID: 12213115DOI: 10.1046/j.1365-2885.2002.00418.xGoogle Scholar: Lookup
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- Journal Article
Summary
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The research explores how two oral antibiotics, trimethoprim (TMP) and sulfadiazine (SDZ), distribute in the body of healthy adult ponies. The study finds that the recommended dosage of these antibiotics can effectively treat susceptible bacterial infections in ponies.
Research Methodology
- The research studied the distribution of TMP and SDZ in healthy adult ponies. Special attention was given to how these drugs were distributed into subcutaneously implanted, non-infected tissue chambers.
- Six ponies were administered an oral paste formulation of TMP/SDZ in specific doses. The doses were repeated every 12 hours for two days to attain steady-state drug concentrations.
- The concentration of these drugs was monitored in the plasma and tissue chamber fluid (TCF) at regular intervals, starting 24 hours after the last administered oral dose.
Results
- The peak concentration of TMP was found to be higher in plasma (2.92 +/- 0.86 microg/mL) than in TCF (1.09 +/- 0.25 microg/mL).
- In contrast, SDZ had a greater peak concentration in plasma (40.20 +/- 14.74 microg/mL) compared to TCF (23.48 +/- 5.84 microg/mL).
- The peak concentrations for TMP were reached faster in plasma (approximately 3.17 hours) compared to TCF (approximately 7.33 hours). A similar trend was observed for SDZ, with peak concentrations in plasma and TCF reached around 1.83 hours and 8.00 hours respectively.
- Furthermore, concentrations of TMP and SDZ in TCF remained above the general breakdown point for susceptibility for approximately 12 hours. This observation suggests the lasting efficacy of the TMP/SDZ combination within the body.
Conclusion
- Based on these findings, researchers found that the oral administration of TMP/SDZ at a dose rate of 30 mg/kg given twice daily in paste form should be suitable for treating infections caused by susceptible bacteria in ponies.
- This study is significant as it provides insights into how these two antibiotics distribute and interact within a pony’s body. This information can guide veterinarians in prescribing accurate dosages for effective treatment.
Cite This Article
APA
van Duijkeren E, Ensink JM, Meijer LA.
(2002).
Distribution of orally administered trimethoprim and sulfadiazine into noninfected subcutaneous tissue chambers in adult ponies.
J Vet Pharmacol Ther, 25(4), 273-277.
https://doi.org/10.1046/j.1365-2885.2002.00418.x Publication
Researcher Affiliations
- Bacteriology Division, Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, the Netherlands. e.duijkeren@vet.uu.nl
MeSH Terms
- Administration, Oral
- Animals
- Anti-Infective Agents, Urinary / administration & dosage
- Anti-Infective Agents, Urinary / blood
- Anti-Infective Agents, Urinary / pharmacokinetics
- Area Under Curve
- Chromatography, High Pressure Liquid
- Drug Combinations
- Female
- Half-Life
- Horses
- Male
- Sulfadiazine / administration & dosage
- Sulfadiazine / blood
- Sulfadiazine / pharmacokinetics
- Tissue Distribution
- Trimethoprim / administration & dosage
- Trimethoprim / blood
- Trimethoprim / pharmacokinetics
Citations
This article has been cited 5 times.- Yu JE, You BH, Bae M, Han SY, Jung K, Choi YH. Evaluation of Pharmacokinetic Feasibility of Febuxostat/L-pyroglutamic Acid Cocrystals in Rats and Mice. Pharmaceutics 2023 Aug 21;15(8).
- Lam KL, Kong WP, Ling PY, Lau TH, Ho KH, Lee FW, Chan PL. Antibiotic-Resistant Bacteria in Hydroponic Lettuce in Retail: A Comparative Survey. Foods 2020 Sep 21;9(9).
- Sadaka C, Kanellos T, Guardabassi L, Boucher J, Watts JL. Evaluation of Veterinary-Specific Interpretive Criteria for Susceptibility Testing of Streptococcus equi Subspecies with Trimethoprim-Sulfamethoxazole and Trimethoprim-Sulfadiazine. J Clin Microbiol 2017 Jan;55(1):326-330.
- Sykes BW, Sykes KM, Hallowell GD. Administration of trimethoprim-sulphadimidine does not improve healing of glandular gastric ulceration in horses receiving omeprazole: a randomised, blinded, clinical study. BMC Vet Res 2014 Aug 23;10:180.
- Kim SY, You BH, Bae M, Han SY, Jung K, Choi YH. Improved Pharmacokinetic Feasibilities of Mirabegron-1,2-Ethanedisulfonic Acid, Mirabegron-1,5-Naphthalenedisulfonic Acid, and Mirabegron-L-Pyroglutamic Acid as Co-Amorphous Dispersions in Rats and Mice. Pharmaceutics 2023 Sep 4;15(9).
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