Combined pharmacokinetics of gentamicin in pony mares after a single intravenous and intramuscular administration.
Abstract: Healthy mature pony mares (n = 6) were given a single dose of gentamicin (5 mg/kg of body weight) IV or IM 8 days apart. Venous blood samples were collected at 0, 5, 10, 20, 30, and 45 minutes and at 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 18, 24, 30, 36, 40, and 48 hours after IV injection of gentamicin, and at 10, 20, 30, and 45 minutes and at 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 18, 24, and 30 hours after IM injection of gentamicin. Gentamicin serum concentration was determined by a liquid-phase radioimmunoassay. The combined data of IV and IM treatments were analyzed by a nonlinear least-square regression analysis program. The kinetic data were best fitted by a 2-compartment open model, as indicated by residual trends and improvements in the correlation of determination. The distribution phase half-life was 0.12 +/- 0.02 hour and postdistribution phase half-life was 1.82 +/- 0.22 hour. The volume of the central compartment was 115.8 +/- 6.0 ml/kg, volume of distribution at steady state was 188 +/- 9.9 ml/kg, and the total body clearance was 1.27 +/- 0.18 ml/min/kg. Intramuscular absorption was rapid with a half-life for absorption of 0.64 +/- 0.14 hour. The extent of absorption was 0.87 +/- 0.14. Kinetic calculations predicted that IM injections of 5 mg of gentamicin/kg every 8 hours would provide average steady-state serum concentrations of 7.0 micrograms/ml, with maximum and minimum steady-state concentrations of 16.8 and 1.1 micrograms/ml, respectively.
Publication Date: 1985-09-01 PubMed ID: 4051305
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article investigates how gentamicin, an antibiotic, is absorbed and distributed in the body of pony mares after single intramuscular and intravenous injections. The researchers tracked the concentration of gentamicin in the blood over time, using a mathematical model to describe the drug’s behaviors.
Research Methodology
- The study involved healthy adult pony mares, where each received an identical dose of gentamicin either intravenously (IV) or intramuscularly (IM), with an 8-day interval between different formats of injection.
- The researchers collected venous blood samples at specific intervals following each injection. For IV injections, the intervals spanned from immediate post-injection to 48 hours later. For the IM injections, sample collection occurred over a 30-hour period.
- The concentration of gentamicin in these samples was then determined using a method known as liquid-phase radioimmunoassay. This technique allows for the detection and measurement of specific proteins (such as the gentamicin molecules) in a sample.
Data Analysis
- The researchers used a form of regression analysis to examine the concentrations of gentamicin over time for both IV and IM methods, combining the data from each to generate a comprehensive understanding of the gentamicin pharmacokinetics.
- The obtained results were best described using a “two-compartment open model”. This is a type of pharmacokinetic model that simulates the body as two separate ‘compartments’ (often represented by the bloodstream and tissue) and calculates how the drug moves between them.
Results and Interpretation
- The analysis indicated specific timing for distribution and post-distribution phase half-lives, the amount of the drug in the central compartment and how quickly it was spread around the body.
- In terms of absorption, gentamicin was quickly absorbed when injected intramuscularly, evidenced by a calculated half-life for absorption.
- Based on their findings, the researchers were able to predict average, maximum, and minimum steady-state concentrations of gentamicin that would be present in the bloodstream if a pony mare were to be administered an IM injection of gentamicin every 8 hours.
This research contributes valuable information to veterinary medicine, particularly in ensuring effective dosing strategies for antibiotics like gentamicin. The results of this pharmacokinetic study could be used to make significant improvements in the treatment of infections in equines.
Cite This Article
APA
Haddad NS, Pedersoli WM, Ravis WR, Fazeli MH, Carson RL.
(1985).
Combined pharmacokinetics of gentamicin in pony mares after a single intravenous and intramuscular administration.
Am J Vet Res, 46(9), 2004-2007.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Female
- Gentamicins / administration & dosage
- Gentamicins / blood
- Gentamicins / metabolism
- Horses / metabolism
- Injections, Intramuscular / veterinary
- Injections, Intravenous / veterinary
- Kinetics
- Radioimmunoassay / veterinary
- Regression Analysis
Citations
This article has been cited 3 times.- Zhao LS, Yin R, Wei BB, Li Q, Jiang ZY, Chen XH, Bi KS. Comparative pharmacokinetics of cefuroxime lysine after single intravenous, intraperitoneal, and intramuscular administration to rats. Acta Pharmacol Sin 2012 Nov;33(11):1348-52.
- Abd El-Aty AM, Goudah A, Ismail M, Shimoda M. Disposition kinetics of difloxacin in rabbit after intravenous and intramuscular injection of Dicural. Vet Res Commun 2005 May;29(4):297-304.
- Garg SK, Garg BD. Disposition kinetics and urinary excretion of gentamicin in buffalo bulls (Bubalus bubalis). Vet Res Commun 1989;13(4):331-7.
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