Literature DB >> 3370552

Pharmacokinetic and pathological evaluation of gentamicin in cats given a small intravenous dose repeatedly for five days.

A D Jernigan1, R C Hatch, J Brown, W A Crowell.   

Abstract

Gentamicin was administered to six cats at a dosage of 3 mg/kg of body weight intravenously every 8 h for five days. Peak and trough serum gentamicin concentrations were measured after each injection. Gentamicin elimination rate and serum half-life were calculated. Serum urea nitrogen, creatinine, biochemistry profile, electrolyte, glucose, total protein, and albumin concentrations were measured daily. Urinalyses were performed before and after the five-day experimental period. The mean +/- SD peak serum gentamicin concentration was 7.19 +/- 1.10 micrograms/mL, and the trough concentration was 0.59 +/- 0.09 microgram/mL. These concentrations are known to be effective against most gentamicin-sensitive bacteria. The mean +/- SD gentamicin elimination rate was 0.0065 +/- 0.0004 min-1. The harmonic mean +/- pseudo standard deviation serum half-life of gentamicin was 107.21 +/- 12.79 min. There were no significant increases (P greater than 0.05) in clinicopathological variables. Microscopic examination of renal sections did not disclose pathological lesions. Signs of vestibular impairment were not observed. A dosage of 3 mg gentamicin/kg given intravenously every 8 h for five days was determined to be safe and to produce therapeutic blood levels in cats.

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Year:  1988        PMID: 3370552      PMCID: PMC1255423     

Source DB:  PubMed          Journal:  Can J Vet Res        ISSN: 0830-9000            Impact factor:   1.310


  26 in total

1.  Comparative ototoxicity of amikacin and gentamicin in cats.

Authors:  E F Christensen; J C Reiffenstein; H Madissoo
Journal:  Antimicrob Agents Chemother       Date:  1977-08       Impact factor: 5.191

Review 2.  Clinical uses of gentamicin.

Authors:  C H Clark
Journal:  Mod Vet Pract       Date:  1977-09

3.  Changes in the apparent half life of gentamicin and tobramycin without detectable changes in creatinine clearance.

Authors:  S Vozeh; P Spring; M Wenk; F Follath
Journal:  Br J Clin Pharmacol       Date:  1979-06       Impact factor: 4.335

4.  Simplified, accurate method for antibiotic assay of clinical specimens.

Authors:  J V Bennett; J L Brodie; E J Benner; W M Kirby
Journal:  Appl Microbiol       Date:  1966-03

5.  Comparative tests of gentamicin ototoxicity.

Authors:  J E Hawkins; L G Johnsson; J M Aran
Journal:  J Infect Dis       Date:  1969 Apr-May       Impact factor: 5.226

6.  Histological and function changes in the ears of cats after subcutaneous administration of gentamicin.

Authors:  T M McGee; J Webster; M Williams
Journal:  J Infect Dis       Date:  1969 Apr-May       Impact factor: 5.226

7.  Prediction of gentamicin serum levels using a one-compartment open linear pharmacokinetic model.

Authors:  M Chow; J Deglin; A Harralson; R Bartlett; R Quintiliani
Journal:  Am J Hosp Pharm       Date:  1978-09

8.  Accuracy of using pre- and postdose gentamicin serum concentrations to estimate pharmacokinetic parameters and adjust doses in children and adolescents.

Authors:  S F Hamilton; W E Evans
Journal:  Ther Drug Monit       Date:  1981       Impact factor: 3.681

9.  Nephrotoxic and ototoxic effects of hydroxygentamicin in cats.

Authors:  R G Slighter; R J Fabian; M R Donikian; R D Rench; M J Neidl; C R Boshart
Journal:  Fundam Appl Toxicol       Date:  1984-08

10.  The influence of dosage regimen on experimental gentamicin nephrotoxicity: dissociation of peak serum levels from renal failure.

Authors:  W M Bennett; C E Plamp; D N Gilbert; R A Parker; G A Porter
Journal:  J Infect Dis       Date:  1979-10       Impact factor: 5.226

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