Literature DB >> 1804014

Effect of isepamicin dosing scheme on concentration in cochlear tissue.

P J Govaerts1, J Claes, P H Van de Heyning, M P Derde, L Kaufman, J F Marquet, M E De Broe.   

Abstract

To investigate the possible effect of the dosing scheme of aminoglycosides on their concentration in the cochlear tissue, we gave two groups of 12 guinea pigs subcutaneous doses of 45 mg of isepamicin (ca. 30 mg of active product) per kg of body weight daily for eight consecutive days. The first group received the drug by continuous infusion, while the second group received it by single daily injection. On the final day of administration, the animals were sacrificed and the cochlear tissue was removed. The tissues from the cochleas of pairs of guinea pigs were pooled. The isepamicin concentrations in the cochlear duct tissue (organ of Corti plus lateral wall) and the cochlear nerve tissue were determined separately. Hearing levels before and after treatment were assessed by means of frequency-specific auditory brain stem responses (ABR). The creatinine level in serum was determined on the last day of the administration. None of the animals in either group showed signs of renal insufficiency or of hearing impairment. The median isepamicin concentration in the cochlear duct was 2.40 micrograms/mg of protein after continuous administration and 2.50 micrograms/mg of protein after once-daily administration, compared with the concentration in the cochlear nerve, where it was 1.93 micrograms/mg of protein after continuous administration and 2.59 micrograms/mg of protein after once-daily administration. These differences are statistically insignificant. The results give evidence for linear uptake kinetics of isepamicin in the inner ear tissue and may be directly relevant to the clinical dosing of the drug.

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Year:  1991        PMID: 1804014      PMCID: PMC245392          DOI: 10.1128/AAC.35.11.2401

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  21 in total

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Authors:  G A Verpooten; R A Giuliano; L Verbist; G Eestermans; M E De Broe
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Authors:  C S Desrochers; J Schacht
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Authors:  R A Giuliano; G A Verpooten; M E De Broe
Journal:  Am J Kidney Dis       Date:  1986-11       Impact factor: 8.860

5.  Morphological changes in the vestibular epithelia and ganglion induced by ototoxic drug.

Authors:  K Sera; Y Harada; N Tagashira; M Suzuki; K Hirakawa; T Ohya
Journal:  Scanning Microsc       Date:  1987-09

6.  Role of high-frequency audiometry in the early detection of ototoxicity. II. Clinical Aspects.

Authors:  W A Dreschler; R J van der Hulst; R A Tange; N A Urbanus
Journal:  Audiology       Date:  1989

7.  Incidence of amikacin ototoxicity: a sigmoid function of total drug exposure independent of plasma levels.

Authors:  A R Beaubien; S Desjardins; E Ormsby; A Bayne; K Carrier; M J Cauchy; R Henri; M Hodgen; J Salley; A St Pierre
Journal:  Am J Otolaryngol       Date:  1989 Jul-Aug       Impact factor: 1.808

8.  Kinetics of gentamicin uptake and release in the rat. Comparison of inner ear tissues and fluids with other organs.

Authors:  P Tran Ba Huy; P Bernard; J Schacht
Journal:  J Clin Invest       Date:  1986-05       Impact factor: 14.808

9.  Choice of drug and dosage regimen. Two important risk factors for aminoglycoside nephrotoxicity.

Authors:  M E De Broe; R A Giuliano; G A Verpooten
Journal:  Am J Med       Date:  1986-06-30       Impact factor: 4.965

10.  Differential susceptibility to gentamicin ototoxicity between albino and pigmented guinea pigs.

Authors:  J W Conlee; S S Gill; P T McCandless; D J Creel
Journal:  Hear Res       Date:  1989-08       Impact factor: 3.208

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  1 in total

Review 1.  Clinical pharmacokinetics and pharmacodynamics of isepamicin.

Authors:  M Tod; C Padoin; O Petitjean
Journal:  Clin Pharmacokinet       Date:  2000-03       Impact factor: 6.447

  1 in total

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