Literature DB >> 8934426

Clarithromycin pharmacokinetics after oral administration with or without fasting in crossbred beagles.

E Vilmànyi1, K Küng, J L Riond, B Trümpi, M Wanner.   

Abstract

Clarithromycin was administered to eight dogs intravenously and orally. A suspension or a tablet was given to animals both immediately after feeding and on an empty stomach. Neither the formulation nor the time of administration in relation to feeding significantly influenced the pharmacokinetic parameters. The lowest mean (+/-SD) maximum plasma concentration (Cmax) of 3.0 +/- 0.6 micrograms/ml, the lowest bioavailability (F) of approximately 69 per cent and the shortest time above the proposed breakpoint of susceptibility (L) of 2.9 +/- 1.3 hours were observed with the suspension after feeding. The highest Cmax of 3.6 +/- 0.8 micrograms/ml, the highest F of 83 per cent and the longest L of 4.5 +/- 2.0 hours were observed with the suspension in the fasted group. The mean time at which Cmax occurred (tmax) was between one and two hours after administration. In conclusion, clarithromycin is potentially suitable for therapeutic use in dogs, pending species-specific studies of safety and therapeutic efficacy.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8934426     DOI: 10.1111/j.1748-5827.1996.tb02314.x

Source DB:  PubMed          Journal:  J Small Anim Pract        ISSN: 0022-4510            Impact factor:   1.522


  1 in total

1.  Preliminary study of effects of multiple oral dosing of clarithromycin on the pharmacokinetics of cyclosporine in dogs.

Authors:  Masaaki Katayama; Yoshiki Kawakami; Rieko Katayama; Shunsuke Shimamura; Yasuhiko Okamura; Yuji Uzuka
Journal:  J Vet Med Sci       Date:  2013-11-05       Impact factor: 1.267

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.