Literature DB >> 20557439

Pharmacokinetics of gamithromycin in cattle with comparison of plasma and lung tissue concentrations and plasma antibacterial activity.

R A Huang1, L T Letendre, N Banav, J Fischer, B Somerville.   

Abstract

The pharmacokinetics (PK) and dose proportionality of gamithromycin (ZACTRAN), a novel azalide, after a single intravenous (i.v.) dose of 3 mg/kg or subcutaneous (s.c.) injection at 3, 6 and 9 mg/kg body weight were studied in 13 male castrate and 13 female Angus cattle. Following i.v. administration, the mean area under the curve extrapolated to infinity (AUC(inf)) was 4.28 +/- 0.536 microgxh/mL, and mean elimination half-life (t(1/2)) was 44.9 +/- 4.67 h, with a large volume of distribution (V(ss)) of 24.9 +/- 2.99 L/kg and a high clearance rate (Cl(obs)) of 712 +/- 95.7 mL/h/kg. For cattle treated with s.c. injection of 3, 6 or 9 mg/kg, mean AUC(inf) values were 4.55 +/- 0.690, 9.42 +/- 1.11 and 12.2 +/- 1.13 microgxh/mL, respectively, and the mean elimination half-lives (t(1/2)) were 51.2 +/- 6.10, 50.8 +/- 3.80 and 58.5 +/- 5.50 h. Gamithromycin was well absorbed and fully bioavailable (97.6-112%) after s.c. administration. No statistically significant (alpha = 0.05) gender differences in the AUC(Inf) or elimination half-life values were observed. Dose proportionality was established based on AUC(Inf) over the range of 0.5 to 1.5 times of the recommended dosage of 6 mg/kg of body weight. Further investigations were conducted to assess plasma PK, lung/plasma concentration ratios and plasma antibacterial activity using 36 cattle. The average maximum gamithromycin concentration measured in whole lung homogenate was 18 500 ng/g at first sampling time of 1 day ( approximately 24 h) after treatment. The ratios of lung to plasma concentration were 265, 410, 329 and 247 at 1, 5, 10 and 15 days postdose. The lung AUC(inf) was 194 times higher than the corresponding plasma AUC(inf). The apparent elimination half-life for gamithromycin in lung was 90.4 h ( approximately 4 days). Antibacterial activity was observed with plasma collected at 6 h postdose with a corresponding average gamithromycin plasma concentration of 261 ng/mL. In vitro plasma protein binding in bovine plasma was determined to be 26.0 +/- 0.60% bound over a range of 0.1-3.0 microg/mL of gamithromycin. The dose proportionality of AUC, high bioavailability, rapid and extensive distribution to lung tissue and low level of plasma protein binding are beneficial PK parameters for an antimicrobial drug used for the treatment and prevention of bovine respiratory disease.

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Year:  2010        PMID: 20557439     DOI: 10.1111/j.1365-2885.2009.01125.x

Source DB:  PubMed          Journal:  J Vet Pharmacol Ther        ISSN: 0140-7783            Impact factor:   1.786


  7 in total

1.  Determination of the duration of antibacterial efficacy following administration of gamithromycin using a bovine Mannheimia haemolytica challenge model.

Authors:  A B Forbes; C Ramage; J Sales; D Baggott; W Donachie
Journal:  Antimicrob Agents Chemother       Date:  2010-11-15       Impact factor: 5.191

2.  Demonstration of the metaphylactic use of gamithromycin against bacterial pathogens associated with bovine respiratory disease in a multicentre farm trial.

Authors:  D Baggott; A Casartelli; F Fraisse; C Manavella; R Marteau; S Rehbein; M Wiedemann; S Yoon
Journal:  Vet Rec       Date:  2011-02-28       Impact factor: 2.695

3.  Overall decrease in the susceptibility of Mycoplasma bovis to antimicrobials over the past 30 years in France.

Authors:  Anne V Gautier-Bouchardon; Séverine Ferré; Dominique Le Grand; Agnès Paoli; Emilie Gay; François Poumarat
Journal:  PLoS One       Date:  2014-02-04       Impact factor: 3.240

4.  Synovial fluid pharmacokinetics of tulathromycin, gamithromycin and florfenicol after a single subcutaneous dose in cattle.

Authors:  Meredyth L Jones; Kevin E Washburn; Virginia R Fajt; Somchai Rice; Johann F Coetzee
Journal:  BMC Vet Res       Date:  2015-02-07       Impact factor: 2.741

5.  Pharmacokinetics and Pharmacodynamics of Gamithromycin Treatment of Pasteurella multocida in a Murine Lung Infection Model.

Authors:  Qingwen Yang; Xuesong Liu; Chenghuan Zhang; Kang Yong; Alancia Carol Clifton; Huanzhong Ding; Yun Liu
Journal:  Front Pharmacol       Date:  2019-09-24       Impact factor: 5.810

6.  Pharmacokinetics and Pharmacodynamics of Tildipirosin Against Pasteurella multocida in a Murine Lung Infection Model.

Authors:  Dongping Zeng; Meizhen Sun; Zhoumeng Lin; Miao Li; Ronette Gehring; Zhenling Zeng
Journal:  Front Microbiol       Date:  2018-05-18       Impact factor: 5.640

7.  Gamithromycin in swine: Pharmacokinetics and clinical evaluation against swine respiratory disease.

Authors:  Dietmar Hamel; Alexandra Richard-Mazet; Florian Voisin; Inge Böhne; Florence Fraisse; Renate Rauh; Rose Huang; Michael Kellermann; Laura Letendre; Pascal Dumont; Steffen Rehbein
Journal:  Vet Med Sci       Date:  2020-10-15
  7 in total

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