Pharmacokinetics, Pharmacodynamic Efficacy Prediction Indexes and Monte Carlo Simulations of Enrofloxacin Hydrochloride Against Bacterial Strains That Induce Common Clinical Diseases in Broiler Chickens

被引:5
作者
Bonassa, Karina P. D. [1 ]
Miragliotta, Miwa Y. [2 ]
Simas, Rosineide C. [3 ]
Eberlin, Marcos N. [4 ]
Anadon, Arturo [5 ]
Moreno, Ronilson A. [1 ]
Reyes, Felix G. R. [1 ]
机构
[1] Univ Estadual Campinas, Sch Food Engn, Dept Food Sci, Campinas, SP, Brazil
[2] AGRIAS Pesquisa & Desenvolvimento SARC Agronegoci, Amparo, Brazil
[3] Univ Fed Goias, Inst Chem, Lab Chromatog & Mass Spectrometry, Goiania, Go, Brazil
[4] Univ Prebiteriana Mackenzie, Sch Engn, MackMass Lab Mass Spectrometry, Sao Paulo, Brazil
[5] Univ Complutense Madrid, Fac Vet Med, Dept Pharmacol & Toxicol, Madrid, Spain
关键词
enrofloxacin hydrochloride; ciprofloxacin; pharmacokinetics; pharmacodynamics; MIC values; PK/PD modeling; Monte Carlo simulations; broiler chicken; METABOLITE CIPROFLOXACIN; RESIDUES; FLUOROQUINOLONES; FORMULATION;
D O I
10.3389/fvets.2020.606872
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Pharmacokinetic parameters and efficacy prediction indexes (C-max/MIC90 and AUC(0-24)/MIC90) of an enrofloxacin hydrochloride (ENR-HCl) veterinary product soluble in water were determined in healthy broiler chickens of both sexes after a single oral dose of ENR-HCl (equivalent to 10 mg ENR base/kg bw). Monte Carlo simulations targeting C-max/MIC90 = 10 and AUC(0-24)/MIC90 =125 were also performed based on a set of MIC (minimum inhibitory concentration) values of bacterial strains that induce common clinical diseases in broiler chickens and that showed to be susceptible to ENR-HCl. Plasma concentrations of ENR and its main metabolite ciprofloxacin (CIP) were determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Plasma concentration-time curves were found to fit a non-compartmental open model. The ratio of the area under the plasma concentration-time curve (AUC) of CIP/ENR was 4.91%. Maximum plasma concentrations of 1.35 +/- 0.15 mu g/mL for ENR-HCl and 0.09 +/- 0.01 mu g/mL for CIP were reached at 4.00 +/- 0.00 h and 3.44 +/- 1.01 h, respectively. Areas under the plasma vs. time concentration curve in 24 h (AUC(0-24)) were 18.91 +/- 1.91 h x mu g/mL and 1.19 +/- 0.12 h x mu g/mL for ENR-HCl and CIP, respectively. Using a microbroth dilution method, the minimum inhibitory concentration (MIC90) values were determined for ENR-HCl for 10 bacterial strains (Mycoplasma gallisepticum, Mycoplasma synoviae, Avibacterium paragallinarum, Clostridium perfringens, Escherichia coli, Pseudomonas aeruginosa, Salmonella ser. Enteritidis, Salmonella ser. Gallinarum, Salmonella ser. Pullorum, and Salmonella ser. Typhimurium), which are the most common causes of infectious clinical diseases in broiler chickens. In summary, the PK/PD ratios and Monte Carlo simulation were carried out for ENR-HCl in poultry, which due to its solubility was administered in drinking water. The PK/PD efficacy prediction indexes and Monte Carlo simulations indicated that the ENR-HCl oral dose used in this study is useful for bacterial infections in treating C. perfringens (Gram-positive), E. coli and S. ser. Enteritidis (Gram-negative) and M. gallisepticum bacteria responsible for systemic infections in poultry, predicting a success rate of 100% when MIC <= 0.06 mu g/mL for E. coli and S. ser. Enteritidis and MIC <= 0.1 mu g/mL for M. gallisepticum. For C. perfringens, the success rate was 98.26% for MIC <= 0.12. However, clinical trials are needed to confirm this recommendation.
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页数:9
相关论文
共 36 条
[1]  
AbdElAziz MI, 1997, BRIT POULTRY SCI, V38, P164, DOI 10.1080/00071669708417963
[2]   Enhancement of enrofloxacin serum antibacterial activity by calcium primed broilers [J].
Aguilera, R. ;
Gutierrez, O. L. ;
Sumano, L. H. .
RESEARCH IN VETERINARY SCIENCE, 2007, 82 (01) :80-84
[3]   Mechanism of Quinolone Action and Resistance [J].
Aldred, Katie J. ;
Kerns, Robert J. ;
Osheroff, Neil .
BIOCHEMISTRY, 2014, 53 (10) :1565-1574
[4]   Some pharmacokinetic parameters of eprinomectin in goats following pour-on administration [J].
Alvinerie, M ;
Lacoste, E ;
Sutra, JF ;
Chartier, C .
VETERINARY RESEARCH COMMUNICATIONS, 1999, 23 (07) :449-455
[5]  
ANADON A, 1995, AM J VET RES, V56, P501
[6]   Pharmacokinetics and residues of ciprofloxacin and its metabolites in broiler chickens [J].
Anadón, A ;
Martínez-Larrañaga, MR ;
Iturbe, J ;
Martínez, MA ;
Díaz, MJ ;
Frejo, MT ;
Martínez, M .
RESEARCH IN VETERINARY SCIENCE, 2001, 71 (02) :101-109
[7]  
[Anonymous], 2008, Performance standards for antimicrobial testing. 18th Informational supplement M100-S18
[8]   Tissue depletion study of enrofloxacin and its metabolite ciprofloxacin in broiler chickens after oral administration of a new veterinary pharmaceutical formulation containing enrofloxacin [J].
Bonassa, Karina P. D. ;
Miragliotta, Miwa Y. ;
Simas, Rosineide C. ;
Monteiro, Diego A. ;
Eberlin, Marcos N. ;
Anadon, Arturo ;
Reyes, Felix G. R. .
FOOD AND CHEMICAL TOXICOLOGY, 2017, 105 :8-13
[9]  
Bonassa KPD, 2016, THESIS
[10]  
Bugyei K, 1999, CAN J VET RES, V63, P193