Optimal regimens based on PK/PD cutoff evaluation of ceftiofur against Actinobacillus pleuropneumoniae in swine

被引:8
作者
Sun, Da [1 ,2 ]
Mi, Kun [3 ]
Hao, Haihong [3 ]
Xie, Shuyu [3 ]
Chen, Dongmei [1 ,2 ,3 ]
Huang, Lingli [1 ,2 ,3 ]
机构
[1] Huazhong Agr Univ, Natl Reference Lab Vet Drug Residues, Wuhan, Peoples R China
[2] Huazhong Agr Univ, MAO Key Lab Detect Vet Drug Residues, Wuhan, Peoples R China
[3] Huazhong Agr Univ, Coll Vet Med, Dept Vet Pharmacol, Wuhan, Peoples R China
关键词
Ceftiofur; Actinobacillus pleuropneumoniae; Epidemiologic cutoff value; Pharmacokinetic; pharmacodynamics cutoff; Dosage; PHARMACOKINETICS; SUSCEPTIBILITY; SODIUM; HYDROCHLORIDE; RESISTANCE; DESFUROYLCEFTIOFUR; PHARMACODYNAMICS; IDENTIFICATION; METABOLISM; PREVENTION;
D O I
10.1186/s12917-020-02589-9
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundActinobacillus pleuropneumoniae formerly known as Haemophilus pleuropneumoniae, can cause pleuropneumoniae in pigs, which lead to significant mortality. Ceftiofur was the first cephalosporin antibiotic used in animals, which was effective against gram-negative and gram-positive bacterium. This study aimed to formulate a rational dosage strategy and review the preceding recommended dosage based on PK/PD modeling and Establish Clinical breakpoint of ceftiofur against Actinobacillus pleuropneumoniae based on the pharmacodynamic-pharmacokinetic cutoff.ResultsThe epidemiologic cutoff value was 0.125 mu g/mL. The results of the pharmacodynamic study showed that the MICs of BW39 were 0.5 mu g/mL and 1 mu g/mL in vitro and ex-vivo, respectively. The minimal bactericidal concentrations (MBCs) under in vitro and ex vivo conditions were both 1 mu g/mL. The time-killing profiles of ceftiofur against BW39 were time-dependent with a partly concentration-dependent pattern. Based on the inhibitory sigmoid E-max model, the AUC(24 h)/MIC values for the bacteriostatic, bactericidal, and elimination effects in serum were 45.73, 63.83, and 69.04h for healthy pigs separately. According to the Monte Carlo simulation, the COPD was calculated as 2 mu g/mL, and the optimized dosage regimen of ceftiofur against Actinobacillus pleuropneumoniae to achieve bacteriostatic, bactericidal, and elimination effects over 24h was 2.13, 2.97, and 3.42mg/kg for the 50% target attainment rate (TAR) and 2.47, 3.21, and 3.70mg/kg for the 90% TAR respectively.ConclusionsIn conclusion, we reveal the EOFF and PK/PD cutoff values of ceftiofur against A. pleuropneumoniae in piglets. However, with the paucity of clinical data for ceftiofur to establish a clinical cutoff against A. pleuropneumoniae, the PK/PD cutoff value of 2 mu g/mL will be recommended as surrogate. According to the PK/PD data and the MIC distribution in China, the single bactericidal dose was 3.21mg/kg for the 90% target, which would be more able to cure Actinobacillus pleuropneumoniae and avoid the emergence of resistance for clinical ceftiofur use in piglet.
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页数:11
相关论文
共 36 条
[1]   Integration of PK/PD for dose optimization of Cefquinome against Staphylococcus aureus causing septicemia in cattle [J].
Ahmad, Ijaz ;
Hao, Haihong ;
Huang, Lingli ;
Sanders, Pascal ;
Wang, Xu ;
Chen, Dongmei ;
Tao, Yanfei ;
Xie, Shuyu ;
Kuang Xiuhua ;
Li, Juan ;
Dan, Wan ;
Yuan, Zonghui .
FRONTIERS IN MICROBIOLOGY, 2015, 6
[2]   Animal model pharmacokinetics and pharmacodynamics: a critical review [J].
Andes, D ;
Craig, WA .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2002, 19 (04) :261-268
[3]  
[Anonymous], 2018, PERFERMANCE STANDARD
[4]   Antimicrobial Susceptibilities and Resistance Genes of Canadian Isolates of Actinobacillus pleuropneumoniae [J].
Archambault, Marie ;
Harel, Josee ;
Goure, Julien ;
Tremblay, Yannick D. N. ;
Jacques, Mario .
MICROBIAL DRUG RESISTANCE, 2012, 18 (02) :198-206
[5]   DETERMINATION OF CEFTIOFUR AND ITS DESFUROYLCEFTIOFUR-RELATED METABOLITES IN SWINE TISSUES BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
BECONIBARKER, MG ;
ROOF, RD ;
MILLERIOUX, L ;
KAUSCHE, FM ;
VIDMAR, TJ ;
SMITH, EB ;
CALLAHAN, JK ;
HUBBARD, VL ;
SMITH, GA ;
GILBERTSON, TJ .
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS, 1995, 673 (02) :231-244
[6]   [C-14] CEFTIOFUR SODIUM-ABSORPTION, DISTRIBUTION, METABOLISM, AND EXCRETION IN SHEEP FOLLOWING INTRAMUSCULAR INJECTIONS [J].
BECONIBARKER, MG ;
DAVIDSON, KL ;
HORNISH, RE ;
ARNOLD, TS ;
CRAIGMILL, AL ;
GILBERTSON, TJ ;
SMITH, EB ;
VIDMAR, TJ ;
HOFFMAN, GA ;
GATCHELL, CL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1995, 43 (06) :1589-1597
[7]   Metabolism of [C-14]ceftiofur hydrochloride in swine after intramuscular injections [J].
BeconiBarker, MG ;
Smith, EB ;
Arnold, TS ;
Hornish, RE ;
Vidmar, TJ ;
Gatchell, CL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (07) :2606-2611
[8]   Killing of Streptococcus pneumoniae by azithromycin, clarithromycin, erythromycin, telithromycin and gemifloxacin using drug minimum inhibitory concentrations and mutant prevention concentrations [J].
Blondeau, J. M. ;
Shebelski, S. D. ;
Hesje, C. K. .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2015, 45 (06) :594-599
[9]   Proposal of serovars 17 and 18 of Actinobacillus pleuropneumoniae based on serological and genotypic analysis [J].
Bosse, Janine T. ;
Li, Yanwen ;
Sarkozi, Rita ;
Fodor, Laszlo ;
Lacouture, Sonia ;
Gottschalk, Marcelo ;
Casas Amoribieta, Maria ;
Angen, Oystein ;
Nedbalcova, Katerina ;
Holden, Matthew T. G. ;
Maskell, Duncan J. ;
Tucker, Alexander W. ;
Wren, Brendan W. ;
Rycroft, Andrew N. ;
Langford, Paul R. .
VETERINARY MICROBIOLOGY, 2018, 217 :1-6
[10]   COMPARATIVE VIRULENCE OF SOME ENGLISH STRAINS OF HAEMOPHILUS-PLEUROPNEUMONIAE SEROTYPE-2 AND SEROTYPE-3 IN THE PIG [J].
BRANDRETH, SR ;
SMITH, IM .
RESEARCH IN VETERINARY SCIENCE, 1987, 42 (02) :187-193