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Pharmacodynamic Parameters of Pharmacokinetic/Pharmacodynamic (PK/PD) Integration Models

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Journal Front Vet Sci
Date 2022 Apr 11
PMID 35400105
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Abstract

Pharmacokinetic/pharmacodynamic (PK/PD) integration models are used to investigate the antimicrobial activity characteristics of drugs targeting pathogenic bacteria through comprehensive analysis of the interactions between PK and PD parameters. PK/PD models have been widely applied in the development of new drugs, optimization of the dosage regimen, and prevention and treatment of drug-resistant bacteria. In PK/PD analysis, minimal inhibitory concentration (MIC) is the most commonly applied PD parameter. However, accurately determining MIC is challenging and this can influence the therapeutic effect. Therefore, it is necessary to optimize PD indices to generate more rational results. Researchers have attempted to optimize PD parameters using mutant prevention concentration (MPC)-based PK/PD models, multiple PD parameter-based PK/PD models, kill rate-based PK/PD models, and others. In this review, we discuss progress on PD parameters for PK/PD models to provide a valuable reference for drug development, determining the dosage regimen, and preventing drug-resistant mutations.

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References
1.
Blondeau J, Fitch S . Mutant prevention and minimum inhibitory concentration drug values for enrofloxacin, ceftiofur, florfenicol, tilmicosin and tulathromycin tested against swine pathogens Actinobacillus pleuropneumoniae, Pasteurella multocida and Streptococcus suis. PLoS One. 2019; 14(1):e0210154. PMC: 6328246. DOI: 10.1371/journal.pone.0210154. View

2.
Yang F, Chen P, Wang H, Xing X, Wang S, Ishaq H . Comparative Minimal Inhibitory and Mutant Prevention Concentration of Eight Antimicrobial Agents Against . Microb Drug Resist. 2021; 28(2):229-235. DOI: 10.1089/mdr.2021.0228. View

3.
Zeng D, Sun M, Lin Z, Li M, Gehring R, Zeng Z . Pharmacokinetics and Pharmacodynamics of Tildipirosin Against in a Murine Lung Infection Model. Front Microbiol. 2018; 9:1038. PMC: 5968193. DOI: 10.3389/fmicb.2018.01038. View

4.
Cui J, Liu Y, Wang R, Tong W, Drlica K, Zhao X . The mutant selection window in rabbits infected with Staphylococcus aureus. J Infect Dis. 2006; 194(11):1601-8. DOI: 10.1086/508752. View

5.
Lees P, Giraudel J, Landoni M, Toutain P . PK-PD integration and PK-PD modelling of nonsteroidal anti-inflammatory drugs: principles and applications in veterinary pharmacology. J Vet Pharmacol Ther. 2004; 27(6):491-502. DOI: 10.1111/j.1365-2885.2004.00618.x. View