Journal List > Infect Chemother > v.40(3) > 1075395

Lee and Shin: Pharmacokinetics and Pharmacodynamics of Antibiotics : General Concepts and Recent Advances

Abstract

Pharmacokinetics (PK) of antibiotics can be considered as the absorption, distribution, and elimination of drug. Pharmacodynamics (PD) is the relationship between concentration of drug and the antimicrobial effect. Time course of antibiotic activity is a reflection of the interrelationship between PK and PD. Over the past decades, considerable data have been derived from in vitro, in vivo models and infected patients. The time course activity characteristics of concentration effect, and postantibiotic effects, determine the typical patterns of antibiotic activity according to the PD classification. Furthermore, the pattern of antibiotic activity over time is an important determinant of optimal dosage regimens. This review will focus on general concepts and the applications of PK/PD to antibiotic therapy.

Figures and Tables

Fig. 1
Schematic presentation of pharmacokinetic/pharmacodynamic indices in antibiotics: Cmax, peak concentration; Cmin, trough concentration; MIC, minimum inhibitory concentration; AUC, area under the curve; T>MIC, time above the MIC.
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Fig. 2
Relationship between three pharmacokinetic/pharmacodynamic indices (peak/MIC, 24-hour AUC/MIC, percentage of time that serum levels exceed the MIC) and the number of Klebsiella pneumoniae ATCC 43816 in the lungs of neutropenic mice after 24-hour of therapy with ceftazidime.
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Table 1
Classification of Antibiotics Based on Pharmacodynamics
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Dong-Gun Lee
https://orcid.org/http://orcid.org/0000-0003-4655-0641

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