Abstract
Variants of the available methods for estimating antimicrobial effect kinetics in an in vitro dynamic model were analyzed. Two integral parameters characterizing antimicrobial effect duration (TE) and intensity (IE) are suggested to define and analyze the concentration-effect relationships in these models, irrespective of the method of recording. TE is defined by the time from the moment of antibiotic administration to the movement when the bacterial count again reaches its initial level. IE is defined by the area between the microbial growth curves in the presence and absence of an antibiotic. TE and IE were used to quantify the antimicrobial effects of sisomicin on Pseudomonas aeruginosa 58, Escherichia coli 93, and Klebsiella pneumoniae 5056, simulating the pharmacokinetic profiles of the drugs observed following intramuscular administration in therapeutic doses, including the variability of aminoglycoside concentrations in human blood.
MeSH Terms
Anti-Bacterial Agents/pharmacokinetics,pharmacology
Bacteria/drug effects,growth & development
Colony Count, Microbial
Escherichia coli/drug effects
Humans
Kinetics
Klebsiella pneumoniae/drug effects
Microbial Sensitivity Tests
Models, Biological
Pseudomonas aeruginosa/drug effects
Sisomicin/pharmacokinetics,pharmacology
Chemicals
Anti-Bacterial Agents
Sisomicin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Firsov A A
Department of Pharmacokinetics, National Research Institute of Antibiotics, Moscow, USSR.
Chernykh V M
Navashin S M
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