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Quantification of antibiotic drug potency by a two-compartment radioassay of bacterial growth.
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 1990 Jun; Vol. 34 (6), pp. 1035-40. - Publication Year :
- 1990
-
Abstract
- The two-compartment radioassay for microbial kinetics based on continuous measurement of the 14CO2 released by bacterial metabolism of 14C-labeled substrate offers a valuable approach to testing the potency of antimicrobial drugs. By using a previously validated radioassay with gram-positive and gram-negative bacteria, a group of protein synthesis inhibitors was evaluated for their effect on microbial growth kinetics. All tested drugs induced changes in both the slopes and intercepts of the growth curves. An exponential growth model was applied to quantify the drug effect on the processes of bacterial 14CO2 liberation and cell generation. The response was measured in terms of a generation rate constant. A linear dependence of the generation rate constant on the dose of spectinomycin was observed with Escherichia coli. Sigmoidal-shaped curves were found in the assays of chloramphenicol and tetracycline. The implications of dose-response curves are discussed on the basis of the receptor site concept for drug action. The assay sensitivities for chloramphenicol and tetracycline were similar to those obtained by the cell counting method, but the sensitivity of the radioassay was at least 10 times greater for spectinomycin.
- Subjects :
- Anti-Bacterial Agents pharmacology
Biological Assay methods
Calibration
Chloramphenicol analysis
Data Interpretation, Statistical
Escherichia coli drug effects
Escherichia coli growth & development
Spectinomycin analysis
Staphylococcus aureus drug effects
Staphylococcus aureus growth & development
Tetracycline analysis
Anti-Bacterial Agents analysis
Carbon Radioisotopes
Subjects
Details
- Language :
- English
- ISSN :
- 0066-4804
- Volume :
- 34
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 2144102
- Full Text :
- https://doi.org/10.1128/AAC.34.6.1035