Using mathematical modelling to predict optimal antibiotic treatment strategies.

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• Dr Pia Abel zur Weisch, University of Tromsø
• Wednesday 04 May 2016, 11:00-12:00
• Lecture Room C, Watson Building.

If you have a question about this talk, please contact David Smith.

Optimal dosing of antibiotics has proven challenging – some antibiotics are most effective when they are administered periodically at high doses, while others work best when minimizing concentration fluctuations. Mechanistic explanations for why antibiotics differ in their optimal dosing are lacking, limiting our ability to predict optimal therapy and leading to long and costly experiments.

We use mathematical models that describe both bacterial growth and intracellular antibiotic-target binding to investigate the effects of fluctuating antibiotic concentrations on individual bacterial cells and bacterial populations.

We show that physicochemical parameters, e.g. the rate of drug transmembrane diffusion and the antibiotic-target complex half-life are sufficient to explain which treatment strategy is most effective. If the drug-target complex dissociates rapidly, the antibiotic must be kept constantly at a concentration that prevents bacterial replication. If antibiotics cross bacterial cell envelopes slowly to reach their target, there is a delay in the onset of action that may be reduced by increasing initial antibiotic concentration. Finally, slow drug-target dissociation and slow diffusion out of cells act to prolong antibiotic effects, thereby allowing for less frequent dosing. Our model can be used as a tool in the rational design of treatment for bacterial infections. It is easily adaptable to other biological systems, e.g. HIV , malaria and cancer, where the effects of physiological fluctuations of drug concentration are also poorly understood.

This talk is part of the Applied Mathematics Seminar Series series.

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• Applied Mathematics Seminar Series
• Lecture Room C, Watson Building
• School of Mathematics events

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