Pharmacokinetics-pharmacodynamics of beta-lactamase inhibitors: are we missing the target?

摘要

ABSTRACT Introduction: beta-lactamase production in Gram-negative bacteria is a leading cause of antimicrobial resistance, beta-lactamase inhibitors are therapeutic agents used in combination with a partner antimicrobial to overcome the production of these enzymes and restore antimicrobial activity. To address the ongoing threat of multi-drug resistant bacteria, a recent wave of beta-lactamase inhibitor development has occurred. Emphasis on the pharmacokinetics and pharmacodynamics of these agents is needed to optimize their clinical impact. Areas covered: This review will describe methods currently used to define the pharmacokinetics/ pharmacodynamics of beta-lactamase inhibitors. Minimal focus will be on the structure and mechanism of p-lactamase inhibitors. Emphasis will be placed on the use of specific thresholds to normalize beta-lactamase inhibitor exposure. In vitro and in vivo pharmacokinetic/pharmacodynamic data specific to FDA approved and pipeline beta-lactamase inhibitors will be explored. Expert opinion: Describing the exposure-response relationship of p-lactamase inhibitors is an ongoing challenge due to the dynamic relationship of the beta-lactamase inhibitor with the active partner compound. Pharmacokinetic/pharmacodynamic indices and target exposures lack generalizability, as they are often specific to the infecting organism and/or p-lactamase, rather than beta-lactamase inhibitor class. Selected dosage regimens of new agents should be validated via the use of population target attainment analyses.