| Literature DB >> 27208767 |
Krisztina M Papp-Wallace1, Robert A Bonomo2.
Abstract
Given the serious medical burden of β-lactamases, many approaches are being used identify candidate agents for β-lactamase inhibition. Here, we review two β-lactam-β-lactamase inhibitor (BL-BLI) combinations, ceftolozane-tazobactam and ceftazidime-avibactam that recently entered the clinic. In addition, we focus on BL-BLI combinations in preclinical development that have demonstrated activity in clinical isolates via susceptibility testing and/or in in vivo models of infection. We highlight only the BLIs that are able to reduce the Clinical Laboratory Standards Institute (CLSI) breakpoints for the BL partner into the susceptible range. Our analysis includes the primary literature, meeting abstracts, as well as the patent literature.Entities:
Keywords: Boronic acids; Carbapenems; Diazabicyclooctanones; Inhibitor; Metallo-beta-lactamases; Monobactams; Sulfones; β-Lactamases
Mesh:
Substances:
Year: 2016 PMID: 27208767 PMCID: PMC4980828 DOI: 10.1016/j.idc.2016.02.007
Source DB: PubMed Journal: Infect Dis Clin North Am ISSN: 0891-5520 Impact factor: 5.982