» Articles » PMID: 8031044

Comparative Activities of Clavulanic Acid, Sulbactam, and Tazobactam Against Clinically Important Beta-lactamases

Overview
Specialty Pharmacology
Date 1994 Apr 1
PMID 8031044
Citations 43
Authors
Affiliations
Soon will be listed here.
Abstract

Clavulanic acid, sulbactam, and tazobactam are inhibitors of a variety of plasmid-mediated beta-lactamases. However, inhibition data for these three inhibitors with a wide range of different plasmid-mediated beta-lactamases have not yet been compared under the same experimental conditions. A number of groups have inferred that clavulanic acid inhibits extended-spectrum TEM and SHV beta-lactamases, but inhibition data have rarely been published. In this study, the 50% inhibitory concentrations of these three beta-lactamase inhibitors for 35 plasmid-mediated beta-lactamases have been determined. Of these 35 beta-lactamases, 20 were extended-spectrum TEM- or SHV-derived beta-lactamases. The other 15 enzymes were conventional-spectrum beta-lactamases such as TEM-1 and SHV-1. Clavulanic acid was a more potent inhibitor than sulbactam for 32 of the 35 plasmid-mediated beta-lactamases tested. In particular, clavulanic acid was 60 and 580 times more potent than sulbactam against TEM-1 and SHV-1, respectively, currently the two most clinically prevalent gram-negative plasmid-mediated beta-lactamases. Statistical analysis of the data of the 50% inhibitory concentrations showed that clavulanic acid was 20 times more active overall than sulbactam against the conventional-spectrum enzymes. In addition, clavulanic acid was 14 times more potent than sulbactam at inhibiting the extended-spectrum enzymes. Tazobactam also showed significantly greater activity than sulbactam against the two groups of beta-lactamases. There were no significant differences between the overall activities of tazobactam and clavulanic acid against the extended-spectrum TEM and SHV enzymes and conventional-spectrum enzymes, although differences in their inhibition profiles were observed.

Citing Articles

Model-Informed Clinical Practice - Determining an Appropriate Ampicillin-Sulbactam Redosing Regimen in Surgical Patients by Utilizing Population Pharmacokinetics and Target Attainment Analysis.

Reeder J, OSullivan C, Xu M, Wu N, Ince D, Rogers W Antimicrob Agents Chemother. 2023; 67(4):e0124822.

PMID: 36920230 PMC: 10112153. DOI: 10.1128/aac.01248-22.


Pharmacokinetic/Pharmacodynamic Evaluation of Aztreonam/Amoxicillin/Clavulanate Combination against New Delhi Metallo-β-Lactamase and Serine-β-Lactamase Co-Producing and .

Zhang J, Wu M, Diao S, Zhu S, Song C, Yue J Pharmaceutics. 2023; 15(1).

PMID: 36678879 PMC: 9865866. DOI: 10.3390/pharmaceutics15010251.


Activity of newest generation β-lactam/β-lactamase inhibitor combination therapies against multidrug resistant Pseudomonas aeruginosa.

Haines R, Putsathit P, Hammer K, Tai A Sci Rep. 2022; 12(1):16814.

PMID: 36207358 PMC: 9547053. DOI: 10.1038/s41598-022-21101-x.


Pharmacokinetics of ceftriaxone-tazobactam (8:1) combination in healthy and induced diarrhoeic birds.

Mithin U, Buragohain R, Das P, Mandal T, Hansda R, Joardar S ADMET DMPK. 2022; 10(3):180-196.

PMID: 36131891 PMC: 9484700. DOI: 10.5599/admet.1170.


A review on the mechanistic details of OXA enzymes of ESKAPE pathogens.

Avci F, Tastekil I, Jaisi A, Sarica P, Sariyar Akbulut B Pathog Glob Health. 2022; 117(3):219-234.

PMID: 35758005 PMC: 10081068. DOI: 10.1080/20477724.2022.2088496.


References
1.
Hedges R, Datta N, KONTOMICHALOU P, Smith J . Molecular specificities of R factor-determined beta-lactamases: correlation with plasmid compatibility. J Bacteriol. 1974; 117(1):56-62. PMC: 246524. DOI: 10.1128/jb.117.1.56-62.1974. View

2.
Bush K, Macalintal C, Rasmussen B, Lee V, Yang Y . Kinetic interactions of tazobactam with beta-lactamases from all major structural classes. Antimicrob Agents Chemother. 1993; 37(4):851-8. PMC: 187782. DOI: 10.1128/AAC.37.4.851. View

3.
Furth A . Purification and properties of a constitutive beta-lactamase from Pseudomonas aeruginosa strain Dalgleish. Biochim Biophys Acta. 1975; 377(2):431-43. DOI: 10.1016/0005-2744(75)90323-x. View

4.
Mathew A, Harris A, Marshall M, Ross G . The use of analytical isoelectric focusing for detection and identification of beta-lactamases. J Gen Microbiol. 1975; 88(1):169-78. DOI: 10.1099/00221287-88-1-169. View

5.
Petrocheilou V, Sykes R, Richmond M . Novel R-plasmid-mediated beta-lactamase from Klebsiella aerogenes. Antimicrob Agents Chemother. 1977; 12(1):126-8. PMC: 352167. DOI: 10.1128/AAC.12.1.126. View