Abstract
CENTA is a newly synthesized, beta-lactamase-labile, chromogenic cephalosporin reagent which changes color from light yellow (lambda maximum ca. 340 nm) to chrome yellow (lambda maximum ca. 405 nm) concomitant with hydrolysis of the beta-lactam ring. This compound offers promise as a diagnostic reagent comparable to other chromogens (PADAC and nitrocefin) for the early detection of beta-lactamase-producing clinical isolates, while retaining some antimicrobial effect against Escherichia coli, Klebsiella spp., Proteus mirabilis, Staphylococcus aureus, and non-enterococcal Streptococcus spp. CENTA is relatively unaffected by commonly used microbiological media and human serum.
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- DeBell R. M., Hickey T. M., Uddin D. E. Partial characterization of a beta-lactamase from Vibrio parahaemolyticus by a new automated microiodometric technique. Antimicrob Agents Chemother. 1978 Feb;13(2):165–169. doi: 10.1128/aac.13.2.165. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fu K. P., Neu H. C. The comparative beta-lactamase resistance and inhibitory activity of 1-oxa cephalosporin, cefoxitin and cefotaxime. J Antibiot (Tokyo) 1979 Sep;32(9):909–914. doi: 10.7164/antibiotics.32.909. [DOI] [PubMed] [Google Scholar]
- Jones R. N., Barry A. L., Thornsberry C., Wilson H. W. In vitro antimicrobial activity evaluation of cefodizime (HR221), a new semisynthetic cephalosporin. Antimicrob Agents Chemother. 1981 Dec;20(6):760–768. doi: 10.1128/aac.20.6.760. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones R. N., Wilson H. W., Novick W. J., Jr In vitro evaluation of pyridine-2-azo-p-dimethylaniline cephalosporin, a new diagnostic chromogenic reagent, and comparison with nitrocefin, cephacetrile, and other beta-lactam compounds. J Clin Microbiol. 1982 Apr;15(4):677–683. doi: 10.1128/jcm.15.4.677-683.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Callaghan C. H., Morris A., Kirby S. M., Shingler A. H. Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate. Antimicrob Agents Chemother. 1972 Apr;1(4):283–288. doi: 10.1128/aac.1.4.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Petrocheilou V., Sykes R. B., Richmond M. H. Novel R-plasmid-mediated beta-lactamase from Klebsiella aerogenes. Antimicrob Agents Chemother. 1977 Jul;12(1):126–128. doi: 10.1128/aac.12.1.126. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richmond M. H., Sykes R. B. The beta-lactamases of gram-negative bacteria and their possible physiological role. Adv Microb Physiol. 1973;9:31–88. doi: 10.1016/s0065-2911(08)60376-8. [DOI] [PubMed] [Google Scholar]
- Rotimi V. O., Turk D. C. Transferable multiple antibiotic resistance in Haemophilus influenzae. J Antimicrob Chemother. 1981 Sep;8(3):187–192. doi: 10.1093/jac/8.3.187. [DOI] [PubMed] [Google Scholar]
- Russel A. D. Interaction of a new cephalosporin, 7-cyanacetamidocephalosporanic acid, with some gram-negative and gram-positive beta-lactamase-producing bacteria. Antimicrob Agents Chemother. 1972 Oct;2(4):255–260. doi: 10.1128/aac.2.4.255. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Seibert G., Biebach A. Eine enzymatische Methode zur Bestimmung von Cefotaxim in Serum- und Harnproben. J Clin Chem Clin Biochem. 1981 May;19(5):279–281. [PubMed] [Google Scholar]