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PMID: 3348609 Published · ppublish English Comparative Study Journal Article

A-61827 (A-60969), a new fluoronaphthyridine with activity against both aerobic and anaerobic bacteria.

Antimicrobial agents and chemotherapy ·Vol. 32 ·No. 1 ·1988-01-00 ·Pages 27-32

Fernandes PB, Chu DT, Swanson RN, Ramer NR, Hanson CW, Bower RR, Stamm JM, Hardy DJ

Abstract

A-61827 (A-60969 is the hydrochloric salt of A-61827) is a new aryl-fluoronaphthyridine which is active against aerobic and anaerobic bacteria. The MICs of A-61827 for 90% of strains (MIC90) of staphylococci and streptococci were less than or equal to 1 microgram/ml and were generally 1 to 4 twofold dilutions less than those of ciprofloxacin for these bacteria. The MIC90S of A-61827 for members of the family Enterobacteriaceae and Pseudomonas aeruginosa were also less than or equal to 1 microgram/ml. Ciprofloxacin was 1 to 3 twofold dilutions more active than A-61827 against these gram-negative bacteria. Neisseria gonorrhoeae, Campylobacter jejuni, and Haemophilus influenzae were susceptible to less than 0.06 microgram of A-61827 per ml. The MIC90 of A-61827 for Legionella pneumophila was 0.25 microgram/ml. A-61827 was as potent or 1 to 2 twofold dilutions more potent than ciprofloxacin against these organisms. The MIC90 of A-61827 for all anaerobic bacteria was less than or equal to 4 micrograms/ml compared with less than or equal to 32 micrograms/ml for ciprofloxacin. In mouse protection tests, A-61827 was as active as ciprofloxacin against Escherichia coli, P. aeruginosa, and Salmonella typhimurium and 5 to 10 times more active than ciprofloxacin against Staphylococcus aureus and Streptococcus pyogenes. A-61827 was as active as ciprofloxacin against P. aeruginosa in a mouse pyelonephritis model and more active than ciprofloxacin and metronidazole in a mouse Bacteroides fragilis abscess model. After oral administration of 100 mg/kg to mice, the peak concentrations of A-61827 and ciprofloxacin in serum were 2.3 and 2.4 micrograms/ml and the half-lives in serum were 3.9 and 1.2 h, respectively.

MeSH Terms
Abscess/drug therapy Animals Anti-Bacterial Agents/pharmacokinetics,pharmacology,therapeutic use Bacteria, Aerobic/drug effects Bacteria, Anaerobic/drug effects Bacteroides Infections/drug therapy Calcium/pharmacology Chemical Phenomena Chemistry Ciprofloxacin/pharmacokinetics,pharmacology Disease Models, Animal Drug Resistance, Microbial Fluoroquinolones Hydrogen-Ion Concentration Magnesium/pharmacology Mice Naphthyridines/pharmacokinetics,pharmacology,therapeutic use Pseudomonas Infections/drug therapy Pyelonephritis/drug therapy
Chemicals
Anti-Bacterial Agents Fluoroquinolones Naphthyridines Ciprofloxacin tosufloxacin Magnesium Calcium
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Fernandes P B
Anti-Infective Research Division, Abbott Laboratories, Abbott Park, Illinois 60064.
Chu D T
Swanson R N
Ramer N R
Hanson C W
Bower R R
Stamm J M
Hardy D J
References (5)
5 references, click to expand
  1. In vitro evaluation of A-56619 (difloxacin) and A-56620: new aryl-fluoroquinolones.
    Antimicrob Agents Chemother. 1986 Feb;29(2):193-200 PMID: 3087274
  2. In vivo evaluation of A-56619 (difloxacin) and A-56620: new aryl-fluoroquinolones.
    Antimicrob Agents Chemother. 1986 Feb;29(2):201-8 PMID: 3521473
  3. The frequency of in-vitro resistance development to fluoroquinolones and the use of a murine pyelonephritis model to demonstrate selection of resistance in vivo.
    J Antimicrob Chemother. 1987 Apr;19(4):449-65 PMID: 3108227
  4. In-vitro and in-vivo potency of five new fluoroquinolones against anaerobic bacteria.
    J Antimicrob Chemother. 1986 Dec;18(6):693-701 PMID: 3818495
  5. The comparative in-vitro activity of eight newer quinolones and nalidixic acid.
    J Antimicrob Chemother. 1986 Nov;18 Suppl D:1-20 PMID: 3468100
Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1988-01-00
Pages
27-32
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC172092
Subset
IM
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