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PMID: 921239 Published · ppublish English Journal Article

In vitro and in vivo antibacterial activity of T-1220, a new semisynthetic penicillin.

Antimicrobial agents and chemotherapy ·Vol. 12 ·No. 4 ·1977-10-00 ·Pages 455-60

Ueo K, Fukuoka Y, Hayashi T, Yasuda T, Taki H, Tai M, Watanabe Y, Saikawa I, Mitsuhashi S

Abstract

T-1220, sodium 6-[d-(-)-alpha-(4-ethyl-2,3-dioxo-1-piperazinylcarbonyl-amino)- alpha-phenylacetamido] penicillanate, is a new semisynthetic penicillin derivative that possesses a broad spectrum of in vitro antibacterial activity against gram-positive and gram-negative bacteria. T-1220 is more effective than carbenicillin (CB-PC) against Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus species, and Serratia marcescens. Addition of human serum to culture media did not significantly alter the antibacterial activity of T-1220. Greater bactericidal activity toward various strains of gram-negative bacteria was demonstrated with T-1220 than with CB-PC. T-1220, like penicillin G, was hydrolyzed by penicillinase, but was sable to a type IV penicillinase produced by P. aeruginosa strains. In vivo antibacterial activities of T-1220, ampicillin (AB-PC), and CB-PC were compared, using systemic infections of mice with P. aeruginosa, K. pneumoniae, and Escherichia coli. The 50% effective doses (milligrams per kilogram) of T-1220 were consistently lower than those of AB-PC and CB-PC.

MeSH Terms
Ampicillin/analogs & derivatives,pharmacology,therapeutic use Animals Bacteria/drug effects Bacterial Infections/drug therapy Culture Media Drug Stability Male Mice Mice, Inbred ICR Microbial Sensitivity Tests beta-Lactamase Inhibitors
Chemicals
Culture Media beta-Lactamase Inhibitors Ampicillin
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Ueo K
Fukuoka Y
Hayashi T
Yasuda T
Taki H
Tai M
Watanabe Y
Saikawa I
Mitsuhashi S
References (11)
11 references, click to expand
  1. Iodometric assay of penicillinase.
    Nature. 1954 Nov 27;174(4439):1012-3 PMID: 13214059
  2. Semisynthetic -lactam antibiotics. 2. Synthesis and properties of D- and L- -sulfobenzylpenicillins.
    J Med Chem. 1972 Nov;15(11):1108-11 PMID: 4631919
  3. Biochemical properties of a cephalosporin beta-lactamase from Pseudomonas aeruginosa.
    Jpn J Microbiol. 1973 Mar;17(2):141-9 PMID: 4198890
  4. Plasmid-mediated penicillin beta-lactamases in Pseudomonas aeruginosa.
    Antimicrob Agents Chemother. 1976 Jan;9(1):55-60 PMID: 4010
  5. Biochemical properties of a penicillin beta-lactamase mediated by R factor from Bordetella bronchiseptica.
    Antimicrob Agents Chemother. 1975 Sep;8(3):238-42 PMID: 241286
  6. Clinical pharmacology of ticarcillin (alpha-carboxyl-3-thienylmethyl penicillin, BRL-2288).
    Antimicrob Agents Chemother. 1973 Jul;4(1):31-6 PMID: 4791480
  7. Changing patterns in surgical infections.
    Ann Surg. 1973 Oct;178(4):436-45 PMID: 4743865
  8. Detection of a beta-lactamase markedly active against carbenicillin in a strain of Pseudomonas aeruginosa.
    J Bacteriol. 1970 Mar;101(3):1079-80 PMID: 4985588
  9. The purification and properties of penicillin beta-lactamases mediated by transmissible R factors in Escherichia coli.
    J Biochem. 1969 Jul;66(1):11-20 PMID: 4980693
  10. Changing ecology of bacterial infections as related to antibacterial therapy.
    J Infect Dis. 1970 Nov;122(5):419-31 PMID: 5476392
  11. New semi-synthetic penicillin active against Pseudomonas pyocyanea.
    Nature. 1967 Jul 1;215(5096):25-30 PMID: 6069557
Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1977-10-00
Pages
455-60
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC429945
Subset
IM
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