FUNDAMENTAL AND CLINICAL STUDIES OF 6059-S IN SURGICAL FIELD

Biliary concentrations of 6059-S after intravenous injection of 1 g were assayed in 3 cases, and high peak level of 139μg/ml in mean value was observed after 2 hours. 6059-S was administered to 12 cases of infection (11 cases of superficial soft tissue infection and one case of perforative peritonit...

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Published inCHEMOTHERAPY Vol. 28; no. Supplement7; pp. 636 - 639
Main Authors TAKENAKA, NOBUO, TANAKA, TOYOHARU, ISHIDA, MOTOHIKO, KATOH, SHIGETSUGU
Format Journal Article
LanguageJapanese
Published Japanese Society of Chemotherapy 01.01.1980
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ISSN0009-3165
1884-5894
DOI10.11250/chemotherapy1953.28.Supplement7_636

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Abstract Biliary concentrations of 6059-S after intravenous injection of 1 g were assayed in 3 cases, and high peak level of 139μg/ml in mean value was observed after 2 hours. 6059-S was administered to 12 cases of infection (11 cases of superficial soft tissue infection and one case of perforative peritonitis) and one case of prophylactic use for burn.The clinical response of the drug in 12 cases of infection was excellent in 6 cases, good in 3 cases and fair in 4 cases with 75.0% of efficacy, and the result of prophylactic use was effective. Bacteriologically, all causative organisms were eradicated in 4 cases of S.aureus, one case of S.epidermidis and one case of E.coli mixed with Bacteroides. No side effect nor adverse reaction on blood and blood chemistry was observed in these cases.
AbstractList Biliary concentrations of 6059-S after intravenous injection of 1 g were assayed in 3 cases, and high peak level of 139μg/ml in mean value was observed after 2 hours. 6059-S was administered to 12 cases of infection (11 cases of superficial soft tissue infection and one case of perforative peritonitis) and one case of prophylactic use for burn.The clinical response of the drug in 12 cases of infection was excellent in 6 cases, good in 3 cases and fair in 4 cases with 75.0% of efficacy, and the result of prophylactic use was effective. Bacteriologically, all causative organisms were eradicated in 4 cases of S.aureus, one case of S.epidermidis and one case of E.coli mixed with Bacteroides. No side effect nor adverse reaction on blood and blood chemistry was observed in these cases.
Author TANAKA, TOYOHARU
TAKENAKA, NOBUO
ISHIDA, MOTOHIKO
KATOH, SHIGETSUGU
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  fullname: KATOH, SHIGETSUGU
  organization: Department of Surgery, Tokyo Dental College
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References 1) NARISADA, M.; et al.: Synthetic studies on P-lactam antibiotics. Part 10. Synthesis of 713-(2-carboxy-2-(4-hydraxyphenyl) acetamido)-7a-methoxy-3-(((1-methyl-1/1-tertazol-5-yl) thio) methyl)-1-oxa-1-dethia-3-cephm-4-carboxylic acid disodium salt (6059-S) and its related 1-oxacephems. J. Med. Chem. 22: 757-759, 1979
2) WISE, R.; J. M. ANDREWS & K. A. BEDFORD: LY127935, a novel oxa-β-lactam: anin vitro comparison withother P-lactam antibiotics. Antlmicr. Agents & Chemoth. 16: 341-445, 1979
3) NEU, H. C.; N. ASWAPOKRE, K. P. Fu & P. ASWAPOKEB: Antibacterial activity of a now 1 oxa cephalosporin compared with that of other β-lactam compounds. Antimicr. Agents & Chemoth. 16: 141-149, 1979
5) FU, K. P. & H. C. Nitu: The comparative β-lactamase resistance and inhibitory activity of 1-oxa cephalosporin, cefoxitin and cefotaxime. J. Antibiot. 32: 909-914, 1979
4) BARZA, M.; F. P. TALLY, N. V. JACOBUS & S. L. GORBACH: In vitro activity of LY127935. Antimicr. Agents & Chemoth. 16: 287-492, 1979
References_xml – reference: 4) BARZA, M.; F. P. TALLY, N. V. JACOBUS & S. L. GORBACH: In vitro activity of LY127935. Antimicr. Agents & Chemoth. 16: 287-492, 1979
– reference: 1) NARISADA, M.; et al.: Synthetic studies on P-lactam antibiotics. Part 10. Synthesis of 713-(2-carboxy-2-(4-hydraxyphenyl) acetamido)-7a-methoxy-3-(((1-methyl-1/1-tertazol-5-yl) thio) methyl)-1-oxa-1-dethia-3-cephm-4-carboxylic acid disodium salt (6059-S) and its related 1-oxacephems. J. Med. Chem. 22: 757-759, 1979
– reference: 2) WISE, R.; J. M. ANDREWS & K. A. BEDFORD: LY127935, a novel oxa-β-lactam: anin vitro comparison withother P-lactam antibiotics. Antlmicr. Agents & Chemoth. 16: 341-445, 1979
– reference: 5) FU, K. P. & H. C. Nitu: The comparative β-lactamase resistance and inhibitory activity of 1-oxa cephalosporin, cefoxitin and cefotaxime. J. Antibiot. 32: 909-914, 1979
– reference: 3) NEU, H. C.; N. ASWAPOKRE, K. P. Fu & P. ASWAPOKEB: Antibacterial activity of a now 1 oxa cephalosporin compared with that of other β-lactam compounds. Antimicr. Agents & Chemoth. 16: 141-149, 1979
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