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CEFAZOLIN, A NEW SEMISYNTHETIC CEPHALOSPORIN ANTIBIOTIC. III
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- NISHIDA MINORU
- Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
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- MATSUBARA TADAO
- Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
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- MURAKAWA TAKEO
- Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
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- MINE YASUHIRO
- Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
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- YOKOTA YOSHIKO
- Research Laboratories, Fujisawa Pharmaceutical Co., Ltd.
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- GOTO SACHIKO
- Department of Microbiology, Toho University, School of Medicine
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- KUWAHARA SHOGO
- Department of Microbiology, Toho University, School of Medicine
Bibliographic Information
- Other Title
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- Cefazolin,a new semisynthetic cephalosporin antibiotic-3-Absorption,excretion and tissue distribution in parenteral administration
- CEFAZOLIN, A NEW SEMISYNTHETIC CEPHALOSPORIN ANTIBIOTIC. II
- ABSORPTION, EXCRETION AND TISSUE DISTRIBUTION IN PARENTERAL ADMINISTRATION
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Description
Cefazolin is a new antibiotic derived from 7-aminocephalosporanic acid, having the structure of 7-[l-(lH)-tetrazolylacetamido]-3-[2-(5-methyl-l, 3, 4-thiadiazolyl)-thiomethyl]-Δ3-cephem-4-carboxylic cid. This substance is a broad-spectrum antibiotic, active in vitro against most of Gram-positive and Gram-negative species of bacteria except for Ps. aeruginosa, and is also active against penicillinase-producing strains of Staph. aureus. The activity of cefazolin against fresh isolates of E. coli and Kl. pneumoniae seems superior to those of other antibiotics used in this study. The in vitro activity of cefazolin is little influenced by size of inoculum, presence of rabbit serum, or kinds or properties of test medium. The activity of cefazolin is apparently bactericidal against both Gram-positive and Gram-negative bacteria at or above the MIC levels. In experiments on the development of resistance in vitro, the MICs of cefazolin against Staph. aureus strain 209P and E. coli strain NIHJ increase slowly in a stepwise over a period of 17 transfers. The rate of resistance development of cefazolin is comparable with that of cepholoridine or ampicillin. Cefazolin is relatively stable to enzymes from Staph. aureus and E. coli, which readily inactivate ampicillin and benzyl penicillin. Cefazolin is not remarkably degraded by the tissue homogenates of rat, although cephalothin is degraded quite rapidly. Cefazolin, in the single subcutaneous dose, shows excellent protecting activity against experimental infections in mice infected with both PC-sensitive and resistant strains of Staph. aureus, and is also fairly effective against infections in mice with Diplococcus pneumoniae, E. coli and Proteus mirabilis.
Journal
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- The Journal of Antibiotics
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The Journal of Antibiotics 23 (4), 184-194, 1970
JAPAN ANTIBIOTICS RESEARCH ASSOCIATION
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Keywords
- Male
- Clostridium perfringens
- Staphylococcus
- Microbial Sensitivity Tests
- Mice
- Drug Stability
- Klebsiella
- Escherichia coli
- Animals
- Bacteria
- Corynebacterium diphtheriae
- Streptococcus
- Drug Resistance, Microbial
- Mycobacterium tuberculosis
- Hydrogen-Ion Concentration
- Neisseria gonorrhoeae
- Anti-Bacterial Agents
- Cephalosporins
- Culture Media
- Rats
- Streptococcus pneumoniae
- Protein Binding
Details 詳細情報について
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- CRID
- 1390001204154745600
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- NII Article ID
- 130003498279
- 130003498272
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- NII Book ID
- AA0069330X
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- COI
- 1:CAS:528:DyaE3cXksVersrc%3D
- 1:CAS:528:DyaE3cXkt1amsLc%3D
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- ISSN
- 18811469
- 00218820
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- NDL BIB ID
- 8510162
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- Text Lang
- en
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- Article Type
- journal article
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- Data Source
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- JaLC
- NDL Search
- Crossref
- PubMed
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed