STUDY ON FOSFOMYCIN-SODIUM-SALT
Basic and clinical studies were conducted on FOM-Na. The MIC was low especially against Proteus spp. High blood concentrations were obtained following intravenous one shot administration, intravenous drip-infusion, and intrathorax administration, being considered effective against most of the organi...
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Published in | CHEMOTHERAPY Vol. 23; no. 11; pp. 3316 - 3326 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
Japanese Society of Chemotherapy
1975
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Abstract | Basic and clinical studies were conducted on FOM-Na. The MIC was low especially against Proteus spp. High blood concentrations were obtained following intravenous one shot administration, intravenous drip-infusion, and intrathorax administration, being considered effective against most of the organisms tested for MIC. FOM was excreted in the urine at high concentration, the excretion rate was good, and more than 90% of the given dose were excreted within 12 hours after administration. The excretion route of FOM is considered through the kidney. The active substance in the blood, urine, saliva, and pleural effusion was inferred to be FOM according to the spot obtained in the bioautogram of TLC. The clinical result showed both effective and poor cases, though the number of cases was small. No side effects. |
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AbstractList | Basic and clinical studies were conducted on FOM-Na. The MIC was low especially against Proteus spp. High blood concentrations were obtained following intravenous one shot administration, intravenous drip-infusion, and intrathorax administration, being considered effective against most of the organisms tested for MIC. FOM was excreted in the urine at high concentration, the excretion rate was good, and more than 90% of the given dose were excreted within 12 hours after administration. The excretion route of FOM is considered through the kidney. The active substance in the blood, urine, saliva, and pleural effusion was inferred to be FOM according to the spot obtained in the bioautogram of TLC. The clinical result showed both effective and poor cases, though the number of cases was small. No side effects. |
Author | SHIMIZU, TATSUNORI SAITO, NAGANORI YOKOYAMA, MICHIO KOBAYASHI, TAKESHI NITTA, HIDEAKI SAITO, NOBUTERU TAKAGI, YASUO ANZAI, TSUTOMU HIRAI, HIDEYUKI ONUMA, HIROAKI |
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References | 4) ZIMMERMAN, S. B..; E. 0. STAPLEY, H. WALLICK & R. BALDWIN : Phosphonomycin. IV. Susceptibility testing method and survey. Antimicr. Agents & Chemoth.-1969 : 303 309, 1970 2) MILLER, A. K., B. M. FROST, M. E. VALIANT, H. KROPP & D. HENDLIN : Phosphonomycin. V. Evaluation in mice. Antimicr. Agents & Chemoth.-1969 : 310-315, 1970 3) STAPLEY, E. O. ; D. HENDLIN, J.M. MATA, M. JACKSON, H. WALLIK, S. HERNANDEZ, S. MOCHALES, S. A. CURRIE & R. M. MILLER : Phosphonomycin. I. Discovery and in vitro biological characterization. Antimicr. Agents & Chemoth.-1969 : 284-290, 1970 1) HENDLIN, D.; B. M. FROST, E. THIELE, H. KROPP, M. E. VAUNT, B. PELAK, B. WEISS BERGER, C. CORIN & A. K. MILLER : Phosphonomycin. III. Evaluation in vitro. Antimicr. Agents & Chemoth.-1969 : 297-302,302, 1970 6) 清水辰典, 高木康夫, 斎藤永憲, 横山道夫, 小林武, 平井英幸, 新田秀昭, 斉藤宣照, 大沼広明, 常松和則 : Fosfomycin-Caに関する研究. Chemotherapy23 : 1700-1708, 1975 8) 清水辰典 : 未発表 7) FOLTZ, E. L & H. WALHCK : Pharmacodynamics of phosphonomycin after intravenous administration in man. Antimicr. Agents & Chemoth.-1969 : 316-321, 1970 5) FOLTZ, E. L.; H. WALLICK & C. ROSENBLUM : Pharmacodynamics of phosphonomycin after oral administration in man. Antimicr. Agents & Chemoth.-1969 : 322-326, 1970 |
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Title | STUDY ON FOSFOMYCIN-SODIUM-SALT |
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