FUNDAMENTAL AND CLINICAL STUDIES ON DL-8280 IN THE SURGICAL FIELD
Fundamental and clinical studies on DL-8280, a newly synthesized antibacterial agent, were conducted in the surgical field. For the fundamental studies, 200 and 400mg of DL-8280 was administered orally to 10 patients with cholelithiasis 3 hours before the operations. The concentration of DL-8280 in...
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Published in | CHEMOTHERAPY Vol. 32; no. Supplement1; pp. 843 - 852 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English Japanese |
Published |
Japanese Society of Chemotherapy
1984
公益社団法人 日本化学療法学会 |
Online Access | Get full text |
ISSN | 0009-3165 1884-5894 |
DOI | 10.11250/chemotherapy1953.32.Supplement1_843 |
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Abstract | Fundamental and clinical studies on DL-8280, a newly synthesized antibacterial agent, were conducted in the surgical field. For the fundamental studies, 200 and 400mg of DL-8280 was administered orally to 10 patients with cholelithiasis 3 hours before the operations. The concentration of DL-8280 in serum was 3.10, 1.87, 1.76μg/ml (200mg), and 5.65, 4.92, 3.88μg/ml (400 mg) at 2, 4, 6 hours after adminitration, respectively. The concentration in choledochal bile was 6.35 (200 mg) and 11.3 (400 mg) μg/ml. The concentration in cholecystic bile was 11.3 (200 mg) and 16.8 (400 mg) μg/ml. The concentration of DL-8280 in bile was studied every 30 minutes after oral administration of 200 mg with food. The peak concentration of DL-8280 in bile was 7.81μg/ml, thereafter the concentration decreased slowly to 3.65, 1.58, 0.45μg/ml at 6, 12, 24 hours after administration. The recovery rate of DL-8280 into bile was 0.53%. The peak concentration of DL-8280 in bile was 1.5 times higher than that of norfloxacin (NFLX), and the recovery rate of DL-8280 was 3 times higher than that of NFLX. So, it was suggested that DL-8280 might be clinically effective, because of the high and prolonged concentration in serum and biliary system. For the clinical studies, DL-8280 was administered to 43 paients with abscess, mastitis, phlegmone, cholangitis, furuncle, carbuncle and etc. The dose of DL-8280 was 100mg×3/day to 40 patients and 200mg×3/day to 3 patients. The clinical effect of DL-8280 was good in 67.4%, fair in 20.9% and poor in 11.6%. Bacteriological effect of DL-8280 was good in 10 out of 17 (58.8%) strains of gram positive cocci, and good in 4 out of 6 (66.7%) strains of gram negative bacilli. The minimal inhibitory concentration of DL-8280 was 0.10-0.78μg/ml against 9 strains of gram positive cocci, and 0.05-0.20μg/ml against 2 strains of gram negative bacilli. Therefore, it was suggested that DL-8280 might be effective not only against infections caused by gram negative bacilli, but also against infections caused by gram positive cocci. No side effect and abnormal findings in laboratory data due to the administration of DL-8280 were experienced. |
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AbstractList | Fundamental and clinical studies on DL-8280, a newly synthesized antibacterial agent, were conducted in the surgical field. For the fundamental studies, 200 and 400mg of DL-8280 was administered orally to 10 patients with cholelithiasis 3 hours before the operations. The concentration of DL-8280 in serum was 3.10, 1.87, 1.76μg/ml (200mg), and 5.65, 4.92, 3.88μg/ml (400 mg) at 2, 4, 6 hours after adminitration, respectively. The concentration in choledochal bile was 6.35 (200 mg) and 11.3 (400 mg) μg/ml. The concentration in cholecystic bile was 11.3 (200 mg) and 16.8 (400 mg) μg/ml. The concentration of DL-8280 in bile was studied every 30 minutes after oral administration of 200 mg with food. The peak concentration of DL-8280 in bile was 7.81μg/ml, thereafter the concentration decreased slowly to 3.65, 1.58, 0.45μg/ml at 6, 12, 24 hours after administration. The recovery rate of DL-8280 into bile was 0.53%. The peak concentration of DL-8280 in bile was 1.5 times higher than that of norfloxacin (NFLX), and the recovery rate of DL-8280 was 3 times higher than that of NFLX. So, it was suggested that DL-8280 might be clinically effective, because of the high and prolonged concentration in serum and biliary system. For the clinical studies, DL-8280 was administered to 43 paients with abscess, mastitis, phlegmone, cholangitis, furuncle, carbuncle and etc. The dose of DL-8280 was 100mg×3/day to 40 patients and 200mg×3/day to 3 patients. The clinical effect of DL-8280 was good in 67.4%, fair in 20.9% and poor in 11.6%. Bacteriological effect of DL-8280 was good in 10 out of 17 (58.8%) strains of gram positive cocci, and good in 4 out of 6 (66.7%) strains of gram negative bacilli. The minimal inhibitory concentration of DL-8280 was 0.10-0.78μg/ml against 9 strains of gram positive cocci, and 0.05-0.20μg/ml against 2 strains of gram negative bacilli. Therefore, it was suggested that DL-8280 might be effective not only against infections caused by gram negative bacilli, but also against infections caused by gram positive cocci. No side effect and abnormal findings in laboratory data due to the administration of DL-8280 were experienced. Fundamental and clinical studies on DL-8280, a newly synthesized antibacterial agent, were conducted in the surgical field.For the fundamental studies, 200 and 400mg of DL-8280 was administered orally to 10 patients with cholelithiasis 3 hours before the operations. The concentration of DL-8280 in serum was 3.10, 1.87, 1.76μg/ml (200mg), and 5.65, 4.92, 3.88μg/ml (400 mg) at 2, 4, 6 hours after adminitration, respectively. The concentration in choledochal bile was 6.35 (200 mg) and 11.3 (400 mg) μg/ml. The concentration in cholecystic bile was 11.3 (200 mg) and 16.8 (400 mg) μg/ml.The concentration of DL-8280 in bile was studied every 30 minutes after oral administration of 200 mg with food. The peak concentration of DL-8280 in bile was 7.81μg/ml, thereafter the concentration decreased slowly to 3.65, 1.58, 0.45μg/ml at 6, 12, 24 hours after administration. The recovery rate of DL-8280 into bile was 0.53%. The peak concentration of DL-8280 in bile was 1.5 times higher than that of norfloxacin (NFLX), and the recovery rate of DL-8280 was 3 times higher than that of NFLX.So, it was suggested that DL-8280 might be clinically effective, because of the high and prolonged concentration in serum and biliary system.For the clinical studies, DL-8280 was administered to 43 paients with abscess, mastitis, phlegmone, cholangitis, furuncle, carbuncle and etc. The dose of DL-8280 was 100mg×3/day to 40 patients and 200mg×3/day to 3 patients. The clinical effect of DL-8280 was good in 67.4%, fair in 20.9% and poor in 11.6%.Bacteriological effect of DL-8280 was good in 10 out of 17 (58.8%) strains of gram positive cocci, and good in 4 out of 6 (66.7%) strains of gram negative bacilli. The minimal inhibitory concentration of DL-8280 was 0.10-0.78μg/ml against 9 strains of gram positive cocci, and 0.05-0.20μg/ml against 2 strains of gram negative bacilli.Therefore, it was suggested that DL-8280 might be effective not only against infections caused by gram negative bacilli, but also against infections caused by gram positive cocci.No side effect and abnormal findings in laboratory data due to the administration of DL-8280 were experienced. 外科領域において, 新合成経口抗菌剤DL-8280に対する基礎的・臨床的検討を行った。本剤投与後2, 4, 6時間後の血中濃度は, 200mg投与では3.10, 1.87, 1。76μg/ml, 400mg投与では5。65, 4.92, 3.88μg/mlであった。術前3時間前に本剤を投与し術中採取した胆嚢組織内濃度は, 200mg投与では3.01μg/g, 400mg投与では5.05μg/gであり, 総胆管胆汁および胆嚢胆汁中濃度は, 200mg投与では6.35, 1183μg/ml, 400mg投与では11.3, 16.8μg/mlであった。本剤の胆汁中への経時的移行を検討した結果, 200mg投与における最高胆汁中濃度は7.81μg/mlであった。ピーク以後の濃度低下は緩徐であり, 6時間後3.65μg/ml, 12時間後1.58μg/ml, 24時間後0.45μg/mlを示した。胆汁中回収率は0.53%であった。Norfloxacinとの比較では, 本剤はピーク濃度で1.5倍, 胆汁中回収率で3倍良好な成績を得た。また, 本剤投与量と胆汁中濃度との間にdose responseの関係を認めた。外科的感染症43例に対する臨床効果は, 有効29, やや有効9, 無効5で, 有効率は67.4%であった。細菌学的検討では, グラム陽性球菌は10/17 (58.8%), グラム陰性桿菌は4/6 (66.7%), 嫌気性菌は0/1 (0%) が有効と判定された。本剤のMICは, グラム陽性球菌9株に対しては0.10~0.78μg/ml, グラム陰性桿菌2株に対しては0.05~0.20μg/mlであった。本剤投与に起因する自他覚的な副作用および臨床検査値の異常は認められなかった。 |
Author | YOKOYAMA, ISAO FUKUTOMI, TAKASHI YAMADA, YOSHINARI SAITO, TOSHIAKI ARAI, TAKEYUKI HANATANI, YUJI |
Author_FL | 新井 健之 斎藤 敏明 山田 良成 花谷 勇治 横山 勲 福富 隆志 |
Author_FL_xml | – sequence: 1 fullname: 花谷 勇治 – sequence: 2 fullname: 福富 隆志 – sequence: 3 fullname: 横山 勲 – sequence: 4 fullname: 新井 健之 – sequence: 5 fullname: 山田 良成 – sequence: 6 fullname: 斎藤 敏明 |
Author_xml | – sequence: 1 fullname: YOKOYAMA, ISAO organization: Department of Surgery, Kawasaki Municipal Hospital – sequence: 1 fullname: SAITO, TOSHIAKI organization: Department of Surgery, Kawasaki Municipal Hospital – sequence: 1 fullname: ARAI, TAKEYUKI organization: Department of Surgery, Kawasaki Municipal Hospital – sequence: 1 fullname: YAMADA, YOSHINARI organization: Department of Surgery, Kawasaki Municipal Hospital – sequence: 1 fullname: HANATANI, YUJI organization: Department of Surgery, Kawasaki Municipal Hospital – sequence: 1 fullname: FUKUTOMI, TAKASHI organization: Department of Surgery, Kawasaki Municipal Hospital |
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References | 4) 花谷勇治, 福富隆志, 横山勲, 新井健之, 山田良成, 斎藤敏明: 外科領域におけるCeftazidimeの基礎的・臨床的検討. Chemotherapy 31 (S-3): 683-690, 1983 1) 第30回日本化学療法学会西日本支部総会, 新薬シンポジウム, DL-8280, 1982 3) 第28回日本化学療法学会総会, 新薬シンポジウム, AM-715, 1980 5) 山田良成, 花谷勇治, 斎藤敏明: 外科領域におけるT-1982の基礎的検討および臨床経験. Chemotherapy 30 (S-3): 662-670, 1982 2) 第23回日本化学療法学会総会, 新薬研究会報告, PIPEMIDICACID, 1975 |
References_xml | – reference: 4) 花谷勇治, 福富隆志, 横山勲, 新井健之, 山田良成, 斎藤敏明: 外科領域におけるCeftazidimeの基礎的・臨床的検討. Chemotherapy 31 (S-3): 683-690, 1983 – reference: 2) 第23回日本化学療法学会総会, 新薬研究会報告, PIPEMIDICACID, 1975 – reference: 1) 第30回日本化学療法学会西日本支部総会, 新薬シンポジウム, DL-8280, 1982 – reference: 5) 山田良成, 花谷勇治, 斎藤敏明: 外科領域におけるT-1982の基礎的検討および臨床経験. Chemotherapy 30 (S-3): 662-670, 1982 – reference: 3) 第28回日本化学療法学会総会, 新薬シンポジウム, AM-715, 1980 |
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