Fundamental and clinical studies of pazufloxacin in respiratory tract infections

Pazufloxacin (PZFX), a newly synthesized pyridoncarboxylic acid antibacterial agent, was administered to 6 patients with chronic bronchitis, 4 with bronchiectasis, 3 with acute bronchitis, 1 with a secondary infection of diffuse panbronchiolitis and 1 with a secondary infection of pulmonary emphysem...

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Published inJapanese Journal of Chemotherapy Vol. 43; no. Supplement2; pp. 202 - 207
Main Authors Nishioka, Kiyo, Shirato, Kunio, Tanno, Yasuo
Format Journal Article
LanguageJapanese
Published Japanese Society of Chemotherapy 1995
公益社団法人 日本化学療法学会
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ISSN1340-7007
1884-5886
DOI10.11250/chemotherapy1995.43.Supplement2_202

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Abstract Pazufloxacin (PZFX), a newly synthesized pyridoncarboxylic acid antibacterial agent, was administered to 6 patients with chronic bronchitis, 4 with bronchiectasis, 3 with acute bronchitis, 1 with a secondary infection of diffuse panbronchiolitis and 1 with a secondary infection of pulmonary emphysema, at a single dose of 100 mg or 200 mg twice or three times daily for 6-15 days. The results were excellent in 2, good in 8, fair in 3 and poor in 2, with a total efficacy rate of 66.7%. Among the causative organisms isolated, i.e., 3 strains of Streptococcus pneumoniae, 3 strains of Moraxella catarrhalis and 1 strain of Pasteurella multocida, 2 strains of S. pneumoniae, 3 strains of M catarrhalis and 1 strain of P. multocida were eradicated, with an eradication rate of 6/7. Neither side effects nor abnormal laboratory findings were observed in any subjects. The antimicrobial activity of PZFX against S. pneumoniae, M catarrhalis, Haemophilus influenzae and Pseudomonas aeruginosa, isolated from respiratory tract infections in our department recent years, was compared with that of tosufloxacin (TFLX), ciprofloxacin (CPFX) and ofloxacin (OFLX)[excluding S. pneumoniae in OFLX]. PZFX showed equal or superior antimicrobial activity against M. catarrhalis, H. influenzae and P. aeruginosa, compared with control drugs.
AbstractList Pazufloxacin (PZFX), a newly synthesized pyridoncarboxylic acid antibacterial agent, was administered to 6 patients with chronic bronchitis, 4 with bronchiectasis, 3 with acute bronchitis, 1 with a secondary infection of diffuse panbronchiolitis and 1 with a secondary infection of pulmonary emphysema, at a single dose of 100 mg or 200 mg twice or three times daily for 6-15 days. The results were excellent in 2, good in 8, fair in 3 and poor in 2, with a total efficacy rate of 66.7%. Among the causative organisms isolated, i.e., 3 strains of Streptococcus pneumoniae, 3 strains of Moraxella catarrhalis and 1 strain of Pasteurella multocida, 2 strains of S. pneumoniae, 3 strains of M catarrhalis and 1 strain of P. multocida were eradicated, with an eradication rate of 6/7. Neither side effects nor abnormal laboratory findings were observed in any subjects. The antimicrobial activity of PZFX against S. pneumoniae, M catarrhalis, Haemophilus influenzae and Pseudomonas aeruginosa, isolated from respiratory tract infections in our department recent years, was compared with that of tosufloxacin (TFLX), ciprofloxacin (CPFX) and ofloxacin (OFLX)[excluding S. pneumoniae in OFLX]. PZFX showed equal or superior antimicrobial activity against M. catarrhalis, H. influenzae and P. aeruginosa, compared with control drugs.
Pazufloxacin (PZFX), a newly synthesized pyridoncarboxylic acid antibacterial agent, was administered to 6 patients with chronic bronchitis, 4 with bronchiectasis, 3 with acute bronchitis, 1 with a secondary infection of diffuse panbronchiolitis and 1 with a secondary infection of pulmonary emphysema, at a single dose of 100 mg or 200 mg twice or three times daily for 6-15 days. The results were excellent in 2, good in 8, fair in 3 and poor in 2, with a total efficacy rate of 66.7%.Among the causative organisms isolated, i.e., 3 strains of Streptococcus pneumoniae, 3 strains of Moraxella catarrhalis and 1 strain of Pasteurella multocida, 2 strains of S. pneumoniae, 3 strains of M catarrhalis and 1 strain of P. multocida were eradicated, with an eradication rate of 6/7.Neither side effects nor abnormal laboratory findings were observed in any subjects.The antimicrobial activity of PZFX against S. pneumoniae, M catarrhalis, Haemophilus influenzae and Pseudomonas aeruginosa, isolated from respiratory tract infections in our department recent years, was compared with that of tosufloxacin (TFLX), ciprofloxacin (CPFX) and ofloxacin (OFLX)[excluding S. pneumoniae in OFLX]. PZFX showed equal or superior antimicrobial activity against M. catarrhalis, H. influenzae and P. aeruginosa, compared with control drugs. 新たに開発された経口用ピリドンカルボン酸系抗菌薬pazufloxacin (PZFX) について基礎的・臨床的検討を行った。15名の呼吸器感染症患者 (慢性気管支炎6例, 気管支拡張症4例, 急性気管支炎3例, びまん性汎細気管支炎二次感染, 肺気腫二次感染各々1例) に, 本剤1回100mgあるいは200mgを1日2~3回, 6~15日間投与した。その結果, 著効2例, 有効8例, やや有効3例, 無効2例で, 有効率は66.7%であった。細菌学的効果判定可能な分離菌は, Streptococcus pneumeniae, Mcraxella catarrhalis各々3株・, Pasteurella multocida 1株で, そのうち消失したものはS.pneumoniae 2株, M. catarrhalis 3株, P.multocida 1株で, 消失率は6/7であった。副作用および臨床検査値異常変動は全例において認められなかった。さらに, 近年当科において呼吸器感染症患者の喀痰より分離されたS.pneumoniae, M. catarrhalis, Haemophilus influeneaeおよびPseudomonas aernginosaに対する本剤の抗菌力を, tosufloxacin (TFLX), ciprofloxacin (CPFX), ofloxacin (OFLX)(OFLXは S, pneumniaeを除く3菌種) と比較した。本剤はS.pneumoniaeを除くM.catarrhalis, H.influeneae, P.aernginosaに対して対照薬と同等あるいはそれ以上の抗菌力を示した。
Author Nishioka, Kiyo
Shirato, Kunio
Tanno, Yasuo
Author_FL 白土 邦男
丹野 恭夫
西岡 きよ
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  fullname: Tanno, Yasuo
  organization: The First Department of Internal Medicine, School of Medicine, Tohoku University
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2) Fukuoka Y, Ikeda Y. Yamashiro Y, Takahata M, Todo Y and Narita H: In vitro and in vivo antibacterial activitk, of T-3761, a new quinolonc derivative. Antimicrob Agents Chemother 37: 384-392, 1993
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1) NIuratani T, Inoue NI and Mitsuhashi S: In vitro activity of T-3761, a II fluoroquinolone. Antimicrob Agents Chemother 36: 2293-2303, 1992
6) 佐藤清紀, 小西一樹, 西岡きよ, 佐藤裕子, 丹野恭夫, 樋渡奈奈子, 井田士朗, 滝島任: 呼吸器感染症に対するDL-8280の臨床的評価. Chemotherapy 32 (S-1): 173-177, 1984
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References_xml – reference: 1) NIuratani T, Inoue NI and Mitsuhashi S: In vitro activity of T-3761, a II fluoroquinolone. Antimicrob Agents Chemother 36: 2293-2303, 1992
– reference: 3) 熊澤淨一, 小林宏行: 第42回日本化学療法学会総会, 新薬シンポジウム. T-3761, 福岡, 1994
– reference: 11) 丹野恭夫, 三浦康子, 滝島任, 杉山正春, 工藤国夫, 石井宗彦, 高橋誠: 呼吸器感染症に対するciprofloxgacinの臨床的検討. 化学療法の領域7: 103-107, 1991
– reference: 12) 大野勲, 西岡きよ, 丹野恭夫, 荻原央子, 滝島任: 呼吸器感染症におけるsparfloxacinの基礎的・臨床的検討. Chemotherapy 39 (S4): 213-218, 1991
– reference: 10) 真宗るり子, 大野勲, 井田士朗, 滝島任: 呼吸器感染症におけるT-3262の臨床的評価. Chemotherapy 36 (S-9): 368-373, 1988
– reference: 13) 丹野恭夫, 西岡きよ, 佐藤るり子, 荻原央子, 佐藤裕子, 滝島任: 呼吸器感染症に対するtemafloxacinの臨床的検討. Chemotherapy 41 (S.5) 1301-307, 1993
– reference: 2) Fukuoka Y, Ikeda Y. Yamashiro Y, Takahata M, Todo Y and Narita H: In vitro and in vivo antibacterial activitk, of T-3761, a new quinolonc derivative. Antimicrob Agents Chemother 37: 384-392, 1993
– reference: 4) 西岡きよ: 喀痰の一般細菌検査. 検査と技術7: 221-227, 1979
– reference: 8) 大野勲, 井田士朗, 西岡きよ, 滝島任: 呼吸器感染症におけるBAYo-9867 (ciprofloxacin) の臨床治験成績. Chemotherapy 33 (S-7): 220-225, 1985
– reference: 5) 日本化学療法学会: 最小発育阻止濃度 (MIC) 測定法再改訂について. Chemotherapy 29: 76-79, 1981
– reference: 9) 井田士朗, 進藤百合予, 滝島任: 呼吸器感染症におけるNY-198の臨床治験成績. Chemothe. rapy 36 (S-2) 1480-485, 1988
– reference: 6) 佐藤清紀, 小西一樹, 西岡きよ, 佐藤裕子, 丹野恭夫, 樋渡奈奈子, 井田士朗, 滝島任: 呼吸器感染症に対するDL-8280の臨床的評価. Chemotherapy 32 (S-1): 173-177, 1984
– reference: 7) 井田士朗, 樋渡奈奈子, 滝島任: 呼吸器感染症に対するAT-2266の臨床試験成績. Chemotherapy 32 (S-3): 381-384, 1984
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Snippet Pazufloxacin (PZFX), a newly synthesized pyridoncarboxylic acid antibacterial agent, was administered to 6 patients with chronic bronchitis, 4 with...
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呼吸器感染症
抗菌力
Title Fundamental and clinical studies of pazufloxacin in respiratory tract infections
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