• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

诺氟沙星。对其抗菌活性、药代动力学特性及治疗用途的综述。

Norfloxacin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.

作者信息

Holmes B, Brogden R N, Richards D M

出版信息

Drugs. 1985 Dec;30(6):482-513. doi: 10.2165/00003495-198530060-00003.

DOI:10.2165/00003495-198530060-00003
PMID:3908074
Abstract

Norfloxacin is one of the new 4-quinolone antibacterial agents. A fluorinated piperazinyl-substituted congener of nalidixic acid, it demonstrates a much wider in vitro antibacterial spectrum and greater potency than the parent compound. Its antibacterial activity against most Gram-negative pathogens is enhanced in comparison to nalidixic acid, but is similar to that of some of the other new 4-quinolones like enoxacin, and slightly less than that of ciprofloxacin. Unlike nalidixic acid, norfloxacin is also active against Pseudomonas aeruginosa and some Gram-positive organisms. In acute or uncomplicated urinary tract infections, norfloxacin has repeatedly been shown to be as effective as co-trimoxazole. Single studies have demonstrated a significantly better bacteriological cure rate with norfloxacin than with pipemidic acid, and similar cure rates with norfloxacin and both a nalidixic acid/sodium citrate mixture and amoxycillin. Similar results were found in a few studies comparing norfloxacin to pipemidic acid or amoxycillin in patients with chronic and/or complicated urinary tract infections. Norfloxacin is as effective as spectinomycin in gonorrhoea due to penicillin-resistant N. gonorrhoeae, and cures bacterial gastroenteritis caused by several gastrointestinal pathogens. Norfloxacin appears to be well tolerated and may have a low propensity to select for bacterial resistance during clinical use, although the latter needs further confirmation.

摘要

诺氟沙星是新型4-喹诺酮类抗菌剂之一。它是萘啶酸的一种氟化哌嗪基取代的同类物,其体外抗菌谱比母体化合物宽得多,效力也更强。与萘啶酸相比,它对大多数革兰氏阴性病原体的抗菌活性有所增强,但与依诺沙星等其他一些新型4-喹诺酮类药物相似,略低于环丙沙星。与萘啶酸不同,诺氟沙星对铜绿假单胞菌和一些革兰氏阳性菌也有活性。在急性或非复杂性尿路感染中,诺氟沙星已多次被证明与复方新诺明疗效相当。单项研究表明,诺氟沙星的细菌学治愈率明显高于吡哌酸,与萘啶酸/柠檬酸钠混合物及阿莫西林的治愈率相似。在一些比较诺氟沙星与吡哌酸或阿莫西林治疗慢性和/或复杂性尿路感染患者的研究中也发现了类似结果。对于由耐青霉素淋病奈瑟菌引起的淋病,诺氟沙星与壮观霉素疗效相当,并且能治愈由多种胃肠道病原体引起的细菌性肠胃炎。诺氟沙星似乎耐受性良好,在临床使用期间产生细菌耐药性的倾向可能较低,不过这一点尚需进一步证实。

相似文献

1
Norfloxacin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.诺氟沙星。对其抗菌活性、药代动力学特性及治疗用途的综述。
Drugs. 1985 Dec;30(6):482-513. doi: 10.2165/00003495-198530060-00003.
2
Norfloxacin: clinical pharmacology and clinical use.诺氟沙星:临床药理学与临床应用。
Pharmacotherapy. 1987;7(4):92-110. doi: 10.1002/j.1875-9114.1987.tb04030.x.
3
[The history of the development and changes of quinolone antibacterial agents].[喹诺酮类抗菌药物的发展与变迁史]
Yakushigaku Zasshi. 2003;38(2):161-79.
4
Enoxacin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.依诺沙星。对其抗菌活性、药代动力学特性及治疗用途的综述。
Drugs. 1988 Jul;36(1):32-66. doi: 10.2165/00003495-198836010-00004.
5
Norfloxacin: a new targeted fluoroquinolone antimicrobial agent.诺氟沙星:一种新型靶向氟喹诺酮类抗菌剂。
Ann Intern Med. 1988 Feb;108(2):238-51. doi: 10.7326/0003-4819-108-2-238.
6
Norfloxacin: a quinoline antibiotic.诺氟沙星:一种喹啉类抗生素。
Drug Intell Clin Pharm. 1986 Apr;20(4):261-6. doi: 10.1177/106002808602000402.
7
Ciprofloxacin and norfloxacin, two fluoroquinolone antimicrobials.环丙沙星和诺氟沙星,两种氟喹诺酮类抗菌药物。
Clin Pharm. 1987 Feb;6(2):105-17.
8
Comparison of the antibacterial in vitro and in vivo activity of ofloxacin (HOE 280 DL 8280) and nalidixic acid analogues.氧氟沙星(HOE 280 DL 8280)与萘啶酸类似物的体外和体内抗菌活性比较。
Eur J Clin Microbiol. 1983 Dec;2(6):548-53. doi: 10.1007/BF02016563.
9
Effects of norfloxacin on the faecal flora in patients with complicated urinary tract infections.
Scand J Infect Dis Suppl. 1986;48:27-31.
10
Clinical trial of norfloxacin in the treatment of uncomplicated gonococcal urethritis: preliminary report.诺氟沙星治疗单纯性淋菌性尿道炎的临床试验:初步报告。
Drugs Exp Clin Res. 1989;15(1):33-5.

引用本文的文献

1
The negligible mutagenic effects of norfloxacin on the genome of the fission yeast ATCC-16979.诺氟沙星对裂殖酵母ATCC - 16979基因组的诱变作用可忽略不计。
Microbiol Spectr. 2025 Sep 2;13(9):e0023325. doi: 10.1128/spectrum.00233-25. Epub 2025 Jul 25.
2
Synergistic Antibacterial Action of Norfloxacin-Encapsulated G4 Hydrogels: The Role of Boronic Acid and Cyclodextrin.载诺氟沙星的G4水凝胶的协同抗菌作用:硼酸和环糊精的作用
Gels. 2025 Jan 4;11(1):35. doi: 10.3390/gels11010035.
3
Effect of Fluorine Atoms and Piperazine Rings on Biotoxicity of Norfloxacin Analogues: Combined Experimental and Theoretical Study.

本文引用的文献

1
In vitro and in vivo activity of DL-8280, a new oxazine derivative.新型恶嗪衍生物DL-8280的体外和体内活性
Antimicrob Agents Chemother. 1982 Oct;22(4):548-53. doi: 10.1128/AAC.22.4.548.
2
In vitro activity of ciprofloxacin, a new carboxyquinoline antimicrobial agent.新型羧基喹啉抗菌剂环丙沙星的体外活性
Antimicrob Agents Chemother. 1984 Mar;25(3):331-5. doi: 10.1128/AAC.25.3.331.
3
Comparative in vitro activities of ten antimicrobial agents against bacterial enteropathogens.十种抗菌剂对细菌性肠道病原体的体外活性比较
氟原子和哌嗪环对诺氟沙星类似物生物毒性的影响:实验与理论相结合的研究
Environ Health (Wash). 2024 Aug 22;2(12):886-901. doi: 10.1021/envhealth.4c00095. eCollection 2024 Dec 20.
4
Contribution of the SOS response and the DNA repair systems to norfloxacin induced mutations in .SOS 应答和 DNA 修复系统对诺氟沙星诱导的……中的突变的贡献 。 (注:原文中“in.”后面内容不完整)
Mar Life Sci Technol. 2023 Sep 21;5(4):538-550. doi: 10.1007/s42995-023-00185-y. eCollection 2023 Nov.
5
Piperazine based antimicrobial polymers: a review.基于哌嗪的抗菌聚合物:综述
RSC Adv. 2021 Apr 23;11(25):15213-15230. doi: 10.1039/d1ra00341k. eCollection 2021 Apr 21.
6
Synbiotic Effects of , Mannan Oligosaccharides, and β-Glucan on Innate Immunity, Antioxidant Status, and Disease Resistance of Nile Tilapia, .甘露寡糖和β-葡聚糖对尼罗罗非鱼先天免疫、抗氧化状态及抗病力的合生元效应
Antibiotics (Basel). 2021 May 12;10(5):567. doi: 10.3390/antibiotics10050567.
7
Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance.喹诺酮类药物:作用机制、致死性及其对抗生素耐药性的贡献。
Molecules. 2020 Dec 1;25(23):5662. doi: 10.3390/molecules25235662.
8
Antimicrobial Activities of Highly Bioavailable Organic Salts and Ionic Liquids from Fluoroquinolones.氟喹诺酮类高生物利用度有机盐和离子液体的抗菌活性
Pharmaceutics. 2020 Jul 23;12(8):694. doi: 10.3390/pharmaceutics12080694.
9
Effect of lactation on single-dose pharmacokinetics of norfloxacin nicotinate in ewes.泌乳对母羊烟酸诺氟沙星单剂量药代动力学的影响。
Antimicrob Agents Chemother. 1994 Oct;38(10):2336-9. doi: 10.1128/AAC.38.10.2336.
10
Problems in identification of Campylobacter jejuni associated with acquisition of resistance to nalidixic acid.空肠弯曲菌鉴定中与获得对萘啶酸耐药性相关的问题。
J Clin Microbiol. 1987 Sep;25(9):1807-8. doi: 10.1128/jcm.25.9.1807-1808.1987.
Antimicrob Agents Chemother. 1983 Oct;24(4):509-13. doi: 10.1128/AAC.24.4.509.
4
The activity of enoxacin against clinical bacterial isolates in comparison with that of five other agents, and factors affecting that activity.
J Antimicrob Chemother. 1984 Sep;14 Suppl C:7-17. doi: 10.1093/jac/14.suppl_c.7.
5
In-vitro activity of enoxacin (CL-919), a new quinoline derivative, compared with that of other antimicrobial agents.新喹啉衍生物依诺沙星(CL-919)的体外活性与其他抗菌剂的比较。
J Antimicrob Chemother. 1984 Mar;13(3):237-44. doi: 10.1093/jac/13.3.237.
6
In vitro antibacterial properties of AT-2266, a new pyridonecarboxylic acid.新型吡啶羧酸AT-2266的体外抗菌特性
Antimicrob Agents Chemother. 1983 May;23(5):641-8. doi: 10.1128/AAC.23.5.641.
7
Comparison of antimicrobial susceptibility patterns of Campylobacter jejuni and Campylobacter coli.空肠弯曲菌和结肠弯曲菌抗菌药敏模式的比较。
Antimicrob Agents Chemother. 1984 Sep;26(3):351-3. doi: 10.1128/AAC.26.3.351.
8
Activity of the newer quinolones against Chlamydia trachomatis.新型喹诺酮类药物对沙眼衣原体的活性。
Br J Vener Dis. 1984 Oct;60(5):350. doi: 10.1136/sti.60.5.350.
9
Comparison of the antibacterial activity of norfloxacin (MK 0366, AM 715), a new organic acid, with that of other orally absorbed chemotherapeutic agents.新型有机酸诺氟沙星(MK 0366,AM 715)与其他口服吸收的化疗药物抗菌活性的比较。
Infection. 1982 Jan;10(1):41-4. doi: 10.1007/BF01640837.
10
In vitro antibacterial activity of AM-715, a new nalidixic acid analog.新型萘啶酸类似物AM - 715的体外抗菌活性
Antimicrob Agents Chemother. 1980 Feb;17(2):103-8. doi: 10.1128/AAC.17.2.103.