• 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

相似文献

1
Biliary excretion of cefixime: assessment in patients provided with T-tube drainage.头孢克肟的胆汁排泄:对行T管引流患者的评估
Antimicrob Agents Chemother. 1993 Jul;37(7):1488-91. doi: 10.1128/AAC.37.7.1488.
2
Role of intrahepatic protein binding in the hepatobiliary extraction profile of cefixime in humans.肝内蛋白结合在头孢克肟人体肝胆提取特征中的作用。
Clin Pharmacol Ther. 1993 Nov;54(5):476-84. doi: 10.1038/clpt.1993.179.
3
[Biliary excretion and hepatic disposal of cefixime: experimental and clinical study].[头孢克肟的胆汁排泄及肝脏处理:实验与临床研究]
Pathol Biol (Paris). 1992 May;40(5):538-44.
4
[Kinetics of cefixime biliary clearance in cholecystectomized patients].
Therapie. 1994 Jan-Feb;49(1):35-9.
5
Evaluation of cefixime biliary disposition in the isolated perfused rabbit liver model and in humans.
Drugs Exp Clin Res. 1992;18(8):329-36.
6
Concentration of cefixime in bile, gallbladder wall and serum after preoperative administration in patients undergoing cholecystectomy.胆囊切除术患者术前给药后胆汁、胆囊壁和血清中头孢克肟的浓度。
Methods Find Exp Clin Pharmacol. 1990 May;12(4):287-90.
7
Biliary excretion of ceftizoxime in humans.
Chemotherapy. 1984;30(4):221-6. doi: 10.1159/000238272.
8
[Pharmacokinetics of cefixime in volunteers and a literature comparison with the new ester prodrug cephalosporins].[头孢克肟在志愿者体内的药代动力学及与新型酯前药头孢菌素的文献比较]
Infection. 1990;18 Suppl 3:S150-4. doi: 10.1007/BF01644636.
9
Effect of ursodeoxycholate on the biliary excretion of cefotiam and sulbenicillin in patients with percutaneous transhepatic biliary drainage.
Antimicrob Agents Chemother. 1988 May;32(5):726-9. doi: 10.1128/AAC.32.5.726.
10
Alternative continuous infusion method for analysis of enterohepatic circulation and biliary excretion of cefixime in the rat.用于分析大鼠体内头孢克肟肝肠循环和胆汁排泄的交替连续输注法
J Pharm Sci. 1994 Jun;83(6):819-23. doi: 10.1002/jps.2600830612.

引用本文的文献

1
Role of cephalosporins in the era of Clostridium difficile infection.艰难梭菌感染时代头孢菌素的作用
J Antimicrob Chemother. 2017 Jan;72(1):1-18. doi: 10.1093/jac/dkw385. Epub 2016 Sep 22.
2
Effects of surgery on the pharmacokinetic parameters of drugs.手术对药物药代动力学参数的影响。
Clin Pharmacokinet. 1998 Oct;35(4):293-312. doi: 10.2165/00003088-199835040-00003.
3
Assessment of biliary excretion of piperacillin-tazobactam in humans.哌拉西林-他唑巴坦在人体中的胆汁排泄评估。
Antimicrob Agents Chemother. 1997 Aug;41(8):1636-40. doi: 10.1128/AAC.41.8.1636.

本文引用的文献

1
Biliary bacteria: significance and alterations after antibiotic therapy.胆道细菌:抗生素治疗后的意义及变化
Arch Surg. 1982 Apr;117(4):445-9. doi: 10.1001/archsurg.1982.01380280037008.
2
beta-Lactam pharmacology in liver disease.肝病中的β-内酰胺类药物药理学
J Antimicrob Chemother. 1983 Jun;11(6):499-501. doi: 10.1093/jac/11.6.499.
3
Comparative in vitro activity and beta-lactamase stability of FR 17027, a new orally active cephalosporin.新型口服活性头孢菌素FR 17027的体外活性及β-内酰胺酶稳定性比较
Antimicrob Agents Chemother. 1984 Aug;26(2):174-80. doi: 10.1128/AAC.26.2.174.
4
The bacteriology of the obstructed biliary tree.梗阻性胆管树的细菌学
Ann R Coll Surg Engl. 1973 May;52(5):316-9.
5
Evidence for the existence of a common transport system of beta-lactam antibiotics in isolated rat hepatocytes.在分离的大鼠肝细胞中存在β-内酰胺类抗生素共同转运系统的证据。
J Antibiot (Tokyo). 1985 Dec;38(12):1774-80. doi: 10.7164/antibiotics.38.1774.
6
Phase I study of cefixime, a new oral cephalosporin.新型口服头孢菌素头孢克肟的I期研究
J Clin Pharmacol. 1987 May-Jun;27(5):425-31. doi: 10.1002/j.1552-4604.1987.tb03043.x.
7
Absolute bioavailability of cefixime in man.头孢克肟在人体中的绝对生物利用度。
J Clin Pharmacol. 1988 Aug;28(8):700-6. doi: 10.1002/j.1552-4604.1988.tb03203.x.
8
High hepatic excretion in humans of cefpiramide, a new cephalosporin.新型头孢菌素头孢匹胺在人体内的高肝脏排泄率。
Antimicrob Agents Chemother. 1988 Sep;32(9):1360-4. doi: 10.1128/AAC.32.9.1360.
9
Comparative in vitro activity of the new oral cephalosporin cefixime.新型口服头孢菌素头孢克肟的体外活性比较
Eur J Clin Microbiol Infect Dis. 1988 Jun;7(3):428-31. doi: 10.1007/BF01962357.
10
Prospective randomized comparison of mezlocillin therapy alone with combined ampicillin and gentamicin therapy for patients with cholangitis.单独使用美洛西林治疗与联合使用氨苄西林和庆大霉素治疗胆管炎患者的前瞻性随机对照研究。
Arch Intern Med. 1989 Jun;149(6):1279-84.

头孢克肟的胆汁排泄:对行T管引流患者的评估

Biliary excretion of cefixime: assessment in patients provided with T-tube drainage.

作者信息

Westphal J F, Jehl F, Schloegel M, Monteil H, Brogard J M

机构信息

Department of Internal Medicine, Medical B Clinic, Strasbourg, France.

出版信息

Antimicrob Agents Chemother. 1993 Jul;37(7):1488-91. doi: 10.1128/AAC.37.7.1488.

DOI:10.1128/AAC.37.7.1488
PMID:8363380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC187999/
Abstract

The biliary excretion profile of cefixime was studied in 10 patients provided with T-tube drainage of the common bile duct after cholecystectomy. Following a single 200-mg oral dose, the peak concentration of cefixime in bile reached 56.9 +/- 70 mg/liter, approximately 20 times as high as the peak concentration in serum, 2.3 +/- 0.85 mg/liter. Cefixime levels in bile proved relatively sustained, since a concentration of 4.3 +/- 3.7 mg/liter was still found 20 h after dosing. The cumulative amount of cefixime recovered in the 24-h bile drainage averaged 10.0 +/- 12.3 mg, which is 5% of the administered dose and positions this beta-lactam antibiotic among the most highly bile-excreted cephalosporins. The presented results show that a single 200-mg oral dose of cefixime provided drug levels in bile consistently higher than the MICs for the most frequently recovered members of the family Enterobacteriaceae in biliary tract infections and maintained these levels for over 20 h after dosing. Accordingly, this cephalosporin deserves further clinical trials to assess its usefulness in both prophylaxis and treatment of biliary tract infections.

摘要

在10例胆囊切除术后行胆总管T管引流的患者中研究了头孢克肟的胆汁排泄情况。单次口服200mg剂量后,胆汁中头孢克肟的峰值浓度达到56.9±70mg/L,约为血清峰值浓度(2.3±0.85mg/L)的20倍。胆汁中头孢克肟水平相对持久,给药20小时后仍发现浓度为4.3±3.7mg/L。24小时胆汁引流中回收的头孢克肟累积量平均为10.0±12.3mg,占给药剂量的5%,使这种β-内酰胺抗生素跻身于胆汁排泄最高的头孢菌素之列。呈现的结果表明,单次口服200mg头孢克肟可使胆汁中的药物水平持续高于胆道感染中最常见的肠杆菌科成员分离株的最低抑菌浓度,并在给药后维持这些水平超过20小时。因此,这种头孢菌素值得进一步进行临床试验,以评估其在预防和治疗胆道感染中的效用。