• 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

Absorption studies of the H2-blocker nizatidine.

作者信息

Knadler M P, Bergstrom R F, Callaghan J T, Obermeyer B D, Rubin A

机构信息

Lilly Research Laboratories, Lilly Laboratory for Clinical Research, Indianapolis, IN.

出版信息

Clin Pharmacol Ther. 1987 Nov;42(5):514-20. doi: 10.1038/clpt.1987.190.

DOI:10.1038/clpt.1987.190
PMID:2890459
Abstract

The absolute and relative bioavailability of nizatidine, an H2-blocker, was studied in healthy male volunteers. The absolute oral bioavailability, relative to that after intravenous administration, was 98% +/- 14%. The bioavailability of single and multiple oral doses of 150 mg nizatidine was unaffected by concurrent food ingestion; nizatidine may be administered either with or without food. The relative bioavailability of nizatidine was compared when given simultaneously with placebo or Gelusil, 30 minutes after propantheline, or 60 minutes before activated charcoal. Gelusil reduced the amount of nizatidine absorbed by about 10%, charcoal reduced it by about 30%, and propantheline did not affect it.

摘要

相似文献

1
Absorption studies of the H2-blocker nizatidine.
Clin Pharmacol Ther. 1987 Nov;42(5):514-20. doi: 10.1038/clpt.1987.190.
2
Oral bioavailability of nizatidine and ranitidine concurrently administered with antacid.尼扎替丁和雷尼替丁与抗酸剂同时给药时的口服生物利用度。
J Int Med Res. 1989 Jan-Feb;17(1):62-7. doi: 10.1177/030006058901700109.
3
A pharmacokinetic profile of nizatidine in man.
Scand J Gastroenterol Suppl. 1987;136:9-17. doi: 10.3109/00365528709094480.
4
Drug interactions of H2-receptor antagonists.H2受体拮抗剂的药物相互作用。
Scand J Gastroenterol Suppl. 1994;206:14-9. doi: 10.3109/00365529409091415.
5
Nizatidine disposition in subjects with normal and impaired renal function.尼扎替丁在肾功能正常和受损受试者中的处置情况。
Clin Pharmacol Ther. 1988 Jun;43(6):688-95. doi: 10.1038/clpt.1988.97.
6
Secretion of nizatidine into human breast milk after single and multiple doses.单次及多次给药后尼扎替丁在人母乳中的分泌情况。
Clin Pharmacol Ther. 1990 Jun;47(6):724-30. doi: 10.1038/clpt.1990.100.
7
Nizatidine, an H2-blocker. Its metabolism and disposition in man.尼扎替丁,一种H2受体阻滞剂。它在人体内的代谢与处置。
Drug Metab Dispos. 1986 Mar-Apr;14(2):175-82.
8
Pharmacokinetics and pharmacodynamics of oral nizatidine.口服尼扎替丁的药代动力学和药效学
J Clin Pharmacol. 1988 Jan;28(1):71-5. doi: 10.1002/j.1552-4604.1988.tb03103.x.
9
A comparison of nizatidine with the three other histamine receptor antagonists for duodenal ulcer therapy.尼扎替丁与其他三种组胺受体拮抗剂治疗十二指肠溃疡的比较。
Nurse Pract. 1989 Feb;14(2):41-2.
10
Nizatidine, and H2-receptor antagonist: disposition and safety in the elderly.尼扎替丁,一种H2受体拮抗剂:在老年人中的处置与安全性。
J Clin Pharmacol. 1987 Aug;27(8):618-24. doi: 10.1002/j.1552-4604.1987.tb03075.x.

引用本文的文献

1
Clinically significant drug interactions with antacids: an update.与抗酸剂有临床意义的药物相互作用:更新。
Drugs. 2011 Oct 1;71(14):1839-64. doi: 10.2165/11593990-000000000-00000.
2
Clinical pharmacokinetics of drugs used to treat urge incontinence.用于治疗急迫性尿失禁药物的临床药代动力学
Clin Pharmacokinet. 2003;42(14):1243-85. doi: 10.2165/00003088-200342140-00004.
3
Modulation of the tight junctions of the Caco-2 cell monolayers by H2-antagonists.H2拮抗剂对Caco-2细胞单层紧密连接的调节作用。
Pharm Res. 1998 Jan;15(1):53-7. doi: 10.1023/a:1011944602662.
4
Pharmacokinetic optimisation in the treatment of gastro-oesophageal reflux disease.胃食管反流病治疗中的药代动力学优化
Clin Pharmacokinet. 1996 Nov;31(5):386-406. doi: 10.2165/00003088-199631050-00005.
5
Gastric fluid volume and pH after nizatidine in adults undergoing elective surgery: influence of timing and dose.
Can J Anaesth. 1995 Aug;42(8):730-4. doi: 10.1007/BF03012673.
6
Nizatidine. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and its therapeutic use in peptic ulcer disease.尼扎替丁。对其药效学和药代动力学特性及其在消化性溃疡疾病中的治疗应用的初步综述。
Drugs. 1988 Nov;36(5):521-39. doi: 10.2165/00003495-198836050-00002.
7
Newer H2-receptor antagonists. Clinical pharmacokinetics and drug interaction potential.新型H2受体拮抗剂。临床药代动力学及药物相互作用潜力。
Clin Pharmacokinet. 1988 Oct;15(4):205-15. doi: 10.2165/00003088-198815040-00001.
8
Clinical pharmacokinetics of drugs used in the treatment of gastrointestinal diseases (Part II).用于治疗胃肠道疾病的药物的临床药代动力学(第二部分)。
Clin Pharmacokinet. 1990 Aug;19(2):94-125. doi: 10.2165/00003088-199019020-00002.