• 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

舒洛芬:一种新型非麻醉性外周镇痛药的药理学及临床疗效

Suprofen: the pharmacology and clinical efficacy of a new non-narcotic peripheral analgesic.

作者信息

Tolman E L, Rosenthale M E, Capetola R J, McGuire J L

出版信息

Clin Rheum Dis. 1984 Aug;10(2):353-68.

PMID:6439459
Abstract

Suprofen is a potent, peripherally-acting, non-narcotic analgesic agent. The mechanism of action of the compound involves inhibition of prostaglandin biosynthesis and, perhaps, direct antagonism of the peripheral, pain inducing actions of prostaglandins, bradykinin and other pain mediators. Suprofen at a dose of 200 mg appears to be equal or greater in efficacy as an analgesic modality than those of ibuprofen, propoxyphene, naproxen and diflunisal or a combination of 650 mg aspirin plus 60 mg codeine. Its clinical utility has been amply demonstrated in the treatment of a number of types of pain including general and orthopedic surgery, episiotomy, post-partum pain, dysmenorrhea, dental pain and musculoskeletal disorders. Suprofen represents a new class of orally effective nonnarcotic analgesics with potential for effective clinical use in the treatment of pain.

摘要

舒洛芬是一种强效的、作用于外周的非麻醉性镇痛药。该化合物的作用机制包括抑制前列腺素生物合成,或许还包括直接拮抗前列腺素、缓激肽及其他疼痛介质在外周的致痛作用。200毫克剂量的舒洛芬作为一种镇痛方式,其疗效似乎等同于或优于布洛芬、丙氧芬、萘普生和二氟尼柳,或等同于650毫克阿司匹林加60毫克可待因的组合。其临床效用已在多种疼痛治疗中得到充分证明,包括普通外科手术和矫形外科手术、会阴切开术、产后疼痛、痛经、牙痛和肌肉骨骼疾病。舒洛芬代表了一类新型口服有效的非麻醉性镇痛药,具有有效治疗疼痛的临床应用潜力。

相似文献

1
Suprofen: the pharmacology and clinical efficacy of a new non-narcotic peripheral analgesic.舒洛芬:一种新型非麻醉性外周镇痛药的药理学及临床疗效
Clin Rheum Dis. 1984 Aug;10(2):353-68.
2
Suprofen, a new peripheral analgesic.舒洛芬,一种新型外周镇痛药。
J Pharmacol Exp Ther. 1980 Jul;214(1):16-23.
3
Introduction to the pharmacology of suprofen.舒洛芬药理学介绍。
Pharmacology. 1983;27 Suppl 1:1-13. doi: 10.1159/000137893.
4
Suprofen. A review of its pharmacodynamic and pharmacokinetic properties, and analgesic efficacy.舒洛芬。对其药效学、药代动力学特性及镇痛疗效的综述。
Drugs. 1985 Dec;30(6):514-38. doi: 10.2165/00003495-198530060-00004.
5
Suprofen, a potent antagonist of acetic acid-induced writhing in rats.舒洛芬,一种对大鼠醋酸诱导扭体反应有强效拮抗作用的物质。
Arzneimittelforschung. 1975 Oct;25(10):1505-9.
6
Potent and selective effects of suprofen on uterine prostaglandin synthesis.舒洛芬对子宫前列腺素合成的强效及选择性作用。
Prostaglandins Leukot Med. 1985 Jun;18(3):367-77. doi: 10.1016/0262-1746(85)90070-8.
7
A clinical trial in oral surgery of the analgesic efficacy of a suprofen/codeine combination.一项关于舒洛芬/可待因组合在口腔外科手术中镇痛效果的临床试验。
Anesth Prog. 1987 Sep-Oct;34(5):177-80.
8
Inhibition by suprofen and other non-narcotic analgesic drugs of the effects of prostaglandin precursor on isolated tissues and platelets.舒洛芬及其他非麻醉性镇痛药对前列腺素前体在离体组织和血小板上作用的抑制作用。
Arch Int Pharmacodyn Ther. 1976 Apr;220(2):297-310.
9
[Effect of alpha-(p-thenoylphenyl)-propionic acid (TN-762) on acute inflammatory reactions and prostaglandin biosynthesis].α-(对噻吩甲酰基苯基)丙酸(TN-762)对急性炎症反应和前列腺素生物合成的影响
Nihon Yakurigaku Zasshi. 1981 Mar;77(3):321-36.
10
Antagonism of arachidonic acid hydroperoxide on isolated gastrointestinal tissues as a measure of the inhibition of prostaglandin biosynthesis.花生四烯酸氢过氧化物对离体胃肠组织的拮抗作用作为前列腺素生物合成抑制的一种衡量指标。
Adv Prostaglandin Thromboxane Res. 1976;1:139-45.

引用本文的文献

1
Suprofen. A review of its pharmacodynamic and pharmacokinetic properties, and analgesic efficacy.舒洛芬。对其药效学、药代动力学特性及镇痛疗效的综述。
Drugs. 1985 Dec;30(6):514-38. doi: 10.2165/00003495-198530060-00004.
2
Effects of systemic non-steroidal anti-inflammatory drugs on nociception during tail ischaemia and on reperfusion hyperalgesia in rats.全身性非甾体抗炎药对大鼠尾部缺血期间伤害感受及再灌注痛觉过敏的影响。
Br J Pharmacol. 1992 Feb;105(2):412-6. doi: 10.1111/j.1476-5381.1992.tb14267.x.