• 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

Arterial and venous blood sampling in pharmacokinetic studies: griseofulvin.

作者信息

Chen M L, Lam G, Lee M G, Chiou W L

出版信息

J Pharm Sci. 1982 Dec;71(12):1386-9. doi: 10.1002/jps.2600711219.

DOI:10.1002/jps.2600711219
PMID:7153889
Abstract

The pharmacokinetics of griseofulvin were evaluated simultaneously using both arterial and venous plasma in three dogs and one rabbit after a rapid bolus intravenous dosing. Initial arterial-venous ratios 20 sec after injection were the highest and ranged from 15- to 752-fold for dogs; the ratio was 3240-fold for the rabbit. Both curves decayed paralleling each other at the terminal phase with the venous levels higher than arterial levels by 14-43 and 8.4% for the dogs and the rabbit, respectively. The use of the instantaneous input principle was found to overestimate the total area under the plasma level-time curve by as much as 166%. An exponential term with a negative coefficient was used to account for the short and steep rising phase of plasma levels after injection. Detailed analyses showed significant differences in various calculated pharmacokinetic parameters based on arterial or venous data. The present study exemplifies the need for careful assessment and interpretation of classical pharmacokinetic parameters. It appeared that short intravenous infusion rather than the instantaneous or rapid bolus intravenous injection should be preferred for routine pharmacokinetic studies.

摘要

相似文献

1
Arterial and venous blood sampling in pharmacokinetic studies: griseofulvin.
J Pharm Sci. 1982 Dec;71(12):1386-9. doi: 10.1002/jps.2600711219.
2
Arterial and venous blood sampling in pharmacokinetic studies: bumetanide in rabbits.药代动力学研究中的动静脉采血:家兔中的布美他尼
Res Commun Mol Pathol Pharmacol. 1997 Dec;98(3):255-64.
3
Arterial-venous plasma concentration differences of six drugs in the dog and rabbit after intravenous administration.
Res Commun Chem Pathol Pharmacol. 1981 Apr;32(1):27-39.
4
Arterial and venous blood sampling in pharmacokinetic studies: azosemide in rabbits.药代动力学研究中的动静脉采血:兔体内的阿佐塞米
Biopharm Drug Dispos. 1994 May;15(4):305-16. doi: 10.1002/bdd.2510150405.
5
Instantaneous input hypothesis in pharmacokinetic studies.
J Pharm Sci. 1981 Sep;70(9):1037-9. doi: 10.1002/jps.2600700918.
6
Arterial and venous blood sampling in pharmacokinetic studies: propranolol in rabbits and dogs.
Res Commun Chem Pathol Pharmacol. 1981 Jul;33(1):33-48.
7
Arterial and venous blood samplings in pharmacokinetic studies: vancomycin in rabbits.
J Clin Pharm Ther. 1993 Apr;18(2):115-22. doi: 10.1111/j.1365-2710.1993.tb00577.x.
8
Effect of arterial-venous plasma concentration differences on the determination of mean residence time of drugs in the body.
Res Commun Chem Pathol Pharmacol. 1982 Jan;35(1):17-26.
9
The phenomenon and rationale of marked dependence of drug concentration on blood sampling site. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics (Part I).药物浓度对采血部位显著依赖的现象及原理。在药代动力学、药效学、毒理学和治疗学中的意义(第一部分)
Clin Pharmacokinet. 1989 Sep;17(3):175-99. doi: 10.2165/00003088-198917030-00004.
10
Assessment of pharmacokinetic constants from postinfusion blood curves obtained after I.V. infusion.通过静脉输注后获得的输注后血药浓度曲线评估药代动力学常数。
J Pharm Sci. 1970 Jan;59(1):53-5. doi: 10.1002/jps.2600590107.

引用本文的文献

1
Pharmacokinetics and pharmacodynamics of furosemide in protein-calorie malnutrition.呋塞米在蛋白质 - 热量营养不良中的药代动力学和药效学
J Pharmacokinet Biopharm. 1993 Feb;21(1):1-17. doi: 10.1007/BF01061772.
2
Pharmacokinetics and pharmacodynamics of bumetanide after intravenous and oral administration to rats: absorption from various GI segments.布美他尼经静脉和口服给药后在大鼠体内的药代动力学和药效学:从胃肠道各段的吸收情况
J Pharmacokinet Biopharm. 1994 Feb;22(1):1-17. doi: 10.1007/BF02353407.
3
Evaluation of potential causes for the incomplete bioavailability of furosemide: gastric first-pass metabolism.
J Pharmacokinet Biopharm. 1983 Dec;11(6):623-40. doi: 10.1007/BF01059061.
4
Pharmacokinetics of methotrexate and 7-hydroxy-methotrexate in rabbits after intravenous administration.静脉注射后甲氨蝶呤和7-羟基甲氨蝶呤在兔体内的药代动力学
J Pharmacokinet Biopharm. 1983 Oct;11(5):499-513. doi: 10.1007/BF01062208.
5
Concentration and pH dependent steady-state volume of distribution of methotrexate estimated by a simple physiologically based method.
J Pharmacokinet Biopharm. 1984 Dec;12(6):597-610. doi: 10.1007/BF01059555.
6
Correlation of unbound plasma clearances of fifteen extensively metabolized drugs between humans and rats.
Pharm Res. 1988 Oct;5(10):668-72. doi: 10.1023/a:1015935206569.
7
The phenomenon and rationale of marked dependence of drug concentration on blood sampling site. Implications in pharmacokinetics, pharmacodynamics, toxicology and therapeutics (Part II).药物浓度对采血部位显著依赖的现象及原理。在药代动力学、药效学、毒理学及治疗学中的意义(第二部分)
Clin Pharmacokinet. 1989 Oct;17(4):275-90. doi: 10.2165/00003088-198917040-00005.