• 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

[地奥司明在大鼠体内的药代动力学研究]

[Studies on pharmacokinetics of diosmin in rats].

作者信息

Ma Ying-Li, Ma Chao

机构信息

School of Pharmacy, Heilongjiang University of Traditional Chinese Medicine, Harbin 150040, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2007 Mar;32(5):418-20.

PMID:17511149
Abstract

OBJECTIVE

To establish a HPLC method for the determination of diosmin in Rats plasma and to study the pharmacokinetics of diosmin in Rats.

METHOD

Rats were given diosmin with 3 doses as 225, 325, 425 mg x kg(-1). Blood samples were collected at different times after oral administration. The plasma concentration of diosmin was determined by HPLC, and the pharmacokinetics parameters were calculated by 3p97 program.

RESULT

The typical equation of diosmin in rats plasma was Y = 3.05 x 10(-3) C + 1.55 x 10(-3), the calibration curves of diosmin was linear in the range from 0.5-100 microg x mL(-1) (R =0. 996 4). The lowest concentration of diosmin in plasma was 0. 2 g x mL(-1). Its recoveries was more than 85%, and the interday and intraday precision, which was expressed as RSD, were all less than 15%. After 3 doses oral administration of diosmin in rats, the mean plasma concentration-time curves were found to fit one compartment model, and the main pharmacokinetics parameters were obtained.

CONCLUSION

It is first time to establish the HPLC method to determine the concentration of diosmin in rats plasma, and the method described in this report has high sensitivity and selectivity, and it was suitable for pharmacokinetics studies of diosmin. The internal process of diosmin in rats is fit to one compartment model.

摘要

目的

建立测定大鼠血浆中地奥司明的高效液相色谱法,并研究地奥司明在大鼠体内的药代动力学。

方法

给大鼠分别灌胃225、325、425mg·kg⁻¹ 3种剂量的地奥司明。口服给药后于不同时间点采集血样。采用高效液相色谱法测定血浆中地奥司明的浓度,并用3p97程序计算药代动力学参数。

结果

大鼠血浆中地奥司明的典型方程为Y = 3.05×10⁻³C + 1.55×10⁻³,地奥司明的标准曲线在0.5 - 100μg·mL⁻¹范围内呈线性(R = 0.996 4)。血浆中地奥司明的最低检测浓度为0.2μg·mL⁻¹。其回收率大于85%,以相对标准偏差(RSD)表示的日间和日内精密度均小于15%。大鼠口服3种剂量地奥司明后,平均血浆浓度 - 时间曲线符合一室模型,并获得了主要药代动力学参数。

结论

首次建立了测定大鼠血浆中地奥司明浓度的高效液相色谱法,本报告所述方法具有高灵敏度和选择性,适用于地奥司明的药代动力学研究。地奥司明在大鼠体内的过程符合一室模型。

相似文献

1
[Studies on pharmacokinetics of diosmin in rats].[地奥司明在大鼠体内的药代动力学研究]
Zhongguo Zhong Yao Za Zhi. 2007 Mar;32(5):418-20.
2
[The pharmacokinetics of rhein in 12 healthy volunteers after oral administration of rhubarb extract].[12名健康志愿者口服大黄提取物后大黄酸的药代动力学]
Zhongguo Zhong Yao Za Zhi. 2005 Sep;30(18):1458-61.
3
[Pharmacokinetics of luteolin from Elsholtzia blanda extracts in rats].[淡黄香薷提取物中木犀草素在大鼠体内的药代动力学]
Yao Xue Xue Bao. 2008 May;43(5):523-7.
4
[Pharmacokinetics and tissue distribution of atractylenolide III in rats].白术内酯III在大鼠体内的药代动力学及组织分布
Zhong Yao Cai. 2006 Aug;29(8):807-9.
5
[Pharmacokinetics of (-)-clausenamide and its major metabolite 6-hydroxyl-clausenamide in beagle dogs by HPLC/MS].
Yao Xue Xue Bao. 2005 Oct;40(10):940-4.
6
Pharmacokinetics and metabolism of oral diosmin in healthy volunteers.健康志愿者口服地奥司明的药代动力学与代谢
Int J Clin Pharmacol Ther Toxicol. 1992 Jan;30(1):29-33.
7
[Studies on pharmacokinetics of nitidine chloride in rabbits].[氯化两面针碱在兔体内的药代动力学研究]
Zhongguo Zhong Yao Za Zhi. 2009 Jun;34(11):1406-9.
8
[RP-HPLC method for determination of protopine in plasma and pharmacokinetics in rats].
Yao Xue Xue Bao. 2001 Oct;36(10):790-2.
9
[Study on pharmacokinetics of glycyrrhetic acid in rats by RP-HPLC].[反相高效液相色谱法研究大鼠体内甘草次酸的药代动力学]
Zhongguo Zhong Yao Za Zhi. 2008 Jun;33(11):1294-6.
10
[Investigation on pharmacokinetics of helicid in rats].
Zhongguo Zhong Yao Za Zhi. 2008 Nov;33(22):2662-6.