您的位置: 专家智库 > >

国家自然科学基金(30772613)

作品数:4 被引量:11H指数:2
相关作者:顾景凯吴秀君高峰崔向勇关鑫更多>>
相关机构:吉林大学辽宁中医药大学附属医院中国医科大学更多>>
发文基金:国家自然科学基金国家科技重大专项更多>>
相关领域:医药卫生农业科学理学更多>>

文献类型

  • 2篇中文期刊文章

领域

  • 1篇医药卫生
  • 1篇农业科学
  • 1篇理学

主题

  • 1篇药代
  • 1篇药代动力学
  • 1篇生物利用度
  • 1篇亮菌甲素
  • 1篇绝对生物利用...
  • 1篇PHARMA...
  • 1篇RANITI...
  • 1篇APPLIC...
  • 1篇CLINIC...
  • 1篇ITS
  • 1篇LC-MS/...

机构

  • 1篇吉林大学
  • 1篇吉林大学第一...
  • 1篇佳木斯大学

作者

  • 1篇刘明远
  • 1篇董雷
  • 1篇顾景凯
  • 1篇王岩
  • 1篇王中华

传媒

  • 1篇吉林大学学报...
  • 1篇Chemic...

年份

  • 1篇2010
  • 1篇2008
4 条 记 录,以下是 1-2
排序方式:
Rapid Determination of Ranitidine in Human Plasma by Liquid Chromatography-Tandem Mass Spectrometry and Its Application to a Clinical Pharmacokinetic Study
2010年
A rapid and sensitive assay based on high performance liquid chromatography-tandem mass spectrometry(LC-MS/MS) was developed for the determination of ranitidine(RAN) in human plasma with codeine as internal standard(IS).After protein precipitation with acetonitrile,the analyte and IS were separated on a Zorbax SB-Aq C18 column(150 mm×4.6 mm i.d.,5 μm) eluted with a mobile phase consisting of methanol/acetonitrile/10 mmol/L ammonium acetate containing 1% formic acid(pH=2.4)(volume ratio 12.5:12.5:75) at a flow rate of 1.0 mL/min.Detection was performed by electrospray ionization in the positive ion mode followed by the multiple reaction monito-ring(MRM) of the transitions of RAN at m/z 315.1→176.3 and of IS at m/z 300.1→165.1.The method was linear over a concentration range of 1―1000 ng/mL(r=0.9991) with a lower limit of quantitation(LLOQ) of 1 ng/mL and a limit of detection(LOD) of 0.3 ng/mL.Accuracy as relative error was from-0.01% to-1.7% and intra-day and inter-day precisions as relative standard deviation were ≤8.9% and ≤5.5%,respectively.The method was successfully applied to a pharmacokinetic study of ranitidine,getting a single oral dose(160 mg) to healthy volunteers.
ZHANG ChaoWANG LuGUAN XinJ. Paul FawcettZHAO Li-meiSUN Yan-tongGU Jing-kai
关键词:RANITIDINEPHARMACOKINETICSLC-MS/MS
亮菌甲素在大鼠体内的绝对生物利用度被引量:2
2008年
采用液相色谱-串联质谱(LC—MS/MS)法测定大鼠血浆中亮菌甲素的浓度,研究亮菌甲素在大鼠体内药动学特征及其绝对生物利用度.结果表明,亮菌甲素灌胃给药(ig)1.44mg和静脉注射给药(iv)0.9mg后,在大鼠体内的主要药动学参数达峰浓度(Cmax)分别为(58.33±23.41),(825.25±92.13)μg/L,半衰期(t1/2)分别为(1.55±0.43),(0.75±0.35)h,血药浓度-时间曲线下面积(AUC0~1)分别为(41.87±7.54),(140.64±19.73)h·(μg/L).经剂量校正后求得亮菌甲素在大鼠体内的绝对生物利用度(Fab)为18.61%.
王岩王中华刘明远董雷顾景凯
关键词:亮菌甲素药代动力学绝对生物利用度
共1页<1>
聚类工具0