J4 ›› 2012, Vol. 38 ›› Issue (3): 598-602.

• 技术交流 • 上一篇    下一篇

姜黄素及姜黄素衍生物A在大鼠血浆中含量的测定

杨 苹1,隋思博2,王艳芳1,杨 晶1,张 敏1,3,李校堃1,3,4|郑 琳5   

  1. 1.吉林农业大学 生物反应器与药物开发教育部工程研究中心,吉林 长春 130118;2.吉林省食品药品检验所|吉林 长春 130033;3. 南京理工大学研究生院|江苏 南京 210094;4.吉林大学白求恩医学院生物化学教研室|吉林 长春 130021;5.辽宁省大连市环境监测中心|辽宁 大连 116023
  • 收稿日期:2011-11-22 出版日期:2012-05-28 发布日期:2012-05-28
  • 通讯作者: 张 敏(Tel:0431-84533428,E-mail:372754079@qq.com);李校堃(Tel:0431-84533348,E-mail:xiaokunli@163.net) E-mail:E-mail:372754079@qq.com;E-mail:xiaokunli@163.net
  • 作者简介:杨 苹(1987-)|女|山西省晋中市人|医学硕士|主要从事中药新药资源研究及开发应用的研究。
  • 基金资助:

    吉林农业大学青年基金资助课题(201127);十一五“863”计划生物反应器重大专项基金资助课题(2007AA100503)

Determination of curcumin and curcumin derivative A in rat plasma

YANG Ping 1,SUI Si-bo 2,WANG Yan-fang 1,YANG Jing 1,ZHANG Min 1|3,LI Xiao-kun 1,3,4,ZHENG Lin 5   

  1. 1.Engineering Research Center of Bioreactor and Pharmaceutical Development,Ministry of Education,Jilin Agricultural University,Changchun 130118,China;2. Jilin Institute for Food and Drug Control,Changchun 130033,China;3.Graduate |School,Nanjing University of Science and Technology,Nanjing 210094,China;4. Department of Biochemistry,Norman Bethune College of Medicine,Jilin University, Changchun 130021,China;5.Environmental Center of Dalian City,Dalian 116023,China
  • Received:2011-11-22 Online:2012-05-28 Published:2012-05-28

摘要:

目的:建立大鼠血浆中姜黄素及姜黄素衍生物A的高效液相色谱(HPLC)测定方法,研究其在大鼠体内的药物动力学,为姜黄素的临床应用提供参考。方法:将姜黄素及姜黄素衍生物A分别灌胃给药,采用HPLC测定其在大鼠血浆中的血药浓度,色谱柱为Hypersil ODS2 C18(5  μm×4.6 mm×200 mm);柱温:30℃;姜黄素流动相,乙腈-水-乙酸(体积比45∶55∶1),姜黄素检测波长为420 nm;姜黄素衍生物A流动相,乙腈-水-乙酸(体积比70∶30∶1);体积流量为1.0 mL?min-1;姜黄素衍生物A检测波长为361 nm。结果:姜黄素及姜黄素衍生物A在0.25~100.00 mg?L-1 范围内与峰面积呈良好的线性关系,姜黄素回归方程为Y=105.90X-22.70,r=0.999 6;姜黄素衍生物A回归方程为Y=71.20X+24.62,r=0.999 4。两者日内、日间精密度RSD均小于4%,平均回收率均大于96%;大鼠灌胃给药后的药动学行为符合单室模型,姜黄素衍生物A的清除率比姜黄素显著降低,约是姜黄素清除率的3.57倍,曲线下面积是姜黄素的4.09倍,半衰期t1/2约为姜黄素的2.79倍。结论:HPLC测定姜黄素及姜黄素衍生物A在大鼠体内血药浓度的方法准确、简单可行、重复性好,为提高姜黄素在体内的稳定性,延长其在体内半衰期提供了依据。 

关键词:  姜黄素;姜黄素衍生物;药物动力学;高效液

Abstract:

Objective
To develop the method of high performance liquid chromatography(HPLC) for determination of curcumin and curcumin derivative A in rat plasma and study their  pharmacokinetics in rats, and to provide basis for  clinical application of curcumin.Methods The curcumin and the curcumin derivative A were lavaged to the rats,and the concentrations of curcumin and curcumin derivative A in rat blood at different time points were determined by HPLC.The curcumin and curcumin derivative A were separated well on a Hypersil ODS2 C18 (5  μm×4.6 mm ×200 mm)under 30℃.The mobile phase of curcumin was a mixture of acetonitrile-water containing 1% acetic acid (45∶55) at a flow rate of 1 mL?min-1.The detective wavelength was 420 nm;the mobile phase of curcumin derivative A was a mixture of acetonitrile-water containing 1% acetic acid (70∶30) at a flow rate of 1 mL?min-1.The detective wavelength was 361 nm.Results The calibration curve was liner at the range of 0.25-100.00 mg?mL-1.The regression equation of curcumin was  Y=105.90X-22.70,r=0.999 6;the regression equation of curcumin derivative A was Y=71.20X+24.62,r=0.999 4.The RSD of intra-day precision and inter-day precision was less than 4%.The average recovery was more than 96%.The plasma concentration-time curves of curcumin and curcumin derivative A in rats  fit to one compartment model respectively.The clearance rate,the area under temperature and t1/2 of curcumin derivative A were 3.57,4.09 and 2.79 times respectively than those of curcumin.Conclusion The method of HPLC for the determination of curcumin and curcumin derivative A in plasma is accurate,simple and reliable,which provides the basis for the improvement of stablility and the extending of the half-time of curcumin.

Key words: curcumin;curcumin derivative;pharmacokinetics;high performance liquid chromatography

中图分类号: 

  • R927.1