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引用本文:冯素香,吴加,李建生,屈凌波,徐会平,杨冉,李建军.大黄5个蒽醌类成分与大鼠血浆蛋白结合率的测定[J].中国现代应用药学,2013,30(1):1-5.
FENG Suxiang,WU Jia,LI Jiansheng,QU Lingbo,XU Huiping,YANG Ran,LI Jianjun.Determination of the Binding Rate of Rat Plasma Protein with Five Anthraquinones in Rhubarb[J].Chin J Mod Appl Pharm(中国现代应用药学),2013,30(1):1-5.
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大黄5个蒽醌类成分与大鼠血浆蛋白结合率的测定
冯素香1,2, 吴加1, 李建生1, 屈凌波2,3, 徐会平2, 杨冉2, 李建军2
1.河南中医学院,郑州 450008;2.郑州大学,郑州 450001;3.河南工业大学,郑州 450001
摘要:
目的 建立测定大黄苷元中芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚5种成分与大鼠血浆蛋白结合率的方法。方法 采用体外平衡透析法,模拟大黄苷元与血浆蛋白的结合过程,以固相萃取柱处理血浆样品,用高效液相色谱法测定大黄苷元中5种蒽醌类成分在透析袋内血浆中的浓度与透析袋外缓冲液中的浓度,计算血浆蛋白结合率。结果 芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚提取回收率分别为68.6%,91.5%,78.6%,88.2%和71.4%,与大鼠体外血浆蛋白结合率分别为93.1%,91.3%,95.2%,87.5%和89.7%。结论 大黄5种苷元与大鼠血浆蛋白结合率较高,且蛋白结合率与血药浓度无明显依赖性。
关键词:  大黄苷元  血浆蛋白结合率  平衡透析法  高效液相色谱法
DOI:
分类号:
基金项目:国家自然科学基金资助项目(81274179);河南省高校青年骨干教师资助项目(2009GGJS-065);河南省教育自然科学研究计划项目(2010A360002)
Determination of the Binding Rate of Rat Plasma Protein with Five Anthraquinones in Rhubarb
FENG Suxiang1,2, WU Jia1, LI Jiansheng1, QU Lingbo2,3, XU Huiping2, YANG Ran2, LI Jianjun2
1.Henan University of Traditional Chinese Medicine, Zhengzhou 450008, China;2.Zhengzhou University, Zhengzhou 450001, China;3.Henan University of Technology, Zhengzhou 450001, China
Abstract:
OBJECTIVE To develop a method for the simultaneous determination of the binding rate of plasma protein with aloe-emodin, rhein, emodin, chrysophanol and physcion. METHODS The equilibrium dialysis method was carried out to imitate the binding process between five anthraquinones and plasma protein. Plasma samples were treated with solid-phase extraction and the binding rate was determined by HPLC. RESULTS The extract recoveries of aloe-emodin, rhein, emodin, chrysophanol and physcion were 68.6%, 91.5%, 78.6%, 88.2% and 71.4%, the binding rates of plasma protein were 93.1%, 91.3%, 95.2%, 87.5% and 89.7%. CONCLUSION This method shows the high binding rate of five anthraquinones to plasma protein. The binding rates of five anthraquinones are not proportionally dependent on plasma concentration.
Key words:  rhubarb aglycone  protein binding rate  equilibrium dialysis  HPLC
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