张秀琴, 徐礼燊. 朱砂七中蒽醌类成分的脉冲极谱测定J. 药学学报, 1984, 19(7): 519-523.
引用本文: 张秀琴, 徐礼燊. 朱砂七中蒽醌类成分的脉冲极谱测定J. 药学学报, 1984, 19(7): 519-523.
ZHANG Xiu-Qin, XU Li-Xin. PULSE POLAROGRAPHIC DETERMINATION OF ANTHRAQUINONE IN POLYGONUM CILLINERVE (NAKAI) OHWIJ. Acta Pharmaceutica Sinica, 1984, 19(7): 519-523.
Citation: ZHANG Xiu-Qin, XU Li-Xin. PULSE POLAROGRAPHIC DETERMINATION OF ANTHRAQUINONE IN POLYGONUM CILLINERVE (NAKAI) OHWIJ. Acta Pharmaceutica Sinica, 1984, 19(7): 519-523.

朱砂七中蒽醌类成分的脉冲极谱测定

PULSE POLAROGRAPHIC DETERMINATION OF ANTHRAQUINONE IN POLYGONUM CILLINERVE (NAKAI) OHWI

  • 摘要: 本文报道用脉冲极谱法测定生药朱砂七中蒽醌甙元及其甙的测定条件。研究了大黄素在氯化锂电解液中的极谱还原波,峰电位为—0.75V(vs SEC),波高与浓度在6.4×10-6~3.1×10-5M范围呈线性关系。并研究了生药的提取及薄层分离方法,为评价生药的质量及蒽醌类化合物的测定提供了有效的定性和定量方法。

     

    Abstract: Pulse polarographic determination of anthraquinone in Polygonum cillinerve (Nakai) Ohwi was reported.The sample was extracted with methanol and separated with thin layer chromatography. The zones of emodin and physcion were removed from the plate, and analysed by pulse polarographic method. 0.1 M lithium chloride solution was used as supporting electrolyte. The peak potential was -0.75 V (vs SEC)The current was proportional to the concentration in the range of 6.4×10-6~3.1×10-5 M. The method is accurate and sensitive. The error is<2%.

     

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