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差分脉冲伏安法同时测定α-山竹黄酮和γ-山竹黄酮

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研究了α-山竹黄酮和γ-山竹黄酮在玻璃碳电极上的电化学行为, 研究了pH和静置时间等因素的影响, 探讨了α-山竹黄酮和γ-山竹黄酮在玻璃碳电极上的氧化机理, 建立了差分脉冲伏安法同时测定α-山竹黄酮和γ-山竹黄酮的方法. 在pH 3.1的BR缓冲介质中, α-山竹黄酮在0.822 V产生灵敏的氧化峰, γ-山竹黄酮在0.426 V和0.700 V产生灵敏的氧化峰. 对α-山竹黄酮, 相应的氧化峰的峰高与浓度在5.00×10~(-6) mol/L~2.00×10~(-4) mol/L范围内呈良好的线性关系, 线性相关系数为0.9950;对γ-山竹黄酮, 其在0.426 V氧化峰的峰高与浓度在2.00×10~(-5) mol/L~6.00×10~(-4) mol/L浓度范围内呈良好的线性关系, 线性相关系数为0.9904. 该方法测量2.00×10~(-4) mol/L 的α-山竹黄酮和γ-山竹黄酮相对标准偏差分别为3.3%和4.1% (n=10).
Differential pulse voltammetry for the simultaneous determination of the α-mangostin and γ-mangostin
Electrochemical behavior of α-mangostin and γ-mangostin on a glassy carbon disk electrode was studied through investigation of the effect of pH, quit time etc. A novel differential pulse voltammetry (DPV) for the simultaneous determination of α-mangostin and γ-mangostin in the mixture was established. In Britton-Robinson buffer (pH 3.1), α-mangostin and γ-mangostin can be oxidized on the electrode to produce oxidative peaks at the potentials of 0.822 V and 0.426 V (vs SCE) respectively. The corresponding peak currents are proportional to the concentration within 5.00×10~(-6)~2.00×10~(-4) mol/L for α-mangostin and within 2.00×10~(-5)~6.00×10~(-4) mol/L for γ-mangostin respectively. The linear correlation coefficients are 0.9950 and 0.9904 for α-mangostin and γ-mangostin respectively. The RSDs are 3.3% and 4.1% (n=10) for 2.00×10~(-4) mol/L α-mangostin and γ-mangostin separately.

α-mangostinγ-mangostinDifferential pulse voltammetrySimultaneous determination

陈墨、魏永锋、王晓莹、赵佳

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西北大学化学与材料科学学院,西安,710069

α-山竹黄酮 γ-山竹黄酮 差分脉冲伏安法 同时测定

2010

分析试验室
北京有色金属研究总院 中国分析测试协会

分析试验室

CSTPCDCSCD北大核心
影响因子:1.171
ISSN:1000-0720
年,卷(期):2010.29(1)
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