Tang Peter H
Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Department of Pathology, Cincinnati, OH 45229-3039, USA.
J AOAC Int. 2006 Jan-Feb;89(1):35-9.
A rapid and sensitive method is described for the determination of coenzyme Q10 (Q10) in over-the-counter dietary supplements by automated high-performance liquid chromatography (HPLC) with coulometric detection. Sample solutions of powder-filled capsules, oil-based softgels, and tablets were prepared by serial dilution with 1-propanol. After dilution, a known volume of sample solution containing Q10 and the internal standard, coenzyme Q9 (Q9), was directly injected into the HPLC system. Most of electrochemically active compounds in the injection were oxidized at the precolumn conditioning cell and postcolumn guard cell. Q9 and Q10 were monitored at an analytical cell that contained 2 coulometric electrodes, where Q9 and Q10 were reduced to the corresponding ubiquinol-9 and -10 and then oxidized to produce currents. This method produced a linear detector response for peak height measurements over the concentration range of 0.05-8 microg/mL (r > 0.999). The lower limit of detection was 5 ng/mL (signal-to-noise ratio, > or =3). The mean recovery was 98.9 +/- 0.6%; coefficients of variation for intra- and interday precisions were 1.8-4.0%. The proposed method was successfully applied to the determination of Q10 in marketed products.
描述了一种通过带电量检测的自动高效液相色谱法(HPLC)测定非处方膳食补充剂中辅酶Q10(Q10)的快速灵敏方法。粉末填充胶囊、油基软胶囊和片剂的样品溶液通过用1-丙醇连续稀释来制备。稀释后,将已知体积的含有Q10和内标辅酶Q9(Q9)的样品溶液直接注入HPLC系统。进样中的大多数电化学活性化合物在柱前调节池和柱后保护池中被氧化。在含有2个电量电极的分析池中监测Q9和Q10,在该池中Q9和Q10被还原为相应的泛醇-9和-10,然后被氧化以产生电流。该方法在0.05 - 8μg/mL的浓度范围内对峰高测量产生线性检测器响应(r > 0.999)。检测下限为5 ng/mL(信噪比≥3)。平均回收率为98.9±0.6%;日内和日间精密度的变异系数为1.8 - 4.0%。所提出的方法成功应用于市售产品中Q10的测定。