Di Youjun, Zhao Min, Nie Yingchun, Wang Fei, Lv Jiagen
Department of Chemistry, Shaanxi Institute of Education, Xi'an 710061, China.
J Autom Methods Manag Chem. 2011;2011:982186. doi: 10.1155/2011/982186. Epub 2011 Jan 20.
A flow method of high-performance liquid chromatography (HPLC) seperation and chemiluminescence (CL) detection for sensitive vardenafil analysis in dietary supplements was developed. The vardenafil separation was achieved on a C18 column at 30°C using ethanol-H(3)PO(4) and ethylenediaminetetraacetic acid disodium salt (Na(2)EDTA) aqueous solution (25 : 75, v/v%) as mobile phase. The followed continuous CL detection was conducted based on the strong CL enhancement by the presence of vardenafil to luminol-K(3)Fe(CN)(6) reaction in alkaline medium. At the flow rate of 0.8 mL/min, the vardenafil retention time (t(R)) was 6.4 min. Factors that affected the HPLC resolution and CL detection were studied and optimized. The calibration curve obtained for vardenafil standard was linear in concentration range of 8.0 × 10(-7) ~ 1.0 × 10(-4) mol/L. The relative standard deviations (RSD) of intraday and interday precision were less than 3.5%. The proposed method was applied to the vardenafil determination in oral liquid, wine, and capsule samples.
建立了一种用于膳食补充剂中伐地那非灵敏分析的高效液相色谱(HPLC)分离与化学发光(CL)检测的流动分析法。伐地那非在C18柱上于30℃下进行分离,以乙醇-H₃PO₄和乙二胺四乙酸二钠盐(Na₂EDTA)水溶液(25 : 75,v/v%)作为流动相。随后基于伐地那非在碱性介质中对鲁米诺-K₃Fe(CN)₆反应的强烈化学发光增强作用进行连续CL检测。在流速为0.8 mL/min时,伐地那非的保留时间(tR)为6.4分钟。研究并优化了影响HPLC分离度和CL检测的因素。伐地那非标准品的校准曲线在8.0×10⁻⁷~1.0×10⁻⁴ mol/L的浓度范围内呈线性。日内和日间精密度的相对标准偏差(RSD)均小于3.5%。所提出的方法应用于口服液、葡萄酒和胶囊样品中伐地那非的测定。