Development of a Robust Method for Screening PDE-5 Inhibitor Additives in Dietary Supplements Using UPLC-MS/MS

Hua Wang
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Abstract

A novel ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) method was developed to detect the illegal additive of phosphodiesterase type 5 (PDE-5) inhibitors in dietary supplements. With the optimized chromatographic program, vardenafil, sildenafil, and tadalafil were separated within 5 minutes. The MS1, MS2, and retention time of PDE-5 inhibitors were acquired simultaneously within the information dependent acquisition mass spectrometry mode. Quantification was achieved via the quantity ion current chromatogram that was extracted from the total ion current. The linear range of vardenafil and sildenafil was 0.5-48 mg/L while the range of tadalafil was 0.3-36 mg/L. The correlation coefficients of the calibration curves of three PDE-5 inhibitors were all greater than 99.9%. At three concentration levels, the RSD values of the five repeat tests were all better than 1.30%. Sildenafil was detected in one dietary supplement. The comprehensive method of this study is reliable and may be a powerful tool for routine PDE-5 inhibitor screening and determination.
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利用 UPLC-MS/MS 开发筛选膳食补充剂中 PDE-5 抑制剂添加剂的可靠方法
建立了一种新型的超高效液相色谱-串联质谱(UPLC-MS/MS)检测膳食补充剂中非法添加磷酸二酯酶5 (PDE-5)抑制剂的方法。在优化的色谱程序下,伐地那非、西地那非和他达拉非在5分钟内分离。在信息依赖获取质谱模式下,同时获得PDE-5抑制剂的MS1、MS2和保留时间。定量是通过从总离子电流中提取的定量离子电流色谱图来实现的。伐地那非和西地那非的线性范围为0.5 ~ 48mg /L,他达拉非的线性范围为0.3 ~ 36mg /L。3种PDE-5抑制剂的标度曲线相关系数均大于99.9%。在3个浓度水平下,5次重复试验的RSD值均优于1.30%。在一种膳食补充剂中检测到西地那非。本研究综合方法可靠,可作为常规PDE-5抑制剂筛选和测定的有力工具。
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