首页> 美国卫生研究院文献>Journal of Chromatographic Science >Multiwalled Carbon Nanotubes-Dispersive Solid-Phase Extraction Coupled with UPLC–ESI-MS-MS for Simultaneous Determination of 10 Illegal Adulterants in Antihypertensive Functional Foods
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Multiwalled Carbon Nanotubes-Dispersive Solid-Phase Extraction Coupled with UPLC–ESI-MS-MS for Simultaneous Determination of 10 Illegal Adulterants in Antihypertensive Functional Foods

机译:多壁碳纳米管分散固相萃取与UPLC-ESI-MS-MS联用同时测定降压功能食品中的10种违法掺假物

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摘要

A reliable method for simultaneous determination of 10 illegal adulterants including chlortalidone, hydrochlorothiazide, indapamide, metoprolol, nifedipine, nimodipine, nitrendipine, reserpine, triamterene and valsartan in antihypertensive functional foods by ultra-high-performance liquid chromatography coupled with electrospray ionization-tandem mass spectrometry is presented in this article. The target chemicals were extracted with acetonitrile ultrasonically and cleaned up using multiwalled carbon nanotubes-dispersive solid-phase extraction. The separation was performed on a Waters ACQUITY UPLC BEH C18 Column (2.1 × 100 mm, 1.7 µm) with acetonitrile, 0.1% formic acid and 10 mmol/L ammonium acetate solution as mobile phase at a flow rate of 0.2 mL/min. Multiple reaction monitoring was applied for detection and sildenafil was used as the internal standard. The correlation coefficients of the method were >0.995, with the limits of detection of 0.022–0.30 ng/mL and the limits of quantification of 0.075–0.99 ng/mL. The interday and intraday relative standard deviations were <9.77% and the recoveries were in the range of 85.8–109%. The established method has been applied for the analysis of real samples, and reserpine was detected in a tonic wine sample with a content of 60.1 ± 3.2 mg/L.
机译:超高效液相色谱-电喷雾串联质谱法同时测定降压功能食品中十种违法掺假物的可靠方法在本文中介绍。用乙腈超声提取目标化学物质,并使用多壁碳纳米管-分散固相萃取法净化。分离在Waters ACQUITY UPLC BEH C18色谱柱(2.1×100 mm,1.7 µm)上,以乙腈,0.1%甲酸和10 mmol / L乙酸铵溶液为流动相,流速为0.2 mL / min。多反应监测用于检测,西地那非用作内标。该方法的相关系数> 0.995,检测限为0.022–0.30 ng / mL,定量限为0.075–0.99 ng / mL。日间和日内相对标准偏差<9.77%,回收率在85.8-109%范围内。所建立的方法已用于实际样品的分析,并在补品酒样品中检出了利血平,含量为60.1±3.2 mg / L。

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