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采用超快速液相色谱-电喷雾串联质谱法同时筛查和测定壮阳类中草药和保健品中的 18 种非法掺杂物。

Simultaneous screening and determination of 18 illegal adulterants in herbal medicines and health foods for male sexual potency by ultra-fast liquid chromatography-electrospray ionization tandem mass spectrometry.

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

出版信息

J Sep Sci. 2012 Nov;35(21):2847-57. doi: 10.1002/jssc.201200280. Epub 2012 Sep 24.

Abstract

An ultra-fast liquid chromatography-electrospray ionization tandem mass spectrometry method was developed and validated to simultaneously screen, confirm, and determine 18 illegal adulterants in herbal medicines and health foods for male sexual potency. The separation was achieved on a Shim-Pack XR-ODS II column (2.0 × 100 mm, 2.2 μm) with acetonitrile and aqueous solution (12 mmol/L ammonium formate, 0.01% acetic acid) as mobile phase at a flow rate of 0.4 mL/min with a gradient elution. The column temperature was maintained at 40°C and the run time was within 18 min. The 18 illegal adulterants were detected in electrospray ionization positive mode by multiple-reaction monitoring. All the calibration curves showed good linearity with correlation coefficient (r) higher than 0.996 within the tested concentration ranges. The extraction recoveries and relative recoveries were in the range of 79.5-114% and 82.0-120%, respectively. The RSD of repeatability and intermediate precision was all less than 18% and the accuracy was in the range of 81.7-118%. The intra-day and inter-day stability was in the range of 86.8-110%. The validated method was successfully applied to screen, confirm, and determine 16 samples. Nine products were confirmed to contain illegal adulterants and the contents of adulterants were related to the therapeutic dosages.

摘要

建立并验证了一种超快速液相色谱-电喷雾串联质谱法,用于同时筛选、确证和测定 18 种用于男性性功能的草药和保健品中的非法掺杂物。分离在 Shim-Pack XR-ODS II 柱(2.0×100mm,2.2μm)上进行,以乙腈和水溶液(12mmol/L 甲酸铵,0.01%乙酸)为流动相,流速为 0.4mL/min,梯度洗脱。柱温保持在 40°C,运行时间在 18min 内。18 种非法掺杂物在电喷雾正离子模式下通过多反应监测进行检测。所有校准曲线在测试浓度范围内均具有良好的线性关系,相关系数(r)均高于 0.996。提取回收率和相对回收率的范围分别为 79.5-114%和 82.0-120%。重复性和中间精密度的 RSD 均小于 18%,准确度在 81.7-118%范围内。日内和日间稳定性均在 86.8-110%范围内。该验证方法成功应用于筛选、确证和测定 16 个样品。有 9 种产品被确认为含有非法掺杂物,掺杂物的含量与治疗剂量有关。

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