UPLC-ESI-MS/MS法测定八子补肾胶囊中14种成分的含量
Determination of 14 components in Bazibushen capsule by UPLC-ESI-MS/MS
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摘要: 建立UPLC-ESI-MS/MS 法测定八子补肾胶囊中14 种成分的含量。Waters ACQUITY BEH C18柱(50mm×2.1 mm, 1.7 μm), 柱温为40℃; 流动相为A(乙腈)-B(0.1% 乙酸), 梯度洗脱; 电喷雾离子源(ESI源), 源温度为 150℃, 毛细管电压为2.0 kV, 离子源补偿电压为 50 V, 脱溶剂气温度为500℃, 脱溶剂气流量为 800 L·h-1,锥孔气流量为150 L·h-1, 雾化气压力为7.0 Bar(1 Bar=100 kPa), 接口处加热, 采用多反应监测模式。在本方法条件下, 14 种成分的线性关系良好(r2 ≥ 0.999 1), 定量限为0.11~4.52 ng·mL-1。精密度为0.8~2.1%。平均回收率范围为97.89%~101.9%。该方法操作简便、快速、准确度高、重现性好, 可用于八子补肾胶囊的质量控制。Abstract: The study developed a method for the determination of 14 components in Bazibushen capsule by UPLC-ESI-MS/MS. Waters ACQUITY BEH C18 column (50 mm×2.1 mm, 1.7 μm) was used and the column temperature was 40℃. A linear gradient elution of eluents A (acetonitrile) and B (0.1% acetic acid) was used for the separation. The source temperature was set at 150℃. The capillary voltage was set at 2.0 kV. The source offset voltage was kept at 50 V. The desolvation temperature was set at 500℃. The desolvation flow was 800 L·h-1. The cone flow was 150 L·h-1. The nebuliser pressure was 7.0 Bar. Multiple reaction monitoring mode (MRM) is adopted. All of the 14 components showed good linearity (r2 > 0.999 1) in the test ranges. The LOQs for the compounds ranged from 0.11-4.52 ng·mL-1, respectively. The RSDs were 0.8%-2.1%. The overall recoveries were between 97.89% and 101.9% for all compounds. The method is simple, rapid, accurate and highly reproducible, and may be used in the determination of 14 components in Bazibushen capsule.
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