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A pretreatment free method for the determination of seven natural products in a high-salt matrix by online guard column extraction coupled with tandem mass spectrometry

机译:在线保护柱萃取-串联质谱法测定高盐基质中七种天然产物的无预处理方法

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摘要

In vitro cell models are easy, reproducible, and cost-effective tools for tracking drug absorption rates and for elucidating related mechanisms. Traditionally, before introduction into an analysis system, samples crossing an in vitro cell membrane usually undergo complicated processes including precipitation, centrifugation, and even filtering. In the current study, a generic, sensitive and rapid method was developed for the determination of natural products in the matrix of in vitro drug absorption systems (HBSS, Hank's balanced salt solution). A guard RP-C_(18) column was used to retain the target compounds, while a tandem mass spectrometry system in the multiple reaction monitoring mode was used to specifically detect the target compounds. In addition, a six-way valve was used to connect the LC and MS systems, and to automatically switch the flow directions between the mass spectrometer and the waste. The method was validated by determining the accuracy, precision and sensitivity using seven natural products including (+)-praeruptorin A (dPA), (-)-praeruptorin A (/PA), (+)-praeruptorin B (dPB), (-)-praeruptorin B (/PB) from Peucedani Radix (Chinese name: Qian-hu), morusin (Mo), sanggenon C (SC), and kuwanon G (KG) from Mori Cortex (Chinese name: Sang-Bai-Pi). The developed method is proposed to be applied for in vitro absorption and transport studies.
机译:体外细胞模型是追踪药物吸收速率和阐明相关机制的简便,可复制且具有成本效益的工具。传统上,在进入分析系统之前,穿过体外细胞膜的样品通常会经历复杂的过程,包括沉淀,离心甚至过滤。在当前的研究中,开发了一种通用,灵敏,快速的方法来测定体外药物吸收系统(HBSS,汉克的平衡盐溶液)基质中的天然产物。使用保护RP-C_(18)色谱柱保留目标化合物,同时使用多反应监测模式的串联质谱系统特异性检测目标化合物。此外,还使用六通阀连接LC和MS系统,并自动在质谱仪和废物之间切换流向。该方法通过使用七种天然产物(包括(+)-普鲁珀林A(dPA),(-)-普鲁珀林A(/ PA),(+)-普鲁珀林B(dPB),(- )-来自Peucedani Radix(中文名称:前胡),桑rus酮(Mo),sanggenon C(SC)和kuwanon G(KG)的Peucedani Radix(中文名称:Sang-Bai-Pi) 。拟将开发的方法用于体外吸收和转运研究。

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