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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Liquid chromatography/tandem mass spectrometry sensitivity enhancement via online sample dilution and trapping: Applications in microdosing and dried blood spot (DBS) bioanalysis
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Liquid chromatography/tandem mass spectrometry sensitivity enhancement via online sample dilution and trapping: Applications in microdosing and dried blood spot (DBS) bioanalysis

机译:通过在线样品稀释和捕集提高液相色谱/串联质谱的灵敏度:在微剂量和干血斑(DBS)生物分析中的应用

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摘要

A simple online sample dilution, enrichment, and cleanup technique was developed for sensitive microdosing and dried blood spot (DBS) liquid chromatography/tandem mass spectrometric (LC/ MS/MS) bioanalysis. Samples are diluted online with water and enriched in a trap column which is subsequently switched inline with the analytical column. Excellent lansoprazole (in acetonitrile) peak shape is maintained even with an 80-μL injection. In comparison, similar chromatographic peaks were observed only when a small volume of the same solution, i.e., 1μL, was injected on a regular high-performance liquid chromatography (HPLC) system, where an injection of 5μL resulted in severe peak fronting. A substantial enhancement in sensitivity is realized in the trapping mode using large injection volumes. The trap column is washed at the beginning and at the end of each injection with aqueous and organic solvent respectively to remove matrix components. This ultimately leads to reduction of matrix effects and mass spectrometer noise, thus facilitating the utilization of protein precipitation as the sample preparation for plasma samples. A lower limit of quantitation (LLOQ) of 0.5 pg/mL was demonstrated for lansoprazole in human plasma with a signalto- noise (S/N) ratio of 13 using a 100μL injection. Excellent intra-day precision and accuracy were established for lansoprazole in human plasma with good linearity (R~2 > 0.999) from 0.5 to 500 pg/mL. This level of LLOQ makes LC/MS/MS a practical alternative for microdosing bioanalysis, where the dose is typically 100 times lower than the therapeutic dose. The same technique was applied to quantitate lansoprazole in human whole blood employing DBS technology. With a single 3-mm punch, i.e. ~2μL of whole blood or ~1μL plasma, a LLOQ of 0.1 ng/mL showed sufficient S/N ratio (40) for lansoprazole when ~75μL of extract was injected. In all, the online sample dilution, cleanup, and enrichment technique demonstrated the practical utility of LC/MS/MS in microdosing and DBS bioanalysis.
机译:开发了一种简单的在线样品稀释,富集和净化技术,用于灵敏的微剂量和干血斑(DBS)液相色谱/串联质谱(LC / MS / MS)生物分析。用水在线稀释样品,并在捕集柱中进行富集,随后将其与分析柱进行在线切换。即使注射80μL,也能保持出色的兰索拉唑(在乙腈中)峰形。相比之下,只有在常规的高效液相色谱(HPLC)系统上注入少量相同溶液(即1μL)时,才能观察到相似的色谱峰,其中注入5μL会导致严重的峰前沿。使用大的进样量,在捕集模式下可显着提高灵敏度。捕集柱在每次进样的开始和结束时分别用水性和有机溶剂洗涤,以除去基质组分。这最终导致基质效应和质谱仪噪音的降低,从而促进蛋白质沉淀作为血浆样品的样品制备的利用。兰索拉唑在人血浆中的定量下限(LLOQ)为0.5 pg / mL,使用100μL进样时信噪比(S / N)为13。兰索拉唑在人血浆中建立了极好的日内精密度和准确性,线性范围从0.5到500 pg / mL(R〜2> 0.999)。 LLOQ的这一水平使LC / MS / MS成为微剂量生物分析的实用替代方法,该剂量通常比治疗剂量低100倍。采用DBS技术将相同技术应用于人全血中兰索拉唑的定量分析。用一个3毫米的冲头,即约2μL的全血或约1μL的血浆,当注射约75μL的提取物时,0.1 ng / mL的LLOQ对兰索拉唑显示出足够的信噪比(40)。总之,在线样品稀释,净化和富集技术证明了LC / MS / MS在微量给药和DBS生物分析中的实际应用。

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