Henion J, Skrabalak D, Dewey E, Maylin G
Drug Metab Rev. 1983;14(5):961-1003. doi: 10.3109/03602538308991418.
LC/MS has become a routine research tool in some laboratories. Although no single approach to LC/MS presently is without limitations, each approach offers encouraging results and prompts continued improvements. The remaining hurdles appear to be the introduction of total LC effluent into the MS, increased sensitivity, and the ability to analyze higher molecular weight, polar molecules. The micro LC/MS results discussed in this paper offer an opportunity for significantly increased sensitivity by allowing total micro LC effluent introduction into the MS. It remains to be seen whether the development of micro LC column and equipment technology will allow practical micro LC/MS. It may someday provide improved separation of drugs, metabolites, and their conjugates from high levels of endogenous materials in reasonable time periods. Currently, the impressive efficiencies demonstrated for micro LC columns involve mixtures containing low molecular weight solutes that are perhaps more amenable to GC analysis. The analyst routinely involved with problem solving must deal with complex mixtures composed of components with large concentration differences. The future of micro LC, and hence micro LC/MS, will depend upon how well the technique helps solve problems. We believe the future is bright for micro LC/MS. The techniques may require some fine tuning of operating procedures, just as with capillary GC/MS, but certainly the potential for increased efficiency and sensitivity is worth the effort. Currently we are testing a new micro LC/MS DLI probe wherein the exit of the micro column is within 1 cm of the MS ion source [82]. The micro LC column is contained within the DLI probe and should offer the lowest dead volume and the least extracolumn effects yet achieved by LC/MS. Initial testing of this new probe is under way, and experimental results will be reported subsequently. The analytical potential of micro LC/MS is receiving considerable interest. Practical micro LC performance can provide increased capabilities to all types of LC/MS reported to date, and perhaps offer new insight into alternative methods of LC/MS not yet reported. We look forward to learning of these breakthroughs as they become available.
液相色谱/质谱联用(LC/MS)在一些实验室已成为常规研究工具。尽管目前尚无一种单一的LC/MS方法毫无局限性,但每种方法都给出了令人鼓舞的结果并促使不断改进。剩下的障碍似乎是将全部液相色谱流出物引入质谱仪、提高灵敏度以及分析更高分子量极性分子的能力。本文讨论的微LC/MS结果通过允许将全部微LC流出物引入质谱仪,提供了显著提高灵敏度的机会。微LC柱和设备技术的发展能否实现实用的微LC/MS还有待观察。有朝一日它可能在合理的时间段内,从大量内源性物质中更好地分离药物、代谢物及其缀合物。目前,微LC柱所展示出的令人印象深刻的效率涉及含有低分子量溶质的混合物,这些混合物可能更适合气相色谱分析。日常参与解决问题的分析人员必须处理由浓度差异很大的组分组成的复杂混合物。微LC以及因此微LC/MS的未来将取决于该技术在解决问题方面的效果如何。我们相信微LC/MS的前景光明。这些技术可能需要对操作程序进行一些微调,就像毛细管气相色谱/质谱联用一样,但提高效率和灵敏度的潜力肯定值得付出努力。目前我们正在测试一种新的微LC/MS直接液体引入(DLI)探头,其中微柱的出口位于距质谱仪离子源1厘米范围内[82]。微LC柱包含在DLI探头内,应该能提供迄今为止LC/MS所实现的最低死体积和最小柱外效应。这种新探头的初步测试正在进行,后续将报告实验结果。微LC/MS 的分析潜力正受到广泛关注。实用的微LC性能可以提升目前所有类型LC/MS的能力,或许还能为尚未报道的LC/MS替代方法提供新的见解。我们期待着了解这些突破的出现。