Sandvoss Martin, Bardsley Ben, Beck Tony L, Lee-Smith Emma, North Stephanie E, Moore Peter J, Edwards Andrew J, Smith Richard J
DMPK Structural ID Group, GlaxoSmithKline R & D, Ware, UK.
Magn Reson Chem. 2005 Sep;43(9):762-70. doi: 10.1002/mrc.1615.
High-performance liquid chromatography-solid phase extraction-NMR spectroscopy (HPLC-SPE-NMR) has recently become commercially available and has been evaluated with regard to its applicability in a pharmaceutical environment. The addition of an automated SPE unit to an HPLC-NMR system for peak trapping results in an improved NMR signal-to-noise ratio (S/N) and also has other practical advantages. The trapping efficiency is shown to depend on compound polarity and is highest for compounds eluting late on reversed-phase HPLC systems. Multiple peak trapping further increases the S/N, again with the best results for less polar compounds. For polar compounds, multiple peak trapping resulted in no S/N gain as the amount of material retained on the SPE cartridge was equivalent to that from a single injection. When compared with conventional HPLC-NMR, a S/N gain of up to five-fold could be achieved for some compounds in a single trapping step. A major advantage of the technique is the independence of the chromatographic step from the NMR step, resulting in greater versatility than conventional HPLC-NMR in the HPLC solvents and NMR solvents that can be used. Practical applications from both drug metabolite and drug impurity identification are presented.
高效液相色谱 - 固相萃取 - 核磁共振波谱联用技术(HPLC - SPE - NMR)最近已实现商业化,并已针对其在制药环境中的适用性进行了评估。在HPLC - NMR系统中添加一个自动固相萃取单元用于峰捕集,可提高核磁共振的信噪比(S/N),并且还有其他实际优势。结果表明,捕集效率取决于化合物的极性,对于在反相高效液相色谱系统中较晚洗脱的化合物,捕集效率最高。多次峰捕集会进一步提高信噪比,对于极性较小的化合物,效果同样最佳。对于极性化合物,多次峰捕集并未使信噪比提高,因为固相萃取柱上保留的物质量与单次进样的量相当。与传统的HPLC - NMR相比,在单次捕集步骤中,某些化合物的信噪比可提高多达五倍。该技术的一个主要优点是色谱步骤与核磁共振步骤相互独立,这使得在可使用的HPLC溶剂和NMR溶剂方面,比传统的HPLC - NMR具有更大的通用性。本文展示了该技术在药物代谢物和药物杂质鉴定方面的实际应用。