Selala M I, Janssens J J, Coucke V, Andries S, Schepens P J
Department of Pharmaceutical Sciences, University of Antwerp, Wilrijk, Belgium.
J Chromatogr. 1989 Apr 7;489(1):51-6. doi: 10.1016/s0378-4347(00)82882-0.
During the past two decades, the use of retention times in gas chromatography has been augmented by mass spectrometric data. By providing both the retention indices and spectrometric data, this technique has greatly improved gas chromatographic identification analysis. However, although gas chromatography-mass spectrometry has become pre-eminent, several drawbacks still remain. The mass spectral library often gives erroneous identifications when concentrations near the detection limit are analysed, when gas chromatographically interfering substances are present, or when structural isomers or compounds exhibiting identical retention behaviour are analysed. Linked with gas chromatography-mass spectrometry, Fourier transform infrared spectroscopy can be a powerful complementary technique in peak identification analysis. Some spectral data to illustrate this point are presented.
在过去二十年中,质谱数据增强了气相色谱中保留时间的应用。通过提供保留指数和光谱数据,这项技术极大地改进了气相色谱的鉴定分析。然而,尽管气相色谱-质谱联用已占据主导地位,但仍存在一些缺点。当分析接近检测限的浓度、存在气相色谱干扰物质或分析结构异构体或具有相同保留行为的化合物时,质谱图库常常会给出错误的鉴定结果。与气相色谱-质谱联用相结合,傅里叶变换红外光谱在峰鉴定分析中可以成为一种强大的补充技术。本文给出了一些光谱数据来说明这一点。