Oleszek W, Bialy Z
Department of Biochemistry, Institute of Soil Science and Plant Cultivation, State Research Institute, ul. Czartoryskich 8, 24-100 Pulawy, Poland.
J Chromatogr A. 2006 Apr 21;1112(1-2):78-91. doi: 10.1016/j.chroma.2006.01.037. Epub 2006 Jan 31.
The developments during 2002-2005 in the methods used for saponin analyses in plant material are presented. There were number of papers published on isolation and identification of new saponins by chromatographic techniques. Some new developments can be found in separation techniques or solid and mobiles phases used. Separation of individual saponins is still complicated and time consuming. This is due to the fact that in most of the plant species saponins occur as a multi-component mixture of compounds of very similar polarities. Thus, to isolate single compound for structure elucidation or biological activity testing, a combination of different chromatographic techniques has to be used, e.g. first separation of the mixture to simpler sub-fractions on reversed phase C18 has to be followed by further purification on normal phase Silica gel column. Especially difficult is determination of saponins in plant material as these compounds do not possess chromophores and their profiles cannot be registered in UV. Most HPLC methods apply not only specific registration at 200-210 nm, but these methods are not applicable for determination of many saponins in plant material at levels lower than 200-300 mg/kg. Some new or improved techniques for quantification of saponins in plant material were published in reviewed period. These include further progress in the application of evaporative light scattering detection (ELSD) for saponin profiling and quantification, which is also not only specific but also more sensitive in comparison to 200-210 nm detection. Some progress in development of new applications for liquid chromatography-electrospray mass spectrometry (LC/ESI/MS) for saponin determination has also been done. This method gives highest sensitivity and on line identification of separated saponins and should be recommended for specialized analyses of extracts and pharmaceutical formulas like the validation of a new assay. From non-chromatographic techniques for saponin determination, a sensitive and compound specific ELISA tests for some saponins were developed.
本文介绍了2002年至2005年期间植物材料中皂苷分析方法的发展情况。有许多关于通过色谱技术分离和鉴定新皂苷的论文发表。在分离技术或所用的固定相和流动相方面可以发现一些新进展。单个皂苷的分离仍然复杂且耗时。这是因为在大多数植物物种中,皂苷以极性非常相似的化合物的多组分混合物形式存在。因此,为了分离单个化合物以进行结构阐明或生物活性测试,必须使用不同色谱技术的组合,例如首先在反相C18上把混合物分离成更简单的亚组分,随后在正相硅胶柱上进一步纯化。特别困难的是测定植物材料中的皂苷,因为这些化合物不具有发色团,其图谱无法在紫外线下记录。大多数高效液相色谱法不仅在200 - 210nm处进行特定检测,但这些方法不适用于测定植物材料中含量低于200 - 300mg/kg的许多皂苷。在所述期间发表了一些用于定量植物材料中皂苷的新的或改进的技术。这些包括蒸发光散射检测(ELSD)在皂苷谱分析和定量应用方面的进一步进展,与200 - 210nm检测相比,它不仅具有特异性,而且更灵敏。在液相色谱 - 电喷雾质谱(LC/ESI/MS)用于皂苷测定的新应用开发方面也取得了一些进展。该方法具有最高的灵敏度,并且可以在线鉴定分离出的皂苷,应该推荐用于提取物和药物配方的专门分析,如新测定方法的验证。在用于皂苷测定的非色谱技术方面,开发了一些针对某些皂苷的灵敏且化合物特异性的酶联免疫吸附测定(ELISA)测试。