Cucinotta Lorenzo, Cannizzaro Francesca, Sciarrone Danilo, Mondello Luigi
Messina Institute of Technology c/o Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, Former Veterinary School, University of Messina, Viale G. Palatucci snc, 98168, Messina, Italy.
Messina Institute of Technology c/o Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, Former Veterinary School, University of Messina, Viale G. Palatucci snc, 98168, Messina, Italy.
Anal Chim Acta. 2025 Sep 15;1367:344271. doi: 10.1016/j.aca.2025.344271. Epub 2025 Jun 3.
The separation of enantiomers via chiral gas chromatography remains a pivotal area of research in analytical chemistry, driven by its critical role in the quality control of high-value products. Recent helium shortages and escalating costs have necessitated the exploration of alternative carrier gases, such as nitrogen and hydrogen. Maintaining optimal resolution is paramount, as co-elution directly impacts the accuracy of enantiomeric ratio determination and, consequently, the reliability of analytical data. Given that resolution is a function of efficiency, selectivity, and retention, a thorough investigation of these parameters is essential to optimize enantiomeric separations when comparing different carrier gases.
In this study, a comprehensive comparison of nitrogen, helium, and hydrogen as carrier gases was conducted using bergamot essential oil as a model sample on a commercially available cyclodextrin (CD) column. The analysis revealed distinct chromatographic profiles, underscoring the importance of selecting the appropriate carrier gas and chromatographic conditions for specific separation challenges. Notably, hydrogen demonstrated superior performance compared to helium, exhibiting higher resolution at elevated linear velocities. However, the analysis of a real sample highlighted significant limitations, including co-elution of chiral components with each other and with achiral compounds. To address these issues, the separation was optimized by joining two chiral stationary phases. The strategic arrangement of chiral selectors within this tandem phase column facilitated enhanced separation of critical enantiomeric pairs. This approach yielded significant improvements in enantiomer resolution, both amongst themselves and in relation to non-chiral compounds, compared to the conventional column.
These findings offer insights into the design and application of tandem chiral stationary phases for the analysis of chiral components in essential oils. The ability to fine-tune separation selectivity through the strategic combination of chiral selectors, optimization of chromatographic parameters, and judicious selection of carrier gas represents a significant advancement. This comprehensive approach provides a powerful tool for tackling challenging separations and holds broad implications for the quality control and authentication of essential oils and related products.
通过手性气相色谱法分离对映体仍然是分析化学中一个关键的研究领域,这是由其在高价值产品质量控制中的关键作用所驱动的。近期的氦气短缺和成本不断上升使得人们有必要探索替代载气,如氮气和氢气。保持最佳分离度至关重要,因为共洗脱直接影响对映体比例测定的准确性,进而影响分析数据的可靠性。鉴于分离度是效率、选择性和保留率的函数,在比较不同载气时,全面研究这些参数对于优化对映体分离至关重要。
在本研究中,以佛手柑精油为模型样品,在市售的环糊精(CD)柱上对氮气、氦气和氢气作为载气进行了全面比较。分析揭示了不同的色谱图,突出了为特定分离挑战选择合适载气和色谱条件的重要性。值得注意的是,与氦气相比,氢气表现出更优的性能,在较高的线性速度下具有更高的分离度。然而,对实际样品的分析突出了显著的局限性,包括手性成分之间以及与非手性化合物的共洗脱。为了解决这些问题,通过连接两个手性固定相优化了分离。在这种串联相柱中手性选择剂的策略性排列促进了关键对映体对的增强分离。与传统柱相比,这种方法在对映体之间以及与非手性化合物的分离度方面都有显著提高。
这些发现为串联手性固定相在精油中手性成分分析的设计和应用提供了见解。通过手性选择剂的策略性组合、色谱参数的优化以及载气的明智选择来微调分离选择性的能力代表了一项重大进展。这种综合方法为解决具有挑战性的分离提供了一个强大的工具,对精油及相关产品的质量控制和鉴定具有广泛的意义。