Vrije Universiteit Brussel (VUB), Department of Chemical Engineering, Brussels, Belgium.
Thermo Fisher Scientific, Germering, Germany.
J Chromatogr A. 2022 Nov 22;1684:463565. doi: 10.1016/j.chroma.2022.463565. Epub 2022 Oct 13.
The present study discusses UHPLC method development allowing to establish ultra-high-resolution separations in gradient mode while operating at the kinetic performance limits, targeting the analysis of complex residual multi-class antibiotic samples in food products. The peak capacity and gradient occupation have been systematically assessed at different flow rates and gradient duration. The small particle size (1.5 µm core-shell particles) used in this study limits the mass-transfer contribution to band broadening when operating at high flow rate. As a result, for high-throughput analysis, high-pressure (1500 bar) operation leads to high resolving power where the gradient steepness dominates the peak capacity generation vs mass-transfer resistance. To reach the highest possible resolving power within a practically acceptable analysis time, one should use coupled-column systems at 1500 bar and adjust the gradient steepness correspondingly. Coupling four columns and applying a shallow gradient at 1500 bar led to a sample peak capacity of 379 in 140 min, allowing to resolve 71% of the analytes in a mixture composed of 61 milk antibiotics.
本研究讨论了 UHPLC 方法的开发,该方法允许在以动力学性能极限运行的梯度模式下建立超高分辨率分离,旨在分析食品中复杂的残留多类抗生素样品。在不同流速和梯度持续时间下系统地评估了峰容量和梯度占据。本研究中使用的小粒径(1.5 µm 核壳颗粒)在高流速下限制了传质对带宽展宽的贡献。因此,对于高通量分析,高压(1500 巴)操作可实现高分辨率,其中梯度陡度主导峰容量生成与传质阻力。为了在可接受的实际分析时间内达到最高可能的分辨率,应在 1500 巴下使用柱联系统并相应地调整梯度陡度。在 1500 巴下耦合四根柱子并采用较浅的梯度,可在 140 分钟内获得 379 个样品峰容量,从而可解析由 61 种牛奶抗生素组成的混合物中 71%的分析物。