Novel Flow-Confinement Concept for LC×LC
A novel flow-confinement concept designed to remove the performance sacrifice associated with current comprehensive two-dimensional liquid chromatography techniques has been tested by researchers.
Photo Credit:deomis/stock.adobe.com
A novel flow-confinement concept designed to remove the performance sacrifice associated with current comprehensive two-dimensional liquid chromatography techniques has been tested by researchers (1).
The characterization of highly complex samples is always a challenge, often requiring a comprehensive two-dimensional liquid chromatographic approach (LC×LC) to solve. However, the compromise made between the first and the second dimensions, specifically in the flow rates and the modulation time, often results in a reduction in performance. To avoid this reduction in performance, a perfectly operated spatial ×LC××LC system is required with rigorous confinement of the flow of the mobile phase and analytes in the desired direction.
A suitable format for spatial separations can be realized through microfluidics devices, which can be designed using computational fluid dynamics to create satisfactory designs that can be rapidly and easily prototyped using 3D-printing methods.
Using this process, researchers designed a novel flow-confinement method titled TWIST (two-dimensional insertable separation tool). The modular device has an internal first-dimension (1D) part that is cylindrical and rotatable. This internal part features a series of through-holes, each of which is perpendicular to the direction of the 1D flow. The internal part is inserted in the cylindrical casing of the external part, which also includes a flow distributor and second dimension (2D) channels. During injection the liquid remains confined within the 1D channel as the rotating piece flow positions the through-holes towards the wall of the external part. During transfer to the second dimension, the rotation of the internal part aligns the through-holes to the external part allowing transversal flow of the 2D mobile phase from the distributor and into the 2D area.
Despite the promise of the device, researchers cautioned that further research is required for device and material optimization, incorporation of stationary phases, and for the performance of actual separations. Furthermore, it is believed the device could be modified to realize flow confinement in spatial three-dimensional liquid chromatography.
Reference
- T. Adamopoulou et al., J. Chroma. A1577, 120–123 (2018).
An LC–HRMS Method for Separation and Identification of Hemoglobin Variant Subunits
March 6th 2025Researchers from Stanford University’s School of Medicine and Stanford Health Care report the development of a liquid chromatography high-resolution mass spectrometry (LC–HRMS) method for identifying hemoglobin (Hb) variants. The method can effectively separate several pairs of normal and variant Hb subunits with mass shifts of less than 1 Da and accurately identify them in intact-protein and top-down analyses.
The Next Frontier for Mass Spectrometry: Maximizing Ion Utilization
January 20th 2025In this podcast, Daniel DeBord, CTO of MOBILion Systems, describes a new high resolution mass spectrometry approach that promises to increase speed and sensitivity in omics applications. MOBILion recently introduced the PAMAF mode of operation, which stands for parallel accumulation with mobility aligned fragmentation. It substantially increases the fraction of ions used for mass spectrometry analysis by replacing the functionality of the quadrupole with high resolution ion mobility. Listen to learn more about this exciting new development.
