In Silico Multifactorial Modeling for Streamlined Development and Optimization of Two-Dimensional Liquid Chromatography.

Autor: Haidar Ahmad IA; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States., Makey DM; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.; Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States., Wang H; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States., Shchurik V; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States., Singh AN; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States., Stoll DR; Department of Chemistry, Gustavus Adolphus College, Saint Peter, Minnesota 56082, United States., Mangion I; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States., Regalado EL; Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
Jazyk: angličtina
Zdroj: Analytical chemistry [Anal Chem] 2021 Aug 24; Vol. 93 (33), pp. 11532-11539. Date of Electronic Publication: 2021 Aug 10.
DOI: 10.1021/acs.analchem.1c01970
Abstrakt: Continued adoption of two-dimensional liquid chromatography (2D-LC) in industrial laboratories will depend on the development of approaches to make method development for 2D-LC more systematic, less tedious, and less reliant on user expertise. In this paper, we build on previous efforts in these directions by describing the use of multifactorial modeling software that can help streamline and simplify the method development process for 2D-LC. Specifically, we have focused on building retention models for second dimension ( 2 D) separations involving variables including gradient time, temperature, organic modifier blending, and buffer concentration using LC simulator (ACD/Labs) software. Multifactorial retention modeling outcomes are illustrated as resolution map planes or cubes that enable straightforward location of 2 D conditions that maximize resolution while minimizing analysis time. We also illustrate the practicality of this approach by identifying conditions that yield baseline separation of all compounds co-eluting from a first dimension ( 1 D) separation using a single combination of 2 D stationary phase and elution conditions. The multifactorial retention models were found to be very accurate for both the 1 D and 2 D separations, with differences between experimental and simulated retention times of less than 0.5%. Pharmaceutical applications of this approach for multiple heartcutting 2D-LC were demonstrated using IEC-IEC or achiral RPLC-chiral RPLC for 2D separations of multicomponent mixtures. The framework outlined here should help make 2D-LC method development more systematic and streamline development and optimization for a variety of 2D-LC applications in both industry and academia.
Databáze: MEDLINE