Chiral chromatography is a crucial technique for separating enantiomers and plays a
vital role in the pharmaceutical industry for drug development and quality control, as many biologically
active compounds are chiral. This study examines the underlying mechanisms governing
enantioseparation, focusing on key interactions such as hydrogen bonding, Van der Waals
forces, and steric effects. Enantiomer separation begins with their binding to the chiral stationary
phase, where their unique three-dimensional structures lead to varying affinities and retention.
This paper explores key factors influencing enantioseparation, including chiral stationary
phases, solvent polarity, temperature, and mobile phase composition. Selection of a chiral stationary
phase is vital for method development and influences enantioseparation. This paper
sheds light on various available chiral stationary phases, their composition, and the mechanism
involved in enantioseparation of various enantiomers in the reported literature. By understanding
these mechanisms, researchers can optimize conditions for effective enantioseparation,
thereby advancing applications in pharmaceuticals, food safety, and environmental analysis.
This review provides an overview of the complex interplay of variables, which guides the researcher
in developing efficient chiral separation techniques.
Profens are chiral nonsteroidal anti-inflammatory drugs (NSAIDs) whose enantiomers may differ in pharmacokinetics, pharmacological activity and pharmacotoxicological profile, making enantioselective analysis relevant for pharmaceutical quality control and bioanalytical applications. Capillary electrophoresis (CE) has b...
G. Hancu, Maria Matean, A. Cârje· Molecules· 0 citations
By integrating selector chemistry with practical analytical requirements, the review provides a framework for application-driven method development and highlights current trends shaping the future of chiral HPLC in biomedical and pharmaceutical sciences.
Mihajlo V. Jakanovski, Mila Č. Lazović, Mirjana Mosić et al.· Journal of chromatography. B...· 0 citations
Chirality, as an inherent property of nature, plays a central role in the complexity and precision of biological systems. The stereochemistry of molecules profoundly impacts their pharmacological activities, metabolic pathways, and toxicological effects. Enantiomers, which are mirror-image forms of the same compou...
Sheng Long, Jia-Yu Chen, Chen Yuan et al.· Se pu = Chinese journal of c...· 0 citations
ABSTRACT Stereochemical impurities can significantly alter a drug's pharmacological profile and compromise patient safety even in small levels. Therefore, the development of selective chiral analytical methods is critical for quality control assurance. In this study, a novel chiral HPLC method was developed for the ena...
Sakine Atila Karaca, Sona Aliyeva, Duygu Yeniceli· Journal of Separation Scienc...· 0 citations
Stereochemistry and substitution jointly influence biological and chromatographic behavior in this thiourea series and provides a useful framework for early enantiomer-resolved developability assessment.
Gergely Molnár, Balázs Simon, A. Mirzahosseini et al.· Pharmaceutics· 0 citations
ABSTRACT The conformationally flexible 2‐methylbutyl structural motif represents a small chiral center, which cannot engage in polar interactions with chiral stationary phases (e.g., hydrogen bonds), which often play a key role in enantioselective recognition. In this contribution, racemic liquid crystalline materials...
T. Jurkovičová, Martin Cigl, Věra Hamplová et al.· Journal of Separation Scienc...· 0 citations
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