ReviewMolecules (Basel, Switzerland)2019
Enantiomeric Recognition and Separation by Chiral Nanoparticles.
Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
19 citing papers in PubMed.
- Advances and Prospects of Chiral Plasmonic Nanomaterials in Emerging Applications.Nanomaterials (Basel, Switzerland) · 2026Review
- High-performance gas-phase chiral enantiomer detectors based on chiral-induced spin selectivity effect.Nature communications · 2025Article
- Intensive Value Utilization of Food-Derived Marine Immunoactive Peptides: Optimizing the Process Yield and Improving the Delivery Efficiency According to the Immune Activity Mechanism and Assisted Enzymatic Hydrolysis.Food science & nutrition · 2025Review
- Defect-engineered chiral metal-organic frameworks.Mikrochimica acta · 2024Review
- Preparation of Chiral Carbon Quantum Dots and its Application.Journal of fluorescence · 2024Review
- Evaluation of Poly(vinyl alcohol)-Xanthan Gum Hydrogels Loaded with Neomycin Sulfate as Systems for Drug Delivery.Gels (Basel, Switzerland) · 2023Article
- Surface modified nanoparticles and their applications for enantioselective detection, analysis, and separation of various chiral compounds.RSC advances · 2023Review
- Laser-Induced Chirality of Plasmonic Nanoparticles Embedded in Porous Matrix.Nanomaterials (Basel, Switzerland) · 2023Article
- Isolation, Detection and Analysis of Circulating Tumour Cells: A Nanotechnological Bioscope.Pharmaceutics · 2023Review
- Hydrothermal synthesis of chiral carbon dots.Chirality · 2022Article
- Enantioselective Separation of Amino Acids Using Chiral Polystyrene Microspheres Synthesized by a Post-Polymer Modification Approach.ACS polymers Au · 2022Article
- Chiral carbon dots: synthesis, optical properties, and emerging applications.Light, science & applications · 2022Review
- Demystifying racemic natural products in the homochiral world.Nature reviews. Chemistry · 2022Review
- Facile separation of enantiomers via covalent organic framework bonded stationary phase.Mikrochimica acta · 2021Article
- Kinetic Resolution of Racemic Mixtures via Enantioselective Photocatalysis.ACS applied materials & interfaces · 2021Article
- Self-Assembly of Supramolecular Architectures by the Effect of Amino Acid Residues of Quaternary Ammonium Pillar[5]arenes.International journal of molecular sciences · 2020Article
- Enantioselective Synthesis, Enantiomeric Separations and Chiral Recognition.Molecules (Basel, Switzerland) · 2020Article
- D-Lactic Acid as a Metabolite: Toxicology, Diagnosis, and Detection.BioMed research international · 2020Review
- Polarimetric Measurements of Surface Chirality Based on Linear and Nonlinear Light Scattering.Frontiers in chemistry · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Chiral molecules are stereoselective with regard to specific biological functions. Enantiomers differ considerably in their physiological reactions with the human body. Safeguarding the quality and safety of drugs requires an efficient analytical platform by which to selectively probe chiral compounds to ensure the extraction of single enantiomers. Asymmetric synthesis is a mature approach to the production of single enantiomers; however, it is poorly suited to mass production and allows for only specific enantioselective reactions. Furthermore, it is too expensive and time-consuming for the evaluation of therapeutic drugs in the early stages of development. These limitations have prompted the development of surface-modified nanoparticles using amino acids, chiral organic ligands, or functional groups as chiral selectors applicable to a racemic mixture of chiral molecules. The fact that these combinations can be optimized in terms of sensitivity, specificity, and enantioselectivity makes them ideal for enantiomeric recognition and separation. In chiral resolution, molecules bond selectively to particle surfaces according to homochiral interactions, whereupon an enantiopure compound is extracted from the solution through a simple filtration process. In this review article, we discuss the fabrication of chiral nanoparticles and look at the ways their distinctive surface properties have been adopted in enantiomeric recognition and separation.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.