Effect of the chiral discrimination on the vibrational properties of (R)-, (S)- and (R,S)-ibuprofen/methyl-β-cyclodextrin inclusion complexes
Author:
Publisher
Informa UK Limited
Subject
Condensed Matter Physics
Link
http://www.tandfonline.com/doi/pdf/10.1080/14786435.2010.512575
Reference23 articles.
1. Pharmacological differences between the optical isomers of ibuprofen: evidence for metabolic inversion of the (—)-isomer
2. Interactions of Poly(vinylpyrrolidone) with Ibuprofen and Naproxen: Experimental and Modeling Studies
3. Characterization of Racemic Species of Chiral Drugs Using Thermal Analysis, Thermodynamic Calculation, and Structural Studies
4. Thermodynamics of Sublimation, Crystal Lattice Energies, and Crystal Structures of Racemates and Enantiomers: (+)- and (±)-Ibuprofen
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2. The study of chiral recognition on ibuprofen enantiomers by a fluorescent probe based on β-cyclodextrin modified ZnS:Mn quantum dots;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2021-02
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5. A characterization study of resveratrol/sulfobutyl ether-β-cyclodextrin inclusion complex and in vitro anticancer activity;Colloids and Surfaces B: Biointerfaces;2014-03
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