Chiral differentiation of l- and d-penicillamine by β-cyclodextrin: Investigated by IRMPD spectroscopy and theoretical simulations.
Chirality
Cyclodextrin
IRMPD spectroscopy
Penicillamine
Theoretical simulations
Journal
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
ISSN: 1873-3557
Titre abrégé: Spectrochim Acta A Mol Biomol Spectrosc
Pays: England
ID NLM: 9602533
Informations de publication
Date de publication:
05 Nov 2020
05 Nov 2020
Historique:
received:
02
05
2020
revised:
24
06
2020
accepted:
24
06
2020
pubmed:
6
7
2020
medline:
15
5
2021
entrez:
6
7
2020
Statut:
ppublish
Résumé
The chirality of penicillamine (Peni) results in different clinic applications. Host-guest complex based drug delivery system that differentiates the two enantiomers and provides delayed release is of significance in medication. We hereby used β-CD to encapsulate d- and l-Peni. IRMPD spectra show different characteristic vibrations to distinguish the two enantiomers. Besides common peaks found at 3000-3100 cm
Identifiants
pubmed: 32623304
pii: S1386-1425(20)30632-6
doi: 10.1016/j.saa.2020.118653
pii:
doi:
Substances chimiques
beta-Cyclodextrins
0
Penicillamine
GNN1DV99GX
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
118653Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.