Separation of racemic compound by nanofibrous composite membranes with chiral selector

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dc.contributor.author Gaálová, Jana
dc.contributor.author Yalcinkaya, Fatma
dc.contributor.author Cuřínová, Petra
dc.contributor.author Kohout, Michal
dc.contributor.author Yalcinkaya, Baturalp
dc.contributor.author Koštejn, Martin
dc.contributor.author Jirsák, Jan
dc.contributor.author Stibor, Ivan
dc.contributor.author Bara, Jason E.
dc.contributor.author Van der Bruggen, Bart
dc.contributor.author Izák, Pavel
dc.date.accessioned 2020-03-02T07:35:10Z
dc.date.available 2020-03-02T07:35:10Z
dc.date.issued 2020-02-15
dc.identifier.uri https://dspace.tul.cz/handle/15240/154593
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S0376738819326419
dc.description.abstract A series of unique composite membranes formed from a nano&fibrous material with different amounts of a chiral selector was used for separation of chiral drugs. The membrane performances were demonstrated through sorption tests, wherein they were soaked in an aqueous solution of racemic D, L-tryptophan (a model chiral drug). The changes in concentration of both enantiomers over time were monitored by HPLC analysis. During 100 days, a blank membrane (without the chiral selector) exhibited no sorption activity. The membranes containing the selector had no influence on the amount of D-enantiomer, while the L-enantiomer was preferentially adsorbed on each membrane. The intensity of the sorption was found to be a direct function of the amount of the selector contained in a particular membrane. The separation of the same model chiral compound was further studied in diffusion cells by pertraction. The preferential sorption of L-tryptophan in the feed underlined the crucial importance of the selector in an active layer in view of chiral recognition of enantiomers. Due to the exclusive membrane material, the retention of L-tryptophan in the membrane materials did not block the passage of D-enantiomer into the permeate at any point during the experiment. Moreover, the nanomaterial in the active layer assured the distribution of the selector to the point that only 50% of (S, S)-1,2-diaminocyclohexane in one part of the active layer was sufficient to achieve 99% of enantioselectivity. The membranes - fresh and used - were analysed by Fourier-transform infrared (FTIR) spectroscopy and characterized by scanning electron microscopy (SEM) confirming the stability of the tested membranes. To complete the study, the role of the polyamide active layer in chiral recognition of tryptophan enantiomers was proposed. cs
dc.format.extent 9 stran cs
dc.language.iso cs cs
dc.publisher ELSEVIER, RADARWEG 29, 1043 NX AMSTERDAM, NETHERLANDS
dc.relation.ispartof JOURNAL OF MEMBRANE SCIENCE
dc.subject Chiral resolution cs
dc.subject Composite membrane cs
dc.subject Pertraction cs
dc.subject Preferential sorption cs
dc.subject Separation of enantiomers cs
dc.title Separation of racemic compound by nanofibrous composite membranes with chiral selector cs
dc.identifier.doi 10.1016/j.memsci.2019.117728
local.relation.volume 596
local.identifier.publikace 7294
dc.identifier.orcid 0000-0002-5057-3718 Yalcinkaya, Fatma
local.article.number 10.1016/j.memsci.2019.117728


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