Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays

Three polyaminocyclodextrin materials, obtained by direct reaction between heptakis(6-deoxy-6-iodo)-β-cyclodextrin and the proper linear polyamines, were investigated for their binding properties, in order to assess their potential applications in biological systems, such as vectors for simultaneous...

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Main Authors: Marco Russo, Daniele La Corte, Annalisa Pisciotta, Serena Riela, Rosa Alduina, Paolo Lo Meo
Format: Article
Language:English
Published: Beilstein-Institut 2017-12-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.13.271
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spelling doaj-7ac7a9a128e6414a9c90fad7f17ee5c12021-02-02T05:10:57ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972017-12-011312751276310.3762/bjoc.13.2711860-5397-13-271Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assaysMarco Russo0Daniele La Corte1Annalisa Pisciotta2Serena Riela3Rosa Alduina4Paolo Lo Meo5Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), University of Palermo, V.le delle Scienze ed. 17, 90128 Palermo, ItalyDipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), University of Palermo, V.le delle Scienze ed. 17, 90128 Palermo, ItalyDipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), University of Palermo, V.le delle Scienze ed. 17, 90128 Palermo, ItalyDipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), University of Palermo, V.le delle Scienze ed. 17, 90128 Palermo, ItalyDipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), University of Palermo, V.le delle Scienze ed. 17, 90128 Palermo, ItalyDipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche (STEBICEF), University of Palermo, V.le delle Scienze ed. 17, 90128 Palermo, ItalyThree polyaminocyclodextrin materials, obtained by direct reaction between heptakis(6-deoxy-6-iodo)-β-cyclodextrin and the proper linear polyamines, were investigated for their binding properties, in order to assess their potential applications in biological systems, such as vectors for simultaneous drug and gene cellular uptake or alternatively for the protection of macromolecules. In particular, we exploited polarimetry to test their interaction with some model p-nitroaniline derivatives, chosen as probe guests. The data obtained indicate that binding inside the host cavity is mainly affected by interplay between Coulomb interactions and conformational restraints. Moreover, simultaneous interaction of the cationic polyamine pendant bush at the primary rim was positively assessed. Insights on quantitative aspects of the interaction between our materials and polyanions were investigated by studying the binding with sodium alginate. Finally, the complexation abilities of the same materials towards polynucleotides were assessed by studying their interaction with the model plasmid pUC19. Our results positively highlight the ability of our materials to exploit both the cavity and the polycationic branches, thus functioning as bimodal ligands.https://doi.org/10.3762/bjoc.13.271aminocyclodextrinsbinding propertiesnitroanilinespDNApolarimetrysupramolecular chemistry
collection DOAJ
language English
format Article
sources DOAJ
author Marco Russo
Daniele La Corte
Annalisa Pisciotta
Serena Riela
Rosa Alduina
Paolo Lo Meo
spellingShingle Marco Russo
Daniele La Corte
Annalisa Pisciotta
Serena Riela
Rosa Alduina
Paolo Lo Meo
Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
Beilstein Journal of Organic Chemistry
aminocyclodextrins
binding properties
nitroanilines
pDNA
polarimetry
supramolecular chemistry
author_facet Marco Russo
Daniele La Corte
Annalisa Pisciotta
Serena Riela
Rosa Alduina
Paolo Lo Meo
author_sort Marco Russo
title Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
title_short Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
title_full Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
title_fullStr Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
title_full_unstemmed Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
title_sort binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2017-12-01
description Three polyaminocyclodextrin materials, obtained by direct reaction between heptakis(6-deoxy-6-iodo)-β-cyclodextrin and the proper linear polyamines, were investigated for their binding properties, in order to assess their potential applications in biological systems, such as vectors for simultaneous drug and gene cellular uptake or alternatively for the protection of macromolecules. In particular, we exploited polarimetry to test their interaction with some model p-nitroaniline derivatives, chosen as probe guests. The data obtained indicate that binding inside the host cavity is mainly affected by interplay between Coulomb interactions and conformational restraints. Moreover, simultaneous interaction of the cationic polyamine pendant bush at the primary rim was positively assessed. Insights on quantitative aspects of the interaction between our materials and polyanions were investigated by studying the binding with sodium alginate. Finally, the complexation abilities of the same materials towards polynucleotides were assessed by studying their interaction with the model plasmid pUC19. Our results positively highlight the ability of our materials to exploit both the cavity and the polycationic branches, thus functioning as bimodal ligands.
topic aminocyclodextrins
binding properties
nitroanilines
pDNA
polarimetry
supramolecular chemistry
url https://doi.org/10.3762/bjoc.13.271
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