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Temperature-responsive mixed-mode column for the modulation of multiple interactions

In this study, mixed-mode chromatography columns have been investigated using multiple analyte interactions. A mixed-mode chromatography column was developed using poly(N-isopropylacrylamide) (PNIPAAm) brush-modified silica beads and poly(3-acrylamidopropyl trimethylammonium chloride) (PAPTAC) brush...

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Autores principales: Nagase, Kenichi, Matsumoto, Kosuke, Kanazawa, Hideko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924202/
https://www.ncbi.nlm.nih.gov/pubmed/35292748
http://dx.doi.org/10.1038/s41598-022-08475-8
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author Nagase, Kenichi
Matsumoto, Kosuke
Kanazawa, Hideko
author_facet Nagase, Kenichi
Matsumoto, Kosuke
Kanazawa, Hideko
author_sort Nagase, Kenichi
collection PubMed
description In this study, mixed-mode chromatography columns have been investigated using multiple analyte interactions. A mixed-mode chromatography column was developed using poly(N-isopropylacrylamide) (PNIPAAm) brush-modified silica beads and poly(3-acrylamidopropyl trimethylammonium chloride) (PAPTAC) brush-modified silica beads. PNIPAAm brush-modified silica beads and PAPTAC brush-modified silica beads were prepared by atom transfer radical polymerization. The beads were then packed into a stainless-steel column in arbitrary compositions. The elution studies evaluated the column performance on hydrophobic, electrostatic, and therapeutic drug samples using steroids, adenosine nucleotide, and antiepileptic drugs as analytes, respectively. Steroids exhibited an increased retention time when the column temperature was increased. The retention of adenosine nucleotides increased with the increasing composition of the PAPTAC-modified beads in the column. The antiepileptic drugs were separated using the prepared mixed-mode columns. An effective separation of antiepileptic drugs was observed on a 10:1 PNIPAAm:PAPTAC column because the balance between the hydrophobic and electrostatic interactions with antiepileptic drugs was optimized for the bead composition. Oligonucleotides were also separated using mixed-mode columns through multiple hydrophobic and electrostatic interactions. These results demonstrate that the developed mixed-mode column can modulate multiple hydrophobic and electrostatic interactions by changing the column temperature and composition of the packed PNIPAAm and PAPTAC beads.
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spelling pubmed-89242022022-03-17 Temperature-responsive mixed-mode column for the modulation of multiple interactions Nagase, Kenichi Matsumoto, Kosuke Kanazawa, Hideko Sci Rep Article In this study, mixed-mode chromatography columns have been investigated using multiple analyte interactions. A mixed-mode chromatography column was developed using poly(N-isopropylacrylamide) (PNIPAAm) brush-modified silica beads and poly(3-acrylamidopropyl trimethylammonium chloride) (PAPTAC) brush-modified silica beads. PNIPAAm brush-modified silica beads and PAPTAC brush-modified silica beads were prepared by atom transfer radical polymerization. The beads were then packed into a stainless-steel column in arbitrary compositions. The elution studies evaluated the column performance on hydrophobic, electrostatic, and therapeutic drug samples using steroids, adenosine nucleotide, and antiepileptic drugs as analytes, respectively. Steroids exhibited an increased retention time when the column temperature was increased. The retention of adenosine nucleotides increased with the increasing composition of the PAPTAC-modified beads in the column. The antiepileptic drugs were separated using the prepared mixed-mode columns. An effective separation of antiepileptic drugs was observed on a 10:1 PNIPAAm:PAPTAC column because the balance between the hydrophobic and electrostatic interactions with antiepileptic drugs was optimized for the bead composition. Oligonucleotides were also separated using mixed-mode columns through multiple hydrophobic and electrostatic interactions. These results demonstrate that the developed mixed-mode column can modulate multiple hydrophobic and electrostatic interactions by changing the column temperature and composition of the packed PNIPAAm and PAPTAC beads. Nature Publishing Group UK 2022-03-15 /pmc/articles/PMC8924202/ /pubmed/35292748 http://dx.doi.org/10.1038/s41598-022-08475-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nagase, Kenichi
Matsumoto, Kosuke
Kanazawa, Hideko
Temperature-responsive mixed-mode column for the modulation of multiple interactions
title Temperature-responsive mixed-mode column for the modulation of multiple interactions
title_full Temperature-responsive mixed-mode column for the modulation of multiple interactions
title_fullStr Temperature-responsive mixed-mode column for the modulation of multiple interactions
title_full_unstemmed Temperature-responsive mixed-mode column for the modulation of multiple interactions
title_short Temperature-responsive mixed-mode column for the modulation of multiple interactions
title_sort temperature-responsive mixed-mode column for the modulation of multiple interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924202/
https://www.ncbi.nlm.nih.gov/pubmed/35292748
http://dx.doi.org/10.1038/s41598-022-08475-8
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