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Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase
Therapeutic drug monitoring is a key technology for effective pharmacological treatment. In the present study, a temperature-responsive chromatography column was developed for safe and simple therapeutic drug monitoring without the use of organic solvents. Poly(N-isopropylacrylamide) (PNIPAAm) hydro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648775/ https://www.ncbi.nlm.nih.gov/pubmed/34873248 http://dx.doi.org/10.1038/s41598-021-02998-2 |
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author | Nagase, Kenichi Nishiyama, Teruno Inoue, Masakazu Kanazawa, Hideko |
author_facet | Nagase, Kenichi Nishiyama, Teruno Inoue, Masakazu Kanazawa, Hideko |
author_sort | Nagase, Kenichi |
collection | PubMed |
description | Therapeutic drug monitoring is a key technology for effective pharmacological treatment. In the present study, a temperature-responsive chromatography column was developed for safe and simple therapeutic drug monitoring without the use of organic solvents. Poly(N-isopropylacrylamide) (PNIPAAm) hydrogel-modified silica beads were prepared via a condensation reaction and radical polymerization. The temperature-dependent elution behavior of the drugs was observed using a PNIPAAm-modified silica-bead packed column and an all-aqueous mobile phase. Sharp peaks with reproducible retention times were observed at temperatures of 30 °C or 40 °C because the PNIPAAm hydrogel on the silica beads shrinks at these temperatures, limiting drug diffusion into the PNIPAAm hydrogel layer. The elution behavior of the sample from the prepared column was examined using a mixture of serum and model drugs. The serum and drugs were separated on the column at 30 °C or 40 °C, and the concentration of the eluted drug was obtained using the calibration curve. The results show that the prepared chromatography column would be useful for therapeutic drug monitoring because the drug concentration in serum can be measured without using organic solvents in the mobile phase and without any need for sample preparation. |
format | Online Article Text |
id | pubmed-8648775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86487752021-12-08 Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase Nagase, Kenichi Nishiyama, Teruno Inoue, Masakazu Kanazawa, Hideko Sci Rep Article Therapeutic drug monitoring is a key technology for effective pharmacological treatment. In the present study, a temperature-responsive chromatography column was developed for safe and simple therapeutic drug monitoring without the use of organic solvents. Poly(N-isopropylacrylamide) (PNIPAAm) hydrogel-modified silica beads were prepared via a condensation reaction and radical polymerization. The temperature-dependent elution behavior of the drugs was observed using a PNIPAAm-modified silica-bead packed column and an all-aqueous mobile phase. Sharp peaks with reproducible retention times were observed at temperatures of 30 °C or 40 °C because the PNIPAAm hydrogel on the silica beads shrinks at these temperatures, limiting drug diffusion into the PNIPAAm hydrogel layer. The elution behavior of the sample from the prepared column was examined using a mixture of serum and model drugs. The serum and drugs were separated on the column at 30 °C or 40 °C, and the concentration of the eluted drug was obtained using the calibration curve. The results show that the prepared chromatography column would be useful for therapeutic drug monitoring because the drug concentration in serum can be measured without using organic solvents in the mobile phase and without any need for sample preparation. Nature Publishing Group UK 2021-12-06 /pmc/articles/PMC8648775/ /pubmed/34873248 http://dx.doi.org/10.1038/s41598-021-02998-2 Text en © The Author(s) 2021 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 Nishiyama, Teruno Inoue, Masakazu Kanazawa, Hideko Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
title | Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
title_full | Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
title_fullStr | Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
title_full_unstemmed | Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
title_short | Temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
title_sort | temperature responsive chromatography for therapeutic drug monitoring with an aqueous mobile phase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648775/ https://www.ncbi.nlm.nih.gov/pubmed/34873248 http://dx.doi.org/10.1038/s41598-021-02998-2 |
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