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Development of a Plasmonic Sensor for a Chemotherapeutic Agent Cabazitaxel
[Image: see text] Drug dosage is a crucial subject in both human and animal treatment. Administering less drug dosage may prevent treatment or make it less effective, and high drug dosage may cause a heightened risk of adverse effects, or in some cases, cost a patient’s life. Also, even when the dos...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835620/ https://www.ncbi.nlm.nih.gov/pubmed/36643531 http://dx.doi.org/10.1021/acsomega.2c05327 |
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author | Aşır, Süleyman Uğur, Buse Jalilzadeh, Mitra Göktürk, Ilgım Türkmen, Deniz |
author_facet | Aşır, Süleyman Uğur, Buse Jalilzadeh, Mitra Göktürk, Ilgım Türkmen, Deniz |
author_sort | Aşır, Süleyman |
collection | PubMed |
description | [Image: see text] Drug dosage is a crucial subject in both human and animal treatment. Administering less drug dosage may prevent treatment or make it less effective, and high drug dosage may cause a heightened risk of adverse effects, or in some cases, cost a patient’s life. Also, even when the dosage is administered carefully, metabolic differences may cause different effects on different patients. Because of these considerations, monitoring drug dosage in the body is a critical and significant requirement in the health industry. Within the scope of this study, a reusable surface plasmon resonance (SPR) chip with fast response, high selectivity, and no pretreatment is produced for the chemotherapeutic agent cabazitaxel. A cabazitaxel-imprinted nanofilm was synthesized on the sensor chip surface and characterized by atomic force microscopy, ellipsometry, and contact angle measurements. Standard cabazitaxel solution and an artificial plasma sample were used for the kinetic analysis. Docetaxel, methylprednisolone, and dexamethasone were analyzed for their selectivity experiment. In addition, the repeatability and storage durability of the sensor were also evaluated. As a result of the adsorption studies, the limit of detection and limit of quantitation values were found to be 0.012 and 0.036 μg/mL, respectively. High-performance liquid chromatography analysis was used to validate the response of the cabazitaxel-imprinted sensor. |
format | Online Article Text |
id | pubmed-9835620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98356202023-01-13 Development of a Plasmonic Sensor for a Chemotherapeutic Agent Cabazitaxel Aşır, Süleyman Uğur, Buse Jalilzadeh, Mitra Göktürk, Ilgım Türkmen, Deniz ACS Omega [Image: see text] Drug dosage is a crucial subject in both human and animal treatment. Administering less drug dosage may prevent treatment or make it less effective, and high drug dosage may cause a heightened risk of adverse effects, or in some cases, cost a patient’s life. Also, even when the dosage is administered carefully, metabolic differences may cause different effects on different patients. Because of these considerations, monitoring drug dosage in the body is a critical and significant requirement in the health industry. Within the scope of this study, a reusable surface plasmon resonance (SPR) chip with fast response, high selectivity, and no pretreatment is produced for the chemotherapeutic agent cabazitaxel. A cabazitaxel-imprinted nanofilm was synthesized on the sensor chip surface and characterized by atomic force microscopy, ellipsometry, and contact angle measurements. Standard cabazitaxel solution and an artificial plasma sample were used for the kinetic analysis. Docetaxel, methylprednisolone, and dexamethasone were analyzed for their selectivity experiment. In addition, the repeatability and storage durability of the sensor were also evaluated. As a result of the adsorption studies, the limit of detection and limit of quantitation values were found to be 0.012 and 0.036 μg/mL, respectively. High-performance liquid chromatography analysis was used to validate the response of the cabazitaxel-imprinted sensor. American Chemical Society 2022-12-26 /pmc/articles/PMC9835620/ /pubmed/36643531 http://dx.doi.org/10.1021/acsomega.2c05327 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Aşır, Süleyman Uğur, Buse Jalilzadeh, Mitra Göktürk, Ilgım Türkmen, Deniz Development of a Plasmonic Sensor for a Chemotherapeutic Agent Cabazitaxel |
title | Development of a Plasmonic Sensor for a Chemotherapeutic
Agent Cabazitaxel |
title_full | Development of a Plasmonic Sensor for a Chemotherapeutic
Agent Cabazitaxel |
title_fullStr | Development of a Plasmonic Sensor for a Chemotherapeutic
Agent Cabazitaxel |
title_full_unstemmed | Development of a Plasmonic Sensor for a Chemotherapeutic
Agent Cabazitaxel |
title_short | Development of a Plasmonic Sensor for a Chemotherapeutic
Agent Cabazitaxel |
title_sort | development of a plasmonic sensor for a chemotherapeutic
agent cabazitaxel |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835620/ https://www.ncbi.nlm.nih.gov/pubmed/36643531 http://dx.doi.org/10.1021/acsomega.2c05327 |
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