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Development of an enzyme-linked immunosorbent assay for camptothecin
The use of camptothecin and its analogues has increased in clinical settings and in agriculture. Therefore, camptothecins and their derivatives, metabolites and degradation products are frequently found in the environment. Therefore, it is important to develop an ELISA for the quantification of camp...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625201/ https://www.ncbi.nlm.nih.gov/pubmed/31173229 http://dx.doi.org/10.3892/mmr.2019.10342 |
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author | Yan, Liting Nan, Xiang Zhang, Cunzheng Wang, Haifang Huang, Xiaoyan Hu, Jun Liu, Yingqian |
author_facet | Yan, Liting Nan, Xiang Zhang, Cunzheng Wang, Haifang Huang, Xiaoyan Hu, Jun Liu, Yingqian |
author_sort | Yan, Liting |
collection | PubMed |
description | The use of camptothecin and its analogues has increased in clinical settings and in agriculture. Therefore, camptothecins and their derivatives, metabolites and degradation products are frequently found in the environment. Therefore, it is important to develop an ELISA for the quantification of camptothecins in human plasma, plants, animal tissues and other matrices. The present study developed a novel competitive indirect ELISA for camptothecin using a monoclonal antibody (MAb). In total, two haptens and various carrier proteins were tested to select the most suitable immunogen for the production of MAbs against camptothecin. Hapten 1 conjugated with keyhole limpet hemocyanin was selected for the preparation of MAb 5A3, and was used to establish a competitive indirect ELISA for camptothecin. A total of three derivatives of camptothecin used in clinical practice were examined. Topotecan showed an IC(50) value of 0.68 µg/ml with a detection limit of 0.19 µg/ml, belotecan showed an IC(50) value of 0.87 µg/ml with a detection limit of 0.22 µg/ml and irinotecan showed an IC(50) value of 2.85 µg/ml with a detection limit of 0.47 µg/ml. The cross-reactivity results suggested that the assay developed in the present study possessed a high sensitivity to camptothecin. Therefore, this immunoassay technique may be suitable for monitoring the levels of camptothecin in compound analysis, clinical applications, and analyses of food and environmental samples. |
format | Online Article Text |
id | pubmed-6625201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-66252012019-07-31 Development of an enzyme-linked immunosorbent assay for camptothecin Yan, Liting Nan, Xiang Zhang, Cunzheng Wang, Haifang Huang, Xiaoyan Hu, Jun Liu, Yingqian Mol Med Rep Articles The use of camptothecin and its analogues has increased in clinical settings and in agriculture. Therefore, camptothecins and their derivatives, metabolites and degradation products are frequently found in the environment. Therefore, it is important to develop an ELISA for the quantification of camptothecins in human plasma, plants, animal tissues and other matrices. The present study developed a novel competitive indirect ELISA for camptothecin using a monoclonal antibody (MAb). In total, two haptens and various carrier proteins were tested to select the most suitable immunogen for the production of MAbs against camptothecin. Hapten 1 conjugated with keyhole limpet hemocyanin was selected for the preparation of MAb 5A3, and was used to establish a competitive indirect ELISA for camptothecin. A total of three derivatives of camptothecin used in clinical practice were examined. Topotecan showed an IC(50) value of 0.68 µg/ml with a detection limit of 0.19 µg/ml, belotecan showed an IC(50) value of 0.87 µg/ml with a detection limit of 0.22 µg/ml and irinotecan showed an IC(50) value of 2.85 µg/ml with a detection limit of 0.47 µg/ml. The cross-reactivity results suggested that the assay developed in the present study possessed a high sensitivity to camptothecin. Therefore, this immunoassay technique may be suitable for monitoring the levels of camptothecin in compound analysis, clinical applications, and analyses of food and environmental samples. D.A. Spandidos 2019-08 2019-06-05 /pmc/articles/PMC6625201/ /pubmed/31173229 http://dx.doi.org/10.3892/mmr.2019.10342 Text en Copyright: © Yan et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Yan, Liting Nan, Xiang Zhang, Cunzheng Wang, Haifang Huang, Xiaoyan Hu, Jun Liu, Yingqian Development of an enzyme-linked immunosorbent assay for camptothecin |
title | Development of an enzyme-linked immunosorbent assay for camptothecin |
title_full | Development of an enzyme-linked immunosorbent assay for camptothecin |
title_fullStr | Development of an enzyme-linked immunosorbent assay for camptothecin |
title_full_unstemmed | Development of an enzyme-linked immunosorbent assay for camptothecin |
title_short | Development of an enzyme-linked immunosorbent assay for camptothecin |
title_sort | development of an enzyme-linked immunosorbent assay for camptothecin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625201/ https://www.ncbi.nlm.nih.gov/pubmed/31173229 http://dx.doi.org/10.3892/mmr.2019.10342 |
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