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Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection
Medical diagnostics is trending towards a more personalized future approach in which multiple tests can be digitized into patient records. In cancer diagnostics, patients can be tested for individual protein and genomic biomarkers that detect cancers at very early stages and also be used to monitor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559629/ https://www.ncbi.nlm.nih.gov/pubmed/32906644 http://dx.doi.org/10.3390/bios10090115 |
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author | Dhanapala, Lasangi Krause, Colleen E. Jones, Abby L. Rusling, James F. |
author_facet | Dhanapala, Lasangi Krause, Colleen E. Jones, Abby L. Rusling, James F. |
author_sort | Dhanapala, Lasangi |
collection | PubMed |
description | Medical diagnostics is trending towards a more personalized future approach in which multiple tests can be digitized into patient records. In cancer diagnostics, patients can be tested for individual protein and genomic biomarkers that detect cancers at very early stages and also be used to monitor cancer progression or remission during therapy. These data can then be incorporated into patient records that could be easily accessed on a cell phone by a health care professional or the patients themselves on demand. Data on protein biomarkers have a large potential to be measured in point-of-care devices, particularly diagnostic panels that could provide a continually updated, personalized record of a disease like cancer. Electrochemical immunoassays have been popular among protein detection methods due to their inherent high sensitivity and ease of coupling with screen-printed and inkjet-printed electrodes. Integrated chips featuring these kinds of electrodes can be built at low cost and designed for ease of automation. Enzyme-linked immunosorbent assay (ELISA) features are adopted in most of these ultrasensitive detection systems, with microfluidics allowing easy manipulation and good fluid dynamics to deliver reagents and detect the desired proteins. Several of these ultrasensitive systems have detected biomarker panels ranging from four to eight proteins, which in many cases when a specific cancer is suspected may be sufficient. However, a grand challenge lies in engineering microfluidic-printed electrode devices for the simultaneous detection of larger protein panels (e.g., 50–100) that could be used to test for many types of cancers, as well as other diseases for truly personalized care. |
format | Online Article Text |
id | pubmed-7559629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75596292020-10-29 Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection Dhanapala, Lasangi Krause, Colleen E. Jones, Abby L. Rusling, James F. Biosensors (Basel) Review Medical diagnostics is trending towards a more personalized future approach in which multiple tests can be digitized into patient records. In cancer diagnostics, patients can be tested for individual protein and genomic biomarkers that detect cancers at very early stages and also be used to monitor cancer progression or remission during therapy. These data can then be incorporated into patient records that could be easily accessed on a cell phone by a health care professional or the patients themselves on demand. Data on protein biomarkers have a large potential to be measured in point-of-care devices, particularly diagnostic panels that could provide a continually updated, personalized record of a disease like cancer. Electrochemical immunoassays have been popular among protein detection methods due to their inherent high sensitivity and ease of coupling with screen-printed and inkjet-printed electrodes. Integrated chips featuring these kinds of electrodes can be built at low cost and designed for ease of automation. Enzyme-linked immunosorbent assay (ELISA) features are adopted in most of these ultrasensitive detection systems, with microfluidics allowing easy manipulation and good fluid dynamics to deliver reagents and detect the desired proteins. Several of these ultrasensitive systems have detected biomarker panels ranging from four to eight proteins, which in many cases when a specific cancer is suspected may be sufficient. However, a grand challenge lies in engineering microfluidic-printed electrode devices for the simultaneous detection of larger protein panels (e.g., 50–100) that could be used to test for many types of cancers, as well as other diseases for truly personalized care. MDPI 2020-09-07 /pmc/articles/PMC7559629/ /pubmed/32906644 http://dx.doi.org/10.3390/bios10090115 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Dhanapala, Lasangi Krause, Colleen E. Jones, Abby L. Rusling, James F. Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection |
title | Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection |
title_full | Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection |
title_fullStr | Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection |
title_full_unstemmed | Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection |
title_short | Printed Electrodes in Microfluidic Arrays for Cancer Biomarker Protein Detection |
title_sort | printed electrodes in microfluidic arrays for cancer biomarker protein detection |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559629/ https://www.ncbi.nlm.nih.gov/pubmed/32906644 http://dx.doi.org/10.3390/bios10090115 |
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