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Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells
To curtail pathogens or tumors, antimicrobial or antineoplastic drugs have been developed. These drugs target microbial/cancer growth and survival, thereby improving the host’s health. In attempts to evade the detrimental effects of such drugs, these cells have evolved several mechanisms over time....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954051/ https://www.ncbi.nlm.nih.gov/pubmed/36832001 http://dx.doi.org/10.3390/bios13020235 |
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author | Jha, Niharika G. Dkhar, Daphika S. Singh, Sumit K. Malode, Shweta J. Shetti, Nagaraj P. Chandra, Pranjal |
author_facet | Jha, Niharika G. Dkhar, Daphika S. Singh, Sumit K. Malode, Shweta J. Shetti, Nagaraj P. Chandra, Pranjal |
author_sort | Jha, Niharika G. |
collection | PubMed |
description | To curtail pathogens or tumors, antimicrobial or antineoplastic drugs have been developed. These drugs target microbial/cancer growth and survival, thereby improving the host’s health. In attempts to evade the detrimental effects of such drugs, these cells have evolved several mechanisms over time. Some variants of the cells have developed resistances against multiple drugs or antimicrobial agents. Such microorganisms or cancer cells are said to exhibit multidrug resistance (MDR). The drug resistance status of a cell can be determined by analyzing several genotypic and phenotypic changes, which are brought about by significant physiological and biochemical alterations. Owing to their resilient nature, treatment and management of MDR cases in clinics is arduous and requires a meticulous approach. Currently, techniques such as plating and culturing, biopsy, gene sequencing, and magnetic resonance imaging are prevalent in clinical practices for determining drug resistance status. However, the major drawbacks of using these methods lie in their time-consuming nature and the problem of translating them into point-of-care or mass-detection tools. To overcome the shortcomings of conventional techniques, biosensors with a low detection limit have been engineered to provide quick and reliable results conveniently. These devices are highly versatile in terms of analyte range and quantities that can be detected to report drug resistance in a given sample. A brief introduction to MDR, along with a detailed insight into recent biosensor design trends and use for identifying multidrug-resistant microorganisms and tumors, is presented in this review. |
format | Online Article Text |
id | pubmed-9954051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99540512023-02-25 Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells Jha, Niharika G. Dkhar, Daphika S. Singh, Sumit K. Malode, Shweta J. Shetti, Nagaraj P. Chandra, Pranjal Biosensors (Basel) Review To curtail pathogens or tumors, antimicrobial or antineoplastic drugs have been developed. These drugs target microbial/cancer growth and survival, thereby improving the host’s health. In attempts to evade the detrimental effects of such drugs, these cells have evolved several mechanisms over time. Some variants of the cells have developed resistances against multiple drugs or antimicrobial agents. Such microorganisms or cancer cells are said to exhibit multidrug resistance (MDR). The drug resistance status of a cell can be determined by analyzing several genotypic and phenotypic changes, which are brought about by significant physiological and biochemical alterations. Owing to their resilient nature, treatment and management of MDR cases in clinics is arduous and requires a meticulous approach. Currently, techniques such as plating and culturing, biopsy, gene sequencing, and magnetic resonance imaging are prevalent in clinical practices for determining drug resistance status. However, the major drawbacks of using these methods lie in their time-consuming nature and the problem of translating them into point-of-care or mass-detection tools. To overcome the shortcomings of conventional techniques, biosensors with a low detection limit have been engineered to provide quick and reliable results conveniently. These devices are highly versatile in terms of analyte range and quantities that can be detected to report drug resistance in a given sample. A brief introduction to MDR, along with a detailed insight into recent biosensor design trends and use for identifying multidrug-resistant microorganisms and tumors, is presented in this review. MDPI 2023-02-07 /pmc/articles/PMC9954051/ /pubmed/36832001 http://dx.doi.org/10.3390/bios13020235 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Jha, Niharika G. Dkhar, Daphika S. Singh, Sumit K. Malode, Shweta J. Shetti, Nagaraj P. Chandra, Pranjal Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells |
title | Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells |
title_full | Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells |
title_fullStr | Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells |
title_full_unstemmed | Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells |
title_short | Engineered Biosensors for Diagnosing Multidrug Resistance in Microbial and Malignant Cells |
title_sort | engineered biosensors for diagnosing multidrug resistance in microbial and malignant cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954051/ https://www.ncbi.nlm.nih.gov/pubmed/36832001 http://dx.doi.org/10.3390/bios13020235 |
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