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Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes
Light-activated molecular nanomachines (MNMs) can be used to drill holes into prokaryotic (bacterial) cell walls and the membrane of eukaryotic cells, including mammalian cancer cells, by their fast rotational movement, leading to cell death. We examined how these MNMs function in multicellular orga...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8189693/ https://www.ncbi.nlm.nih.gov/pubmed/32091877 http://dx.doi.org/10.1021/acsami.9b22595 |
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author | Gunasekera, Richard S. Galbadage, Thushara Ayala-Orozco, Ciceron Liu, Dongdong García-López, Victor Troutman, Brian E. Tour, Josiah J. Pal, Robert Krishnan, Sunil Cirillo, Jeffrey D. Tour, James M. |
author_facet | Gunasekera, Richard S. Galbadage, Thushara Ayala-Orozco, Ciceron Liu, Dongdong García-López, Victor Troutman, Brian E. Tour, Josiah J. Pal, Robert Krishnan, Sunil Cirillo, Jeffrey D. Tour, James M. |
author_sort | Gunasekera, Richard S. |
collection | PubMed |
description | Light-activated molecular nanomachines (MNMs) can be used to drill holes into prokaryotic (bacterial) cell walls and the membrane of eukaryotic cells, including mammalian cancer cells, by their fast rotational movement, leading to cell death. We examined how these MNMs function in multicellular organisms and investigated their use for treatment and eradication of specific diseases by causing damage to certain tissues and small organisms. Three model eukaryotic species, Caenorhabditis elegans, Daphnia pulex, and Mus musculus (mouse), were evaluated. These organisms were exposed to light-activated fast-rotating MNMs and their physiological and pathological changes were studied in detail. Slow rotating MNMs were used to control for the effects of rotation rate. We demonstrate that fast-rotating MNMs caused depigmentation and 70% mortality in C. elegans while reducing the movement as well as heart rate and causing tissue damage in Daphnia. Topically applied light-activated MNMs on mouse skin caused ulceration and microlesions in the epithelial tissue, allowing MNMs to localize into deeper epidermal tissue. Overall, this study shows that the nanomechanical action of light-activated MNMs is effective against multicellular organisms, disrupting cell membranes and damaging tissue in vivo. Customized MNMs that target specific tissues for therapy combined with spatial and temporal control could have broad clinical applications in a variety of benign and malignant disease states including treatment of cancer, parasites, bacteria, and diseased tissues. |
format | Online Article Text |
id | pubmed-8189693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-81896932021-06-09 Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes Gunasekera, Richard S. Galbadage, Thushara Ayala-Orozco, Ciceron Liu, Dongdong García-López, Victor Troutman, Brian E. Tour, Josiah J. Pal, Robert Krishnan, Sunil Cirillo, Jeffrey D. Tour, James M. ACS Appl Mater Interfaces Article Light-activated molecular nanomachines (MNMs) can be used to drill holes into prokaryotic (bacterial) cell walls and the membrane of eukaryotic cells, including mammalian cancer cells, by their fast rotational movement, leading to cell death. We examined how these MNMs function in multicellular organisms and investigated their use for treatment and eradication of specific diseases by causing damage to certain tissues and small organisms. Three model eukaryotic species, Caenorhabditis elegans, Daphnia pulex, and Mus musculus (mouse), were evaluated. These organisms were exposed to light-activated fast-rotating MNMs and their physiological and pathological changes were studied in detail. Slow rotating MNMs were used to control for the effects of rotation rate. We demonstrate that fast-rotating MNMs caused depigmentation and 70% mortality in C. elegans while reducing the movement as well as heart rate and causing tissue damage in Daphnia. Topically applied light-activated MNMs on mouse skin caused ulceration and microlesions in the epithelial tissue, allowing MNMs to localize into deeper epidermal tissue. Overall, this study shows that the nanomechanical action of light-activated MNMs is effective against multicellular organisms, disrupting cell membranes and damaging tissue in vivo. Customized MNMs that target specific tissues for therapy combined with spatial and temporal control could have broad clinical applications in a variety of benign and malignant disease states including treatment of cancer, parasites, bacteria, and diseased tissues. 2020-03-13 2020-03-25 /pmc/articles/PMC8189693/ /pubmed/32091877 http://dx.doi.org/10.1021/acsami.9b22595 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Article Gunasekera, Richard S. Galbadage, Thushara Ayala-Orozco, Ciceron Liu, Dongdong García-López, Victor Troutman, Brian E. Tour, Josiah J. Pal, Robert Krishnan, Sunil Cirillo, Jeffrey D. Tour, James M. Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes |
title | Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes |
title_full | Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes |
title_fullStr | Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes |
title_full_unstemmed | Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes |
title_short | Molecular Nanomachines Can Destroy Tissue or Kill Multicellular Eukaryotes |
title_sort | molecular nanomachines can destroy tissue or kill multicellular eukaryotes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8189693/ https://www.ncbi.nlm.nih.gov/pubmed/32091877 http://dx.doi.org/10.1021/acsami.9b22595 |
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