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Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin
BACKGROUND: We proposed a method of using electrical stimulation for treatment of malignant melanoma through directly spray-printing liquid metal on skin as soft electrodes to deliver low intensity, intermediate frequency electric fields. METHODS: With patterned conductive liquid metal components on...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919201/ https://www.ncbi.nlm.nih.gov/pubmed/27339426 http://dx.doi.org/10.1186/s40169-016-0102-9 |
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author | Li, Jun Guo, Cangran Wang, Zhongshuai Gao, Kai Shi, Xudong Liu, Jing |
author_facet | Li, Jun Guo, Cangran Wang, Zhongshuai Gao, Kai Shi, Xudong Liu, Jing |
author_sort | Li, Jun |
collection | PubMed |
description | BACKGROUND: We proposed a method of using electrical stimulation for treatment of malignant melanoma through directly spray-printing liquid metal on skin as soft electrodes to deliver low intensity, intermediate frequency electric fields. METHODS: With patterned conductive liquid metal components on mice skin and under assistance of a signal generator, a sine wave electrical power with voltage of 5 V and 300 kHz could be administrated on treating malignant melanoma tumor. FINDINGS: The experiments demonstrated that tumor volume was significantly reduced compared with that of the control group. Under the designed parameters (signal: sine wave, signal amplitude Vpp: 5 V and Vpp: 4 V, frequency: 300 kHz) of Tumor treating fields (TTFields) with the sprayed liquid metal electrode, four mice tumor groups became diminishing after 1 week of treatment. The only device-related side effect as seen was a mild to moderate contact dermatitis underneath the field delivering electrodes. The SEM images and pathological analysis demonstrated the targeted treating behavior of the malignant melanoma tumor. Further, thermal infrared imaging experiments indicated that there occur no evident heating effects in the course of treatment. Besides, the liquid metal is easy to remove through medical alcohol. CONCLUSIONS: Tumor treating fields through liquid metal electrode could offer a safe, straightforward and effective treatment modality which evidently slows down tumor growth in vivo. These promising results also raised the possibility of applying spray-printing TTFields as an easy going physical way for future cancer therapy. |
format | Online Article Text |
id | pubmed-4919201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-49192012016-07-06 Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin Li, Jun Guo, Cangran Wang, Zhongshuai Gao, Kai Shi, Xudong Liu, Jing Clin Transl Med Short Report BACKGROUND: We proposed a method of using electrical stimulation for treatment of malignant melanoma through directly spray-printing liquid metal on skin as soft electrodes to deliver low intensity, intermediate frequency electric fields. METHODS: With patterned conductive liquid metal components on mice skin and under assistance of a signal generator, a sine wave electrical power with voltage of 5 V and 300 kHz could be administrated on treating malignant melanoma tumor. FINDINGS: The experiments demonstrated that tumor volume was significantly reduced compared with that of the control group. Under the designed parameters (signal: sine wave, signal amplitude Vpp: 5 V and Vpp: 4 V, frequency: 300 kHz) of Tumor treating fields (TTFields) with the sprayed liquid metal electrode, four mice tumor groups became diminishing after 1 week of treatment. The only device-related side effect as seen was a mild to moderate contact dermatitis underneath the field delivering electrodes. The SEM images and pathological analysis demonstrated the targeted treating behavior of the malignant melanoma tumor. Further, thermal infrared imaging experiments indicated that there occur no evident heating effects in the course of treatment. Besides, the liquid metal is easy to remove through medical alcohol. CONCLUSIONS: Tumor treating fields through liquid metal electrode could offer a safe, straightforward and effective treatment modality which evidently slows down tumor growth in vivo. These promising results also raised the possibility of applying spray-printing TTFields as an easy going physical way for future cancer therapy. Springer Berlin Heidelberg 2016-06-23 /pmc/articles/PMC4919201/ /pubmed/27339426 http://dx.doi.org/10.1186/s40169-016-0102-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Short Report Li, Jun Guo, Cangran Wang, Zhongshuai Gao, Kai Shi, Xudong Liu, Jing Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
title | Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
title_full | Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
title_fullStr | Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
title_full_unstemmed | Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
title_short | Electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
title_sort | electrical stimulation towards melanoma therapy via liquid metal printed electronics on skin |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919201/ https://www.ncbi.nlm.nih.gov/pubmed/27339426 http://dx.doi.org/10.1186/s40169-016-0102-9 |
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