Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.

Continuous monitoring of physiological parameters inside a living cell will lead to major advances in our understanding of biology and complex diseases, such as cancer. It also enables the development of new medical diagnostics and therapeutics. Progress in nanofabrication and wireless communication...

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Main Authors: Kokab B Parizi, Demir Akin, H-S Philip Wong
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5877870?pdf=render
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spelling doaj-33b51f9b1da2441ba114001b8ab98cda2020-11-25T02:06:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01133e019471210.1371/journal.pone.0194712Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.Kokab B PariziDemir AkinH-S Philip WongContinuous monitoring of physiological parameters inside a living cell will lead to major advances in our understanding of biology and complex diseases, such as cancer. It also enables the development of new medical diagnostics and therapeutics. Progress in nanofabrication and wireless communication has opened up the potential of making a wireless chip small enough that it can be wholly inserted into a living cell. To investigate how such chips could be internalized into various types of living single cells and how this process might affect cells' physiology, we designed and fabricated a series of multilayered micron-scale tag structures with different sizes as potential RFID (Radio Frequency IDentification) cell trackers. While the present structures are test structures that do not resonate, the tags that do resonate have similar structure from device fabrication, material properties, and device size point of view. The structures are in four different sizes, the largest with the lateral dimension of 9 μm × 21 μm. The thickness for these structures is kept constant at 1.5 μm. We demonstrate successful delivery of our fabricated chips into various types of living cells, such as melanoma skin cancer, breast cancer, colon cancer and healthy/normal fibroblast skin cells. To our surprise, we observed a remarkable internalization rate difference between each cell type; the uptake rate was faster for more aggressive cancer cells than the normal/healthy cells. Cell viability before and after tag cellular internalization and persistence of the internalized tags have also been recorded over the course of five days of incubation. These results establish the foundations of the possibility of long term, wireless, intracellular physiological signal monitoring.http://europepmc.org/articles/PMC5877870?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kokab B Parizi
Demir Akin
H-S Philip Wong
spellingShingle Kokab B Parizi
Demir Akin
H-S Philip Wong
Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
PLoS ONE
author_facet Kokab B Parizi
Demir Akin
H-S Philip Wong
author_sort Kokab B Parizi
title Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
title_short Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
title_full Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
title_fullStr Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
title_full_unstemmed Internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
title_sort internalization of subcellular-scale microfabricated chips by healthy and cancer cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Continuous monitoring of physiological parameters inside a living cell will lead to major advances in our understanding of biology and complex diseases, such as cancer. It also enables the development of new medical diagnostics and therapeutics. Progress in nanofabrication and wireless communication has opened up the potential of making a wireless chip small enough that it can be wholly inserted into a living cell. To investigate how such chips could be internalized into various types of living single cells and how this process might affect cells' physiology, we designed and fabricated a series of multilayered micron-scale tag structures with different sizes as potential RFID (Radio Frequency IDentification) cell trackers. While the present structures are test structures that do not resonate, the tags that do resonate have similar structure from device fabrication, material properties, and device size point of view. The structures are in four different sizes, the largest with the lateral dimension of 9 μm × 21 μm. The thickness for these structures is kept constant at 1.5 μm. We demonstrate successful delivery of our fabricated chips into various types of living cells, such as melanoma skin cancer, breast cancer, colon cancer and healthy/normal fibroblast skin cells. To our surprise, we observed a remarkable internalization rate difference between each cell type; the uptake rate was faster for more aggressive cancer cells than the normal/healthy cells. Cell viability before and after tag cellular internalization and persistence of the internalized tags have also been recorded over the course of five days of incubation. These results establish the foundations of the possibility of long term, wireless, intracellular physiological signal monitoring.
url http://europepmc.org/articles/PMC5877870?pdf=render
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