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Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound
Controlling cell functions for research and therapeutic purposes may open new strategies for the treatment of many diseases. An efficient and safe introduction of membrane impermeable molecules into target cells will provide versatile means to modulate cell fate. We introduce a new transfection tech...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740885/ https://www.ncbi.nlm.nih.gov/pubmed/26843283 http://dx.doi.org/10.1038/srep20477 |
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author | Yoon, Sangpil Kim, Min Gon Chiu, Chi Tat Hwang, Jae Youn Kim, Hyung Ham Wang, Yingxiao Shung, K. Kirk |
author_facet | Yoon, Sangpil Kim, Min Gon Chiu, Chi Tat Hwang, Jae Youn Kim, Hyung Ham Wang, Yingxiao Shung, K. Kirk |
author_sort | Yoon, Sangpil |
collection | PubMed |
description | Controlling cell functions for research and therapeutic purposes may open new strategies for the treatment of many diseases. An efficient and safe introduction of membrane impermeable molecules into target cells will provide versatile means to modulate cell fate. We introduce a new transfection technique that utilizes high frequency ultrasound without any contrast agents such as microbubbles, bringing a single-cell level targeting and size-dependent intracellular delivery of macromolecules. The transfection apparatus consists of an ultrasonic transducer with the center frequency of over 150 MHz and an epi-fluorescence microscope, entitled acoustic-transfection system. Acoustic pulses, emitted from an ultrasonic transducer, perturb the lipid bilayer of the cell membrane of a targeted single-cell to induce intracellular delivery of exogenous molecules. Simultaneous live cell imaging using HeLa cells to investigate the intracellular concentration of Ca(2+) and propidium iodide (PI) and the delivery of 3 kDa dextran labeled with Alexa 488 were demonstrated. Cytosolic delivery of 3 kDa dextran induced via acoustic-transfection was manifested by diffused fluorescence throughout whole cells. Short-term (6 hr) cell viability test and long-term (40 hr) cell tracking confirmed that the proposed approach has low cell cytotoxicity. |
format | Online Article Text |
id | pubmed-4740885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47408852016-02-09 Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound Yoon, Sangpil Kim, Min Gon Chiu, Chi Tat Hwang, Jae Youn Kim, Hyung Ham Wang, Yingxiao Shung, K. Kirk Sci Rep Article Controlling cell functions for research and therapeutic purposes may open new strategies for the treatment of many diseases. An efficient and safe introduction of membrane impermeable molecules into target cells will provide versatile means to modulate cell fate. We introduce a new transfection technique that utilizes high frequency ultrasound without any contrast agents such as microbubbles, bringing a single-cell level targeting and size-dependent intracellular delivery of macromolecules. The transfection apparatus consists of an ultrasonic transducer with the center frequency of over 150 MHz and an epi-fluorescence microscope, entitled acoustic-transfection system. Acoustic pulses, emitted from an ultrasonic transducer, perturb the lipid bilayer of the cell membrane of a targeted single-cell to induce intracellular delivery of exogenous molecules. Simultaneous live cell imaging using HeLa cells to investigate the intracellular concentration of Ca(2+) and propidium iodide (PI) and the delivery of 3 kDa dextran labeled with Alexa 488 were demonstrated. Cytosolic delivery of 3 kDa dextran induced via acoustic-transfection was manifested by diffused fluorescence throughout whole cells. Short-term (6 hr) cell viability test and long-term (40 hr) cell tracking confirmed that the proposed approach has low cell cytotoxicity. Nature Publishing Group 2016-02-04 /pmc/articles/PMC4740885/ /pubmed/26843283 http://dx.doi.org/10.1038/srep20477 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yoon, Sangpil Kim, Min Gon Chiu, Chi Tat Hwang, Jae Youn Kim, Hyung Ham Wang, Yingxiao Shung, K. Kirk Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
title | Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
title_full | Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
title_fullStr | Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
title_full_unstemmed | Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
title_short | Direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
title_sort | direct and sustained intracellular delivery of exogenous molecules using acoustic-transfection with high frequency ultrasound |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740885/ https://www.ncbi.nlm.nih.gov/pubmed/26843283 http://dx.doi.org/10.1038/srep20477 |
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