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Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble
The conjunction of low intensity ultrasound and encapsulated microbubbles can alter the permeability of cell membrane, offering a promising theranostic technique for non-invasive gene/drug delivery. Despite its great potential, the biophysical mechanisms of the delivery at the cellular level remains...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4775856/ https://www.ncbi.nlm.nih.gov/pubmed/26941839 http://dx.doi.org/10.7150/thno.13518 |
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author | Nejad, S. Moosavi Hosseini, Hamid Akiyama, Hidenori Tachibana, Katsuro |
author_facet | Nejad, S. Moosavi Hosseini, Hamid Akiyama, Hidenori Tachibana, Katsuro |
author_sort | Nejad, S. Moosavi |
collection | PubMed |
description | The conjunction of low intensity ultrasound and encapsulated microbubbles can alter the permeability of cell membrane, offering a promising theranostic technique for non-invasive gene/drug delivery. Despite its great potential, the biophysical mechanisms of the delivery at the cellular level remains poorly understood. Here, the first direct high-speed micro-photographic images of human lymphoma cell and microbubble interaction dynamics are provided in a completely free suspension environment without any boundary parameter defect. Our real-time images and theoretical analyses prove that the negative divergence side of the microbubble's dipole microstreaming locally pulls the cell membrane, causing transient local protrusion of 2.5 µm in the cell membrane. The linear oscillation of microbubble caused microstreaming well below the inertial cavitation threshold, and imposed 35.3 Pa shear stress on the membrane, promoting an area strain of 0.12%, less than the membrane critical areal strain to cause cell rupture. Positive transfected cells with pEGFP-N1 confirm that the interaction causes membrane poration without cell disruption. The results show that the overstretched cell membrane causes reparable submicron pore formation, providing primary evidence of low amplitude (0.12 MPa at 0.834 MHz) ultrasound sonoporation mechanism. |
format | Online Article Text |
id | pubmed-4775856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-47758562016-03-03 Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble Nejad, S. Moosavi Hosseini, Hamid Akiyama, Hidenori Tachibana, Katsuro Theranostics Research Paper The conjunction of low intensity ultrasound and encapsulated microbubbles can alter the permeability of cell membrane, offering a promising theranostic technique for non-invasive gene/drug delivery. Despite its great potential, the biophysical mechanisms of the delivery at the cellular level remains poorly understood. Here, the first direct high-speed micro-photographic images of human lymphoma cell and microbubble interaction dynamics are provided in a completely free suspension environment without any boundary parameter defect. Our real-time images and theoretical analyses prove that the negative divergence side of the microbubble's dipole microstreaming locally pulls the cell membrane, causing transient local protrusion of 2.5 µm in the cell membrane. The linear oscillation of microbubble caused microstreaming well below the inertial cavitation threshold, and imposed 35.3 Pa shear stress on the membrane, promoting an area strain of 0.12%, less than the membrane critical areal strain to cause cell rupture. Positive transfected cells with pEGFP-N1 confirm that the interaction causes membrane poration without cell disruption. The results show that the overstretched cell membrane causes reparable submicron pore formation, providing primary evidence of low amplitude (0.12 MPa at 0.834 MHz) ultrasound sonoporation mechanism. Ivyspring International Publisher 2016-02-03 /pmc/articles/PMC4775856/ /pubmed/26941839 http://dx.doi.org/10.7150/thno.13518 Text en © Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions. |
spellingShingle | Research Paper Nejad, S. Moosavi Hosseini, Hamid Akiyama, Hidenori Tachibana, Katsuro Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble |
title | Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble |
title_full | Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble |
title_fullStr | Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble |
title_full_unstemmed | Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble |
title_short | Reparable Cell Sonoporation in Suspension: Theranostic Potential of Microbubble |
title_sort | reparable cell sonoporation in suspension: theranostic potential of microbubble |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4775856/ https://www.ncbi.nlm.nih.gov/pubmed/26941839 http://dx.doi.org/10.7150/thno.13518 |
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