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Intracellular nanomaterial delivery via spiral hydroporation

Intracellular nanomaterial delivery via spiral hydroporation
Intracellular nanomaterial delivery via spiral hydroporation
In recent nanobiotechnology developments, a wide variety of functional nanomaterials and engineered biomolecules have been created, and these have numerous applications in cell biology. For these nanomaterials to fulfill their promises completely, they must be able to reach their biological targets at the subcellular level and with a high level of specificity. Traditionally, either nanocarrier- or membrane disruption-based method has been used to deliver nanomaterials inside cells; however, these methods are suboptimal due to their toxicity, inconsistent delivery, and low throughput, and they are also labor intensive and time-consuming, highlighting the need for development of a next-generation, intracellular delivery system. This study reports on the development of an intracellular nanomaterial delivery platform, based on unexpected cell-deformation phenomena via spiral vortex and vortex breakdown exerted in the cross- and T-junctions at moderate Reynolds numbers. These vortex-induced cell deformation and sequential restoration processes open cell membranes transiently, allowing effective and robust intracellular delivery of nanomaterials in a single step without the aid of carriers or external apparatus. By using the platform described here (termed spiral hydroporator), we demonstrate the delivery of different nanomaterials, including gold nanoparticles (200 nm diameter), functional mesoporous silica nanoparticles (150 nm diameter), dextran (hydrodynamic diameters between 2–55 nm), and mRNA, into different cell types. We demonstrate here that the system is highly efficient (up to 96.5%) with high throughput (up to 1 × 106 cells/min) and rapid delivery (∼1 min) while maintaining high levels of cell viability (up to 94%).
1936-0851
Kang, GeoumYoung
04dc299b-b7b2-475d-8571-323eb12eafad
Carlson, Daniel W.
c0f88797-732c-46ef-8e74-a5186d4733bf
Kang, Tae Ho
65010772-634a-4b1e-8e59-3076e223a7c9
Lee, Seungki
56800d30-6ca7-4f75-be2d-0cb57db7e954
Haward, Simon J.
5693ac8d-5d84-4519-869f-9ba04077e160
Choi, Inhee
e5a6fe49-dd88-4823-983d-da3d1c5ca95c
Shen, Amy Q.
f04513a5-fedd-4759-958a-674855da2600
Chung, Aram J.
ceaf9aa3-a452-4b4c-92a3-5a809dbf3cde
Kang, GeoumYoung
04dc299b-b7b2-475d-8571-323eb12eafad
Carlson, Daniel W.
c0f88797-732c-46ef-8e74-a5186d4733bf
Kang, Tae Ho
65010772-634a-4b1e-8e59-3076e223a7c9
Lee, Seungki
56800d30-6ca7-4f75-be2d-0cb57db7e954
Haward, Simon J.
5693ac8d-5d84-4519-869f-9ba04077e160
Choi, Inhee
e5a6fe49-dd88-4823-983d-da3d1c5ca95c
Shen, Amy Q.
f04513a5-fedd-4759-958a-674855da2600
Chung, Aram J.
ceaf9aa3-a452-4b4c-92a3-5a809dbf3cde

Kang, GeoumYoung, Carlson, Daniel W., Kang, Tae Ho, Lee, Seungki, Haward, Simon J., Choi, Inhee, Shen, Amy Q. and Chung, Aram J. (2020) Intracellular nanomaterial delivery via spiral hydroporation. ACS Nano, 14 (3). (doi:10.1021/acsnano.9b07930).

Record type: Article

Abstract

In recent nanobiotechnology developments, a wide variety of functional nanomaterials and engineered biomolecules have been created, and these have numerous applications in cell biology. For these nanomaterials to fulfill their promises completely, they must be able to reach their biological targets at the subcellular level and with a high level of specificity. Traditionally, either nanocarrier- or membrane disruption-based method has been used to deliver nanomaterials inside cells; however, these methods are suboptimal due to their toxicity, inconsistent delivery, and low throughput, and they are also labor intensive and time-consuming, highlighting the need for development of a next-generation, intracellular delivery system. This study reports on the development of an intracellular nanomaterial delivery platform, based on unexpected cell-deformation phenomena via spiral vortex and vortex breakdown exerted in the cross- and T-junctions at moderate Reynolds numbers. These vortex-induced cell deformation and sequential restoration processes open cell membranes transiently, allowing effective and robust intracellular delivery of nanomaterials in a single step without the aid of carriers or external apparatus. By using the platform described here (termed spiral hydroporator), we demonstrate the delivery of different nanomaterials, including gold nanoparticles (200 nm diameter), functional mesoporous silica nanoparticles (150 nm diameter), dextran (hydrodynamic diameters between 2–55 nm), and mRNA, into different cell types. We demonstrate here that the system is highly efficient (up to 96.5%) with high throughput (up to 1 × 106 cells/min) and rapid delivery (∼1 min) while maintaining high levels of cell viability (up to 94%).

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More information

Accepted/In Press date: 12 February 2020
e-pub ahead of print date: 18 February 2020
Published date: 24 March 2020

Identifiers

Local EPrints ID: 507253
URI: http://eprints.soton.ac.uk/id/eprint/507253
ISSN: 1936-0851
PURE UUID: d894c880-b8f9-4504-9d7c-724065f601e2
ORCID for Daniel W. Carlson: ORCID iD orcid.org/0000-0002-0171-1934

Catalogue record

Date deposited: 02 Dec 2025 18:04
Last modified: 03 Dec 2025 03:06

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Contributors

Author: GeoumYoung Kang
Author: Daniel W. Carlson ORCID iD
Author: Tae Ho Kang
Author: Seungki Lee
Author: Simon J. Haward
Author: Inhee Choi
Author: Amy Q. Shen
Author: Aram J. Chung

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