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Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator

BACKGROUND: Controllable and multiple DNA release is critical in modern gene-based therapies. Current approaches require complex assistant molecules for combined release. To overcome the restrictions on the materials and environment, a novel and versatile DNA release method using a nano-electromecha...

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Autores principales: Guo, Xinyi, Zhang, Hongxiang, Wang, Yanyan, Pang, Wei, Duan, Xuexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683436/
https://www.ncbi.nlm.nih.gov/pubmed/31387581
http://dx.doi.org/10.1186/s12951-019-0518-7
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author Guo, Xinyi
Zhang, Hongxiang
Wang, Yanyan
Pang, Wei
Duan, Xuexin
author_facet Guo, Xinyi
Zhang, Hongxiang
Wang, Yanyan
Pang, Wei
Duan, Xuexin
author_sort Guo, Xinyi
collection PubMed
description BACKGROUND: Controllable and multiple DNA release is critical in modern gene-based therapies. Current approaches require complex assistant molecules for combined release. To overcome the restrictions on the materials and environment, a novel and versatile DNA release method using a nano-electromechanical (NEMS) hypersonic resonator of gigahertz (GHz) frequency is developed. RESULTS: The micro-vortexes excited by ultra-high frequency acoustic wave can generate tunable shear stress at solid–liquid interface, thereby disrupting molecular interactions in immobilized multilayered polyelectrolyte thin films and releasing embedded DNA strands in a controlled fashion. Both finite element model analysis and experiment results verify the feasibility of this method. The release rate and released amount are confirmed to be well tuned. Owing to the different forces generated at different depth of the films, release of two types of DNA molecules with different velocities is achieved, which further explores its application in combined gene therapy. CONCLUSIONS: Our research confirmed that this novel platform based on a nano-electromechanical hypersonic resonator works well for controllable single and multi-DNA release. In addition, the unique features of this resonator such as miniaturization and batch manufacturing open its possibility to be developed into a high-throughput, implantable and site targeting DNA release and delivery system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0518-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-66834362019-08-09 Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator Guo, Xinyi Zhang, Hongxiang Wang, Yanyan Pang, Wei Duan, Xuexin J Nanobiotechnology Research BACKGROUND: Controllable and multiple DNA release is critical in modern gene-based therapies. Current approaches require complex assistant molecules for combined release. To overcome the restrictions on the materials and environment, a novel and versatile DNA release method using a nano-electromechanical (NEMS) hypersonic resonator of gigahertz (GHz) frequency is developed. RESULTS: The micro-vortexes excited by ultra-high frequency acoustic wave can generate tunable shear stress at solid–liquid interface, thereby disrupting molecular interactions in immobilized multilayered polyelectrolyte thin films and releasing embedded DNA strands in a controlled fashion. Both finite element model analysis and experiment results verify the feasibility of this method. The release rate and released amount are confirmed to be well tuned. Owing to the different forces generated at different depth of the films, release of two types of DNA molecules with different velocities is achieved, which further explores its application in combined gene therapy. CONCLUSIONS: Our research confirmed that this novel platform based on a nano-electromechanical hypersonic resonator works well for controllable single and multi-DNA release. In addition, the unique features of this resonator such as miniaturization and batch manufacturing open its possibility to be developed into a high-throughput, implantable and site targeting DNA release and delivery system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0518-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-06 /pmc/articles/PMC6683436/ /pubmed/31387581 http://dx.doi.org/10.1186/s12951-019-0518-7 Text en © The Author(s) 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Guo, Xinyi
Zhang, Hongxiang
Wang, Yanyan
Pang, Wei
Duan, Xuexin
Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
title Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
title_full Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
title_fullStr Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
title_full_unstemmed Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
title_short Programmable multi-DNA release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
title_sort programmable multi-dna release from multilayered polyelectrolytes using gigahertz nano-electromechanical resonator
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683436/
https://www.ncbi.nlm.nih.gov/pubmed/31387581
http://dx.doi.org/10.1186/s12951-019-0518-7
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