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Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis

[Image: see text] Nonviral gene delivery holds great promise not just as a safer alternative to viral vectors in traditional gene therapy applications, but also for regenerative medicine, induction of pluripotency in somatic cells, and RNA interference for gene silencing. Although it continues to be...

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Autores principales: Beh, Cyrus W., Pan, Deng, Lee, Jason, Jiang, Xuan, Liu, Kelvin J., Mao, Hai-Quan, Wang, Tza-Huei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134141/
https://www.ncbi.nlm.nih.gov/pubmed/25054542
http://dx.doi.org/10.1021/nl5018404
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author Beh, Cyrus W.
Pan, Deng
Lee, Jason
Jiang, Xuan
Liu, Kelvin J.
Mao, Hai-Quan
Wang, Tza-Huei
author_facet Beh, Cyrus W.
Pan, Deng
Lee, Jason
Jiang, Xuan
Liu, Kelvin J.
Mao, Hai-Quan
Wang, Tza-Huei
author_sort Beh, Cyrus W.
collection PubMed
description [Image: see text] Nonviral gene delivery holds great promise not just as a safer alternative to viral vectors in traditional gene therapy applications, but also for regenerative medicine, induction of pluripotency in somatic cells, and RNA interference for gene silencing. Although it continues to be an active area of research, there remain many challenges to the rational design of vectors. Among these, the inability to characterize the composition of nanoparticles and its distribution has made it difficult to probe the mechanism of gene transfection process, since differences in the nanoparticle-mediated transfection exist even when the same vector is used. There is a lack of sensitive methods that allow for full characterization of DNA content in single nanoparticles and its distribution among particles in the same preparation. Here we report a novel spectroscopic approach that is capable of interrogating nanoparticles on a particle-by-particle basis. Using PEI/DNA and PEI-g-PEG/DNA nanoparticles as examples, we have shown that the distribution of DNA content among these nanoparticles was relatively narrow, with the average numbers of DNA of 4.8 and 6.7 per particle, respectively, in PEI/DNA and PEI-g-PEG/DNA nanoparticles. This analysis enables a more accurate description of DNA content in polycation/DNA nanoparticles. It paves the way toward comparative assessments of various types of gene carriers and provides insights into bridging the efficiency gap between viral and nonviral vehicles.
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spelling pubmed-41341412015-07-23 Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis Beh, Cyrus W. Pan, Deng Lee, Jason Jiang, Xuan Liu, Kelvin J. Mao, Hai-Quan Wang, Tza-Huei Nano Lett [Image: see text] Nonviral gene delivery holds great promise not just as a safer alternative to viral vectors in traditional gene therapy applications, but also for regenerative medicine, induction of pluripotency in somatic cells, and RNA interference for gene silencing. Although it continues to be an active area of research, there remain many challenges to the rational design of vectors. Among these, the inability to characterize the composition of nanoparticles and its distribution has made it difficult to probe the mechanism of gene transfection process, since differences in the nanoparticle-mediated transfection exist even when the same vector is used. There is a lack of sensitive methods that allow for full characterization of DNA content in single nanoparticles and its distribution among particles in the same preparation. Here we report a novel spectroscopic approach that is capable of interrogating nanoparticles on a particle-by-particle basis. Using PEI/DNA and PEI-g-PEG/DNA nanoparticles as examples, we have shown that the distribution of DNA content among these nanoparticles was relatively narrow, with the average numbers of DNA of 4.8 and 6.7 per particle, respectively, in PEI/DNA and PEI-g-PEG/DNA nanoparticles. This analysis enables a more accurate description of DNA content in polycation/DNA nanoparticles. It paves the way toward comparative assessments of various types of gene carriers and provides insights into bridging the efficiency gap between viral and nonviral vehicles. American Chemical Society 2014-07-23 2014-08-13 /pmc/articles/PMC4134141/ /pubmed/25054542 http://dx.doi.org/10.1021/nl5018404 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Beh, Cyrus W.
Pan, Deng
Lee, Jason
Jiang, Xuan
Liu, Kelvin J.
Mao, Hai-Quan
Wang, Tza-Huei
Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis
title Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis
title_full Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis
title_fullStr Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis
title_full_unstemmed Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis
title_short Direct Interrogation of DNA Content Distribution in Nanoparticles by a Novel Microfluidics-Based Single-Particle Analysis
title_sort direct interrogation of dna content distribution in nanoparticles by a novel microfluidics-based single-particle analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134141/
https://www.ncbi.nlm.nih.gov/pubmed/25054542
http://dx.doi.org/10.1021/nl5018404
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