Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly

[Image: see text] A process for 3D programmed self-assembly of lithographically printable microscale polymer particles using ssDNA hybridization as the associative force is described. We report our progress in establishing the unit processes required for 3D programmed self-assembly and demonstrate t...

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Autores principales: Deschner, Ryan, Tang, Hao, Allen, Peter, Hall, Cecilia, Hlis, Rocco, Ellington, Andrew, Willson, C. Grant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985930/
https://www.ncbi.nlm.nih.gov/pubmed/24803723
http://dx.doi.org/10.1021/cm403637v
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author Deschner, Ryan
Tang, Hao
Allen, Peter
Hall, Cecilia
Hlis, Rocco
Ellington, Andrew
Willson, C. Grant
author_facet Deschner, Ryan
Tang, Hao
Allen, Peter
Hall, Cecilia
Hlis, Rocco
Ellington, Andrew
Willson, C. Grant
author_sort Deschner, Ryan
collection PubMed
description [Image: see text] A process for 3D programmed self-assembly of lithographically printable microscale polymer particles using ssDNA hybridization as the associative force is described. We report our progress in establishing the unit processes required for 3D programmed self-assembly and demonstrate the successful fabrication and sequence-specific self-assembly of covalent ssDNA-functionalized parallelepipeds with dimensions in the sub 10 μm regime characterized by optical microscopy and imaging flow cytometry. This technology has the potential to produce parallelepiped particles with different ssDNA on each facet.
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spelling pubmed-39859302015-01-13 Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly Deschner, Ryan Tang, Hao Allen, Peter Hall, Cecilia Hlis, Rocco Ellington, Andrew Willson, C. Grant Chem Mater [Image: see text] A process for 3D programmed self-assembly of lithographically printable microscale polymer particles using ssDNA hybridization as the associative force is described. We report our progress in establishing the unit processes required for 3D programmed self-assembly and demonstrate the successful fabrication and sequence-specific self-assembly of covalent ssDNA-functionalized parallelepipeds with dimensions in the sub 10 μm regime characterized by optical microscopy and imaging flow cytometry. This technology has the potential to produce parallelepiped particles with different ssDNA on each facet. American Chemical Society 2014-01-13 2014-02-11 /pmc/articles/PMC3985930/ /pubmed/24803723 http://dx.doi.org/10.1021/cm403637v Text en Copyright © 2014 American Chemical Society
spellingShingle Deschner, Ryan
Tang, Hao
Allen, Peter
Hall, Cecilia
Hlis, Rocco
Ellington, Andrew
Willson, C. Grant
Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly
title Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly
title_full Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly
title_fullStr Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly
title_full_unstemmed Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly
title_short Progress Report on the Generation of Polyfunctional Microscale Particles for Programmed Self-Assembly
title_sort progress report on the generation of polyfunctional microscale particles for programmed self-assembly
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985930/
https://www.ncbi.nlm.nih.gov/pubmed/24803723
http://dx.doi.org/10.1021/cm403637v
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