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Gene delivery with nanofibrous scaffolds

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

Extracellular and intracellular barriers typically prevent non-viral gene vectors from having an effective transfection efficiency. Formulation of a gene delivery vehicle that can overcome the barriers is a key step for successful tissue regeneration. We have developed a novel core-shelled DNA nanoparticle by invoking solvent-induced condensation of plasmid DNA (β-galactosidase or GFP) in a solvent mixture (94% DMF + 6% 1xTE buffer) and subsequent encapsulation of the condensed DNA globule in a triblock copolymer, polylactide-poly(ethylene glycol)-polylactide (L8E78L 8), in the same solvent environment. The polylactide shell protects the encapsulated DNA from degradation during electrospinning of a mixture of encapsulated DNA nanoparticles and biodegradable PLGA (a random copolymer of lactide and glycolide) to form a nanofibrous non-woven scaffold using the same solution mixture. The bioactive plasmid DNA can then be released in an intact form from the scaffold with a controlled release rate and transfect cells in vitro.

Original languageEnglish
Title of host publicationICAFPM 2009 - Proceedings of 2009 International Conference on Advanced Fibers and Polymer Materials
PublisherChemical Industry Press
Pages554-558
Number of pages5
ISBN (Print)9787122067876
StatePublished - 2009
Event2009 International Conference on Advanced Fibers and Polymer Materials, ICAFPM 2009 - Shanghai, China
Duration: Oct 21 2009Oct 24 2009

Publication series

NameICAFPM 2009 - Proceedings of 2009 International Conference on Advanced Fibers and Polymer Materials
Volume1

Conference

Conference2009 International Conference on Advanced Fibers and Polymer Materials, ICAFPM 2009
Country/TerritoryChina
CityShanghai
Period10/21/0910/24/09

Keywords

  • Electrospinning
  • Gene delivery
  • Light scattering
  • Nanofiber
  • Non-viral

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