Engineering substrate-mediated gene delivery with self-assembled monolayers

Angela K. Pannier, Lonnie D. Shea

Research output: Contribution to conferencePaper

Abstract

Gene transfer has many potential applications in basic and applied sciences, including functional genomics, gene therapy, and tissue engineering. Substrate-mediated delivery, also termed solid phase delivery, describes the immobilization of DNA, complexed with nonviral vectors, to a biomaterial or substrate that supports cell adhesion. A critical component to this process is designing the appropriate interactions between the DNA complexes and substrate. The objective of this study was to investigate gene transfer as a function of i) complex formation and deposition conditions and ii) non-specific and specific binding interactions between the complexes and substrate. The volume and time of complex formation, and incubation time and volume were investigated for their effects on transfection efficiency. While nonspecific immobilization strategies have been used to enhance transfection in vitro, translating the substrate-mediated delivery approach to biomaterials for in vivo applications requires that the complexes be more effectively retained at the biomaterial surface. Self-assembled monolayers (SAMs) of alkanethiols on gold were used to study the mechanisms of transfection by complexes nonspecifically immobilized on chemically specific substrates, to determine appropriate biomaterial surface properties for efficient gene delivery. Surface hydrophilicity and ionization were found to mediate both immobilization and transfection. Furthermore, the ability of specifically tethered complexes to mediate transfection was investigated. DNA, complexed with polyethylenimine (PEI), was covalently linked to SAMs presenting appropriate functional groups through a fraction of the functional groups available on the PEI present in the complex. Complexes were directly coupled to the SAMs through degradable and non-degradable tethers. Covalently tethered complexes provide an approach to retain the complexes at the surface, particularly following exposure to serum. SAMs provide a versatile approach to identify covalent tethering strategies with the potential to be translated to biomaterial surfaces for use in tissue engineering applications.

Original languageEnglish (US)
Number of pages1
StatePublished - Dec 1 2005
Event05AIChE: 2005 AIChE Annual Meeting and Fall Showcase - Cincinnati, OH, United States
Duration: Oct 30 2005Nov 4 2005

Conference

Conference05AIChE: 2005 AIChE Annual Meeting and Fall Showcase
CountryUnited States
CityCincinnati, OH
Period10/30/0511/4/05

Fingerprint

Self assembled monolayers
Biomaterials
Genes
Substrates
Gene transfer
DNA
Tissue engineering
Functional groups
Gene therapy
Cell adhesion
Hydrophilicity
Ionization
Surface properties
Gold

ASJC Scopus subject areas

  • Engineering(all)

Cite this

Pannier, A. K., & Shea, L. D. (2005). Engineering substrate-mediated gene delivery with self-assembled monolayers. Paper presented at 05AIChE: 2005 AIChE Annual Meeting and Fall Showcase, Cincinnati, OH, United States.

Engineering substrate-mediated gene delivery with self-assembled monolayers. / Pannier, Angela K.; Shea, Lonnie D.

2005. Paper presented at 05AIChE: 2005 AIChE Annual Meeting and Fall Showcase, Cincinnati, OH, United States.

Research output: Contribution to conferencePaper

Pannier, AK & Shea, LD 2005, 'Engineering substrate-mediated gene delivery with self-assembled monolayers', Paper presented at 05AIChE: 2005 AIChE Annual Meeting and Fall Showcase, Cincinnati, OH, United States, 10/30/05 - 11/4/05.
Pannier AK, Shea LD. Engineering substrate-mediated gene delivery with self-assembled monolayers. 2005. Paper presented at 05AIChE: 2005 AIChE Annual Meeting and Fall Showcase, Cincinnati, OH, United States.
Pannier, Angela K. ; Shea, Lonnie D. / Engineering substrate-mediated gene delivery with self-assembled monolayers. Paper presented at 05AIChE: 2005 AIChE Annual Meeting and Fall Showcase, Cincinnati, OH, United States.1 p.
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