Fabrication of a Biocompatible Liquid Crystal Graphene Oxide-Gold Nanorods Electro- and Photoactive Interface for Cell Stimulation.
Daniela DucPaul R StoddartSally L McArthurRobert M I KapsaAnita F QuigleyMitchell Boyd-MossSimon E MoultonPublished in: Advanced healthcare materials (2019)
For decades, electrode-tissue interfaces are pursued to establish electrical stimulation as a reliable means to control neuronal cells behavior. However, spreading of electrical currents in tissues limits its spatial precision. Thus, optical cues, such as near-infrared (NIR) light, are explored as alternatives. Presently, NIR stimulation requires higher energy input than electrical methods despite introduction of light absorbers, e.g., gold nanoparticles. As potential solution, NIR and electrical costimulation are proposed but with limited interfaces capable of sustaining this stimulation technique. Here, a novel electroactive nanocomposite with photoactive properties in the NIR range is constructed by N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride/N-hydroxysulfosuccinimide sodium (EDC)/NHS conjugation of liquid crystal graphene oxide (LCGO) to protein-coated gold nanorods (AuNR). The liquid crystal graphene oxide-gold nanorod nanocomposite (LCGO-AuNR) is fabricated into a hydrophilic electrode-coating via drop-casting, making it appropriate for versatile electrode-tissue interface fabrication. UV-vis spectrophotometry results demonstrate that LCGO-AuNR presents an absorbance peak at 798 nm (NIR range). Cyclic voltammetry measurements further confirm its electroactive capacitive properties. Furthermore, LCGO-AuNR coating supports cell adhesion, proliferation, and differentiation of NG108-15 neuronal cells. This biocompatible interface is anticipated, with ideal electrical and optical properties for NIR and electrical costimulation, to enable further development of the technique for energy-efficient and precise neuronal cell modulation.
Keyphrases
- drug release
- photodynamic therapy
- fluorescence imaging
- fluorescent probe
- induced apoptosis
- reduced graphene oxide
- drug delivery
- carbon nanotubes
- cell adhesion
- cell cycle arrest
- single cell
- quantum dots
- signaling pathway
- gene expression
- cell therapy
- spinal cord injury
- endoplasmic reticulum stress
- cerebral ischemia
- solid phase extraction
- high speed
- brain injury
- gold nanoparticles
- binding protein
- bone marrow
- small molecule
- cell death
- low cost
- highly efficient