Sarunya Bangsaruntip

Novel nanomaterials for bioassay applications represent a rapidly progressing field of nanotechnology and nanobiotechnology. Here, we present an exploration of single-walled carbon nanotubes as a platform for investigating surface-protein and protein-protein binding and developing highly specific electronic biomolecule detectors. Nonspecific binding on nanotubes, a phenomenon found with a wide range of proteins, is overcome by immobilization of polyethylene oxide chains. A general approach is then advanced to enable the selective recognition and binding of target proteins by conjugation of their specific receptors to polyethylene oxide-functionalized nanotubes. This scheme, combined with the sensitivity of nanotube electronic devices, enables highly specific electronic sensors for detecting clinically important biomolecules such as antibodies associated with human autoimmune diseases.

Nanotube/nanoparticle hybrid structures are prepared by forming Au and Pt nanoparticles on the sidewalls of single-walled carbon nanotubes. Reducing agent or catalyst-free electroless deposition, which purely utilizes the redox potential difference between Au3+, Pt2+, and the carbon nanotube, is the main driving force for this reaction. It is also shown that carbon nanotubes act as a template for wire-like metal structures. The successful formation of the hybrid structures is monitored by atomic force microscopy (AFM) and electrical measurements.

Metallic and semiconducting carbon nanotubes generally coexist in as-grown materials. We present a gas-phase plasma hydrocarbonation reaction to selectively etch and gasify metallic nanotubes, retaining the semiconducting nanotubes in near-pristine form. With this process, 100% of purely semiconducting nanotubes were obtained and connected in parallel for high-current transistors. The diameter- and metallicity-dependent "dry" chemical etching approach is scalable and compatible with existing semiconductor processing for future integrated circuits.

It has been reported that protein adsorption on single-walled carbon nanotube field effect transistors (FETs) leads to appreciable changes in the electrical conductance of the devices, a phenomenon that can be exploited for label-free detection of biomolecules with a high potential for miniaturization. This work presents an elucidation of the electronic biosensing mechanisms with a newly developed microarray of nanotube "micromat" sensors. Chemical functionalization schemes are devised to block selected components of the devices from protein adsorption, self-assembled monolayers (SAMs) of methoxy(poly(ethylene glycol))thiol (mPEG-SH) on the metal electrodes (Au, Pd) and PEG-containing surfactants on the nanotubes. Extensive characterization reveals that electronic effects occurring at the metal-nanotube contacts due to protein adsorption constitute a more significant contribution to the electronic biosensing signal than adsorption solely along the exposed lengths of the nanotubes.

We report the use of fluorescein−polyethylene glycol (Fluor-PEG) to noncovalently functionalize single-walled carbon nanotubes (SWNTs) for obtaining water-soluble nanotube conjugates (Fluor-PEG/SWNT) and simultaneously affording fluorescence labels to nanotubes. We find serendipitously that fluorescein, a widely used fluorophore, can strongly adsorb onto the sidewall of the SWNTs, likely via π-stacking, and the hydrophilic PEG chain imparts high aqueous solubility. Interaction between fluorescein and SWNT is pH dependent; it weakens as the pH is increased, causing the Fluor-PEG/SWNT conjugate to be less stable at high pHs. Fluorescein molecules bound to SWNTs exhibit interesting pH-dependent optical absorbance and fluorescence properties that are distinct from free molecules, as a result of pH-dependent interactions with SWNT sidewalls. Fluorescence emission from fluorescein adsorbed on SWNT is quenched by ∼67%, but remains sufficient and useful as a fluorescent label. The utility of Fluor-PEG/SWNT as a simultaneous fluorescent marker and an intracellular transporter is demonstrated by uptake of Fluor-PEG/SWNT by mammalian cells and detection of fluorescence inside the cells. Raman detection of SWNTs in the cells is also carried out and used to prove the co-localization of fluorescein and SWNT.