A bottom-up approach was the key to the successful fabrication of this memory. This approach both minimized the number of processing steps following deposition of the molecular monolayer, as well as protected the molecules from remaining processing steps. In the following paragraphs, we briefly describe the nanofabrication procedures utilized to construct the memory circuit. A full paper describing these procedures in more detail will be submitted for publication in the near future. form an array of top Ti NW electrodes, and the crossbar structure is complete.
The quantitative, real time detection of single stranded oligonucleotides with silicon nanowires (SiNWs) in physiologically relevant electrolyte solution is demonstrated. Debye screening of the hybridization event is minimized by utilizing electrostatically adsorbed primary DNA on an amine-terminated NW surface. Two surface functionalization chemistries are compared: an amine terminated siloxane monolayer on the native SiO 2 surface of the SiNW, and an amine terminated alkyl monolayer grown directly on a hydrogen-terminated SiNW surface. The SiNWs without the native oxide exhibit improved solution-gated field-effect transistor characteristics and a significantly enhanced sensitivity to single stranded DNA detection, with an accompanying two orders of magnitude improvement in the dynamic range of sensing. A model for the detection of analyte by SiNW sensors is developed and utilized to extract DNA binding kinetic parameters. Those values are directly compared with values obtained by the standard method of surface plasmon resonance (SPR), and demonstrated to be similar. The nanowires, however, are characterized by higher detection sensitivity. The implication is that Si NWs can be utilized to quantitate the solution phase concentration of biomolecules at low concentrations. This work also demonstrates the importance of surface chemistry for optimizing biomolecular sensing with silicon nanowires.
Microreactor technology has shown potential for optimizing synthetic efficiency, particularly in preparing sensitive compounds. We achieved the synthesis of an [
18
F]fluoride-radiolabeled molecular imaging probe, 2-deoxy-2-[
18
F]fluoro-
d
-glucose ([
18
F]FDG), in an integrated microfluidic device. Five sequential processes—[
18
F]fluoride concentration, water evaporation, radiofluorination, solvent exchange, and hydrolytic deprotection—proceeded with high radio-chemical yield and purity and with shorter synthesis time relative to conventional automated synthesis. Multiple doses of [
18
F]FDG for positron emission tomography imaging studies in mice were prepared. These results, which constitute a proof of principle for automated multistep syntheses at the nanogram to microgram scale, could be generalized to a range of radiolabeled substrates.
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