Theoretical analysis of the characteristic impedance in metal-insulator-metal plasmonic transmission lines.

We propose a closed form formulation for the impedance of the metal-insulator-metal (MIM) plasmonic transmission lines by solving the Maxwell's equations. We provide approximations for thin and thick insulator layers sandwiched between metallic layers. In the case of very thin dielectric layer, the surface waves on both interfaces are strongly coupled resulting in an almost linear dependence of the impedance of the plasmonic transmission line on the thickness of the insulator layer. On the other hand, for very thick insulator layer, the impedance does not vary with the insulator layer thickness due to the weak-coupling/decoupling of the surface waves on each metal-insulator interface. We demonstrate the effectiveness of our proposed formulation using two test scenarios, namely, almost zero reflection in T-junction and reflection from line discontinuity in the design of Bragg reflectors, where we compare our formulation against previously published results.

A fluorescence sandwich immunoassay for the real-time continuous detection of glucose and insulin in live animals.

Biosensors that continuously measure circulating biomolecules in real time could provide insights into the health status of patients and their response to therapeutics. But biosensors for the continuous real-time monitoring of analytes in vivo have only reached nanomolar sensitivity and can measure only a handful of molecules, such as glucose and blood oxygen. Here we show that multiple analytes can be continuously and simultaneously measured with picomolar sensitivity and sub-second resolution via the integration of aptamers and antibodies into a bead-based fluorescence sandwich immunoassay implemented in a custom microfluidic chip. After an incubation time of 30 s, bead fluorescence is measured using a high-speed camera under spatially multiplexed two-colour laser illumination. We used the assay for continuous quantification of glucose and insulin concentrations in the blood of live diabetic rats to resolve inter-animal differences in the pharmacokinetic response to insulin as well as discriminate pharmacokinetic profiles from different insulin formulations. The assay can be readily modified to continuously and simultaneously measure other blood analytes in vivo.