Sensitivity Optimization of Plain Silver Surface Plasmon Resonance Imaging Sensor

Plain silver surface plasmon resonance imaging (SPRi) sensor has been studied extensively due to its high sensitivity and desirable stability in liquid environments. To further enhance sensitivity performance of the sensor, angular sensitivity, angular slope and depth-width ratio (DWR) of SPR curve, and imaging sensitivity are evaluated at different thickness combinations of the gold and silver films respectively. In this work, the angular slope of SPR curve is found to be the critical factor to the optimized imaging sensitivity of plain silver SPRi sensor. In the comparative study, the above parameters of the plain silver SPR sensor, single gold film and bimetallic SPRi sensors are compared. Plain silver SPRi sensor is proved to be of the highest imaging sensitivity, which is 4.08 and 1.18 times imaging sensitivity of the single gold film and bimetallic SPRi sensors separately.

Dropwise Condensation Mechanism on Smooth Hydrophilic Surfaces

The objective of this work is to identify the mechanism of dropwise condensation on a smooth solid surface. We investigate the stable dropwise condensation that occurs at a droplet growth rate of 1 µm/s in diameter on a gold-coated glass surface. Additionally, we present our observations on unstable dropwise condensation, i.e., degradation of dropwise condensation of steam on a gold surface. Surface Plasmon Resonance Imaging (SPRi) is used to evaluate the existence and structure of thin films and occurrence of initial nuclei during condensation. SPRi approach used in this study has lateral resolutions of 4–10 µm, thickness resolutions of 0.1–1 nm, and temporal resolutions of 200–10,000 frames per second (FPS). Visualization of the onset of stable dropwise condensation suggests droplets form at heterogeneous nucleation sites and that no film greater than a monolayer exists on the surface before the formation of droplets. Observation of the unstable dropwise condensation of steam shows the existence of water films that are several nanometers thick between droplets. This work shows that neither the nucleation theory nor film rupture theory can individually explain the physics of dropwise condensation. Therefore, there is a need for a more comprehensive theory that can explain the mechanism of dropwise condensation.

Dropwise Condensation Mechanism on Smooth Hydrophilic Surfaces

The objective of this work is to identify the mechanism of dropwise condensation on a smooth solid surface. We investigate the stable dropwise condensation that occurs at a droplet growth rate of 1 µm/s in diameter on a gold-coated glass surface. Additionally, we present our observations on unstable dropwise condensation, i.e., degradation of dropwise condensation of steam on a gold surface. The Surface Plasmon Resonance Imaging (SPRi) approach used in this study has lateral resolutions of 4-10 µm, thickness resolutions of 0.1-1 nm, and temporal resolutions of 200-10,000 frames per second (FPS). SPRi is used to evaluate the existence and structure of thin films and occurrence of initial nuclei during condensation. Visualization of the onset of stable dropwise condensation suggests droplets form at heterogeneous nucleation sites and that no film greater than a monolayer exists on the surface before the formation of droplets. Observation of the unstable dropwise condensation of steam shows the existence of water films that are several nanometers thick between droplets. This work shows that neither the nucleation theory or film rupture theory can individually explain the physics of dropwise condensation. Therefore, there is a need for a more comprehensive theory that can explain the mechanism of dropwise condensation.

The determination of cystatin C in biological samples via the surface plasmon resonance method

Surface plasmon resonance imaging biosensors have a number of advantages that make them superior to other analytical methods. These include the possibility of label-free detection, speed and high sensitivity to low protein concentrations. The aim of this study was to create and analyze biochips, with the help of which it is possible to test cystatin C in patient urine samples and compare the results with the one-time traditional ELISA method. The main advantage of the surface plasmon resonance imaging method is the possibility of repeated measurements over a long period of time in accordance with clinical practice. The surface of the biochip was spotted with anticystatin C and a negative control of mouse IgG at a ratio of 1:1. The aforementioned biochip was first verified using standard tests and then with patient samples, which clearly confirmed the required sensitivity even for very low concentrations of cystatin C.