Platform for enhanced detection efficiency in luminescence-based sensors

Luminescence-based biochip measurement platforms are employed in a wide range of biological applications, such as biomedical diagnostics. Based on an understanding of the anisotropic emission properties of luminescence emitters close to a dielectric interface, a simple strategy for producing a better than 25-fold enhancement of the detected luminescence is presented. This strategy is demonstrated for low cost polymer platforms compatible with mass-production

Novel polymer platform for enhanced biochip performance

We report the development of enhanced optical platforms for fluorescence-based biosensors. A previous analysis by us has shown that the emission of fluorescence in such a system is highly anisotropic and is preferentially emitted into the substrate over a well-defined angular range, with the result that the light is guided along the substrate via total internal reflection. However, conventional optical biosensors based on fluorescence detection typically employ a detector that is positioned either directly above or directly below the biochip. As a consequence, only a small fraction of the total emitted fluorescence is detected, which impacts adversely on sensor performance. The enhanced biosensor presented here is based on a novel, generic platform specifically designed to overcome the inherent limitations of planar substrates. The platform incorporates custom-designed optical elements, the purpose of which is to redirect the emitted fluorescence onto a detector positioned beneath the biochip. Platforms were fabricated using the polymer processing technique of microinjection moulding. In this paper we demonstrate the ability of this optical system to achieve a 80-fold luminescence capture enhancement. We also demonstrate its effectiveness as an enhanced biosensor platform by carrying out a proof of principle BSA/antiBSA competitive assay. This work has significant implications for the development of mass-producible, highly efficient optical biosensors

Highly sensitive fluorescence detection on a biochip

A novel, generic lab-on-a-chip platform and associated readout instrumentation is presented. This high-sensitivity system has been developed for the efficient detection of surface-generated fluorescence in biomedical diagnostic applications. The proofof-principle polymer chip contains a 3×3 array of paraboloid elements designed to capture supercritical angle fluorescence (SAF) emitted from biorecognition zones on the top of each paraboloid. Each such element exhibits a fluorescence collection efficiency of 32%, comparable only to sophisticated microscope objectives of high numerical aperture. Furthermore, the chip optical design results in strict confinement of the fluorescence excitation to the surface. Consequently, this inexpensive chip combines the collecting power of modern microscopy optics with strong discrimination between surface and bulk fluorescence. The chip allows for simultaneous detection of 9 different targets (e.g. biomarkers) with very high sensitivity and also facilitates monitoring of receptor-ligand binding in real time. The chip is fabricated in the low fluorescence polymer Zeonor and is compatible with mass production via micro-injection moulding. The performance of the platform is demonstrated by application to a standard bioassay

Sol–gel based optical carbon dioxide sensor employing dual luminophore referencing for application in food packaging technology

An optical sensor for the measurement of carbon dioxide in Modified Atmosphere Packaging (MAP) applications has been developed. It is based on the fluorescent pH indicator 1-hydroxypyrene-3,6,8-trisulfonate (HPTS) immobilised in a hydrophobic organically modified silica (ormosil) matrix. Cetyltrimethylammonium hydroxide was used as an internal buffer system. Fluorescence is measured in the phase domain by means of the Dual Luminophore Referencing (DLR) sensing scheme which provides many of the advantages of lifetime-based fluorometric sensors and makes it compatible with established optical oxygen sensor technology. The long-term stability of the sensor membranes has been investigated. The sensor displays 13.5 degrees phase shift between 0 and 100% CO2 with a resolution of better than 1% and a limit of detection of 0.08%. Oxygen cross-sensitivity is minimised (0.6% quenching in air) by immobilising the reference luminophore in polymer nano-beads. Cross-sensitivity towards chloride and pH was found to be negligible. Temperature effects were studied, and a linear Arrhenius correlation between ln k and 1/T was found. The sensor is stable over a period of at least seven months and its output is in excellent agreement with a standard reference method for carbon dioxide analysis