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Continuous glucose monitoring enables an improved disease management for people with diabetes. However, state-of-the-art, enzyme-based, minimally invasive sensors lose their sensitivity over time and have to be replaced periodically. Here, we present the in vitro investigation of a quantum cascade laser-based measurement scheme that conceptually should be applicable over elongated periods of time due to its reagent-free nature and may therefore be considered as an approach towards long-term implantation. The method uses a miniaturized optofluidic interface in transflection geometry to measure the characteristic mid-infrared absorption properties of glucose. A glucose sensitivity of 3.2 mg dL-1 is achieved in aqueous glucose solutions. While this sensitivity drops to 12 mg dL-1 in the presence of biologically plausible, maximum concentrations of other monosaccharides, it is still well within the medically acceptable range according to Parkes error grid analysis. With a response time of less than five minutes, our sensor should be able to react adequately fast to physiological changes in glucose concentration. Finally, no drift or deterioration was found during an extended, 42 days in vitro experiment. These results underline the potential of this technique for its conceivable applicability in vivo as a long-term glucose monitoring implant.

A laser's high degree of coherence leads to interferences, which-in the absence of precautions-can cause severe image distortions such as fringes and speckles and which thereby strongly hamper a meaningful interpretation of hyperspectral images in laser-based widefield microspectroscopy. While images and spectra of homogenous samples may already suffer from interferences, any structured object such as a tissue thin section will add to these distortions due to wavelength- and, in particular, sample-dependent phase shifts (structure sizes, absorption coefficients, refractive indices). This effect is devastating for the universal applicability of laser-based microspectroscopy especially in the mid-infrared (MIR), where cell sizes are of the same dimension as the wavelength of the illumination source. Here, we show that the impact of interferences is strongly mitigated by reducing the time-averaged spatiotemporal coherence properties of the illumination using a moving plus a stationary scatterer. In this case, the illumination path provides a pseudothermal radiation source and spatially resolved spectra can be obtained at the quality of the reference method, that is, Fourier-transform infrared microspectroscopy, without compromising spectral or spatial resolution., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Today's minimally invasive biosensors are often based on chemical reagents and suffer from, e.g., oxygen dependence, toxic reaction products, excess analyte consumption, and/or degradation of the reagents. Here, we show the first successful analyte quantification by means of a minimally invasive sensor in vivo, which does not use chemical reactions. The concentration of glucose is determined continuously in vivo using transcutaneous, fiber-based mid-infrared laser spectroscopy. When comparing the infrared data measured in vivo with the 127 reference readings of glucose obtained in vitro, an overall standard deviation of 17.5% and a median of the absolute values of the relative deviations of 11.0% are achieved. The encouraging results open up the path toward a reagent-free long-term implant for the continuous surveillance of metabolites. In addition, the high sampling rate facilitates important research in body metabolism as well as its application outside the field of medicine such as real-time analyte sensing during fermentation.

Infrared vibrations of molecular species can be enhanced by several orders of magnitude with plasmonic nanoantennas. Based on the confined electromagnetic near-fields of resonantly excited metal nanoparticles, this antenna-assisted surface-enhanced infrared spectroscopy enables the detection of minute amounts of analytes localized in the nanometer-scale vicinity of the structure. Among other important parameters, the distance of the vibrational oscillator of the analyte to the nanoantenna surface determines the signal enhancement. For sensing applications, this is a particularly important issue since the vibrating dipoles of interest may be located far away from the antenna surface because of functional layers and the large size of biomolecules, proteins, or bacteria. The relation between distance and signal enhancement is thus of paramount importance and measured here with in situ infrared spectroscopy during the growth of a probe layer. Our results indicate a diminishing signal enhancement and the effective saturation of the plasmonic resonance shift beyond 100 nm. The experiments carried out under ultra-high-vacuum conditions are supported by numerical calculations.

In this article we show that linear nanoantennas can be used as shared substrates for surface-enhanced Raman and infrared spectroscopy (SERS and SEIRS, respectively). This is done by engineering the plasmonic properties of the nanoantennas, so to make them resonant in both the visible (transversal resonance) and the infrared (longitudinal resonance), and by rotating the excitation field polarization to selectively take advantage of each resonance and achieve SERS and SEIRS on the same nanoantennas. As a proof of concept, we have fabricated gold nanoantennas by electron beam lithography on calcium difluoride (1-2 μm long, 60 nm wide, 60 nm high) that exhibit a transverse plasmonic resonance in the visible (640 nm) and a particularly strong longitudinal dipolar resonance in the infrared (tunable in the 1280-3100 cm(-1) energy range as a function of the length). SERS and SEIRS detection of methylene blue molecules adsorbed on the nanoantenna's surface is accomplished, with signal enhancement factors of 5×10(2) for SERS (electromagnetic enhancement) and up to 10(5) for SEIRS. Notably, we find that the field enhancement provided by the transverse resonance is sufficient to achieve SERS from single nanoantennas. Furthermore, we show that by properly tuning the nanoantenna length the signals of a multitude of vibrational modes can be enhanced with SEIRS. This simple concept of plasmonic nanosensor is highly suitable for integration on lab-on-a-chip schemes for label-free chemical and biomolecular identification with optimized performances.

The continuous surveillance of glucose concentration reduces short-term risks and long-term complications for people with diabetes mellitus, a disorder of glucose metabolism. As a first step towards the continuous monitoring of glucose, reagent-free transmission spectroscopy in the mid-infrared region has been carried out in vitro using a quantum cascade laser and an optical silver halide fiber. A 30 μm gap in the fiber allowed for transmission spectroscopy of aqueous glucose solutions at a wavelength of 9.69 μm, which is specific to a molecular vibration of glucose. A noise-equivalent concentration as low as 4 mg/dL was achieved at an average power of 1.8 mW and an integration time of 50 s. This is among the most precise of glucose measurements using mid-infrared spectroscopy. Even with the very low average laser power of 0.07 mW the sensitivity of previous results (using a fiber optical evanescent field analysis) has been improved upon by almost one order of magnitude. Finally, the impact of potentially interfering substances such as other carbohydrates was analyzed., (This journal is © The Royal Society of Chemistry 2011)

A novel resonant mechanism involving the interference of a broadband plasmon with the narrowband vibration from molecules is presented. With the use of this concept, we demonstrate experimentally the enormous enhancement of the vibrational signals from less than one attomol of molecules on individual gold nanowires, tailored to act as plasmonic nanoantennas in the infrared. By detuning the resonance via a change in the antenna length, a Fano-type behavior of the spectral signal is observed, which is clearly supported by full electrodynamical calculations. This resonant mechanism can be a new paradigm for sensitive infrared identification of molecular groups.