Mid-infrared dual-comb spectroscopy with absolute frequency calibration using a passive optical reference.

We demonstrate an absolute-frequency-calibrated mid-infrared dual-comb spectrometer by using a reference absorption cell. The source is based on a singly-resonant OPO containing two MgO:PPLN crystals in a common ring cavity, synchronously pumped by two mode-locked Yb-fiber lasers. The repetition-rate of the two pumps are stabilized while their offset frequencies and the OPO cavity length are not actively controlled. The reference spectrum is used to correct the frequency fluctuations in the sample spectrum providing a high-quality averaged spectrum with spectral resolution of 6 GHz and calibration precision of 120 MHz, without adding any complexity to the experimental setup or signal processing.

External cavity diode laser-based detection of trace gases with NICE-OHMS using current modulation.

We combine an external cavity diode laser with noise-immune cavity-enhanced optical heterodyne molecular spectroscopy (NICE-OHMS) using current modulation. With a finesse of 1600, we demonstrate noise equivalent absorption sensitivities of 4.1 x 10(-10) cm(-1) Hz(-1/2), resulting in sub-ppbv detection limits for Doppler-broadened transitions of CH(4) at 6132.3 cm(-1), C(2)H(2) at 6578.5 cm(-1) and HCN at 6541.7 cm(-1). The system is used for hydrogen cyanide detection from sweet almonds.

Sensitivity enhancement in off-axis integrated cavity output spectroscopy.

We report on a detailed model of an improved three mirror off-axis integrated cavity output spectroscopy (OA-ICOS) setup, which re-injects the light reflected by the optical cavity. The model simulates the impact of design parameters on instrument sensitivity and can be used for any off-axis configuration. We demonstrate the application of this model for the real-time detection of ethylene with a pulsed quantum cascade laser (QCL). The three mirror OA-ICOS scheme provides a 10 times increase in signal-to-noise ratio as compared to standard OA-ICOS, resulting in a noise equivalent absorption sensitivity of 1.5 x 10(-8) cm(-1) Hz(-1/2).

Pulmonary infection, and not systemic inflammation, accounts for increased concentrations of exhaled nitric oxide in patients with septic shock.

Nitric oxide (NO) is a key mediator in the pathophysiology of septic shock that can be measured in exhaled breath. To assess whether a pulmonary infection itself or systemic inflammation is responsible for NO production, we determined exhaled NO in ventilated patients with respiratory and non-respiratory septic shock and compared it with the concentration in ventilated intensive care patients without systemic inflammation. In addition, the change of NO production over time and correlations with haemodynamic instability were evaluated. The controls without systemic inflammation, as witnessed by the absence of systemic inflammatory response syndrome criteria and low levels of interleukin-6, had similar concentrations of NO as the patients with non-respiratory septic shock. The respiratory sepsis patients exhaled more NO than the non-respiratory sepsis patients (p = 0.05), and a time dependent decline in time in both groups (p = 0.04). Exhaled NO did not correlate with markers of disease severity, systemic inflammation and haemodynamic instability. These data indicate that the infected lungs are the source of exhaled NO.

Methods of NO detection in exhaled breath.

There is still an unexplored potential for exhaled nitric oxide (NO) in many clinical applications. This study presents an overview of the currently available methods for monitoring NO in exhaled breath and the use of the modelling of NO production and transport in the lung in clinical practice. Three technologies are described, namely chemiluminescence, electrochemical sensing and laser-based detection with their advantages and limitations. Comparisons are made in terms of sensitivity, time response, size, costs and suitability for clinical purposes. The importance of the flow rate for NO sampling is discussed from the perspective of the recent recommendations for standardized procedures for online and offline NO measurement. The measurement of NO at one flow rate, such as 50 ml s(-1), can neither determine the alveolar site/peripheral contribution nor quantify the difference in NO diffusion from the airways walls. The use of NO modelling (linear or non-linear approach) can solve this problem and provide useful information about the source of NO. This is of great value in diagnostic procedures of respiratory diseases and in treatment with anti-inflammatory drugs.

Infrared frequency combs and supercontinua for multiplex high sensitivity spectroscopy.

An infrared high-brightness light source based on supercontinuum generation through a SF6 photonic crystal fiber seeded by a Cr(4+):YAG femtosecond oscillator is developed for high resolution multiplex spectroscopy in the 1.5 µm region. Moreover, a multiplex high resolution approach based on a Cr(4+):YAG frequency comb enables to probe large spectral domains, with simultaneous sensitive measurement of the absorption and the dispersion associated with all individual spectral features.

Sensitive multiplex spectroscopy in the molecular fingerprint 2.4 mum region with a Cr(2+):ZnSe femtosecond laser.

An ultrashort-pulse Cr(2+):ZnSe laser is a novel broadband source for sensitive high resolution molecular spectroscopy. A 130-fs pulse allows covering of up to 380 cm(-1) spectral domain around 2.4 mum which is analyzed simultaneously with a 0.12 cm(-1) (3.6 GHz) resolution by a Fouriertransform spectrometer. Recorded in 13 s, from 70-cm length absorption around 4150 cm(-1), acetylene and ammonia spectra exhibit a 3800 signal-tonoise ratio and a 2.4.10(-7) cm(-1).Hz(-1/2) noise equivalent absorption coefficient at one second averaging per spectral element, suggesting a 0.2 ppbv detection level for HF molecule. With the widely practiced classical tungsten lamp source instead of the laser, identical spectra would have taken more than one hour.