In order to compare our data with those reported in the literature ( Baumgardner et al., 2002 and Shi et al., 2011), the AL300 sensor was also connected to a light intensity measurement system (USB 2000 spectrometer, Ocean Optics, Dunedin, FL, USA), interfaced to a computer through the A/D board. Data were recorded on a computer by means of a custom program (LabView, National Instruments, Austin, TX, USA). A flowing blood test system was used to generate rapid PO2PO2 oscillations in vitro  . Full technical details of this system Selleckchem Pexidartinib have been presented in this journal ( Chen et al., 2012b). Briefly, two standard medical paediatric oxygenators (Medos Hilite 1000LT,

Medos Medizintechnik AG, Stolberg, Germany) were arranged to provide two parallel and independent extracorporeal circuits, where blood PO2PO2 was maintained at 5 kPa (37 mmHg) or 50 kPa (375 mmHg), and PCO2PCO2 at 5 kPa (37 mmHg), and pH at 7.4. The PO2PO2 reference values were confirmed through blood gas analysis (ABL710, Radiometer, Copenhagen, Denmark) for sensor calibration purposes and for monitoring before each experiment.

Two peristaltic pumps maintained blood flow through the circuits. selleck chemicals In order to simulate body temperature in a pig, sheep or lamb animal model, and to record data that are comparable with the published literature, blood temperature was maintained at 39 °C by circulating temperature-controlled water (Grant Instruments, Cambridge, UK) through the two oxygenators. Blood temperature was continuously monitored with a

thermocouple (TES130, TES Electrical Electronic Corp., Taipei, Taiwan). Flow from either circuit was diverted alternately towards the sensor being tested by means of computer-controlled rapid switchover solenoid valves that exposed the sensor to abrupt blood PO2PO2 changes. The frequency of the switchover was controlled by a PC together with a digital to analogue board (National Instruments USB-6251, National Instruments, Austin, Tau-protein kinase TX, USA) and an electronic power switch, and was programmed to simulate RR of 10, 20, 30, 40, 50, and 60 bpm, with an inspired to expired (I:E) ratio of 1:1. For RR of 10 and 30 bpm, I:E ratios of 1:3 and 1:2, respectively were tested in order to investigate other clinically relevant conditions. Whole lambs’ blood (physiological temperature ∼39 °C) was collected from a local abattoir and heparinised immediately. Bench studies were conducted for a continuous period of 5 h. The PMMA in-house sensors were specifically tested over a 24 h period for anti-fouling properties in two separate non-heparinised in vivo animal studies. None of the sensors had any anticoagulant constituents embedded into their polymer materials ( Chen et al., 2012a and Chen et al., 2012b), and since the animals (pigs, weight circa 38 kg) were non-heparinised, these conditions presented a realistic challenge to the sensors. The in vivo experiments were performed at the Faculty of Medicine, Charles University, Pilsen, Czech Republic.