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1.
Article in English | MEDLINE | ID: mdl-29132023

ABSTRACT

The determination of regional blood flow via the accumulation of fluorescent microspheres is a concept regularly used in medical research. Typically, the microbeads get extracted from the tissue of interest and are then quantified by measuring the absorption or fluorescence of the incorporated dyes without further separation from the medium. However, in that case the absorption spectra of different dyes can overlap when used simultaneously, leading to an overestimation of the concentration. Additionally, background absorption from the medium can be problematic. Therefore, a high performance liquid chromatography method for the simultaneous detection of four dyes (orange, crimson, yellow-green and red) incorporated in different microbeads in samples from biological media such as organ tissue (brain, heart and kidneys) was developed. Since for biological samples often a large sample size is required for sufficient statistics, the method was optimized to yield very short run times. With this method it was possible to detect very low concentrations of only one microsphere per gram of organ tissue. By applying this sensitive quantification technique, it was demonstrated that the application of microbeads for perfusion measurements might not be reliable due to different organ distributions in each animal.


Subject(s)
Chromatography, High Pressure Liquid/methods , Fluorescent Dyes/analysis , Animals , Brain/metabolism , Fluorescent Dyes/pharmacokinetics , Kidney/metabolism , Limit of Detection , Linear Models , Male , Microspheres , Myocardium/metabolism , Regional Blood Flow , Swine , Tissue Distribution
2.
Anaesthesia ; 70(10): 1171-9, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26179167

ABSTRACT

Novel devices for small-lumen ventilation may enable effective inspiration and expiratory ventilation assistance despite airway obstruction. In this study, we investigated a porcine model of complete upper airway obstruction. After ethical approval, we randomly assigned 13 anaesthetised pigs either to small-lumen ventilation following airway obstruction (n = 8) for 30 min, or to volume-controlled ventilation (sham setting, n = 5). Small-lumen ventilation enabled adequate gas exchange over 30 min. One animal died as a result of a tension pneumothorax in this setting. Redistribution of ventilation from dorsal to central compartments and significant impairment of the distribution of ventilation/perfusion occurred. Histopathology demonstrated considerable lung injury, predominantly through differences in the dorsal dependent lung regions. Small-lumen ventilation maintained adequate gas exchange in a porcine airway obstruction model. The use of this technique for 30 min by inexperienced clinicians was associated with considerable end-expiratory collapse leading to lung injury, and may also carry the risk of severe injury.


Subject(s)
Airway Obstruction/therapy , Respiration, Artificial/methods , Acute Lung Injury/etiology , Airway Obstruction/blood , Airway Obstruction/physiopathology , Animals , Disease Models, Animal , Hemodynamics/physiology , Male , Oxygen/blood , Partial Pressure , Pulmonary Gas Exchange/physiology , Respiration, Artificial/adverse effects , Sus scrofa , Tidal Volume/physiology , Tracheotomy/methods
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