Cornelia Wiegand | PubMed Health

PubMed2005

Influence of selected wound dressings on PMN elastase in chronic wound fluid and their antioxidative potential in vitro.

Exudates from non-healing wounds contain elevated levels of proteolytic enzymes, like elastase from polymorphonuclear granulocytes (PMN elastase), reactive oxygen species (ROS) and reactive nitrogen species (RNS). The overproduction of proteolytic enzymes leads to reduced concentrations of growth factors and proteinase inhibitors, resulting in an imbalance between degradation and remodelling processes. Thus, the reduction of protein-degrading enzymes and scavenging of ROS and RNS seem to be suitable ways to support the healing process of chronic stagnating wounds. The aim of this study was to test selected wound dressings from different biomaterials (collagen, oxidized regenerated cellulose (ORC) and ORC/collagen mixture), regarding their antioxidative potential in vitro and their influence on the concentration and activity of PMN elastase in chronic wound fluid. Antioxidant capacity of the investigated wound dressing was determined by a pholasin-based chemiluminescent assay. PMN elastase concentration was determined by means of ELISA. Enzyme activities could be measured by a fluorescence assay. As the presented data demonstrates, all tested materials showed antioxidant capacity. In addition, the investigated materials were able to reduce the concentration and activity of PMN elastase. Beside other aspects, such as biocompatibility, biodegradability, fluid absorption and clinical effects (e.g. angiogenesis and microcirculation), the understanding of these properties may help to support the further refinement of wound dressings for improved wound healing.

Antioxidants↗

PubMed2003

Glomerular filtration rate measured by using triphasic helical CT with a two-point Patlak plot technique.

PURPOSE: To determine the accuracy of the two-point Patlak plot in the calculation of glomerular filtration rate (GFR). MATERIALS AND METHODS: Fifty patients without acute renal disorder were included. GFR was calculated by using a two-point Patlak plot technique. The computed tomography (CT) protocol consisted of a plain examination followed by two contrast material-enhanced examinations in the arterial and portovenous phase. Each examination included the entire kidneys and was performed after injection of 120 mL iopromide and 300 mg of iodine per milliliter given per 75 kg of body weight. All examinations were performed with a standard abdominal protocol. Section thickness was 4 x 2.5 mm, and table advance was 12.5 mm. Bolus triggering commenced 10 seconds after the start of contrast medium injection. Twelve dynamic scans were obtained with reduced tube current every 3 seconds to obtain sufficient arterial input function data. Correction for hematocrit level was made by using the unenhanced attenuation of the aorta. As a reference method, plasma clearance of the contrast medium injected for CT was calculated from three iodine plasma concentration measurements obtained 3, 4, and 5 hours after injection. Linear correlation was performed. RESULTS: GFR was calculated from CT data in 48 patients. Two patients were excluded because of breathing errors. Mean GFR was 80 mL/min (range, 17-153 mL/min) as measured with iopromide plasma clearance and 82 mL/min (range, 28-148 mL/min) as measured with CT. Linear correlation between the two methods was r = 0.889; GFR calculated with the two-point Patlak plot was equal to 15 plus 0.83 times GFR (plasma clearance). The mean difference between GFRs as determined with the two methods was -1.2 mL/min (95% CI: -27.1, 24.6). CONCLUSION: Total GFR can be measured accurately with minimally extended triphasic CT in patients without acute renal disorder by using a two-point Patlak plot technique.

Adult↗