Besides precise timing, optical counting enabled to detect the inception and development of the
event through a steep and simultaneous increase of both coarse and fine particle number densities. Although the former increase was much more relevant, the latter occurrence is much less frequently documented for Saharan Dust events: a clear increase of particles in all the diameter ranges from 0.3 mu m (lower limit of an OPC) up to 5.0 mu m was observed during the event The spatial extension of the event was also examined by means of the analysis of the AERONET ground-based sun photometer data from the Venice station for the event Results confirmed a relevant increase of coarse particles over a distance of more than 150 km. Interestingly AERONET data indicates a more significant variation in the scattering properties of the aerosol rather Selleckchem AG-881 than in the absorbing CX-6258 chemical structure ones in connection with the arrival of the Saharan dust, an observation that within the intrinsic limitations of inverse methods to derive aerosol’s optical properties is in agreement with some previous observations showing that dust in the Saharan desert region is much less absorbing than previously measured. (C) 2015 Elsevier Ltd. All rights
reserved.”
“Background: Increased collagenolytic activity, characteristic of uncontrolled diabetes, may compromise collagen membrane (CM) survival. Tetracycline (TCN) possesses Selleck CBL0137 anticollagenolytic properties and delays CM degradation in healthy animals. This study evaluates the degradation of TCN-immersed and -non-immersed CMs in rats with diabetes compared to those with normoglycemia.\n\nMethods: Diabetes was induced in 15 12-week-old male Wistar rats by injection of 65 mg/kg
streptozotocin. The control group consisted of 15 rats with normoglycemia. Sixty bilayered CM disks were labeled before implantation with aminohexanoyl-biotin-N-hydroxy-succinimide ester, of which 30 were immersed in 50 mg/mL TCN solution (experimental) or phosphate-buffered saline (PBS) (control). In each animal, two disks (control and experimental) were implanted in two midsagittal calvarial defects in the parietal bone. Similar non-implanted disks served as baseline. After 3 weeks, animals were euthanized, and the calvaria and overlying soft tissues were processed for demineralized histologic analysis. Horseradish peroxidase-conjugated streptavidin was used to detect the biotinylated collagen. The area of residual collagen within the membrane disks was measured and analyzed with a digital image analysis system. Several slides from each specimen were also stained with hematoxylin and eosin. Statistical analysis consisted of paired and unpaired t tests.