Volatile diterpene emission by two Mediterranean Cistaceae shrubs

Mediterranean vegetation emits a wide range of biogenic volatile organic compounds (BVOCs) among which isoprenoids present quantitatively the most important compound class. Here, we investigated the isoprenoid emission from two Mediterranean Cistaceae shrubs, Halimium halimifolium and Cistus ladanifer, under controlled and natural conditions, respectively. For the first time, diurnal emission patterns of the diterpene kaurene were detected in real-time by Proton-Transfer-Reaction-Timeof- Flight-Mass-Spectrometer. Kaurene emissions were strongly variable among H. halimifolium plants, ranging from 0.01 ± 0.003 to 0.06 ± 0.01 nmol m−2 s−1 in low and high emitting individuals, respectively. They were in the same order of magnitude as monoterpene (0.01 ± 0.01 to 0.11 ± 0.04 nmol m−2 s−1) and sesquiterpene (0.01 ± 0.01 to 0.52 nmol m−2 s−1) emission rates. Comparable range and variability was found for C. ladanifer under natural conditions. Labelling with 13C-pyruvate suggested that emitted kaurene was not derived from de novo biosynthesis. The high kaurene content in leaves, the weak relationship with ecophysiological parameters and the tendency of higher emissions with increasing temperatures in the field indicate an emission from storage pools. This study highlights significant emissions of kaurene from two Mediterranean shrub species, indicating that the release of diterpenes into the atmosphere should probably deserve more attention in the futureinfo:eu-repo/semantics/publishedVersio

The effect of blood contamination on the compressive strength and surface microstructure of mineral trioxide aggregate

Aim To investigate the effects of whole, fresh human blood contamination on compressive strength and surface microstructure of grey and tooth-coloured mineral trioxide aggregate (MTA). Methodology The materials investigated were grey ProRoot (R) MTA Original (Dentsply Tulsa Dental, Johnson City, TN, USA) and tooth-coloured ProRoot (R) MTA (Dentsply Tulsa Dental). Three groups of 10 custom-made cylindrical moulds (internal dimensions 6 +/- 0.1 mm length and 4 +/- 0.1 mm diameter) were filled with tooth-coloured MTA. In the control group, MTA was mixed with water and exposed to water. In the second group, MTA was mixed with water and exposed to whole, fresh human blood. In the third group, MTA was mixed with and exposed to whole, fresh human blood. These three groups were then duplicated using grey MTA, creating a total of 60 samples. A predetermined amount of MTA and appropriate liquid were triturated in a plastic mixing capsule then subjected to ultrasonic energy after placement in the moulds. After 4 days of incubation, specimens were subjected to compressive strength testing. The surface microstructure of one extra specimen in each group was examined using scanning electron microscopy. Data were subjected to a two-way anova. Results Regardless of MTA type, the mean compressive strength values of both experimental groups, which were in contact with blood, were significantly less than that of the control groups (P < 0.0001). In experimental groups in which MTA was mixed with water and exposed to blood, there was a significant difference (P < 0.0001) in compressive strength between tooth-coloured MTA (30.37 +/- 10.16 MPa) and grey MTA (13.92 +/- 3.80 MPa). Conclusion When blood becomes incorporated into MTA, its compressive strength is reduced. In clinical situations in which blood becomes mixed with MTA, its physical properties are likely to be compromised

Capillary Electrophoresis of Tropane Alkaloids and Glycoalkaloids Occurring in Solanaceae Plants

This chapter examines the role of capillary electrophoresis (CE) in the separation of tropane alkaloids, glycoalkaloids, and closely related compounds that have either pharmaceutical value or toxicological effects on humans. The latest significant developments in CE analysis have been selected and critically discussed. When the conventional CE mode was found unable to provide an acceptable selectivity towards the analytes, the addition of either an organic solvent, a chiral selector, or a surfactant to the running buffers was exploited. Likewise, nonaqueous CE (NACE) was also employed to increase solute solubilities and for a better compatibility of this media with mass spectrometry. It turns out that, upon selecting the most appropriate experimental conditions, the CE separation of tropane alkaloids and steroidal glycoalkaloids of Solanaceae plants was successfully accomplished. All major steps involved in the separation and detection of these secondary metabolites in complex samples are described and the relevant aspects of each application are examined with emphasis on the main aspects entailed a typical assay. More applications have yet to be developed in order to encourage more labs to exploit the tremendous potential of capillary electrophoresis