“Background: Conventional mouse or rat pharmacokinetic/tox


“Background: Conventional mouse or rat pharmacokinetic/toxicokinetic (PK/TK) studies frequently require sacrifice or 3-deazaneplanocin A supplier use of multiple animals for a full time-course in order to obtain adequate blood volume. Currently accepted LC-MS/MS analyses require tedious sample preparation and large blood volume, therefore, a bioanalytical method with a simpler blood-sampling procedure using fewer animals, lower sample volume and no additional sample preparation is desirable.

Results: We have developed a method that combines the direct analysis in real time (DART) open-air ambient ionization source and MS/MS to directly analyze dried blood spots (DBS) on glass from low volume whole blood samples without additional sample preparation or manipulation of the spots. Single mouse serial bleeding was performed for sample collection for DART-MS/MS and the results were comparable to the conventional terminal bleeding method for LC-MS/MS. Conclusion: The DART-MS/MS method was applied to DBS sampling for PK/TK studies and also for in vitro screening of absorption, distribution, metabolism and excretion properties. The results from the DART-MS/MS approach correlated well with the LC-MS/MS analyses for comparison.”
“A ‘picket calix[4]pyrrole’ bearing a well-defined

binding domain has allowed the stabilization of a monohydrated fluoride anion. The monohydrated F- was observed only when CsF (not the TBAF) was treated with a host in aqueous acetonitrile. The structure of the receptor-bound, monohydrated F- was fully characterized by single crystal X-ray diffraction analysis as well as by low temperature H-1 PHA-739358 ic50 and F-19 NMR spectroscopy. Further analysis revealed that the complex formed a three-dimensional, salt mediated organic framework in the solid

state.”
“Two Al-Mg-Ge alloys with compositions Al-0.87Mg-0.43Ge (at. pct) and Al-0.59Mg-0.71Ge (at. pct) were investigated and compared using high-resolution transmission electron microscopy, annular dark-field scanning transmission electron microscopy, and nano-beam electron diffraction. The alloys contained fine needle- and lath-shaped precipitates after aging at 473 K (200 A degrees p53 inhibitor C) for 16 hours, which produced hardnesses similar to those measured in comparable Al-Mg-Si alloys. The beta aEuro(3) phase was not observed. Instead, hardness was achieved by beta’-like and disordered precipitates in the Mg-rich alloy, and U1-like and disordered precipitates in the Ge-rich alloy. In all cases, the fine precipitates had structures containing an ordered near-hexagonal network of Ge atoms with a = b a parts per thousand 0.4 nm, which could be visualized directly in annular dark-field mode. The network is very similar to the recently discovered Si network that relates all precipitate structures in the Al-Mg-Si alloys. The orientation of the precipitate unit cells and the Ge network relative to the Al matrix differed from what has been observed for beta’ and U1 in the Al-Mg-Si system.

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