We perform a set of experiments on photo-heating in a water droplet containing gold nanoparticles (NPs). Using photo-calorimetric methods, we determine efficiency of light-to-heat conversion (η) which turns out to be remarkable close to 1, (0.97< η <1.03). Detailed studies reveal a complex character of heat transfer in an optically-stimulated droplet. The main mechanism of equilibration is due to convectional flow. Theoretical modeling is performed to describe thermal effects at both nano- and millimeter-scales. Theory shows that the collective photo-heating is the main mechanism. For a large concentration of NPs and small laser intensity, an averaged temperature increase (at the millimeter-scale) is significant (~ 7 °C) whereas, on the nanometer scale, the temperature increase at the surface of a single NP is small (0.02 °C). In the opposite regime, a small NP concentration and intense laser irradiation, we find an opposite pictures: a temperature increase at the millimeter-scale is small (0.1 °C) but a local, nanoscale temperature has strong local spikes at the surfaces of NPs (3 °C). These studies are crucial for the understanding of photo-thermal effects in NPs and for their potential and current applications in nano-and bio -technologies.

The human cytochrome P4503A forms show expression patterns subject to developmental influence. CYP3A7 and CYP3A4 are generally classified as the major fetal and adult liver forms, respectively. However, characterization of CYP3A4, -3A5, and -3A7 developmental expression has historically been confounded by the lack of CYP3A isoform-specific antibodies or marker enzyme activities. Therefore, the objective of this study was to characterize the developmental expression of hepatic CYP3A forms from early gestation to 18 years of age using up to 212 fetal and pediatric liver samples. Based on immunoquantitation, CYP3A5 protein expression was found to be highly variable, generally independent of age, and more frequently observed for African-American individuals. For differentiation of CYP3A4 and -3A7 levels, dehydroepiandrosterone metabolite patterns for expressed CYP3A forms were characterized and used for simultaneous quantitation of protein levels within liver microsome samples. The major metabolite formed by CYP3A4, 7␤-hydroxy-dehydroepiandrosterone, was identified based on cochromatography and mass spectra matching with the authentic standard. Kinetic analysis showed a 34-fold greater intrinsic clearance of 7␤-hydroxy-dehydroepiandrosterone by CYP3A4 versus -3A7, whereas CYP3A7 showed the highest 16␣-hydroxy-dehydroepiandrosterone intrinsic clearance. Metabolite profiles for the expressed enzymes were fit to a multiple response model and CYP3A4 and -3A7 levels in fetal and pediatric liver microsome samples were calculated. Fetal liver microsomes showed extremely high CYP3A7 levels (311-158 pmol/mg protein) and significant expression through 6 months postnatal age. Low CYP3A4 expression was noted for fetal liver (Յ10 pmol/mg), with mean levels increasing with postnatal age.

The relationship of rotatable bond count (N(rot)) and polar surface area (PSA) with oral bioavailability in rats was examined for 434 Pharmacia compounds and compared with an earlier report from Veber et al. (J. Med. Chem. 2002, 45, 2615). N(rot) and PSA were calculated with QikProp or Cerius2. The resulting correlations depended on the calculation method and the therapeutic class within the data superset. These results underscore that such generalizations must be used with caution.