Visualization of reflectance, transmittance, and application amount distribution of the cosmetic foundation layer on skin.

We developed a method for visualization of makeup finishing with structured lighting. By analyzing images with a sequence of projection patterns, reflectance and transmittance of the cosmetic foundation (FD) layer were extracted as spatial maps using the difference between the light spread of bare skin and made-up skin. The spatial maps reflect conditions and distribution of applied FD under real situations.

Impact of local luminance contrast on facial skin lightness perception: A psychophysical reverse correlation study using sub-band contrast modulation noise.

In conventional psychophysical reverse correlation methods using white or pink noise, the luminance noise is added to every pixel. Thus, the image features correlated with perception are often biased toward local mean luminance. Furthermore, spatial frequencies and orientations are represented in the primary visual cortex, which forms the basis of various visual perception.

Estimation of reflectance, transmittance, and absorbance of cosmetic foundation layer on skin using translucency of skin.

We developed a method to estimate the reflectance, transmittance, and absorbance of a layer of cosmetic foundation (FD) applied to skin from the reflectance of bare skin and FD applied to skin under two measurement conditions using the translucency of skin. Conversely, using the relationship between the applied amount of FD and the reflectance of the FD layer, the applied amount could be estimated. These values could be measured stably regardless of the similarity of reflectance and color between bare skin and made-up skin.

An automated fluorescence protein sequencer using 7-methylthio-4-(2,1,3-benzoxadiazolyl) isothiocyanate (MTBD-NCS) as an Edman reagent.

An automated fluorescence protein sequencer using 7-methylthio-5-(2,1,3-benzoxadiazolyl) isithiocyanate (MTBD-NCS), a fluorescent Edman reagent, is developed by the modification of a commercial protein sequencer. The generated MTBD-thiohydantoin amino acids fluoresced strongly, whereas the by-products such as MTBD-thiocarbamoyl amino acids and MTBD-carbamoly amino acids did not fluoresce. A few interfering peaks were observed in the chromatogram and amino acid sequence was easily determined.