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Baulin, V.

Publications and source records attributed to Baulin, V..

2 recordsLinked to original sources

Topological changes in telechelic micelles: flowers versus stars

Micellization and morphology of spherical telechelic micelles formed by tri-block copolymers with short solvophobic end blocks at low concentrations is discussed within scaling argumentsand Single Chain Mean Field Theory (SCMFT). In ultra-dilute regime, individual telechelic polymer chains can exist in solution in two distinct states: open linear chain conformation with two free ends and closed loop conformation, when two ends are connected by the effective attraction between two solvophobic ends. At concentrations below gelation point, closed loops tend to form micelles comprised mostly of loops in flower-like micelles, while linear polymers in open conformations tend to form star-shaped aggregates with one hydrophobic dangling end. Resulting two kinds of micelles have remarkably different topology and dimensions, while the transition between them can be driven by the entropy, namely conformation changes between domination of the looped and linear conformations. The transition between two types of micelles lies in a narrow interaction parameters range. Thus, these topological micelles are very sensitive to the changes in external environment and they can serve as a very sensitive stimuli-responsive smart materials. Graphical TOC Entry O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=81 SRC="FIGDIR/small/455870v2_ufig1.gif" ALT="Figure 1"> View larger version (10K): org.highwire.dtl.DTLVardef@16b8279org.highwire.dtl.DTLVardef@142fb97org.highwire.dtl.DTLVardef@938fc5org.highwire.dtl.DTLVardef@1c3e145_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics

Deep learning image analysis for in vivo shortwave infrared imaging

Shortwave infrared window (SWIR: 1000-1700 nm) represents a major improvement compared to the NIR-I region (700-900 nm) in terms of temporal and spatial resolutions in depths down to 4 mm. SWIR is a fast and cheap alternative to more precise methods such as X-ray and opto-acoustic imaging. Main obstacles in SWIR imaging are the noise and scattering from tissues and skin that reduce the precision of the method. We demonstrate that the combination of SWIR in vivo imaging in the NIRIIb region (1500-1700 nm) with advanced deep learning image analysis allows to overcome these obstacles and making a large step forward to high resolution imaging: it allows to precisely segment vessels from tissues and noise, provides morphological structure of the vessels network, with learned pseudo-3D shape, their relative position, dynamic information of blood vascularization in depth in small animals and distinguish the vessels types: artieries and veins. For demonstration we use neural network IterNet that exploits structural redundancy of the blood vessels, which provides a useful analysis tool for raw SWIR images.

cancer biology