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HyperSpectral Skin Imaging Tianchen Shi, Prof. Charles A. DiMarzio

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Presentation on theme: "HyperSpectral Skin Imaging Tianchen Shi, Prof. Charles A. DiMarzio"— Presentation transcript:

1 HyperSpectral Skin Imaging Tianchen Shi, Prof. Charles A. DiMarzio
Department of Electrical and Computer Engineering, Northeastern University, Boston, MA 02115 “This work was supported in part by CenSSIS, the Center for Subsurface Sensing and Imaging Systems, under the Engineering Research Centers Program of the National Science Foundation ( Award Number EEC ), “ scar veins Light Source CCD Camera Liquid Crystal Filter (build-in LP) Lens Linear Polarizer(LP) Subject’s Palm CenSISS Value Added Current Status Achieved fast imaging ability to obtain reasonable skin chromospheres concentrations, and oxygen saturation. Obtained blood vessel’s general geometry information: average diameter and depth of blood vessels. Future Plans Extend to a spatially resolved concentration mapping. Explore blood vessels diameter and depth distributions Obtain better light source and detection arrays for high accuracy measurements,and increase the accuracy and stability of the information extraction procedures. Take more in-vivo data for different skin subjects. References L.O.Svaasand, et.al., Lasers Med. Sci., 10: , 1995 M. Shimada, et.al., Phys. Med. Biol., 46: , 2001 R.L.P. van Veen, et.al., Opt. Lett. , 27: ,2002 Izumi Nishidate, et.al., J. Bio. Opt., 9(4): , 2004 PI Contact Information Prof. Charles A. DiMarzio: Northeastern University, 360 Huntington Avenue Stearns Building 302,Boston, MA 02115 Phone : (617) , Fax: (617) 400um 100um 5000um + Epidermis: (melanin) Dermis: (upper part contains hemoglobin in blood vessels) Abstract Chromosphere monitoring is an important aspect in most of skin studies, especially for hemoglobin in human skin, which is closely related to development and diagnosis of various skin diseases. However, recent studies reveals that hemoglobin concentration obtained by assuming homogeneous distribution may deviate from its true value. On the other hand, diameter and distribution of blood vessels in skin are also crucial in monitoring of blood pressure and body temperature. Among various optical skin imaging techniques, HyperSpectral Imaging is a fast, stable method to provide spatial and spectral information of skin tissue. In this poster, we present a Monte Carlo assisted HyperSpectral imaging method to meet both of the challenges mentioned above. Reflection spectrum measurements are used to determine absolute concentration of chromospheres with aid from a Monte Carlo model, and blood vessel information can be further derived by a correction model for the inhomogeneity in skin layers. State of the Art Izumi Nishidate, Muroran Institute of Technology, Japan [4]. The group used a multiple regression analysis assisted by a homogeneous Monte Carlo model to extract chromospheres concentration for point based total reflection measurement. W. Verkruysse, Department of Radiation Oncology, University hospital Rotterdam, Rotterdam, The Netherlands [3]. The group was using a correction factor obtained by a single blood vessel assumption for a fiber based skin measurement. Significance and Challenges Linear multiple regression based HyperSpectral imaging may provide possibility of fast imaging over an area of skin. Pre-computed inhomogeneous Monte Carlo model may allow to obtain general information of blood vessels at superficial skin layer. The method may need very high accuracy and stability of the Monte Carlo model to solve the non-linear and inter dependent relationship between chromosphere concentration and obtained multiple regression coefficients. Technical Approaches Orthogonal polarization detection with incoherent HyperSpectral imaging for in-vivo human skin measurement. Monte Carlo simulation for inhomogeneous layered skin model with very carefully selected parameters. Fast 2-D imaging with linear multiple regression analysis and non- linear conversion by pre-computed Monte Carlo results. R1 R2 Overview of the Strategic Research Plan Fundamental Science Validating TestBEDs L1 L2 L3 R3 S1 S4 S5 S3 S2 Bio-Med Enviro-Civil Figure 2, Experiment Setup Layout Figure 1, Two-layer skin model: randomly distributed blood vessels with diffusively incident photon packets. wavelength 480nm 100 200 300 400 500 0.6 0.7 0.8 0.9 1 wavelength 560nm 0.5 wavelength 620nm 0.4 wavelength 690nm 0.3 Scar tissue Skin Model Modified Lambert-Beer’s Law: where A is absorption, S is scattering term,  is molar concentration of prevailing chromospheres (melanin, hemoglobin), and L is mean free transport path length. Monte Carlo assisted Multiple Regression Analysis: where am is linear multiple regression coefficients, a is a vector consisting of the combination of am for the first and the third order, and b is a conversion vector nonlinearly relating Cm and am , obtained with an inhomogeneous Monte Carlo skin model. Inhomogeneity in skin model (blood vessels) : where D is the average diameter of blood vessels, Z is the average depth of blood vessels, bD and bZ are corresponding conversion vectors obtained from the Monte Carlo model. Figure 3, In-vivo human skin absorption data cube blood oxygen saturation map 100 200 300 400 500 50 150 250 350 450 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 Figure 4, Extracted oxygen saturation map, average chromospheres volume concentration: melanin (4.30%), total hemoglobin(0.32%), average blood vessels diameter (101um) and depth (164um) 450 500 550 600 650 700 750 0.45 0.5 0.55 0.6 0.65 0.7 0.75 wavelength (nm) Absorption (a.u.) measurement Monte Carlo Figure 5, Comparison of in-vivo spectrum and Monte Carlo simulation with extracted parameters:


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