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Double Integrating Sphere Characterization of PVA-CryogelsFiee, Peter Q 26 January 2015 (has links)
Proper functioning of instruments requires precise calibration and routine quality assurance. In a clinical setting, this is achieved through the use of phantoms, which mimic the physical characteristics of tissues. Polyvinyl alcohol (PVA), a non-toxic, water-soluble polymer is well-suited for use as clinical phantom material. Through successive freezing and thawing, solutions of PVA in water can be solidified into rigid cryogels (PVA-C). The number of freeze-thaw cycles affects the properties of the material, including its optical characteristics.
A double integrating sphere system was used in conjunction with the Inverse Adding Doubling (IAD) algorithm to characterize the optical properties of thin slab samples. The setup was evaluated using liquid phantoms. Liquid emulsion and food colouring were used to impart scattering and absorbing properties in the range characteristic of human tissue. Measured values of normalized reflectances and transmittances were entered into IAD, and a set of optical properties (μ′s,μa,g) retrieved. The reduced scattering coefficient was found to increase linearly with increasing lipid concentration, while a consistent overestimation of the absorption coefficient was observed.
Measurements of PVA cryogels revealed a linear increase in the reduced scattering coefficient with an increasing number of freeze-thaw cycles up to five cycles. Scattering was also observed to increase with concentration up to PVA concentrations of 15%, and to spontaneously increase during the lifetime of the slab samples. These findings suggest it is possible to tune the optical scattering of PVA-C via different purely physical mechanisms. / Thesis / Master of Science (MSc)
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Double integrating spheres: A method for assessment of optical properties of biological tissues / Double integrating spheres: A method for assessment of optical properties of biological tissuesPoppendieck, Wigand January 2004 (has links)
<p>The determination of the optical properties of biological tissue is an important issue in laser medicine. The optical properties define the tissue´s absorption and scattering behaviour, and can be expressed by quantities such as the albedo, the optical thickness and the anisotropy coefficient. During this project, a measurement system for the determination of the optical properties was built up. The system consists of a double integrating sphere set-up to perform the necessary reflection and transmission measurements, and a computer algorithm to calculate the optical properties from the measured data. This algorithm is called Inverse Adding Doubling method, and is based on a one-dimensional transport model. First measurements were conducted with the system, including measurements with phantom media (Intralipid-ink solutions) and with cartilage samples taken from the human knee joint. This work also includes an investigation about the preparation of tissue samples for optical measurements.</p>
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Double integrating spheres: A method for assessment of optical properties of biological tissues / Double integrating spheres: A method for assessment of optical properties of biological tissuesPoppendieck, Wigand January 2004 (has links)
The determination of the optical properties of biological tissue is an important issue in laser medicine. The optical properties define the tissue´s absorption and scattering behaviour, and can be expressed by quantities such as the albedo, the optical thickness and the anisotropy coefficient. During this project, a measurement system for the determination of the optical properties was built up. The system consists of a double integrating sphere set-up to perform the necessary reflection and transmission measurements, and a computer algorithm to calculate the optical properties from the measured data. This algorithm is called Inverse Adding Doubling method, and is based on a one-dimensional transport model. First measurements were conducted with the system, including measurements with phantom media (Intralipid-ink solutions) and with cartilage samples taken from the human knee joint. This work also includes an investigation about the preparation of tissue samples for optical measurements.
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