Frequency domain photon migration consists of launching an intensitymodulated near-infrared light into the powder medium and measuring the amplitude, mean-intensity, and phase shift of detected intensity modulated light for extracting both the isotropic scattering and absorption coefficients of the powder bed. The dependence of absorption coefficient upon the active pharmaceutical ingredient (API) concentration of powder blend enables FDPM to monitor blending homogeneity. The volume sampled by FDPM in powder blend was investigated through a designed heterogeneity experiments. A model which describes the visitation probability of a local region by migrating photons was developed to theoretically determine the sampled volume of FDPM in terms of signal-to-noise ratio. The applicability of FDPM in monitoring blending homogeneity was directly verified by measuring the API contents in a series of industrial samples, which were retrieved from various locations at various times in an actual pharmaceutical blending process. The FDPM measurement results were consistent with the traditional analysis using high performance liquid chromatography. The homogeneity evolution revealed through FDPM agreed with the well-established first order model of blending. A simulation method was developed which consisted of (i) dynamic simulation for generating the powder structure; (ii) the completely-randommixture model for predicting the spatial distribution of API particles within the powder bed; and (iii) Monte Carlo simulation for tracking photon trajectories within the powder bed. The simulation of photon migration in powder blend revealed that while both the isotropic scattering and absorption coefficients increased with the solid-volume fraction, the ratio of absorption coefficient to the isotropic scattering coefficient is (i) independent of the solid-volume fraction; (ii) linearly dependent upon the API concentration; and (iii) appropriate for monitoring the powder blending homogeneity under simultaneous variations of solid-volume fraction and API content. Finally, a rigorous two-speed diffusion equation for describing photon migration in powders was derived from the two-group radiative transfer equations and the analytical expression of the isotropic scattering coefficient was provided. The theoretical results agreed well with the experimental measurements in resin powder media and resin suspensions.

A new molecular imaging modality has been developed to detect and locate positive axillary and sentinel lymph nodes non-invasively in breast cancer patients undergoing lymphoscintigraphy. The modality is based on fluorescent photon detection to locate the presence of indocyanine green (ICG) in the lymph subsequent to peritumoral injection of ICG into the breast. The imaging system consists of a gain-modulated intensified charge-coupled device (ICCD) camera, which captures low-intensity, near-infrared, and frequency-modulated photons. A four-fold ‘optical lymphography’ study was conducted to (1) examine fluorescence depth penetration and ICCD system accuracy at clinically relevant depths, (2) compare image quality of the ICCD system vs. conventional gamma imaging, (3) measure ICG pharmacokinetics in vivo, and (4) develop a clinical protocol while examining pre-clinical factors such as the outcome of combining ICG with sulfur colloids used in lymphoscintigraphy. The frequency-domain ICCD system was found to precisely detect modulation amplitude, IAC, and phase, θ, at depths up to 9 cm and with IAC accuracy less than 20% and θ less than 2º using an 80-mW laser incident on phantoms having ranging tissue optical properties. Significant differences in the mean depth of penetration owing to 0.62-ns lifetime and 100-MHz frequency increases were detected. An in vivo optical vs. nuclear image quality comparison demonstrated statistically similar (α=0.05) target-to-background ratios for optical (1.4+/-0.3) and nuclear (1.5+/-0.2). Alternatively, resulting image signal-to-noise ratios (SNR) from the ICCD system were greater than that achieved with a conventional gamma camera (pvalue<<0.01). Analysis of SNR versus contrast showed greater sensitivity of optical over nuclear imaging for subcutaneous tumors. In vivo and rapid detection of ICG in the blood-stream of nude mice was accomplished with a home-built avalanche photodiode dynamic fluorescence measurement system. Intensity data upon i.v. injection were regressed with a pharmacokinetic model describing the partitioning of ICG from the blood to the surrounding tissues. ICG blood-clearance was detected approximately 15 min after injection. Lastly, a human subject protocol was written, practiced, and federally approved for the application of optical lymphography. Furthermore, ICG was unaffected when mixed with sulfur colloids thus supporting the feasibility for combining fluorescence imaging with lymphoscintigraphy in breast cancer patients.

A new molecular imaging modality has been developed to detect and locate positive axillary and sentinel lymph nodes non-invasively in breast cancer patients undergoing lymphoscintigraphy. The modality is based on fluorescent photon detection to locate the presence of indocyanine green (ICG) in the lymph subsequent to peritumoral injection of ICG into the breast. The imaging system consists of a gain-modulated intensified charge-coupled device (ICCD) camera, which captures low-intensity, near-infrared, and frequency-modulated photons. A four-fold ‘optical lymphography’ study was conducted to (1) examine fluorescence depth penetration and ICCD system accuracy at clinically relevant depths, (2) compare image quality of the ICCD system vs. conventional gamma imaging, (3) measure ICG pharmacokinetics in vivo, and (4) develop a clinical protocol while examining pre-clinical factors such as the outcome of combining ICG with sulfur colloids used in lymphoscintigraphy. The frequency-domain ICCD system was found to precisely detect modulation amplitude, IAC, and phase, θ, at depths up to 9 cm and with IAC accuracy less than 20% and θ less than 2º using an 80-mW laser incident on phantoms having ranging tissue optical properties. Significant differences in the mean depth of penetration owing to 0.62-ns lifetime and 100-MHz frequency increases were detected. An in vivo optical vs. nuclear image quality comparison demonstrated statistically similar (α=0.05) target-to-background ratios for optical (1.4+/-0.3) and nuclear (1.5+/-0.2). Alternatively, resulting image signal-to-noise ratios (SNR) from the ICCD system were greater than that achieved with a conventional gamma camera (pvalue<<0.01). Analysis of SNR versus contrast showed greater sensitivity of optical over nuclear imaging for subcutaneous tumors. In vivo and rapid detection of ICG in the blood-stream of nude mice was accomplished with a home-built avalanche photodiode dynamic fluorescence measurement system. Intensity data upon i.v. injection were regressed with a pharmacokinetic model describing the partitioning of ICG from the blood to the surrounding tissues. ICG blood-clearance was detected approximately 15 min after injection. Lastly, a human subject protocol was written, practiced, and federally approved for the application of optical lymphography. Furthermore, ICG was unaffected when mixed with sulfur colloids thus supporting the feasibility for combining fluorescence imaging with lymphoscintigraphy in breast cancer patients.

Herein we present the development of a fluorescence-enhanced, frequency-domain radiative transport reconstruction system designed for small animal optical tomography. The system includes a time-dependent data acquisition instrument, a radiative transport based forward model for prediction of time-dependent propagation of photons in small, non-diffuse volumes, and an algorithm which utilizes the forward model to reconstruct fluorescent yields from air/tissue boundary measurements. The major components of the instrumentation include a charge coupled device camera, an image intensifier, signal generators, and an optical switch. Time-dependent data were obtained in the frequency-domain using homodyne techniques on phantoms with 0.2% to 3% intralipid solutions. Through collaboration with Transpire, Inc., a fluorescence-enhanced, frequency-domain, radiative transport equation (RTE) solver was developed. This solver incorporates the discrete ordinates, source iteration with diffusion synthetic acceleration, and linear discontinuous finite element differencing schemes, to predict accurately the fluence of excitation and emission photons in diffuse and transport limited systems. Additional techniques such as the first scattered distributed source method and integral transport theory are used to model the numerical apertures of fiber optic sources and detectors. The accuracy of the RTE solver was validated against diffusion and Monte Carlo predictions and experimental data. The comparisons were favorable in both the diffusion and transport limits, with average errors of the RTE predictions, as compared to experimental data, typically being less than 8% in amplitude and 7% in phase. These average errors are similar to those of the Monte Carlo and diffusion predictions. Synthetic data from a virtual mouse were used to demonstrate the feasibility of using the RTE solver for reconstructing fluorescent heterogeneities in small, non-diffuse volumes. The current version of the RTE solver limits the reconstruction to one iteration and the reconstruction of marginally diffuse, frequency-domain experimental data using RTE was not successful. Multiple iterations using a diffusion solver successfully reconstructed the fluorescent heterogeneities, indicating that, when available, multiple iterations of the RTE based solver should also reconstruct the heterogeneities.

Herein we present the development of a fluorescence-enhanced, frequency-domain radiative transport reconstruction system designed for small animal optical tomography. The system includes a time-dependent data acquisition instrument, a radiative transport based forward model for prediction of time-dependent propagation of photons in small, non-diffuse volumes, and an algorithm which utilizes the forward model to reconstruct fluorescent yields from air/tissue boundary measurements. The major components of the instrumentation include a charge coupled device camera, an image intensifier, signal generators, and an optical switch. Time-dependent data were obtained in the frequency-domain using homodyne techniques on phantoms with 0.2% to 3% intralipid solutions. Through collaboration with Transpire, Inc., a fluorescence-enhanced, frequency-domain, radiative transport equation (RTE) solver was developed. This solver incorporates the discrete ordinates, source iteration with diffusion synthetic acceleration, and linear discontinuous finite element differencing schemes, to predict accurately the fluence of excitation and emission photons in diffuse and transport limited systems. Additional techniques such as the first scattered distributed source method and integral transport theory are used to model the numerical apertures of fiber optic sources and detectors. The accuracy of the RTE solver was validated against diffusion and Monte Carlo predictions and experimental data. The comparisons were favorable in both the diffusion and transport limits, with average errors of the RTE predictions, as compared to experimental data, typically being less than 8% in amplitude and 7% in phase. These average errors are similar to those of the Monte Carlo and diffusion predictions. Synthetic data from a virtual mouse were used to demonstrate the feasibility of using the RTE solver for reconstructing fluorescent heterogeneities in small, non-diffuse volumes. The current version of the RTE solver limits the reconstruction to one iteration and the reconstruction of marginally diffuse, frequency-domain experimental data using RTE was not successful. Multiple iterations using a diffusion solver successfully reconstructed the fluorescent heterogeneities, indicating that, when available, multiple iterations of the RTE based solver should also reconstruct the heterogeneities.

Interparticle interactions determine the microstructure, stability, rheology, and optical properties of concentrated colloidal suspensions involved in paint, paper, cosmetic, and pharmaceutical industries, etc. Frequency domain photon migration (FDPM) involves modeling the photon transport in a multiple scattering medium as a diffusion process in order to simultaneously determine isotropic scattering and absorption coefficients from measured amplitude attenuation and phase shift of the propagating photon density wave. Using FDPM, we investigated the impact of electrostatic interaction upon the optical properties and structure of dense charged suspensions. We demonstrated that electrostatic interactions among charged polystyrene latex may significantly affect the light scattering properties and structure of dense suspensions at low ionic strength (<0.06 mM NaCl equivalent) by actual FDPM measurement. We showed that the structure factor models addressing electrostatic interaction can be used to describe the microstructure of charged suspensions and quenched scattering due to electrostatics, and demonstrated that FDPM has the potential to be a novel structure and surface charge probe for dense suspensions. We also showed that the FDPM measured isotropic scattering coefficients may respond to the change in effective particle surface charge, and displayed the potential of using FDPM for probing particle surface charge in concentrated suspensions. We presented that the interference approximation implies a linear relationship between the absorption coefficient and volume fraction of suspension. We illustrated that FDPM measured absorption coefficient varies linearly with suspension volume fraction and affirmed the interference approximation from a perspective of light absorption. The validation of the interference approximation enables us to develop the methodology for estimating absorption efficiencies and imaginary refractive indices for both particles and suspending fluid simultaneously using FDPM. We further demonstrated a novel application of FDPM measured absorption coefficients in determining pigment absorption spectra, and displayed the potential of using FDPM as a novel analytical tool in pigment and paint industry.

A new optical imaging modality has been developed for small animal in vivo imaging of near-infrared fluorescence resulting from fluorescent contrast agents specifically targeted to molecular markers of cancer. The imaging system is comprised of an intensified charge-coupled device (ICCD) for the detection of ultra-low levels of re-emitted fluorescence following the delivery of an expanded beam of excitation light. The design of the ICCD detection system allows for both continuous wave (CW) and frequency-domain modes of operation. Since the accurate acquisition of frequency-domain photon migration (FDPM) data is important for tomographic imaging, the imaging system was also validated using experimentally obtained FDPM measurements of homogenous turbid media and diffusion theory to obtain estimates of the optical properties characteristic of the media. The experiments demonstrated that the absorption and reduced scattering coefficients are determined least accurately when relative rel measurements of average light intensity IDC are employed either alone or in a rel combination with relative modulation amplitude data IAC and/or relative phase shift data rel . However, when FDPM measurements of are employed either alone or in rel combination with IAC data, the absorption and reduced scattering coefficients may be found accurate to within 15% and 11%, respectively, of the values obtained from standard single-pixel measurements; a result that suggests that FDPM data obtained from an ICCD detection system may in fact be useful in tomographic imaging. Furthermore, intensified-detection allows for sub-second exposure times, permitting the acquisition of dynamic fluorescence images immediately following administration of the contrast agent. Experimental results demonstrate that when coupled with a suitable pharmacokinetic model describing targeted dye distribution throughout the body, dynamic fluorescence imaging may be used to discriminate spontaneous canine adenocarcinoma from normal mammary tissue. A separate experiment demonstrates that pharmacokinetic analysis of dynamic fluorescence images enables one to estimate the rate constant governing Kaposi's sarcoma tumor uptake of an integrin-targeted dye and integrin receptor turnover rate. The rate constant for uptake was calculated to be 0.16-sec-1 while the turnover rate of the integrin receptor was estimated to occur within 24-hours.

Abstract The thesis clearly demonstrates that photon migration measurements allow characterization of pulp and paper properties, especially the fines and filler content of pulp, and the basis weight, thickness and porosity of paper. Pulp and paper are materials with a worldwide significance. Their properties strongly depend on the manufacturing process used. For efficient process control, the employed monitoring and measuring has to be fast. Therefore it is worthwhile to try to develop new approaches and techniques for such measurements. Recent advancements in optics offer new possibilities for such development. If two samples have different optical properties their photon migration distributions are different. The measurement of a photon migration distribution allows some features between two optically slightly dissimilar samples to be distinguished. Some simple measurements, which only yielded the photons' average time of flight, were made with an oscilloscope and a time-of-flight lidar. More precise measurements yielding photon pathway distribution or some selected characteristics like light pulse rise time, broadening, or fall time were measured with a streak camera. Two methods to assess photon path length distribution were introduced: particle determination with simulation, and streak camera with deconvolution. The basic properties for pulp are consistency and fines content and for paper the basic properties are thickness, basis weight and porosity. The influence on photon migration caused by changes in these basic properties was determined. As pulp and paper are rarely very basic, an additional property was demonstrated for both materials. For pulp it was the content of filler talc, and for paper it was the use of beaten pulp as a raw material. These additional properties were also distinguishable.

No description available.

Frequency domain photon migration (FDPM) measurements are used to study the properties of dense colloidal dispersions with hard sphere and electrostatic interactions, which are otherwise difficult to analyze due to multiple scattering effects. Hard sphere interactions were studied using a theoretical model based upon a polydisperse mixture of particles using the hard sphere Percus Yevick theory. The particle size distribution and volume fraction were recovered by solving a non linear inverse problem using genetic algorithms. The mean sizes of the particles of 144 and 223 nm diameter were recovered within an error range of 0-15.53% of the mean diameters determined from dynamic light scattering measurements. The volume fraction was recovered within an error range of 0-24% of the experimentally determined volume fractions. At ionic strengths varying between 0.5 and 4 mM, multiple wavelength (660, 685, 785 and 828 nm) FDPM measurements of isotropic scattering coefficients were made of 144 and 223 nm diameter, monodisperse dispersions varying between 15% - 22% volume fraction, as well as of bidisperse mixtures of 144 and 223 nm diameter latex particles in 1:3, 1:1 and 3:1 mixtures varying between volume fractions of 15% - 24%. Structure factor models with Yukawa potential were computed by Monte Carlo (MC) simulations and numerical solution of the coupled Ornstein Zernike equations. In monodisperse dispersions of particle diameter 144 nm the isotropic scattering coefficient versus ionic strength show an increase with increasing ionic strength consistent with model predictions, whereas there was a reversal of trends and fluctuations for the particle diameter of 223 nm. In bidisperse mixtures for the case of maximum number of smaller particles, the isotropic scattering coefficient increased with increasing ionic strength and the trends were in conformity with MC simulations of binary Yukawa potential models. As the number of larger diameter particles increased in the dispersions, the isotropic scattering coefficients depicted fluctuations, and no match was found between the models and measurements for a number ratio of 1:3. The research lays the foundation for the determination of particle size distribution, volume fractions and an estimate of effective charge for high density of particles.