Although conventional autofluorescence spectroscopy, in which fluorescence emission spectra are recorded for fixed excitation wavelengths, has demonstrated good performance in tissue diagnosis, it suffers from prolonged data acquisition time and broad-band fluorescence features. Synchronous spectroscopy has been proposed to overcome the limitations of conventional fluorescence spectroscopy but has not been applied to imaging for tissue diagnosis in vivo. Our group has developed a synchronous fluorescence imaging system to combine the great diagnostic potential of synchronous spectroscopy and the large field of view of imaging for cancer diagnosis. This system has been tested in a mouse skin model to capture synchronous fluorescence images. A simple discriminant analysis method and a more complicated multi-variate statistical method have been developed to generate a single diagnostic image from a large number of raw fluorescence images. Moreover, it was demonstrated that the diagnostic image generated from synchronous data is comparable to that generated from full spectral data in classification accuracy.
A limited number of techniques are employed in clinical medicine for regional tissue perfusion assessment. These methods are marginally effective and are not well suited for implantation due to the inability to miniaturize the associated technologies. Consequently, no standardized techniques exist for real-time, continuous monitoring of organ perfusion following transplantation. In this paper, a brief overview of the relevant clinical techniques employed for regional tissue perfusion assessment is given with particular emphasis on post-surgical monitoring of transplanted organs. The ideal characteristics for a perfusion monitoring system are discussed and the development of a new, completely implanted local tissue monitoring system is summarized. In vivo and in vitro data are presented that establish the efficacy of this new technology, which is a photonics-based sensor system uniquely suited for continuous tissue monitoring and real-time data reporting. The suitablity of this sensor technology for miniaturization, which enables implantation for monitoring localized tissue perfusion, is discussed.
This report characterizes for the first time an easy, reproducible means of standardizing the relative fluorescent units normally reported for flow microfluorometry. Absolute values for deoxyribonucleic acid/cell are obtained by using nucleated red blood cells as references. Cell were selected and characterized for the quantitative analysis of deoxyribonucleic acid per cell over a range from 2 pg/cell to 93 pg/cell using literature values for species having nucleated erythrocytes. Fluorescence staining by either acridine-orange (green wavelength) or propidium iodide (red wavelength) gave linear curves over the entire range investigated only when "gain controls" and current are optimized. The range was equivalent to mammalian cell values from 1 N (=3.5 pg deoxyribonucleic acid/cell) to 28 N (=91 pg deoxyribonucleic acid/cell). The standard curves obtained with nonmammalian erythrocytes were compared to mammalian free-cell preparations of bovine thymus and liver cells which fell at 6.8 and 6.9 pg deoxyribonucleic acid/cell, respectively. The routine use of these easily obtainable red blood cells will allow ready comparisons on the basis of absolute values for deoxyribonucleic acid per cell for work between experiments, work between staining procedures and dye types and work between laboratories.
This paper describes a self-contained, portable Raman instrument that has been developed for environmental and homeland defense applications. The instrument consists of a 830-nm diode laser for excitation, an acousto-optic tunable filter (AOTF) for wavelength discrimination, and an avalanche photodiode for detection. The primary component of this system is the AOTF and it has been selected based on its spectral range along with its high resolution, ~7.5 cm -1 . Software has been developed in house using C programming language for controlling the instrument (i.e. the AOTF frequency, the signal acquisition, etc.). Evaluation of this instrument has been performed by analyzing several standard samples and comparing to a conventional Raman system. In addition to system evaluation, this paper will also discuss potential applications of this instrument to trace detection of hazardous chemicals using the Raman Integrated Tunable Sensor (RAMiTs) coupled with surface-enhance Raman scattering process.
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