Cancer diagnosis and classification is extremely complicated and, for the most part, relies on subjective interpretation of biopsy material. Such methods are laborious and in some cases might result in different results depending on the histopathologist doing the examination. Automated, real-time diagnostic procedures would greatly facilitate cancer diagnosis and classification. Laser-induced breakdown spectroscopy (LIBS) is used for the first time to our knowledge to distinguish normal and malignant tumor cells from histological sections. We found that the concentration of trace elements in normal and tumor cells was significantly different. For comparison, the tissue samples were also analyzed by an inductively coupled plasma emission spectroscopy (ICPES) system. The results from the LIBS measurement and ICPES analysis were in good agreement.
Laser-induced breakdown spectrometry (LIBS) has been used to detect atomic and molecular species in various environments. LIBS has the capability to be used as a continuous-emission monitor to monitor toxic-metal concentrations in stack emissions. Recently a mobile LIBS system was calibrated in our laboratory and tested as a multimetal continuous-emission monitor during a joint U.S. Department of Energy-Environmental Protection Agency (EPA) test. LIBS measurements were performed with three sets of metal concentrations at the EPA Rotary Kiln Incinerator Simulator. The LIBS system successfully measured concentrations of Cr, Pb, Cd, and Be in near real time in this test. Real-time LIBS data were averaged and compared with data obtained from an EPA reference method that was conducted concurrently with LIBS. The details of the LIBS calibration and results of these LIBS measurements are described.
The optical properties of laser-induced plasma generated firm solid (Al alloy) and liquid (Mn, Cr, Mg, or Ti solutions) samples expanded across an external, steady magnetic field have been studied by atomic-emission spectroscopy. Various line emissions obtained from the constituents of the Al alloy and of the aqueous solution show an enhancement in intensity in the presence of an approximately 5-kG magnetic field. The enhancement of the signal was nearly a factor of 2 for the minor constituents of the solid samples and a factor of 1.5 for the elements in liquid phase. Temporal evolution of the emission from the solid sample showed maximum enhancement in emission intensity at 3-10-micros time delay after plasma formation in the laser energy range 10-50 mJ. However, for the liquid sample the maximum signal was for a gate delay of 3-25 micros the energy range 50-200 mJ. This enhancement in the emission intensity was found to be due to an increase in effective density of the plasma as a result of magnetic confinement when the plasma cooled after expansion. This enhanced emission was due to an increase in the rate of radiative recombination in the plasma.
The application of laser-induced breakdown spectroscopy to liquid samples, by use of a Nd:YAG laser in double-pulse excitation mode, is described. It is found that the line emission from a magnesium ion or atom is more than six times greater for double-pulse excitation than for single-pulse excitation. The effect of interpulse separation on the emission intensity of a magnesium ion and a neutral atom showed an optimum enhancement at a delay of 2.5-3 micros. The intensity of neutral atomic line emission dominates the ion emission from the plasma for higher interpulse (>10 micros) separation. A study of the temporal evolution of the line emission from the plasma shows that the background as well as line emission decays faster in double-pulse excitation than in single-pulse excitation. The enhancement in the emission seems to be dominated by an increase in the volume of the emitting gas. The limit of detection for a magnesium solution improved from 230 parts per billion (ppb) in single-pulse mode to 69 ppb in double-pulse mode.
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