Abstract:
A system and method for metered dosage illumination in a bioanalysis or other system. In accordance with an embodiment, an illumination system or subsystem is described that can provide optimized amounts of excitation light within the short exposure times necessary to measure fast biological activity. The amount of light can be precisely measured to provide quantitative results. The light flux can also be precisely controlled to generate only a prescribed minimum amount of light, in order to reduce adverse lighting effects on both fluors and samples. Although the examples herein illustrate the providing of metered dosage illumination in the context of a bioanalysis system, the techniques can be similarly used to provide metered dosage illumination in the context of other types of system.
Abstract:
The present invention relates to a system for detection and identification of airborne biological, chemical and/or nuclear threats such as toxins, spores, bacteria, and viruses in real time at distances from a few meters to several kilometers. Compact femtosecond terawatt laser technology is combined with spectroscopic and mathematical methods for spectral sensing of airborne warfare agents such as bio-aerosols. Trigger sensors and standoff devices based on mobile terawatt femtosecond laser systems are provided that may be placed at strategic monitoring locations. Furthermore, the invention relates to the propagation of airborne ultra-short, ultra-intense laser pulses giving rise to plasma channels (filamentation) producing white light supercontinuum ranging from the ultraviolet (UV), visible (VIS), near infra-red (NIR) and middle infra-red (MIR). According to this invention, the supercontinuum can be directly produced in a particle cloud and hence is uniquely suitable for multi-spectral long-range atmospheric agent and radioactive isotope detection.
Abstract:
Radioactive materials are used to assist in starting a discharge in an electrodeless light source. The radioactive emissions predispose on the inner surface of the lamp envelope loosely bound charges which thereafter assist in initiating discharge. The radioactive material can be enclosed within the lamp envelope in gaseous or non-gaseous form. Preferred materials are krypton 85 and americium 241. In addition, the radioactive material can be dispersed in the lamp envelope material or can be a pellet imbedded in the envelope material. Finally, the radioactive material can be located in the termination fixture. Sources of alpha particles, beta particles, or gamma rays are suitable. Because charges accumulate with time on the inner surface of the lamp envelope, activity levels as low as 10.sup.-8 curie are effective as starting aids.
Abstract:
An aiming device of the general type shown in U.S. Pat. No. 2,488,541 is disclosed. The device comprises a tubular housing for mounting on a gun or other device which must be manually aimed and the housing contains a spot source of light which is projected rearwardly toward one eye of the user through a collimator contained within the housing. The light source is preferably a radiation activated phosphor of one color housed in a filter of a different color in order to present automatically a spot source of light of the color of the filter during high ambient lighting intensity and a spot source of light the color of the phosphor during low ambient lighting intensity.
Abstract:
Disclosed is a laser-driven photon source comprising drive optics which focus drive radiation so as to maintain a plasma. The point spread function of the drive optics has a point spread function (75) which is configured such that a spectral position of a peak output wavelength of a black body portion of output radiation emitted by said plasma within a desired wavelength band.
Abstract:
A component of a motor vehicle comprising a photoluminescent interior member formed of a plastic composition, wherein the plastic composition comprises at least one polymer and a plurality of additives comprising at least one photoluminescent material and at least a first ultraviolet protector, wherein the at least one photoluminescent material absorbs electromagnetic radiation in a first ultraviolet range of an electromagnetic spectrum, and thereafter emits electromagnetic radiation in a visible radiation range of the electromagnetic spectrum, and wherein the first ultraviolet protector is an ultraviolet absorber, wherein the ultraviolet absorber absorbs electromagnetic radiation in a second ultraviolet range of the electromagnetic spectrum and does not absorb electromagnetic radiation in the first ultraviolet range of the electromagnetic spectrum.
Abstract:
A method for enhancing contrast in fluorescence imaging is provided. The method comprises providing a patterned illumination source for illuminating one or more regions corresponding to a scan step, scanning at least a portion of a surface of a subject using a plurality of scan steps, acquiring image frames corresponding to two or more scan steps, deducting a background fluorescence from the image frames corresponding to the two or more scan steps to form one or more processed image frames, and reconstructing an image using one or more of the processed image frames.
Abstract:
There is provided a scanning molecule counting method using an optical measurement with a confocal microscope or a multiphoton microscope, enabling characterization of a light-emitting particle or identification of a light-emitting particle with emitted light intensity of a single light-emitting particle measured individually. In the inventive optical analysis technique, with reference to the ratio of the intensities of simultaneously generated signals of the lights of at least two light-emitting sites having mutually different emission wavelengths, possessed by a light-emitting particle contained in a sample solution, the intensities being measured with moving the position of the light detection region of an optical system by changing the optical path of the optical system, a single light-emitting particle corresponding to the signals is identified, and the kind, the size, etc. of the light-emitting particle is identified.
Abstract:
The invention concerns methods and apparatuses for quantitatively determining the concentration of fluorophores of a substance in a sample. A constant portion of the reference light of a reference light wave length (λr) emitted by a reference light source is coupled in by an optical element in the direction of a receiving element. A first value corresponding to the portion of the reference light coupled in which is incident on the receiving element is detected. The sample is irradiated with the excitation light of an excitation wave length (λex) emitted by an excitation light source. A second value corresponding to the portion of the fluorescent light of an emission wave length (λem) emitted by the sample which is incident on the receiving element. The ratio of the second value to the first value is determined. The number of fluorophores in the substance is determined based on the ratio.