Abstract:
The disclosure relates generally to methods and apparatus for using a fiber array spectral translator-based (“FAST”) spectroscopic system for improved imaging, spectral analysis, and interactive probing of a sample. In an embodiment, the confocality of a fiber array spectral translator-based spectroscopic system is improved through the use of structured illumination and/or structured collection of photons. User input may be received and acted upon to allow a user to interactively in real time and/or near real time view and analyze specific regions of the sample.
Abstract:
The disclosure relates to a portable and/or handheld bioagent detector and methodology described herein that is based in part on advanced Raman Chemical Imaging (“RCI”) technology. According to one embodiment of the present disclosure, the detection system may include a fiber array spectral translator (“FAST”) and may also include a probe which may include a complementary metal oxide semiconductor (CMOS) camera. The probe alleviates the need to place the main instrument close to an unconfined release of a potentially hazardous material and facilitates analysis of a sample that is situated in a hard-to-reach location while minimizing contamination of the detector and operator.
Abstract:
Real time biofilm monitoring systems are provided. Said systems comprise single or multiple fiber-optic probes detecting wavelength-specific fluorescence from biomarkers of fouling organisms; a compact optoelectronic interface and data acquisition system interfaced with said probes, wherein said probe or probes are bifurcated and contain at least one excitation and at least one emission filter permitting the simultaneous resolution of multiple biomarkers.
Abstract:
Method and apparatus for detecting biomolecular interactions. The use of labels is not required and the methods may be performed in a high-throughput manner. An apparatus for detecting biochemical interactions occurring on the surface of a biosensor includes a light source. A first optical fiber is coupled to the light source and illuminates the biosensor. A second optical fiber detects a wavelength reflected from the biosensor. A spectrometer determines spectra of a reflected signal from the biosensor.
Abstract:
A microsphere-based analytic chemistry system is disclosed in which self-encoding microspheres having distinct characteristic optical response signatures to specific target analytes may be mixed together while the ability is retained to identify the sensor type and location of each sensor in a random dispersion of large numbers of such sensors in a sensor array using an optically interrogatable encoding scheme. An optical fiber bundle sensor is also disclosed in which individual microsphere sensors are disposed in microwells at a distal end of the fiber bundle and are optically coupled to discrete fibers or groups of fibers within the bundle. The identities of the individual sensors in the array are self-encoded by exposing the array to a reference analyte while illuminating the array with excitation light energy. A single sensor array may carry thousands of discrete sensing elements whose combined signal provides for substantial improvements in sensor detection limits, response times and signal-to-noise ratios.
Abstract:
A method of evaluating the surface of a material that has a distinguishable infrared spectrum comprising (a) positioning an infrared fiber optic probe to be in contact with a surface of the sample or material at a region of interest for detecting attenuated total reflectance or within a sufficient distance from the surface of the region for detecting reflection, (b) detecting mid- or near-infrared radiation attenuated total reflectance or reflection off of the surface of the sample or the material, (c) analyzing the infrared radiation from step (b) for at least one of peak height, peak area, frequency and chemometric parameters, and (d) actuating the removal device when a signal from the infrared fiber optic probe is between pre-selected values for at least one of peak height, peak area, frequency and chemometric parameters for the sample of the material.
Abstract:
A microsphere-based analytic chemistry system is disclosed in which self-encoding microspheres having distinct characteristic optical response signatures to specific target analytes may be mixed together while the ability is retained to identify the sensor type and location of each sensor in a random dispersion of large numbers of such sensors in a sensor array using an optically interrogatable encoding scheme. An optical fiber bundle sensor is also disclosed in which individual microsphere sensors are disposed in microwells at a distal end of the fiber bundle and are optically coupled to discrete fibers or groups of fibers within the bundle. The identities of the individual sensors in the array are self-encoded by exposing the array to a reference analyte while illuminating the array with excitation light energy. A single sensor array may carry thousands of discrete sensing elements whose combined signal provides for substantial improvements in sensor detection limits, response times and signal-to-noise ratios.
Abstract:
A fiber-optic probe is formed by a pair of optical fibers one of which delivers light to a target zone and the other collects light from a field of view in the target zone. One of these fibers is provided with a window that opens substantially perpendicular to the longitudinal axis of the fiber and with a transverse surface oriented at an angle to the longitudinal axis of the fiber to reflect light through the window or from the window longitudinally of the axis of this fiber. Two fibers are physically interconnected to position the window on one side of and immediately adjacent to the target zone and the axial end of other fiber to deliver or receive light from another side of the target zone preferably substantially perpendicular to the one side.
Abstract:
개선점들은 액체 샘플들을 수용하기 위한 장치들에 관한 것이다. 액체 샘플을 수용하기 위한 장치는 분광광도계와 같은 기구를 위한 마이크로 샘플링 헤드의 일부를 형성할 수 있다. 상기 장치는 샘플을 통해 전자기 방사선을 통과시키는 것을 포함하는 공정에 의해 분석될 액체 샘플을 수용하며, 전자기 방사선을 샘플의 내측으로 지향시키기 위한 광 입구 가이드(20), 및 상기 가이드와 대향 관계로 위치되며 사용시, 샘플로 충전되는 일정한 경로 길이의 갭(21)을 형성하도록 일정한 거리만큼 가이드로부터 이격되는 광 수용 요소(23)를 포함한다. 사용시, 방사선은 광 입구 가이드로부터 광 수용 요소(23)로 통과하며, 샘플을 통한 방사선의 경로 길이는 상기 갭(23)에 의해 형성된다. 상기 장치는 샘플의 액적이 갭 내에 직접적으로 놓이게 허용하도록 개방 또는 개방될 수 있다.