A Scanning Beam Time-Resolved Imaging System for Fingerprint Detection

2000 ◽  
Vol 45 (3) ◽  
pp. 14729J ◽  
Author(s):  
Robert D. Roorda ◽  
Alfonso C. Ribes ◽  
Savvas Damaskinos ◽  
A.E. (Ted) (Ted) Dixon ◽  
E. Roland Menzel
2002 ◽  
Vol 2 ◽  
pp. 542-545 ◽  
Author(s):  
Kimberly K. Bouldin ◽  
E. Roland Menzel

Lanthanide complexes are employed in photoluminescence detection of fingerprints because their long luminescence lifetimes allow use of time-resolved imaging techniques to suppress problematic background fluorescence. To date, however, these complexes have been unsuccessful when used in developing old fingerprints on porous substrates. SYPRO®Rose Plus Protein Blot Stain remedies this shortcoming; it lends itself to smooth surfaces as well, thus having potential as a universal fingerprint reagent.


2010 ◽  
Vol 18 (1) ◽  
Author(s):  
M. Kacprzak ◽  
A. Liebert ◽  
P. Sawosz ◽  
N. Żołek ◽  
D. Milej ◽  
...  

AbstractWe present results of application of a time-resolved optical system for imaging of fluorescence excited in an inclusion containing indocyanine green (ICG), and located in optically turbid medium. The developed imaging system enabled simultaneous acquisition of fluorescence and diffusive reflectance. Eight independent time-resolved measurement channels based on time-correlated single photon counting technique were applied. In four of these channels, used for the fluorescence detection, sets of filters were applied in order to block the excitation light. Fast optomechanical switches allowed us to illuminate sequentially nine different spots on the surface of the studied object and finally 4×4 pixels maps at excitation and emission wavelengths were obtained. A liquid phantom used in this study consists of the fish tank filed with a solution ofmilk and water with black ink added to obtain optical properties in the range of the optical properties typical for the living tissue. A gel ball of a diameter of 5 mm with precisely controlled concentration of ICG was immersed in the liquid. The measurements were performed for inclusion located at different depths and for various ICG concentrations in the gel ball and in the surrounding liquid. The recorded distributions of times of arrival (DTA) of fluorescence photons and times of flight (DTOF) of diffusely reflected photons were analyzed by calculation of their statistical moments. We observed specific changes in moments of the measured DTAs as a function of depth of immersion of the fluorescent inclusion in the medium. We noted also that the changes of moments depend significantly on concentration of the dye in the fluorescence inclusion as well as in the surrounding liquid.


2018 ◽  
Vol 61 (2) ◽  
pp. 391-398 ◽  
Author(s):  
Kevin Tewey ◽  
Alan M. Lefcourt ◽  
Uri Tasch ◽  
Patrick Shilts ◽  
Moon S. Kim

Abstract. To reduce the risk of foodborne illnesses resulting from fecal contamination in produce fields, a hyperspectral, line-scan, laser-induced fluorescence imaging system was developed with the goal of eventually incorporating the imaging system into a pre-harvest detection apparatus for fecal contamination. The imaging system includes an intensified, gated camera, a spectral adapter, a 355 nm pulsed laser, and laser expansion optics that produce a line-illumination profile. To validate and test the system, spinach leaves inoculated with dilutions of bovine fecal material were imaged repeatedly using a predefined set of imaging parameters. These images were used to evaluate methods for detecting fecal contamination. Methods investigated included ratio, edge, threshold, and slope detection. Differences in the magnitude of averaged intensities for the spectral range of 450-500 nm for regions within fecal contamination sites and in nearby uncontaminated surface areas suggested that the 450-500 nm waveband would be a good region for use in detection tests. Validation tests that used threshold or slope detection, the 450-500 nm waveband, and that took advantage of the slower fluorescence decay rates of fecal contamination sites relative to uncontaminated surface areas showed almost 100% detection of 1:2, 1:10, and 1:100 dilution sites and over 70% detection of 1:200 dilution sites with essentially zero false positives. These results suggest that the imaging system has potential for development of a commercially viable apparatus for pre-harvest detection of fecal contamination in produce fields and for detection of fecal contamination of leafy green vegetables in general. Keywords: Fecal detection, Fluorescence imaging, Food safety, Machine vision, Spinach, Time-resolved imaging.


2006 ◽  
Vol 11 (5) ◽  
pp. 054006 ◽  
Author(s):  
Ichiro Sase ◽  
Akira Takatsuki ◽  
Junji Seki ◽  
Toshio Yanagida ◽  
Akitoshi Seiyama

2021 ◽  
Vol 92 (12) ◽  
pp. 123507
Author(s):  
Jack W. D. Halliday ◽  
Simon N. Bland ◽  
Jack. D. Hare ◽  
Susan Parker ◽  
Lee G. Suttle ◽  
...  

2001 ◽  
Vol 41 (supplement) ◽  
pp. S90
Author(s):  
I. Sase ◽  
H. Eda ◽  
A. Takatsuki ◽  
A Seiyama ◽  
T. Yanagida

2010 ◽  
Vol 2 (1) ◽  
pp. 194 ◽  
Author(s):  
Aurélie Laidevant ◽  
Lionel Hervé ◽  
Mathieu Debourdeau ◽  
Jérôme Boutet ◽  
Nicolas Grenier ◽  
...  

2014 ◽  
Author(s):  
F. Powolny ◽  
K. Homicsko ◽  
R. Sinisi ◽  
Claudio E. Bruschini ◽  
E. Grigoriev ◽  
...  

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