Abstract:The use of intrinsic fluorescence to characterise airborne particles is often applied to the detection of biological materials, particularly micro-organisms. However, as a number of particles which are found in the atmosphere also fluoresce (whether natural or artificially generated), simple measures of particle fluorescence alone may not be sufficient to indicate the presence of biological agents in the atmosphere. An instrument has been developed for the real-time measurement of aerosols using UV induced flu… Show more
“…The problem is summarised in Figure 20.22 where it is shown how a combination of measurement of particle size, particle shape and particle nature (biological versus nonbiological) can provide options for rapid detection and identification Figure 20.22 Diagram to indicate how a combination of measurement of particle size, particle shape and particle nature (biological versus nonbiological) can provide options for rapid detection and identification of bioaerosols of bioaerosols and narrow down the discrimination process (Foot et al, 2004). The 'fluorescent aerosol particle sizer' approach allows identification of the presence of biological material but not specific biological species.…”
“…The problem is summarised in Figure 20.22 where it is shown how a combination of measurement of particle size, particle shape and particle nature (biological versus nonbiological) can provide options for rapid detection and identification Figure 20.22 Diagram to indicate how a combination of measurement of particle size, particle shape and particle nature (biological versus nonbiological) can provide options for rapid detection and identification of bioaerosols of bioaerosols and narrow down the discrimination process (Foot et al, 2004). The 'fluorescent aerosol particle sizer' approach allows identification of the presence of biological material but not specific biological species.…”
“…These detectors can reach close to real-time warning. Multiple excitations (266 and 355 nm) for the detection of bioaerosols have been reported [5] as well as the spectral characteristics of fluorescence from particles excited at 266 nm [6][7][8]. In order to increase the specificity and lower the false positive alarms, we are developing an early-warning system measuring the fluorescence spectrum of individual BWA aerosol particles excited with dual wavelengths (about 290 nm and 340 nm) ultraviolet (UV) laser pulses.…”
We present initial results of a measurement system designed for detecting the fluorescence spectrum of individual particles of biological warfare agent (BWA). A compact optical parametric oscillator with intracavity sum-frequency mixing and a commercial Nitrogen gas laser was used as excitation sources to generate 293 nm or 337 nm UV laser irradiation. The pulsed lasers and a photomultiplier tube (PMT) array based spectrometer were triggered by a red laserdiode and a PMT detector that sensed the presence of a particle typical of size 5-20 µm in diameter. The spectral detection part of the system consisted of a grating and a PMT array with 32 channels, which measured fluorescence in the wavelength from 280 nm to 800 nm. The detector system was used to demonstrate the measurement of laser induced fluorescence spectra of individual BWA simulant particles by excitation of single UV laser pulses. The spectrum obtained by averaging spectra from several BWA aerosol simulant particles were found generally similar, but not identical, to the fluorescence spectrum obtained from water solutions containing the same particles dissolved.
“…In the earliest systems, continuous wave lasers were employed, for example 1,2 , though these were usually large and fragile and operated at wavelengths which were too long for efficient excitation of some of the important bio-fluorophores such as tryptophan, for which optimal excitation occurred at wavelengths of ~260-280 nm. Hence the use of various solid-state lasers employing harmonic generation, such as frequency quadrupled Nd-YAG lasers, has gained acceptance [3][4][5][6][7][8][9][10][11] , both for the output wavelength of 266nm and because they offered a generally smaller form-factor than continuous-wave gas lasers.…”
Original article can be found at: http://spie.org/x306.xml Copyright SPIE DOI: 10.1117/12.629868 [Full text of this article is not available in the UHRA]Laser diodes and light-emitting diodes capable of continuous sub-300 nm radiation emission will ultimately represent optimal excitation sources for compact and fieldable bio-aerosol monitors. However, until such devices are routinely available and whilst solid-state UV lasers remain relatively expensive, other low-cost sources of UV can offer advantages. This paper describes one such prototype that employs compact xenon discharge UV sources to excite intrinsic fluorescence from individual particles within an ambient aerosol sample. The prototype monitor samples ambient air via a laminar sheathed-flow arrangement such that particles within the sample flow column are rendered in single file as they intersect the beam from a continuous-wave 660nm diode laser. Each individual particle produces a scattered light signal from which an estimate of particle size (down to ~1 um) may be derived. This same signal also initiates the sequential firing (~10 us apart) of two xenon sources which irradiate the particle with UV pulses centred upon ~280 nm and ~370 nm wavelength, optimal for excitation of bio-fluorophores tryptophan and NADH respectively. For each excitation wavelength, fluorescence is detected across two bands embracing the peak emissions of the same bio-fluorophores. Thus, for each particle, a 2-dimensional fluorescence excitation-emission matrix is recorded together with an estimate of particle size. Current measurement rates are up to ~125 particles/s (limited by the xenon recharge time), corresponding to all particles for concentrations up to ~2 x 10^4 particles/l. Developments to increase this to ~500 particles/s are in hand. Analysis of results from aerosols of E.coli, BG spores, and a variety of non-biological materials are given
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