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Low-picomolar limits of detection using high-power light-emitting diodes for fluorescence.
Analyst. 2006 May; 131(5):664-9.A

Abstract

Fluorescence detectors are ever more frequently being used with light-emitting diodes (LEDs) as the light source. Technological advances in the solid-state lighting industry have produced LEDs which are also suitable tools in analytical measurements. LEDs are now available which deliver 700 mW of radiometric power. While this greater light power can increase the fluorescence signal, it is not trivial to make proper use of this light. This new generation of LEDs has a large emitting area and a highly divergent beam. This presents a classic problem in optics where one must choose between either a small focused light spot, or high light collection efficiency. We have selected for light collection efficiency, which yields a light spot somewhat larger than the emitting area of the LED. This light is focused onto a flow cell. Increasing the detector cell internal diameter (i.d.) produces gains in (sensitivity)3. However, since the detector cell i.d. is smaller than the LED spot size, scattering of excitation light towards the detector remains a significant source of background signal. This can be minimized through the use of spectral filters and spatial filters in the form of pinholes. The detector produced a limit of detection (LOD) of 3 pM, which is roughly three orders of magnitude lower than other reports of LED-based fluorescence detectors. Furthermore, this LOD comes within a factor of six of much more expensive laser-based fluorescence systems. This detector has been used to monitor a separation from a gel filtration column of fluorescently labeled BSA from residual labeling reagent. The LOD of fluorescently labeled BSA is 25 pM.

Authors+Show Affiliations

Department of Chemistry, Gunning/Lemieux Chemistry Centre, University of Alberta, Edmonton, Alberta T6G 2G2, Canada.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

16633580

Citation

de Jong, Ebbing P., and Charles A. Lucy. "Low-picomolar Limits of Detection Using High-power Light-emitting Diodes for Fluorescence." The Analyst, vol. 131, no. 5, 2006, pp. 664-9.
de Jong EP, Lucy CA. Low-picomolar limits of detection using high-power light-emitting diodes for fluorescence. Analyst. 2006;131(5):664-9.
de Jong, E. P., & Lucy, C. A. (2006). Low-picomolar limits of detection using high-power light-emitting diodes for fluorescence. The Analyst, 131(5), 664-9.
de Jong EP, Lucy CA. Low-picomolar Limits of Detection Using High-power Light-emitting Diodes for Fluorescence. Analyst. 2006;131(5):664-9. PubMed PMID: 16633580.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Low-picomolar limits of detection using high-power light-emitting diodes for fluorescence. AU - de Jong,Ebbing P, AU - Lucy,Charles A, Y1 - 2006/04/05/ PY - 2006/4/25/pubmed PY - 2006/4/25/medline PY - 2006/4/25/entrez SP - 664 EP - 9 JF - The Analyst JO - Analyst VL - 131 IS - 5 N2 - Fluorescence detectors are ever more frequently being used with light-emitting diodes (LEDs) as the light source. Technological advances in the solid-state lighting industry have produced LEDs which are also suitable tools in analytical measurements. LEDs are now available which deliver 700 mW of radiometric power. While this greater light power can increase the fluorescence signal, it is not trivial to make proper use of this light. This new generation of LEDs has a large emitting area and a highly divergent beam. This presents a classic problem in optics where one must choose between either a small focused light spot, or high light collection efficiency. We have selected for light collection efficiency, which yields a light spot somewhat larger than the emitting area of the LED. This light is focused onto a flow cell. Increasing the detector cell internal diameter (i.d.) produces gains in (sensitivity)3. However, since the detector cell i.d. is smaller than the LED spot size, scattering of excitation light towards the detector remains a significant source of background signal. This can be minimized through the use of spectral filters and spatial filters in the form of pinholes. The detector produced a limit of detection (LOD) of 3 pM, which is roughly three orders of magnitude lower than other reports of LED-based fluorescence detectors. Furthermore, this LOD comes within a factor of six of much more expensive laser-based fluorescence systems. This detector has been used to monitor a separation from a gel filtration column of fluorescently labeled BSA from residual labeling reagent. The LOD of fluorescently labeled BSA is 25 pM. SN - 0003-2654 UR - https://www.unboundmedicine.com/medline/citation/16633580/Low_picomolar_limits_of_detection_using_high_power_light_emitting_diodes_for_fluorescence_ DB - PRIME DP - Unbound Medicine ER -
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