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Journal ArticleDOI

An internal standardization procedure for spectrally resolved fluorescence lifetime imaging.

Quentin S. Hanley, +1 more
- 01 Feb 2005 - 
- Vol. 59, Iss: 2, pp 261-266
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TLDR
Excimer laser fragmentation fluorescence spectroscopy using a 193 nm ArF excimer laser was used to detect atomic Pb emission from solid Pb NO3 and PbNO3 mixed into a soil, holding promise as a rapid and sensitive method for processing soil samples for assessing exposures or the effectiveness of soil remediation.
Abstract
Excimer laser fragmentation fluorescence spectroscopy using a 193 nm ArF excimer laser was used to detect atomic Pb emission from solid PbNO3 and PbNO3 mixed into a soil. The detection method differs from other solid ablation processes in that lower laser fluences can be used where there is no plasma generation and subsequent broadband emission; fluences above 2 J/cm2 resulted in plasma formation. The detection limit for PbNO3 in a single soil type is about 200 ppm, achieved with minimal sample preparation and an analysis time on the order of a minute. The technique holds promise as a rapid and sensitive method for processing soil samples for assessing exposures or the effectiveness of soil remediation.

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Citations
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Journal ArticleDOI

Imaging molecular interactions in living cells by FRET microscopy

TL;DR: FRET imaging provides information about all these molecular processes with high specificity and sensitivity via probes expressed by or introduced from the external medium into the cell, tissue or organism.
Journal Article

Time-gated fluorescence lifetime imaging and microvolume spectroscopy using two-photon excitation

TL;DR: In this paper, a two-photon excitation in combination with fluorescence lifetime contrast is presented, which can be used to quantify concentrations of ions, such as pH and Ca2+, or pO2 and pCO2.
Book ChapterDOI

Quantitative fluorescence microscopy techniques.

TL;DR: Quantitative fluorescence microscopy techniques offer powerful tools for understanding the physiological and pathological roles of molecular machineries in the living cell.
Journal ArticleDOI

Spectrally resolved frequency domain analysis of multi-fluorophore systems undergoing energy transfer.

TL;DR: This work systematically investigates systems of multiple fluorophores with and without energy transfer to provide insight into frequency domain investigations of complex systems of fluorophore.
Journal ArticleDOI

Spectrally resolved fluorescent lifetime imaging

TL;DR: Spectrally resolved fluorescence lifetime imaging (SFLIM) as discussed by the authors is a method that uses a spectrograph or related components capable of generating a spectrum between a microscope and the image intensifier of a conventional FLIM system, which provides a number of opportunities not readily available to conventional systems using bandpass filters.
References
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Journal ArticleDOI

Quantitative Imaging of Lateral ErbB1 Receptor Signal Propagation in the Plasma Membrane

TL;DR: The rapid and extensive propagation of receptor phosphorylation over the entire cell after focal stimulation demonstrates a signaling wave at the plasma membrane resulting in full activation of all receptors.
Journal ArticleDOI

Graphical representation and multicomponent analysis of single‐frequency fluorescence lifetime imaging microscopy data

TL;DR: Graphical representation of fluorescence lifetime imaging microscopy data demonstrates that a mixture of two components with single exponential decays can be resolved by single frequency measurements and derives a method based on linear fitting that allows the calculation of the fluorescence lifetimes of the two components.
Journal ArticleDOI

Theoretical investigation of the signal-to-noise ratio in fluorescence lifetime imaging.

TL;DR: For a given number of detected photons, it is found that frequency-domain and time-domain methods are equally good for fluorescence lifetime imaging.
Journal ArticleDOI

Fluorescence lifetime imaging: multi-point calibration, minimum resolvable differences, and artifact suppression.

TL;DR: A multi-point calibration method is described and applied to demonstrate a previously unreported degree of lifetime resolution in a FLIM microscope, applicable to any system consisting of single-component lifetimes.
Journal ArticleDOI

Time-gated fluorescence lifetime imaging and microvolume spectroscopy using two-photon excitation

TL;DR: In this article, a two-photon excitation in combination with fluorescence lifetime contrast is presented, which can be used to quantify concentrations of ions, such as pH and Ca2+, or pO2 and pCO2.
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