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Fluorescence lifetime biosensing with DNA microarrays and a CMOS-SPAD imager

Authors :
Giraud, G. (author)
Schulze, H. (author)
Li, D.U. (author)
Bachmann, T.T. (author)
Crain, J. (author)
Tyndall, D. (author)
Richardson, J. (author)
Walker, R. (author)
Stoppa, D. (author)
Charbon, E. (author)
Henderson, R. (author)
Arlt, J. (author)
Giraud, G. (author)
Schulze, H. (author)
Li, D.U. (author)
Bachmann, T.T. (author)
Crain, J. (author)
Tyndall, D. (author)
Richardson, J. (author)
Walker, R. (author)
Stoppa, D. (author)
Charbon, E. (author)
Henderson, R. (author)
Arlt, J. (author)
Publication Year :
2010

Abstract

Fluorescence lifetime of dye molecules is a sensitive reporter on local microenvironment which is generally independent of fluorophores concentration and can be used as a means of discrimination between molecules with spectrally overlapping emission. It is therefore a potentially powerful multiplexed detection modality in biosensing but requires extremely low light level operation typical of biological analyte concentrations, long data acquisition periods and on-chip processing capability to realize these advantages. We report here fluorescence lifetime data obtained using a CMOS-SPAD imager in conjunction with DNA microarrays and TIRF excitation geometry. This enables acquisition of single photon arrival time histograms for a 320 pixel FLIM map within less than 26 seconds exposure time. From this, we resolve distinct lifetime signatures corresponding to dye-labelled HCV and quantum-dot-labelled HCMV nucleic acid targets at concentrations as low as 10 nM.<br />Micro Electronics<br />Electrical Engineering, Mathematics and Computer Science

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1011351165
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1364.BOE.1.001302