2003Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIERequires access

Time-delayed fluorescence imaging of a porphycene derivative

Sarah L. Gundy, Wilhelm J. van der Putten, A. Shearer, Daniel J. Buckton, Alan George Ryder, Michael Ball

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Abstract

Porphycenes are currently under investigation for use in Photodynamic therapy, which is a promising treatment for cancer. These materials, which display preferential uptake in cancerous cells, also exhibit high fluorescence yields, and can be used for tumour detection. Problems with steady-state fluorescence techniques such as background autofluorescence can be eliminated by the use of time-resolved techniques. Improved contrast can be obtained with time-resolved techniques because of the differing fluorescence lifetimes between autofluorescence and longer-living exogenous photosensitisers. An imaging system was constructed using a fast (200 ps) gated CCD camera and a pulsed 635 nm laser diode. A tissue phantom composed of polymethyl methacrylate (PMMA) with thirty-six wells of varying diameter and depth (10 mm to 1 mm) was assembled to test the system. The system was used to record images of a porphycene derivative within the wells at differing concentrations in an organic solvent. A tissue imitator was placed on top of the PMMA block at varying thickness. 10-4 M zinc phthalocyanine tetrasulfonate was also placed on top of the block to mimic autofluorescence. The results indicate that the time-gated imaging system can prevent background excitation scatter and fluorescence from a shorter-lived fluorophore from distorting the fluorescence signal from a longer-lived photosensitiser.

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What this paper is about

Porphycenes are currently under investigation for use in Photodynamic therapy, which is a promising treatment for cancer. These materials, which display preferential uptake in cancerous cells, also exhibit high fluorescence yields, and can be used for tumour detection. Problems with steady-state fluorescence techniques such as background autofluorescence can be eliminated by the use of time-resolved techniques. Improved contrast can be obtained with time-resolved techniques because of the differing fluorescence lifetimes between autofluorescence and longer-living exogenous photosensitisers. An imaging system was constructed using a fast (200 ps) gated CCD camera and a pulsed 635 nm laser diode. A tissue phantom composed of polymethyl methacrylate (PMMA) with thirty-six wells of varying diameter and depth (10 mm to 1 mm) was assembled to test the system. The system was used to record images of a porphycene derivative within the wells at differing concentrations in an organic solvent. A tissue imitator was placed on top of the PMMA block at varying thickness. 10-4 M zinc phthalocyanine tetrasulfonate was also placed on top of the block to mimic autofluorescence. The results indicate that the time-gated imaging system can prevent background excitation scatter and fluorescence from a shorter-lived fluorophore from distorting the fluorescence signal from a longer-lived photosensitiser.

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Available abstract

Porphycenes are currently under investigation for use in Photodynamic therapy, which is a promising treatment for cancer. These materials, which display preferential uptake in cancerous cells, also exhibit high fluorescence yields, and can be used for tumour detection. Problems with steady-state fluorescence techniques such as background autofluorescence can be eliminated by the use of time-resolved techniques. Improved contrast can be obtained with time-resolved techniques because of the differing fluorescence lifetimes between autofluorescence and longer-living exogenous photosensitisers. An imaging system was constructed using a fast (200 ps) gated CCD camera and a pulsed 635 nm laser diode. A tissue phantom composed of polymethyl methacrylate (PMMA) with thirty-six wells of varying diameter and depth (10 mm to 1 mm) was assembled to test the system. The system was used to record images of a porphycene derivative within the wells at differing concentrations in an organic solvent. A tissue imitator was placed on top of the PMMA block at varying thickness. 10-4 M zinc phthalocyanine tetrasulfonate was also placed on top of the block to mimic autofluorescence. The results indicate that the time-gated imaging system can prevent background excitation scatter and fluorescence from a shorter-lived fluorophore from distorting the fluorescence signal from a longer-lived photosensitiser.

Key concepts: Autofluorescence, Fluorescence, Fluorophore, Materials science, Fluorescence-lifetime imaging microscopy, Luminescence, Optics, Time-resolved spectroscopy

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