2006
DOI: 10.1562/2006-04-14-ir-874
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Symposium‐in‐Print: Singlet Oxygen Invited Review

Abstract: Singlet oxygen (1O2) is unique amongst reactive oxygen species formed in cells in that it is an excited state molecule with an inherent upper lifetime of 4 micros in water. Whether the lifetime of 1O2 in cells is shortened by reactions with cellular molecules or reaches the inherent maximum value is still unclear. However, even with the maximum lifetime, the diffusion radius is only approximately 220 nm during three lifetimes (approximately 5% 1O2 remaining), much shorter than cellular dimensions indicating th… Show more

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Cited by 387 publications
(385 citation statements)
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References 80 publications
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“…Such approaches can be categorized into several different data types, as outlined in table 1. These [7][8][9] spectral derivative data multiple analyte analysis [10][11][12] fluorescence/excitation ratio fluorescence imaging [13][14][15] multi-distance data estimation of slopes with linear approximations robust tissue spectroscopy systems insensitive to slight shape changes [16][17][18] small-volume sampling scatter spectroscopy fibre probes with size less than effective scatter distance [19][20][21][22] absorption spectroscopy fibre probes sensitive to absorption only [23,24] fluorescence spectroscopy fibre probes sensitive to fluorescence and not tissue [25,26] temporal signals millisecond variations in tissue oxygen saturation and haemodynamic sampling [8,27,28] microsecond sampling flash photolysis analysis of biochemical changes in vivo [29,30] picosecond sampling ultrafast signals to reduce model dependence [31][32][33][34][35] high-frequency phase shift derivative with distance frequency-domain spectroscopy of tissue [36,37] lifetime-based signals fluorophore identification or microenvironment analysis [38] include: (i) ratiometric or derivative data at two or more different wavelengths, (ii) multiple-distance ratio or derivative data, (iii) small spatial volumes that either limit the effect of physical boundaries through scatter and/or absorption, or allow simpler empirical modelling, and (iv) temporal signals that are less sensitive to boundaries and/or more robustly insensitive to shape changes. The use of prior information about the tissue to be sampled is still essential in the design process with these systems, but can be implemented in the very first step o...…”
Section: Prior Information: Structure (A) External Shape and Internalmentioning
confidence: 99%
“…Such approaches can be categorized into several different data types, as outlined in table 1. These [7][8][9] spectral derivative data multiple analyte analysis [10][11][12] fluorescence/excitation ratio fluorescence imaging [13][14][15] multi-distance data estimation of slopes with linear approximations robust tissue spectroscopy systems insensitive to slight shape changes [16][17][18] small-volume sampling scatter spectroscopy fibre probes with size less than effective scatter distance [19][20][21][22] absorption spectroscopy fibre probes sensitive to absorption only [23,24] fluorescence spectroscopy fibre probes sensitive to fluorescence and not tissue [25,26] temporal signals millisecond variations in tissue oxygen saturation and haemodynamic sampling [8,27,28] microsecond sampling flash photolysis analysis of biochemical changes in vivo [29,30] picosecond sampling ultrafast signals to reduce model dependence [31][32][33][34][35] high-frequency phase shift derivative with distance frequency-domain spectroscopy of tissue [36,37] lifetime-based signals fluorophore identification or microenvironment analysis [38] include: (i) ratiometric or derivative data at two or more different wavelengths, (ii) multiple-distance ratio or derivative data, (iii) small spatial volumes that either limit the effect of physical boundaries through scatter and/or absorption, or allow simpler empirical modelling, and (iv) temporal signals that are less sensitive to boundaries and/or more robustly insensitive to shape changes. The use of prior information about the tissue to be sampled is still essential in the design process with these systems, but can be implemented in the very first step o...…”
Section: Prior Information: Structure (A) External Shape and Internalmentioning
confidence: 99%
“…The cellular response to PDT also depends on the primary organelle targeted by the photosensitiser. 7, 8 Most clinical photosensitisers induce apoptosis, generally via direct damage to the mitochondria; 7 however, a secondary apoptotic response can be achieved by initial damage to the lysosomes. 7 Photofrin ® , on the 60 other hand, localises in cell membranes and PDT with this photosensitiser is reported to induce necrosis.…”
Section: Introductionmentioning
confidence: 99%
“…From this viewpoint, reaction involving homolytic fission is advantageous because the reaction can be terminated by cessation of irradiation of γ-ray, ultraviolet ligh or ultrasound. Since hydroxyl radicals have a very short lifetime (approximately 10 À9 s) [44,45,25], residual toxicity would be negligible after the termination of reaction. On the other hand, it might be difficult to control the reaction of one-electron reduction of H 2 O 2 during the disinfection treatment.…”
Section: Application Of Hydroxyl Radicals To Disinfection Treatmentmentioning
confidence: 99%
“…Our recent study demonstrated that hydroxyl radicals would not induce bacterial resistance as singlet oxygen does not [36]. In addition, hydroxyl radicals have higher oxidation power than singlet oxygen [25], resulting in higher antimicrobial activity. In this chapter, the generation systems of hydroxyl radicals and their microbicidal activity are discussed based on our recent works.…”
Section: Introductionmentioning
confidence: 97%
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