TY - JOUR
T1 - Temperature dependent fluorescence of A2-E, the main fluorescent lipofuscin component in the RPE
AU - Framme, Carsten
AU - Schüle, Georg
AU - Birngruber, Reginald
AU - Roider, Johann
AU - Schütt, Florian
AU - Kopitz, Jürgen
AU - Holz, Frank G.
AU - Brinkmann, Ralf
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2004/10
Y1 - 2004/10
N2 - Purpose. A2-E is the dominant fluorophore of lipofuscin in the retinal pigment epithelium. In an in-vitro setup, we determined the temperature- dependent changes of the A2-E fluorescence with the aim of also assessing the potential value of such measurements for determining retinal temperature by autofluorescence measurements during laser treatment. Methods. A2-E was biosynthesized and diluted in Dimethyl Sulfoxide (DMSO) to 1 μM. Fluorescence measurements were performed with a photospectrometer under various temperatures ranging from 20°C to 75°C. Autofluorescence was excited at 467 nm, and emission was detected around 632 nm. Results. A2-E fluorescence intensity showed a linear decrease concomitant with temperature increment. At 75°C, the fluorescence intensity decreased by 43% compared to at 20°C. Fluorescence intensity was completely reversible dependent on the temperature, which cannot be explained by thermal A2-E alteration. Conclusions. If the A2-E temperature-dependent fluorescence in-vitro is transferable to human fundus autofluorescence, then it may be possible to apply an autofluorescence-based online detection device for noninvasive determination of fundus temperature during in vivo laser treatment. This is of clinical relevance, especially for the application of photodynamic therapy (PDT) and transpupillary thermotherpy (TTT).
AB - Purpose. A2-E is the dominant fluorophore of lipofuscin in the retinal pigment epithelium. In an in-vitro setup, we determined the temperature- dependent changes of the A2-E fluorescence with the aim of also assessing the potential value of such measurements for determining retinal temperature by autofluorescence measurements during laser treatment. Methods. A2-E was biosynthesized and diluted in Dimethyl Sulfoxide (DMSO) to 1 μM. Fluorescence measurements were performed with a photospectrometer under various temperatures ranging from 20°C to 75°C. Autofluorescence was excited at 467 nm, and emission was detected around 632 nm. Results. A2-E fluorescence intensity showed a linear decrease concomitant with temperature increment. At 75°C, the fluorescence intensity decreased by 43% compared to at 20°C. Fluorescence intensity was completely reversible dependent on the temperature, which cannot be explained by thermal A2-E alteration. Conclusions. If the A2-E temperature-dependent fluorescence in-vitro is transferable to human fundus autofluorescence, then it may be possible to apply an autofluorescence-based online detection device for noninvasive determination of fundus temperature during in vivo laser treatment. This is of clinical relevance, especially for the application of photodynamic therapy (PDT) and transpupillary thermotherpy (TTT).
UR - http://www.scopus.com/inward/record.url?scp=11844255441&partnerID=8YFLogxK
U2 - 10.1080/02713680490516846
DO - 10.1080/02713680490516846
M3 - Journal articles
C2 - 15590474
AN - SCOPUS:11844255441
SN - 0271-3683
VL - 29
SP - 287
EP - 291
JO - Current Eye Research
JF - Current Eye Research
IS - 4-5
ER -