Development of a handheld fluorescence imaging device to investigate the characteristics of protoporphyrin IX fluorescence in healthy and diseased skin.

Autor: Kulyk O; Organic Semiconductor Centre, SUPA, School of Physics and Astronomy, The University of St Andrews, North Haugh, St Andrews, Fife KY16 9SS, UK., Ibbotson SH; The Photobiology Unit, University of Dundee, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK; The Scottish Photodynamic Therapy Centre, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK. Electronic address: s.h.ibbotson@dundee.ac.uk., Moseley H; The Photobiology Unit, University of Dundee, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK; The Scottish Photodynamic Therapy Centre, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK., Valentine RM; The Photobiology Unit, University of Dundee, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK; The Scottish Photodynamic Therapy Centre, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK., Samuel ID; Organic Semiconductor Centre, SUPA, School of Physics and Astronomy, The University of St Andrews, North Haugh, St Andrews, Fife KY16 9SS, UK. Electronic address: idws@st-andrews.ac.uk.
Jazyk: angličtina
Zdroj: Photodiagnosis and photodynamic therapy [Photodiagnosis Photodyn Ther] 2015 Dec; Vol. 12 (4), pp. 630-9. Date of Electronic Publication: 2015 Oct 20.
DOI: 10.1016/j.pdpdt.2015.10.002
Abstrakt: Background: Topical Photodynamic therapy (PDT) is an effective treatment for superficial non-melanoma skin cancers (NMSC) and dysplasia. During PDT light activates the photosensitiser (PpIX), metabolised from a topical pro-drug. A combination of PpIX, light and molecular oxygen results in inflammation and cell death. However, the outcomes of the treatment could be better. Insufficient biosynthesis of PpIX may be one of the causes of incomplete response or recurrence. Measuring surface fluorescence is usually employed as a means of studying PpIX formation. The aim of this work was to develop a device and a method for convenient fluorescence imaging in clinical settings to gather information on PpIX metabolism in healthy skin and NMSC with a view to improving PDT regimes.
Methods: A handheld fluorescence camera and a time course imaging method was developed and used in healthy volunteers and patients diagnosed with basal cell carcinoma (BCC) and actinic keratosis (AK). The photosensitiser (precursor) creams used were 5-aminolaevulinic acid (ALA; Ameluz(®)) and methyl aminolevulinate (MAL; Metvix(®)). Pain was assessed using a visual analogue score immediately after the PDT.
Results: Fluorescence due to PpIX increases over three hours incubation in healthy skin and in lesional BCC and AK. Distribution of PpIX fluorescence varies between the lesion types and between subjects. There was no significant correlation between PpIX fluorescence characteristics and pro-drug, diagnosis or pain experienced. However, there was a clear dependence on body site.
Conclusion: The device and the method developed can be used to assess the characteristics of PpIX fluorescence, quantitative analysis and time course. Our findings show that body site influences PpIX fluorescence which we suggest may be due to the difference in skin temperature at different body sites.
(Copyright © 2015. Published by Elsevier B.V.)
Databáze: MEDLINE
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