2016
DOI: 10.1111/bjd.14221
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Review of applications of fluorescence excitation spectroscopy to dermatology

Abstract: Endogenous molecules that exhibit fluorescence hold the potential to serve as reporters of tissue structure, activity and physiology. Fluorescence excitation spectroscopy is one means to measure and express tissue's innate fluorescence. This review focuses on the application of endogenous fluorescence ultraviolet excitation spectroscopy to dermatology.

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Cited by 37 publications
(39 citation statements)
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“…In our small sample, the 330 nm excitation band tended to increase with age, consistent with a progressive accumulation of pentosidine, which is in agreement with results reported by Handl et al [23], Uchiyama et al [39] and Senolt [41], in which the concentrations of pentosidine in serum and synovial fluids were observed to be elevated in patients with rheumatoid arthritis (RA) and osteoarthritis. It has also been shown in skin that the fluorescence intensity of this band changes with age [42]. Indentation stiffness E' showed a modest increase with age in our study, but this increase was not statistically significant [R = 0.77, (p = 0.07)].…”
Section: Discussioncontrasting
confidence: 61%
“…In our small sample, the 330 nm excitation band tended to increase with age, consistent with a progressive accumulation of pentosidine, which is in agreement with results reported by Handl et al [23], Uchiyama et al [39] and Senolt [41], in which the concentrations of pentosidine in serum and synovial fluids were observed to be elevated in patients with rheumatoid arthritis (RA) and osteoarthritis. It has also been shown in skin that the fluorescence intensity of this band changes with age [42]. Indentation stiffness E' showed a modest increase with age in our study, but this increase was not statistically significant [R = 0.77, (p = 0.07)].…”
Section: Discussioncontrasting
confidence: 61%
“…This emission band is most likely due to aromatic amino acids: tyrosine, tryptophan, and phenylalanine . As radiation with wavelengths shorter than 300 nm does not propagate significantly into the dermis, the sampled tissue volume for 280 nm radiation resides in the epidermis . Therefore, the observed peak at 340/280 nm (peak emission/peak excitation wavelength) should originate primarily from proteins located in the epidermis of human skin.…”
Section: Discussionmentioning
confidence: 99%
“…The 325 nm excitation generates skin autofluorescence in the region between 360 and 480 nm, apparently consisting of several partially or fully overlapping fluorescence bands with maxima at approximately 390, 420, and 450 nm. The 325 nm excitation can penetrate down to dermis . The most abundant dermis fluorophore is collagen, which, on excitation at 325 nm gives intensive emission peaked at 390‐400 nm with shoulders at around 420 and 460 nm .…”
Section: Discussionmentioning
confidence: 99%
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“…Our group previously developed a UV fluorescence imaging prototype capable of producing images of intrinsic UV fluorescence of tissue 1,2 . Several fluorescence excitation/emission pairs have been identified with molecules that are associated with the structure and function of the skin 3,4 .…”
Section: Introductionmentioning
confidence: 99%