Literature DB >> 19207664

Combined non-linear laser imaging (two-photon excitation fluorescence microscopy, fluorescence lifetime imaging microscopy, multispectral multiphoton microscopy) in cutaneous tumours: first experiences.

V De Giorgi1, D Massi, S Sestini, R Cicchi, F S Pavone, T Lotti.   

Abstract

BACKGROUND: Two-photon excitation (TPE) fluorescence microscopy is a high-resolution laser-scanning imaging technique enabling deep imaging inside biological tissues. TPE microscopy has the triple advantage of offering high spatial resolution (250 nm radially, 800 nm axially), high penetration depth inside skin (200 mm ), and low photodamage effects. Further, cells and extracellular matrix intrinsically contain a variety of fluorescent molecules (NADH, tryptophan, keratins, melanin, elastin, cholecalciferol and others), so that biological tissues can be imaged by TPE microscopy without any exogenous probe. The time-resolved analysis of the fluorescence signal, known as fluorescence lifetime imaging microscopy (FLIM), is an additional non-invasive microscopy technique useful to characterize endogenous fluorescence species and their surrounding medium by measuring the mean lifetime of fluorescent emission. Finally, multispectral (MTPE) tissue imaging can also be used to identify different endogenous fluorescent species by measuring their two photon emission spectra. Those techniques offer functional information about the relative quantities of fluorescent molecules, which are correlated with tissue structure in physiological and pathological states.
OBJECTIVE: We have decided to apply these three methods at the same time for cutaneous tumors in order to evaluate their possible future use.
METHOD: We have analyzed a melanoma and a basal cell carcinoma, with their surrounding healthy skin, to evaluate any difference in healthy skin and neoplasia. The samples were excised during dermatological surgery, then cut, saving some healthy skin in both, to obtain a regular shape, allowing its positioning either with the skin surface parallel to the optical axis (horizontal optical sectioning), or perpendicular (vertical optical sectioning).
CONCLUSION: This first result demonstrates that FLIM is effective in discriminating healthy skin from MM, while MTPE is effective in discriminating healthy skin from BCC.

Entities:  

Mesh:

Year:  2009        PMID: 19207664     DOI: 10.1111/j.1468-3083.2008.03045.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   6.166


  15 in total

1.  Deconvolution of fluorescence lifetime imaging microscopy by a library of exponentials.

Authors:  Daniel U Campos-Delgado; O Gutierrez Navarro; E R Arce-Santana; Alex J Walsh; Melissa C Skala; Javier A Jo
Journal:  Opt Express       Date:  2015-09-07       Impact factor: 3.894

2.  Blind deconvolution estimation of fluorescence measurements through quadratic programming.

Authors:  Daniel U Campos-Delgado; Omar Gutierrez-Navarro; Edgar R Arce-Santana; Melissa C Skala; Alex J Walsh; Javier A Jo
Journal:  J Biomed Opt       Date:  2015-07       Impact factor: 3.170

3.  In vivo nonlinear spectral imaging as a tool to monitor early spectroscopic and metabolic changes in a murine cutaneous squamous cell carcinoma model.

Authors:  Giju Thomas; Johan van Voskuilen; Hoa Truong; Ji-Ying Song; Hans C Gerritsen; H J C M Sterenborg
Journal:  Biomed Opt Express       Date:  2014-11-13       Impact factor: 3.732

Review 4.  Molecular probes for fluorescence lifetime imaging.

Authors:  Pinaki Sarder; Dolonchampa Maji; Samuel Achilefu
Journal:  Bioconjug Chem       Date:  2015-05-22       Impact factor: 4.774

Review 5.  Intravital imaging of anti-tumor immune response and the tumor microenvironment.

Authors:  Tomasz Zal; Grzegorz Chodaczek
Journal:  Semin Immunopathol       Date:  2010-07-22       Impact factor: 9.623

Review 6.  Reflectance confocal microscopy of skin in vivo: From bench to bedside.

Authors:  Milind Rajadhyaksha; Ashfaq Marghoob; Anthony Rossi; Allan C Halpern; Kishwer S Nehal
Journal:  Lasers Surg Med       Date:  2016-10-27       Impact factor: 4.025

Review 7.  Two-photon and second harmonic microscopy in clinical and translational cancer research.

Authors:  Seth W Perry; Ryan M Burke; Edward B Brown
Journal:  Ann Biomed Eng       Date:  2012-01-19       Impact factor: 3.934

8.  Fluorescence lifetime imaging of alterations to cellular metabolism by domain 2 of the hepatitis C virus core protein.

Authors:  Nirmal Mazumder; Rodney K Lyn; Ragunath Singaravelu; Andrew Ridsdale; Douglas J Moffatt; Chih-Wei Hu; Han-Ruei Tsai; John McLauchlan; Albert Stolow; Fu-Jen Kao; John Paul Pezacki
Journal:  PLoS One       Date:  2013-06-24       Impact factor: 3.240

9.  Multiphoton laser microscopy and fluorescence lifetime imaging for the evaluation of the skin.

Authors:  Stefania Seidenari; Federica Arginelli; Sara Bassoli; Jennifer Cautela; Paul M W French; Mario Guanti; Davide Guardoli; Karsten König; Clifford Talbot; Chris Dunsby
Journal:  Dermatol Res Pract       Date:  2011-11-28

10.  Multiphoton multispectral fluorescence lifetime tomography for the evaluation of basal cell carcinomas.

Authors:  Rakesh Patalay; Clifford Talbot; Yuriy Alexandrov; Martin O Lenz; Sunil Kumar; Sean Warren; Ian Munro; Mark A A Neil; Karsten König; Paul M W French; Anthony Chu; Gordon W H Stamp; Chris Dunsby
Journal:  PLoS One       Date:  2012-09-11       Impact factor: 3.240

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