In vivo multiphoton tomography of skin during wound healing and scar formation

Multiphoton tomography based on femtosecond laser NIR (near infrared) pulses was used to perform non-invasive optical sectioning of skin with high spatial and intracellular resolution. Scar formation due to formation of collagen fibers is an important aspect during wound healing processes in skin and tissues and was monitored in vivo using the system DermaInspect. Multiphoton tomography was performed of a dermal wound after nevi extraction. The healing process and the aggregation of collagen fibers could be long term monitored due to the autofluorescence of endogenous fluorophores and SHG of collagen. The system DermaInspect might become a high resolution diagnostic tool for dermatological diagnostics and monitoring therapeutic effects.

[1]  Martin Kaatz,et al.  In vivo multiphoton tomography of inflammatory tissue and melanoma , 2005, SPIE BiOS.

[2]  Colin J. R. Sheppard,et al.  Comparison of three‐dimensional imaging properties between two‐photon and single‐photon fluorescence microscopy , 1995 .

[3]  K. Fujita [Two-photon laser scanning fluorescence microscopy]. , 2007, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[4]  John White,et al.  Long-term two-photon fluorescence imaging of mammalian embryos without compromising viability , 1999, Nature Biotechnology.

[5]  Peter Fischer,et al.  Optical tomography of pigmented human skin biopsies , 2004, SPIE BiOS.

[6]  F. A. Navarro,et al.  Two-Photon Confocal Microscopy: A Nondestructive Method for Studying Wound Healing , 2004, Plastic and reconstructive surgery.

[7]  Peter Fischer,et al.  Optical tomography of human skin with subcellular spatial and picosecond time resolution using intense near infrared femtosecond laser pulses , 2002, SPIE BiOS.

[8]  B R Masters,et al.  Multiphoton Excitation Microscopy of In Vivo Human Skin: Functional and Morphological Optical Biopsy Based on Three‐Dimensional Imaging, Lifetime Measurements and Fluorescence Spectroscopy a , 1998, Annals of the New York Academy of Sciences.

[9]  P. So,et al.  Two-Photon deep tissue ex vivo imaging of mouse dermal and subcutaneous structures. , 1998, Optics express.

[10]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[11]  K J Halbhuber,et al.  Pulse-length dependence of cellular response to intense near-infrared laser pulses in multiphoton microscopes. , 1999, Optics letters.

[12]  B. Tromberg,et al.  Imaging cells and extracellular matrix in vivo by using second-harmonic generation and two-photon excited fluorescence , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Gerald W. Lucassen,et al.  Two-photon fluorescence microscopy of in-vivo human skin , 2000, European Conference on Biomedical Optics.

[14]  Iris Riemann,et al.  High-resolution multiphoton tomography of human skin with subcellular spatial resolution and picosecond time resolution. , 2003, Journal of biomedical optics.

[15]  Iris Riemann,et al.  In vivo multiphoton tomography of skin as a tool to study the effects of topically applied probes and UV exposure , 2005, SPIE BiOS.

[16]  Guy Cox,et al.  3-dimensional imaging of collagen using second harmonic generation. , 2003, Journal of structural biology.