Application of Nonlinear Optical Microscopy for Imaging Skin

被引:43
作者
Hanson, Kerry M. [1 ]
Bardeen, Christopher J. [1 ]
机构
[1] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
基金
美国国家科学基金会;
关键词
HUMAN STRATUM-CORNEUM; 2-PHOTON CONFOCAL MICROSCOPY; VIVO HUMAN SKIN; IN-VIVO; 2ND-HARMONIC GENERATION; MULTIPHOTON FLUORESCENCE; OLEIC-ACID; PH GRADIENT; EX-VIVO; TRANSDERMAL DIFFUSION;
D O I
10.1111/j.1751-1097.2008.00508.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Recent advances in the use of nonlinear optical microscopy (NLOM) in skin microscopy are presented. Nonresonant spectroscopies including second harmonic generation, coherent anti-Stokes Raman and two-photon absorption are described and applications to problems in skin biology are detailed. These nonlinear techniques have several advantages over traditional microscopy methods that rely on one-photon excitation: intrinsic 3D imaging with < 1 mu m spatial resolution, decreased photodamage to tissue samples and penetration depths up to 1000 mu m with the use of near-infrared lasers. Thanks to these advantages, nonlinear optical spectroscopy has become a powerful tool to study the physical and biochemical properties of the skin. Structural information can be obtained using the response of endogenous chemical species in the skin, such as collagen or lipids, indicating that optical biopsy may replace current invasive, time-consuming traditional histology methods. Insertion of specific probe molecules into the skin provides the opportunity to monitor specific biochemical processes such as skin transport, molecular penetration, barrier homeostasis and ultraviolet radiation-induced reactive oxygen species generation. While the field is quite new, it seems likely that the use of NLOM to probe structure and biochemistry of live skin samples will only continue to grow.
引用
收藏
页码:33 / 44
页数:12
相关论文
共 103 条
[1]
*AAD, 2004, BURD SKIN DIS
[2]
ALCALA JR, 1985, ANAL INSTRUM, V14, P225
[3]
Interaction of human apolipoprotein A-I with model membranes exhibiting lipid domains [J].
Arnulphi, C ;
Sánchez, SA ;
Tricerri, MA ;
Gratton, E ;
Jonas, A .
BIOPHYSICAL JOURNAL, 2005, 89 (01) :285-295
[4]
Two photon fluorescence microscopy of coexisting lipid domains in giant unilamellar vesicles of binary phospholipid mixtures [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :290-305
[5]
Neonatal development of the stratum corneum pH gradient: Localization and mechanisms leading to emergence of optimal barrier function [J].
Behne, MJ ;
Barry, NP ;
Hanson, KM ;
Aronchik, I ;
Clegg, RW ;
Gratton, E ;
Feingold, K ;
Holleran, WM ;
Elias, PM ;
Mauro, TM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (06) :998-1006
[6]
NHE1 regulates the stratum corneum permeability barrier homeostasis - Microenvironment acidification assessed with fluorescence lifetime imaging [J].
Behne, MJ ;
Meyer, JW ;
Hanson, KM ;
Barry, NP ;
Murata, S ;
Crumrine, D ;
Clegg, RW ;
Gratton, E ;
Holleran, WM ;
Elias, PM ;
Mauro, TM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (49) :47399-47406
[7]
Bennett BD, 1996, J BIOL CHEM, V271, P3647
[8]
Multifocal multiphoton microscopy [J].
Bewersdorf, J ;
Pick, R ;
Hell, SW .
OPTICS LETTERS, 1998, 23 (09) :655-657
[9]
Navigating transdermal diffusion with multiphoton fluorescence lifetime imaging [J].
Bird, D. K. ;
Schneider, A. L. ;
Watkinson, A. C. ;
Finnin, B. ;
Smith, T. A. .
JOURNAL OF MICROSCOPY-OXFORD, 2008, 230 (01) :61-69
[10]
Real-time two-photon confocal microscopy using a femtosecond, amplified Ti:sapphire system [J].
Brakenhoff, GJ ;
Squier, J ;
Norris, T ;
Bliton, AC ;
Wade, MH ;
Athey, B .
JOURNAL OF MICROSCOPY, 1996, 181 :253-259