Published August 2015 | Version v1
Journal article

Technical parameters of vertical in vivo multiphoton microscopy: a critical evaluation of the flyscanning method

  • 1. Department of Dermatology, Venerology and Allergology, Charité-Universitätsmedizin Berlin, Berlin (Germany)
  • 2. W.O.M. WORLD OF MEDICINE GmbH, Berlin (Germany)
  • 3. Dermatologie am Regierungsviertel, Berlin (Germany)
  • 4. Department of Dermatology and Venerology, Otto-von-Guericke University, Magdeburg (Germany)

Description

The optical biopsy could be a quick and painless support or alternative to a punch biopsy. In this letter the first in vivo vertical wide field two photon microscopy (2PM) images of healthy volunteers are shown. The 2PM images are fused images of two photon excited auto fluorescence (AF) and second harmonic generation (SHG) signals given as false-color images of 200 μm  ×  7 mm in size. By using these two nonlinear effects, the epidermis can be easily distinguished from the dermis at a glance. The auto fluorescence provides cellular resolution of the epidermal cells, and elastin fibers are partly visible in the dermis. Collagen, visible by SHG signal, is the dominant structure in the dermis. As contact agent water was evaluated to increase the AF signal, especially in the deeper layers of epidermis and dermis. For further improvement any terminal hairs should be removed by shaving and by taking tape strips of the first five layers of the stratum corneum. The first images illustrated that young skin compared to aged skin shows remarkably different dermal elastin and collagen signals in the dermis. (letter)

Availability note (English)

Available from http://dx.doi.org/10.1088/1612-2011/12/8/085602

Additional details

Publishing Information

Journal Title
Laser Physics Letters (Internet)
Journal Volume
12
Journal Issue
8
Journal Page Range
[7 p.]
ISSN
1612-202X