Abstract

We use optical coherence tomography (OCT) to systematically study the dependence of the optical attenuation coefficient μ <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">t</sub> upon the applied pressure P in different depth regions of the human skin in vivo. We find that the same OCT data can be used to estimate thicknesses of the epidermis layer and the epidermis-dermis junction and obtain the thickness changes in these skin layers induced by the pressure. We further propose and demonstrate using the correlation map to identify depth regions in which μ <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">t</sub> has positive and negative correlations with the applied pressure and study in detail the changes of μ <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">t</sub> in dermis with the applied pressure. By using a low-cost thin-film pressure sensor to monitor the applied pressure accurately, we are able to quantitatively obtain the pressure dependence of μ <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">t</sub> in different skin layers in vivo with the following interesting findings: When a pressure ranging from 0 to 20 kPa is applied on the volar side of the forearm skin, μ <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">t</sub> increases with the applied pressure in the epidermis layer, which coincides with the thickness decrease and increase of the epidermis and the epidermis-dermis junction, respectively. In contrast, μ <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">t</sub> decreases with applied pressure in the upper dermis but increases again in the deeper dermis with applied pressure. Our results demonstrate that the OCT correlation map and the thin-film sensor are effective tools to study the optical scattering properties of human skin under pressure. We anticipate that our experimental and analytical methods reported in this paper can be useful for clinical diagnostic applications, such as noninvasive blood glucose monitoring.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call