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  4. Visualizing radiofrequency-skin interaction using multiphoton microscopy in vivo
 
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Visualizing radiofrequency-skin interaction using multiphoton microscopy in vivo

Journal
Journal of Dermatological Science
Journal Volume
65
Journal Issue
2
Pages
95-101
Date Issued
2012
Author(s)
Tsai, T.-H.
SUNG-JAN LIN  
Lee, W.-R.
Wang, C.-C.
Hsu, C.-T.
Chu, T.
CHEN-YUAN DONG  
DOI
10.1016/j.jdermsci.2011.10.011
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84856454995&doi=10.1016%2fj.jdermsci.2011.10.011&partnerID=40&md5=cd903d533e82bec8df6668d90e5c30fa
https://scholars.lib.ntu.edu.tw/handle/123456789/620699
Abstract
Redundant skin laxity is a major feature of aging. Recently, radiofrequency has been introduced for nonablative tissue tightening by volumetric heating of the deep dermis. Despite the wide range of application based on this therapy, the effect of this technique on tissue and the subsequent tissue remodeling have not been investigated in detail. Our objective is to evaluate the potential of non-linear optics, including multiphoton autofluorescence and second harmonic generation (SHG) microscopy, as a non-invasive imaging modality for the real-time study of radiofrequency-tissue interaction. Electro-optical synergy device (ELOS) was used as the radiofrequency source in this study. The back skin of nude mouse was irradiated with radiofrequency at different passes. We evaluated the effect on skin immediately and 1 month after treatment with multiphoton microscopy. Corresponding histology was performed for comparison. We found that SHG is negatively correlated to radiofrequency passes, which means that collagen structural disruption happens immediately after thermal damage. After 1 month of collagen remodeling, SHG signals increased above baseline, indicating that collagen regeneration has occurred. Our findings may explain mechanism of nonablative skin tightening and were supported by histological examinations. Our work showed that monitoring the dermal heating status of RF and following up the detailed process of tissue reaction can be imaged and quantified with multiphoton microscopy non-invasively in vivo.
Type
journal article

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