Visualizing radiofrequency–skin interaction using multiphoton microscopy in vivo
Abstract Background 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...
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description | Abstract Background 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. Objective 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. Methods 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. Results 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. Conclusions 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. |
doi_str_mv | 10.1016/j.jdermsci.2011.10.011 |
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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. Objective 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. Methods 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. Results 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. Conclusions 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.</description><identifier>ISSN: 0923-1811</identifier><identifier>EISSN: 1873-569X</identifier><identifier>DOI: 10.1016/j.jdermsci.2011.10.011</identifier><identifier>PMID: 22209318</identifier><language>eng</language><publisher>Netherlands: Elsevier Ireland Ltd</publisher><subject>Animals ; Collagen ; Collagen - metabolism ; Dermatology ; Hot Temperature ; Lasers, Semiconductor - adverse effects ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Microscopy, Fluorescence, Multiphoton ; Multiphoton microscopy ; Radiofrequency ; Skin - metabolism ; Skin - pathology ; Skin - radiation effects ; Time Factors</subject><ispartof>Journal of dermatological science, 2012-02, Vol.65 (2), p.95-101</ispartof><rights>2011</rights><rights>Copyright © 2011. Published by Elsevier Ireland Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-7c700776e262666ecd6d0869cc0eeec531c1dcd42bd9b81e6f5b3a30c2c3c6833</citedby><cites>FETCH-LOGICAL-c446t-7c700776e262666ecd6d0869cc0eeec531c1dcd42bd9b81e6f5b3a30c2c3c6833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jdermsci.2011.10.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22209318$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsai, Tsung-Hua</creatorcontrib><creatorcontrib>Lin, Sung-Jan</creatorcontrib><creatorcontrib>Lee, Woan-Ruoh</creatorcontrib><creatorcontrib>Wang, Chun-Chin</creatorcontrib><creatorcontrib>Hsu, Chih-Ting</creatorcontrib><creatorcontrib>Chu, Thomas</creatorcontrib><creatorcontrib>Dong, Chen-Yuan</creatorcontrib><title>Visualizing radiofrequency–skin interaction using multiphoton microscopy in vivo</title><title>Journal of dermatological science</title><addtitle>J Dermatol Sci</addtitle><description>Abstract Background 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. Objective 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. Methods 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. Results 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. Conclusions 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.</description><subject>Animals</subject><subject>Collagen</subject><subject>Collagen - metabolism</subject><subject>Dermatology</subject><subject>Hot Temperature</subject><subject>Lasers, Semiconductor - adverse effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Microscopy, Fluorescence, Multiphoton</subject><subject>Multiphoton microscopy</subject><subject>Radiofrequency</subject><subject>Skin - metabolism</subject><subject>Skin - pathology</subject><subject>Skin - radiation effects</subject><subject>Time Factors</subject><issn>0923-1811</issn><issn>1873-569X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-O00AMxkcIxJaFV1j1xinFnmknyQWBVvyTVkLin7iNUo8LziaZMpNUKifegTfkSZjQXQ5cOFn69PNn-7NSFwgrBLRP2lXrOfaJZKUBMYurXO6oBValKTa2_nxXLaDWpsAK8Uw9SKkFgI1e1_fVmdYaaoPVQr37JGlqOvkuw5dlbLyEXeRvEw90_PXjZ7qWYSnDyLGhUcKwnNLM9VM3yv5rGLPSC8WQKOyPGVwe5BAeqnu7pkv86Kaeq48vX3y4fF1cvX315vL5VUHrtR2LkkqAsrSsrbbWMnnrobI1ETAzbQwSevJrvfX1tkK2u83WNAZIkyFbGXOuHp989zHkjdPoeknEXdcMHKbkag3aoEbMpD2R86op8s7to_RNPDoEN8fpWncbp5vjnHX403hxM2La9uz_tt3ml4FnJ4DzoQfh6LJFDo-9RKbR-SD_n_H0HwvqZBBqums-cmrDFIcco0OXtAP3fn7q_FNEAIMWzW-F4KHL</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Tsai, Tsung-Hua</creator><creator>Lin, Sung-Jan</creator><creator>Lee, Woan-Ruoh</creator><creator>Wang, Chun-Chin</creator><creator>Hsu, Chih-Ting</creator><creator>Chu, Thomas</creator><creator>Dong, Chen-Yuan</creator><general>Elsevier Ireland Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120201</creationdate><title>Visualizing radiofrequency–skin interaction using multiphoton microscopy in vivo</title><author>Tsai, Tsung-Hua ; Lin, Sung-Jan ; Lee, Woan-Ruoh ; Wang, Chun-Chin ; Hsu, Chih-Ting ; Chu, Thomas ; Dong, Chen-Yuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-7c700776e262666ecd6d0869cc0eeec531c1dcd42bd9b81e6f5b3a30c2c3c6833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Collagen</topic><topic>Collagen - metabolism</topic><topic>Dermatology</topic><topic>Hot Temperature</topic><topic>Lasers, Semiconductor - adverse effects</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Microscopy, Fluorescence, Multiphoton</topic><topic>Multiphoton microscopy</topic><topic>Radiofrequency</topic><topic>Skin - metabolism</topic><topic>Skin - pathology</topic><topic>Skin - radiation effects</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsai, Tsung-Hua</creatorcontrib><creatorcontrib>Lin, Sung-Jan</creatorcontrib><creatorcontrib>Lee, Woan-Ruoh</creatorcontrib><creatorcontrib>Wang, Chun-Chin</creatorcontrib><creatorcontrib>Hsu, Chih-Ting</creatorcontrib><creatorcontrib>Chu, Thomas</creatorcontrib><creatorcontrib>Dong, Chen-Yuan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dermatological science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsai, Tsung-Hua</au><au>Lin, Sung-Jan</au><au>Lee, Woan-Ruoh</au><au>Wang, Chun-Chin</au><au>Hsu, Chih-Ting</au><au>Chu, Thomas</au><au>Dong, Chen-Yuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visualizing radiofrequency–skin interaction using multiphoton microscopy in vivo</atitle><jtitle>Journal of dermatological science</jtitle><addtitle>J Dermatol Sci</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>65</volume><issue>2</issue><spage>95</spage><epage>101</epage><pages>95-101</pages><issn>0923-1811</issn><eissn>1873-569X</eissn><abstract>Abstract Background 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. Objective 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. Methods 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. Results 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. Conclusions 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.</abstract><cop>Netherlands</cop><pub>Elsevier Ireland Ltd</pub><pmid>22209318</pmid><doi>10.1016/j.jdermsci.2011.10.011</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Collagen Collagen - metabolism Dermatology Hot Temperature Lasers, Semiconductor - adverse effects Male Mice Mice, Inbred BALB C Mice, Nude Microscopy, Fluorescence, Multiphoton Multiphoton microscopy Radiofrequency Skin - metabolism Skin - pathology Skin - radiation effects Time Factors |
title | Visualizing radiofrequency–skin interaction using multiphoton microscopy in vivo |
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