In vivo multiphoton‐microscopy of picosecond‐laser‐induced optical breakdown in human skin
Importance Improvements in skin appearance resulting from treatment with fractionated picosecond‐lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non‐invasive laser imaging techniques in conjunction wi...
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Published in | Lasers in surgery and medicine Vol. 49; no. 6; pp. 555 - 562 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.08.2017
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0196-8092 1096-9101 1096-9101 |
DOI | 10.1002/lsm.22655 |
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Abstract | Importance
Improvements in skin appearance resulting from treatment with fractionated picosecond‐lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non‐invasive laser imaging techniques in conjunction with laser therapy can potentially provide feedback for guidance and optimizing clinical outcome.
Objective
The purpose of this study was to demonstrate the capability of multiphoton microscopy (MPM), a high‐resolution, label‐free imaging technique, to characterize in vivo the skin response to a fractionated non‐ablative picosecond‐laser treatment.
Design, Setting, and Participants
Two areas on the arm of a volunteer were treated with a fractionated picosecond laser at the Dermatology Clinic, UC Irvine. The skin response to treatment was imaged in vivo with a clinical MPM‐based tomograph at 3 hours and 24 hours after treatment and seven additional time points over a 4‐week period.
Main Outcomes and Measures
MPM revealed micro‐injuries present in the epidermis. Pigmented cells were particularly damaged in the process, suggesting that melanin is likely the main absorber for laser induced optical breakdown.
Results
Damaged individual cells were distinguished as early as 3 hours post pico‐laser treatment with the 532 nm wavelength, and 24 hours post‐treatment with both 532 and 1064 nm wavelengths. At later time points, clusters of cellular necrotic debris were imaged across the treated epidermis. After 24 hours of treatment, inflammatory cells were imaged in the proximity of epidermal micro‐injuries. The epidermal injuries were exfoliated over a 4‐week period.
Conclusions and Relevance
This observational and descriptive pilot study demonstrates that in vivo MPM imaging can be used non‐invasively to provide label‐free contrast for describing changes in human skin following a fractionated non‐ablative laser treatment. The results presented in this study represent the groundwork for future longitudinal investigations on an expanded number of subjects to understand the response to treatment in different skin types with different laser parameters, critical factors in optimizing treatment outcome. Lasers Surg. Med. 49:555–562, 2017. © 2017 The Authors. Lasers in Surgery and Medicine Published by Wiley Periodicals, Inc. |
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AbstractList | Improvements in skin appearance resulting from treatment with fractionated picosecond-lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non-invasive laser imaging techniques in conjunction with laser therapy can potentially provide feedback for guidance and optimizing clinical outcome.
The purpose of this study was to demonstrate the capability of multiphoton microscopy (MPM), a high-resolution, label-free imaging technique, to characterize in vivo the skin response to a fractionated non-ablative picosecond-laser treatment.
Two areas on the arm of a volunteer were treated with a fractionated picosecond laser at the Dermatology Clinic, UC Irvine. The skin response to treatment was imaged in vivo with a clinical MPM-based tomograph at 3 hours and 24 hours after treatment and seven additional time points over a 4-week period.
MPM revealed micro-injuries present in the epidermis. Pigmented cells were particularly damaged in the process, suggesting that melanin is likely the main absorber for laser induced optical breakdown.
Damaged individual cells were distinguished as early as 3 hours post pico-laser treatment with the 532 nm wavelength, and 24 hours post-treatment with both 532 and 1064 nm wavelengths. At later time points, clusters of cellular necrotic debris were imaged across the treated epidermis. After 24 hours of treatment, inflammatory cells were imaged in the proximity of epidermal micro-injuries. The epidermal injuries were exfoliated over a 4-week period.
This observational and descriptive pilot study demonstrates that in vivo MPM imaging can be used non-invasively to provide label-free contrast for describing changes in human skin following a fractionated non-ablative laser treatment. The results presented in this study represent the groundwork for future longitudinal investigations on an expanded number of subjects to understand the response to treatment in different skin types with different laser parameters, critical factors in optimizing treatment outcome. Lasers Surg. Med. 49:555-562, 2017. © 2017 Wiley Periodicals, Inc. Improvements in skin appearance resulting from treatment with fractionated picosecond-lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non-invasive laser imaging techniques in conjunction with laser therapy can potentially provide feedback for guidance and optimizing clinical outcome.IMPORTANCEImprovements in skin appearance resulting from treatment with fractionated picosecond-lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non-invasive laser imaging techniques in conjunction with laser therapy can potentially provide feedback for guidance and optimizing clinical outcome.The purpose of this study was to demonstrate the capability of multiphoton microscopy (MPM), a high-resolution, label-free imaging technique, to characterize in vivo the skin response to a fractionated non-ablative picosecond-laser treatment.OBJECTIVEThe purpose of this study was to demonstrate the capability of multiphoton microscopy (MPM), a high-resolution, label-free imaging technique, to characterize in vivo the skin response to a fractionated non-ablative picosecond-laser treatment.Two areas on the arm of a volunteer were treated with a fractionated picosecond laser at the Dermatology Clinic, UC Irvine. The skin response to treatment was imaged in vivo with a clinical MPM-based tomograph at 3 hours and 24 hours after treatment and seven additional time points over a 4-week period.DESIGN, SETTING, AND PARTICIPANTSTwo areas on the arm of a volunteer were treated with a fractionated picosecond laser at the Dermatology Clinic, UC Irvine. The skin response to treatment was imaged in vivo with a clinical MPM-based tomograph at 3 hours and 24 hours after treatment and seven additional time points over a 4-week period.MPM revealed micro-injuries present in the epidermis. Pigmented cells were particularly damaged in the process, suggesting that melanin is likely the main absorber for laser induced optical breakdown.MAIN OUTCOMES AND MEASURESMPM revealed micro-injuries present in the epidermis. Pigmented cells were particularly damaged in the process, suggesting that melanin is likely the main absorber for laser induced optical breakdown.Damaged individual cells were distinguished as early as 3 hours post pico-laser treatment with the 532 nm wavelength, and 24 hours post-treatment with both 532 and 1064 nm wavelengths. At later time points, clusters of cellular necrotic debris were imaged across the treated epidermis. After 24 hours of treatment, inflammatory cells were imaged in the proximity of epidermal micro-injuries. The epidermal injuries were exfoliated over a 4-week period.RESULTSDamaged individual cells were distinguished as early as 3 hours post pico-laser treatment with the 532 nm wavelength, and 24 hours post-treatment with both 532 and 1064 nm wavelengths. At later time points, clusters of cellular necrotic debris were imaged across the treated epidermis. After 24 hours of treatment, inflammatory cells were imaged in the proximity of epidermal micro-injuries. The epidermal injuries were exfoliated over a 4-week period.This observational and descriptive pilot study demonstrates that in vivo MPM imaging can be used non-invasively to provide label-free contrast for describing changes in human skin following a fractionated non-ablative laser treatment. The results presented in this study represent the groundwork for future longitudinal investigations on an expanded number of subjects to understand the response to treatment in different skin types with different laser parameters, critical factors in optimizing treatment outcome. Lasers Surg. Med. 49:555-562, 2017. © 2017 Wiley Periodicals, Inc.CONCLUSIONS AND RELEVANCEThis observational and descriptive pilot study demonstrates that in vivo MPM imaging can be used non-invasively to provide label-free contrast for describing changes in human skin following a fractionated non-ablative laser treatment. The results presented in this study represent the groundwork for future longitudinal investigations on an expanded number of subjects to understand the response to treatment in different skin types with different laser parameters, critical factors in optimizing treatment outcome. Lasers Surg. Med. 49:555-562, 2017. © 2017 Wiley Periodicals, Inc. Importance Improvements in skin appearance resulting from treatment with fractionated picosecond‐lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non‐invasive laser imaging techniques in conjunction with laser therapy can potentially provide feedback for guidance and optimizing clinical outcome. Objective The purpose of this study was to demonstrate the capability of multiphoton microscopy (MPM), a high‐resolution, label‐free imaging technique, to characterize in vivo the skin response to a fractionated non‐ablative picosecond‐laser treatment. Design, Setting, and Participants Two areas on the arm of a volunteer were treated with a fractionated picosecond laser at the Dermatology Clinic, UC Irvine. The skin response to treatment was imaged in vivo with a clinical MPM‐based tomograph at 3 hours and 24 hours after treatment and seven additional time points over a 4‐week period. Main Outcomes and Measures MPM revealed micro‐injuries present in the epidermis. Pigmented cells were particularly damaged in the process, suggesting that melanin is likely the main absorber for laser induced optical breakdown. Results Damaged individual cells were distinguished as early as 3 hours post pico‐laser treatment with the 532 nm wavelength, and 24 hours post‐treatment with both 532 and 1064 nm wavelengths. At later time points, clusters of cellular necrotic debris were imaged across the treated epidermis. After 24 hours of treatment, inflammatory cells were imaged in the proximity of epidermal micro‐injuries. The epidermal injuries were exfoliated over a 4‐week period. Conclusions and Relevance This observational and descriptive pilot study demonstrates that in vivo MPM imaging can be used non‐invasively to provide label‐free contrast for describing changes in human skin following a fractionated non‐ablative laser treatment. The results presented in this study represent the groundwork for future longitudinal investigations on an expanded number of subjects to understand the response to treatment in different skin types with different laser parameters, critical factors in optimizing treatment outcome. Lasers Surg. Med. 49:555–562, 2017. © 2017 The Authors. Lasers in Surgery and Medicine Published by Wiley Periodicals, Inc. Importance Improvements in skin appearance resulting from treatment with fractionated picosecond-lasers have been noted, but optimizing the treatment efficacy depends on a thorough understanding of the specific skin response. The development of non-invasive laser imaging techniques in conjunction with laser therapy can potentially provide feedback for guidance and optimizing clinical outcome. Objective The purpose of this study was to demonstrate the capability of multiphoton microscopy (MPM), a high-resolution, label-free imaging technique, to characterize in vivo the skin response to a fractionated non-ablative picosecond-laser treatment. Design, Setting, and Participants Two areas on the arm of a volunteer were treated with a fractionated picosecond laser at the Dermatology Clinic, UC Irvine. The skin response to treatment was imaged in vivo with a clinical MPM-based tomograph at 3 hours and 24 hours after treatment and seven additional time points over a 4-week period. Main Outcomes and Measures MPM revealed micro-injuries present in the epidermis. Pigmented cells were particularly damaged in the process, suggesting that melanin is likely the main absorber for laser induced optical breakdown. Results Damaged individual cells were distinguished as early as 3 hours post pico-laser treatment with the 532nm wavelength, and 24 hours post-treatment with both 532 and 1064nm wavelengths. At later time points, clusters of cellular necrotic debris were imaged across the treated epidermis. After 24 hours of treatment, inflammatory cells were imaged in the proximity of epidermal micro-injuries. The epidermal injuries were exfoliated over a 4-week period. Conclusions and Relevance This observational and descriptive pilot study demonstrates that in vivo MPM imaging can be used non-invasively to provide label-free contrast for describing changes in human skin following a fractionated non-ablative laser treatment. The results presented in this study represent the groundwork for future longitudinal investigations on an expanded number of subjects to understand the response to treatment in different skin types with different laser parameters, critical factors in optimizing treatment outcome. Lasers Surg. Med. 49:555-562, 2017. © 2017 The Authors. Lasers in Surgery and Medicine Published by Wiley Periodicals, Inc. |
Author | Kelly, Kristen M. Tromberg, Bruce J. Balu, Mihaela Lentsch, Griffin Korta, Dorota Z. Zachary, Christopher B. König, Karsten |
AuthorAffiliation | 1 Beckman Laser Institute Laser Microbeam and Medical Program University of California Irvine Irvine California 92612 2 Department of Dermatology University of California Irvine California 92697 3 JenLab GmbH Schillerstrasse 1 Jena Germany 4 Department of Biophotonics and Laser Technology Saarland University Saarbrücken Germany |
AuthorAffiliation_xml | – name: 3 JenLab GmbH Schillerstrasse 1 Jena Germany – name: 2 Department of Dermatology University of California Irvine California 92697 – name: 4 Department of Biophotonics and Laser Technology Saarland University Saarbrücken Germany – name: 1 Beckman Laser Institute Laser Microbeam and Medical Program University of California Irvine Irvine California 92612 |
Author_xml | – sequence: 1 givenname: Mihaela surname: Balu fullname: Balu, Mihaela email: mbalu@uci.edu organization: University of California Irvine – sequence: 2 givenname: Griffin surname: Lentsch fullname: Lentsch, Griffin organization: University of California Irvine – sequence: 3 givenname: Dorota Z. surname: Korta fullname: Korta, Dorota Z. organization: University of California – sequence: 4 givenname: Karsten surname: König fullname: König, Karsten organization: Saarland University – sequence: 5 givenname: Kristen M. surname: Kelly fullname: Kelly, Kristen M. organization: University of California – sequence: 6 givenname: Bruce J. surname: Tromberg fullname: Tromberg, Bruce J. organization: University of California Irvine – sequence: 7 givenname: Christopher B. surname: Zachary fullname: Zachary, Christopher B. organization: University of California |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28333369$$D View this record in MEDLINE/PubMed |
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Keywords | noninvasive multiphoton microscopy laser induced optical breakdown in vivo imaging |
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License | Attribution-NonCommercial http://creativecommons.org/licenses/by-nc/4.0 2017 Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Undefined-3 This article was modified on 14 August 2017 after initial online publication in order to update the copyright line. Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and have disclosed the following: Karsten König is cofounder of JenLab GmbH (Jena, Germany). |
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Improvements in skin appearance resulting from treatment with fractionated picosecond‐lasers have been noted, but optimizing the treatment efficacy... Improvements in skin appearance resulting from treatment with fractionated picosecond-lasers have been noted, but optimizing the treatment efficacy depends on... Importance Improvements in skin appearance resulting from treatment with fractionated picosecond-lasers have been noted, but optimizing the treatment efficacy... |
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SubjectTerms | Ablation Breakdown Clinical Report Clinical Reports Clusters Damage Dermatology Epidermis Epidermis - diagnostic imaging Epidermis - radiation effects Feedback Healthy Volunteers High resolution Humans Image resolution Imaging techniques in vivo imaging In vivo methods and tests Inflammation Injuries laser induced optical breakdown Lasers Lasers, Solid-State Melanin Microscopy Microscopy, Fluorescence, Multiphoton noninvasive multiphoton microscopy Pilot Projects Skin Surgery |
Title | In vivo multiphoton‐microscopy of picosecond‐laser‐induced optical breakdown in human skin |
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