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 inLasers in surgery and medicine Vol. 49; no. 6; pp. 555 - 562
Main Authors Balu, Mihaela, Lentsch, Griffin, Korta, Dorota Z., König, Karsten, Kelly, Kristen M., Tromberg, Bruce J., Zachary, Christopher B.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.08.2017
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN0196-8092
1096-9101
1096-9101
DOI10.1002/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.
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
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  surname: Balu
  fullname: Balu, Mihaela
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  organization: University of California Irvine
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  givenname: Griffin
  surname: Lentsch
  fullname: Lentsch, Griffin
  organization: University of California Irvine
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  givenname: Dorota Z.
  surname: Korta
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  surname: König
  fullname: König, Karsten
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  givenname: Christopher B.
  surname: Zachary
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Issue 6
Keywords noninvasive multiphoton microscopy
laser induced optical breakdown
in vivo imaging
Language English
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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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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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PublicationTitle Lasers in surgery and medicine
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Snippet Importance 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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StartPage 555
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Flsm.22655
https://www.ncbi.nlm.nih.gov/pubmed/28333369
https://www.proquest.com/docview/1919407265
https://www.proquest.com/docview/1880470164
https://pubmed.ncbi.nlm.nih.gov/PMC5513776
Volume 49
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