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Rapid fibrin plug formation within cutaneous ablative fractional CO2 laser lesions
Background Ablative fractional laser procedures have been shown to facilitate topical drug delivery into the skin. Past studies have mainly used ex vivo models to demonstrate enhanced drug delivery and in vivo studies have investigated laser created channels over a time course of days and weeks rath...
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Published in: | Lasers in surgery and medicine 2016-02, Vol.48 (2), p.125-132 |
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creator | Kositratna, Garuna Evers, Michael Sajjadi, Amir Manstein, Dieter |
description | Background
Ablative fractional laser procedures have been shown to facilitate topical drug delivery into the skin. Past studies have mainly used ex vivo models to demonstrate enhanced drug delivery and in vivo studies have investigated laser created channels over a time course of days and weeks rather than within the first few minutes and hours after exposures. We have noticed rapid in vivo fibrin plug formation within ablative fractional laser lesions impairing passage through the laser created channels.
Material and Methods
In vivo laser exposures were performed in a porcine model. A fractional CO2 laser (AcuPulse™ system, AcuScan 120™ handpiece, Lumenis, Inc., Yokneam, Israel) was programmed in quasi‐continuous wave (QCW) mode, at 40W, 50 mJ per pulse, 5% coverage, nominal 120 µm spot size, 8 × 8 mm square pattern, 169 MTZs per scan. Six millimeters punch biopsies were procured at 0, 2, 5, 10, 15, 30, 60, 90 minutes after completion of each scan, then fixed in 10% formalin. 12 repeats were performed of each time point. Skin samples were processed for serial vertically cut paraffin sections (5 μm collected every 25 μm) then H&E and special immunohistochemistry staining for fibrin and platelet. Dimensions of Microscopic Treatment Zones (MTZs) and extent of fibrin plug were assessed and quantified histologically. Ex vivo laser exposures of the identical laser parameter were performed on porcine and human skin at different storage conditions.
Results
Histology procured at various predetermined time intervals after in vivo fractional CO2 laser exposures revealed a rapidly forming fibrin plug initiating at the bottom of the MTZ lesions. At longer time intervals, the fibrin plug was extending towards the superficial sections. Within the first 5 minutes, more than 25% length of the entire laser‐ablated channel was filled with a fibrin plug. With increased time intervals, the cavity was progressively filled with a fibrin plug. At 90 minutes, more than 90% length of the entire laser‐ablated channel was occluded. Ex vivo exposures failed to produce any significant fibrin plug formation.
Conclusions
The current study has demonstrated rapid fibrin plug formation after ablative fractional laser procedures. It was shown that the passage through laser created pathways is critically time dependent for in vivo exposures. In contrast, ex vivo exposures do not exhibit such time dependent passage capacity. In particular, drug, substance, and cell delivery studies for ablati |
doi_str_mv | 10.1002/lsm.22412 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1769620040</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3965905721</sourcerecordid><originalsourceid>FETCH-LOGICAL-g4242-9e2d633f4e2b8a09b99df6a079027548b39ded58f7839f76a99d58f65fea1ef33</originalsourceid><addsrcrecordid>eNpdkU1PGzEQhi3UCtKUA38AWeqFy8LY3vXHsYr4EilRQxBHy5u1qak3G-zdAv8ek1AOnDye93lHo3kROiBwTADoSUjtMaUloTtoREDxQhEgX9AISK4lKLqHvqX0AACMgthFe5QzKQnjIzSfm7VvsPN19Cu8DsM9dl1sTe-7FX7y_Z_cXQ69WdluSNjUISv_LHbRLN8QE_BkRnEwyUYcbMqt9B19dSYku__-jtHt2eliclFMZ-eXk5_T4r6kJS2UpQ1nzJWW1tKAqpVqHDcgFFBRlbJmqrFNJZ2QTDnBTdbzj1fOGmIdY2N0tJ27jt3jYFOvW5-WNoTtspoIrjgFKCGjPz6hD90Q8_YbSpayEkpk6vCdGurWNnodfWvii_5_rQycbIEnH-zLh05Av8Wgcwx6E4Oe3vzaFNlRbB0-9fb5w2HiX80FE5W-uz7XV2e_6eJiArpirxm-iBg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1768485797</pqid></control><display><type>article</type><title>Rapid fibrin plug formation within cutaneous ablative fractional CO2 laser lesions</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Kositratna, Garuna ; Evers, Michael ; Sajjadi, Amir ; Manstein, Dieter</creator><creatorcontrib>Kositratna, Garuna ; Evers, Michael ; Sajjadi, Amir ; Manstein, Dieter</creatorcontrib><description>Background
Ablative fractional laser procedures have been shown to facilitate topical drug delivery into the skin. Past studies have mainly used ex vivo models to demonstrate enhanced drug delivery and in vivo studies have investigated laser created channels over a time course of days and weeks rather than within the first few minutes and hours after exposures. We have noticed rapid in vivo fibrin plug formation within ablative fractional laser lesions impairing passage through the laser created channels.
Material and Methods
In vivo laser exposures were performed in a porcine model. A fractional CO2 laser (AcuPulse™ system, AcuScan 120™ handpiece, Lumenis, Inc., Yokneam, Israel) was programmed in quasi‐continuous wave (QCW) mode, at 40W, 50 mJ per pulse, 5% coverage, nominal 120 µm spot size, 8 × 8 mm square pattern, 169 MTZs per scan. Six millimeters punch biopsies were procured at 0, 2, 5, 10, 15, 30, 60, 90 minutes after completion of each scan, then fixed in 10% formalin. 12 repeats were performed of each time point. Skin samples were processed for serial vertically cut paraffin sections (5 μm collected every 25 μm) then H&E and special immunohistochemistry staining for fibrin and platelet. Dimensions of Microscopic Treatment Zones (MTZs) and extent of fibrin plug were assessed and quantified histologically. Ex vivo laser exposures of the identical laser parameter were performed on porcine and human skin at different storage conditions.
Results
Histology procured at various predetermined time intervals after in vivo fractional CO2 laser exposures revealed a rapidly forming fibrin plug initiating at the bottom of the MTZ lesions. At longer time intervals, the fibrin plug was extending towards the superficial sections. Within the first 5 minutes, more than 25% length of the entire laser‐ablated channel was filled with a fibrin plug. With increased time intervals, the cavity was progressively filled with a fibrin plug. At 90 minutes, more than 90% length of the entire laser‐ablated channel was occluded. Ex vivo exposures failed to produce any significant fibrin plug formation.
Conclusions
The current study has demonstrated rapid fibrin plug formation after ablative fractional laser procedures. It was shown that the passage through laser created pathways is critically time dependent for in vivo exposures. In contrast, ex vivo exposures do not exhibit such time dependent passage capacity. In particular, drug, substance, and cell delivery studies for ablative fractional laser treatments should take early fibrin plug formation into consideration and further investigate the impact on transdermal delivery. Lasers Surg. Med. 48:125–132, 2016. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0196-8092</identifier><identifier>EISSN: 1096-9101</identifier><identifier>DOI: 10.1002/lsm.22412</identifier><identifier>PMID: 26388136</identifier><identifier>CODEN: LSMEDI</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>ablative fractional lasers ; Administration, Cutaneous ; Animals ; Biomarkers - metabolism ; Biopsy ; cell delivery ; drug delivery ; Drug Delivery Systems - instrumentation ; Drug Delivery Systems - methods ; Female ; Fibrin - metabolism ; fibrin plug formation ; gateways ; Humans ; laser-assisted ; Lasers, Gas ; Skin - metabolism ; Skin - pathology ; substance delivery ; Swine ; time course ; time dependence ; Time Factors ; transcutaneous ; transdermal ; transport</subject><ispartof>Lasers in surgery and medicine, 2016-02, Vol.48 (2), p.125-132</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26388136$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kositratna, Garuna</creatorcontrib><creatorcontrib>Evers, Michael</creatorcontrib><creatorcontrib>Sajjadi, Amir</creatorcontrib><creatorcontrib>Manstein, Dieter</creatorcontrib><title>Rapid fibrin plug formation within cutaneous ablative fractional CO2 laser lesions</title><title>Lasers in surgery and medicine</title><addtitle>Lasers Surg. Med</addtitle><description>Background
Ablative fractional laser procedures have been shown to facilitate topical drug delivery into the skin. Past studies have mainly used ex vivo models to demonstrate enhanced drug delivery and in vivo studies have investigated laser created channels over a time course of days and weeks rather than within the first few minutes and hours after exposures. We have noticed rapid in vivo fibrin plug formation within ablative fractional laser lesions impairing passage through the laser created channels.
Material and Methods
In vivo laser exposures were performed in a porcine model. A fractional CO2 laser (AcuPulse™ system, AcuScan 120™ handpiece, Lumenis, Inc., Yokneam, Israel) was programmed in quasi‐continuous wave (QCW) mode, at 40W, 50 mJ per pulse, 5% coverage, nominal 120 µm spot size, 8 × 8 mm square pattern, 169 MTZs per scan. Six millimeters punch biopsies were procured at 0, 2, 5, 10, 15, 30, 60, 90 minutes after completion of each scan, then fixed in 10% formalin. 12 repeats were performed of each time point. Skin samples were processed for serial vertically cut paraffin sections (5 μm collected every 25 μm) then H&E and special immunohistochemistry staining for fibrin and platelet. Dimensions of Microscopic Treatment Zones (MTZs) and extent of fibrin plug were assessed and quantified histologically. Ex vivo laser exposures of the identical laser parameter were performed on porcine and human skin at different storage conditions.
Results
Histology procured at various predetermined time intervals after in vivo fractional CO2 laser exposures revealed a rapidly forming fibrin plug initiating at the bottom of the MTZ lesions. At longer time intervals, the fibrin plug was extending towards the superficial sections. Within the first 5 minutes, more than 25% length of the entire laser‐ablated channel was filled with a fibrin plug. With increased time intervals, the cavity was progressively filled with a fibrin plug. At 90 minutes, more than 90% length of the entire laser‐ablated channel was occluded. Ex vivo exposures failed to produce any significant fibrin plug formation.
Conclusions
The current study has demonstrated rapid fibrin plug formation after ablative fractional laser procedures. It was shown that the passage through laser created pathways is critically time dependent for in vivo exposures. In contrast, ex vivo exposures do not exhibit such time dependent passage capacity. In particular, drug, substance, and cell delivery studies for ablative fractional laser treatments should take early fibrin plug formation into consideration and further investigate the impact on transdermal delivery. Lasers Surg. Med. 48:125–132, 2016. © 2015 Wiley Periodicals, Inc.</description><subject>ablative fractional lasers</subject><subject>Administration, Cutaneous</subject><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Biopsy</subject><subject>cell delivery</subject><subject>drug delivery</subject><subject>Drug Delivery Systems - instrumentation</subject><subject>Drug Delivery Systems - methods</subject><subject>Female</subject><subject>Fibrin - metabolism</subject><subject>fibrin plug formation</subject><subject>gateways</subject><subject>Humans</subject><subject>laser-assisted</subject><subject>Lasers, Gas</subject><subject>Skin - metabolism</subject><subject>Skin - pathology</subject><subject>substance delivery</subject><subject>Swine</subject><subject>time course</subject><subject>time dependence</subject><subject>Time Factors</subject><subject>transcutaneous</subject><subject>transdermal</subject><subject>transport</subject><issn>0196-8092</issn><issn>1096-9101</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpdkU1PGzEQhi3UCtKUA38AWeqFy8LY3vXHsYr4EilRQxBHy5u1qak3G-zdAv8ek1AOnDye93lHo3kROiBwTADoSUjtMaUloTtoREDxQhEgX9AISK4lKLqHvqX0AACMgthFe5QzKQnjIzSfm7VvsPN19Cu8DsM9dl1sTe-7FX7y_Z_cXQ69WdluSNjUISv_LHbRLN8QE_BkRnEwyUYcbMqt9B19dSYku__-jtHt2eliclFMZ-eXk5_T4r6kJS2UpQ1nzJWW1tKAqpVqHDcgFFBRlbJmqrFNJZ2QTDnBTdbzj1fOGmIdY2N0tJ27jt3jYFOvW5-WNoTtspoIrjgFKCGjPz6hD90Q8_YbSpayEkpk6vCdGurWNnodfWvii_5_rQycbIEnH-zLh05Av8Wgcwx6E4Oe3vzaFNlRbB0-9fb5w2HiX80FE5W-uz7XV2e_6eJiArpirxm-iBg</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Kositratna, Garuna</creator><creator>Evers, Michael</creator><creator>Sajjadi, Amir</creator><creator>Manstein, Dieter</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201602</creationdate><title>Rapid fibrin plug formation within cutaneous ablative fractional CO2 laser lesions</title><author>Kositratna, Garuna ; Evers, Michael ; Sajjadi, Amir ; Manstein, Dieter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g4242-9e2d633f4e2b8a09b99df6a079027548b39ded58f7839f76a99d58f65fea1ef33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>ablative fractional lasers</topic><topic>Administration, Cutaneous</topic><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Biopsy</topic><topic>cell delivery</topic><topic>drug delivery</topic><topic>Drug Delivery Systems - instrumentation</topic><topic>Drug Delivery Systems - methods</topic><topic>Female</topic><topic>Fibrin - metabolism</topic><topic>fibrin plug formation</topic><topic>gateways</topic><topic>Humans</topic><topic>laser-assisted</topic><topic>Lasers, Gas</topic><topic>Skin - metabolism</topic><topic>Skin - pathology</topic><topic>substance delivery</topic><topic>Swine</topic><topic>time course</topic><topic>time dependence</topic><topic>Time Factors</topic><topic>transcutaneous</topic><topic>transdermal</topic><topic>transport</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kositratna, Garuna</creatorcontrib><creatorcontrib>Evers, Michael</creatorcontrib><creatorcontrib>Sajjadi, Amir</creatorcontrib><creatorcontrib>Manstein, Dieter</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Lasers in surgery and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kositratna, Garuna</au><au>Evers, Michael</au><au>Sajjadi, Amir</au><au>Manstein, Dieter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid fibrin plug formation within cutaneous ablative fractional CO2 laser lesions</atitle><jtitle>Lasers in surgery and medicine</jtitle><addtitle>Lasers Surg. Med</addtitle><date>2016-02</date><risdate>2016</risdate><volume>48</volume><issue>2</issue><spage>125</spage><epage>132</epage><pages>125-132</pages><issn>0196-8092</issn><eissn>1096-9101</eissn><coden>LSMEDI</coden><abstract>Background
Ablative fractional laser procedures have been shown to facilitate topical drug delivery into the skin. Past studies have mainly used ex vivo models to demonstrate enhanced drug delivery and in vivo studies have investigated laser created channels over a time course of days and weeks rather than within the first few minutes and hours after exposures. We have noticed rapid in vivo fibrin plug formation within ablative fractional laser lesions impairing passage through the laser created channels.
Material and Methods
In vivo laser exposures were performed in a porcine model. A fractional CO2 laser (AcuPulse™ system, AcuScan 120™ handpiece, Lumenis, Inc., Yokneam, Israel) was programmed in quasi‐continuous wave (QCW) mode, at 40W, 50 mJ per pulse, 5% coverage, nominal 120 µm spot size, 8 × 8 mm square pattern, 169 MTZs per scan. Six millimeters punch biopsies were procured at 0, 2, 5, 10, 15, 30, 60, 90 minutes after completion of each scan, then fixed in 10% formalin. 12 repeats were performed of each time point. Skin samples were processed for serial vertically cut paraffin sections (5 μm collected every 25 μm) then H&E and special immunohistochemistry staining for fibrin and platelet. Dimensions of Microscopic Treatment Zones (MTZs) and extent of fibrin plug were assessed and quantified histologically. Ex vivo laser exposures of the identical laser parameter were performed on porcine and human skin at different storage conditions.
Results
Histology procured at various predetermined time intervals after in vivo fractional CO2 laser exposures revealed a rapidly forming fibrin plug initiating at the bottom of the MTZ lesions. At longer time intervals, the fibrin plug was extending towards the superficial sections. Within the first 5 minutes, more than 25% length of the entire laser‐ablated channel was filled with a fibrin plug. With increased time intervals, the cavity was progressively filled with a fibrin plug. At 90 minutes, more than 90% length of the entire laser‐ablated channel was occluded. Ex vivo exposures failed to produce any significant fibrin plug formation.
Conclusions
The current study has demonstrated rapid fibrin plug formation after ablative fractional laser procedures. It was shown that the passage through laser created pathways is critically time dependent for in vivo exposures. In contrast, ex vivo exposures do not exhibit such time dependent passage capacity. In particular, drug, substance, and cell delivery studies for ablative fractional laser treatments should take early fibrin plug formation into consideration and further investigate the impact on transdermal delivery. Lasers Surg. Med. 48:125–132, 2016. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26388136</pmid><doi>10.1002/lsm.22412</doi><tpages>8</tpages></addata></record> |
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subjects | ablative fractional lasers Administration, Cutaneous Animals Biomarkers - metabolism Biopsy cell delivery drug delivery Drug Delivery Systems - instrumentation Drug Delivery Systems - methods Female Fibrin - metabolism fibrin plug formation gateways Humans laser-assisted Lasers, Gas Skin - metabolism Skin - pathology substance delivery Swine time course time dependence Time Factors transcutaneous transdermal transport |
title | Rapid fibrin plug formation within cutaneous ablative fractional CO2 laser lesions |
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