Biocompatibility evaluation of bioprinted decellularized collagen sheet implanted in vivo cornea using swept‐source optical coherence tomography

Corneal transplantation by full‐thickness penetrating keratoplasty with human donor tissue is a widely accepted treatment for damaged or diseased corneas. Although corneal transplantation has a high success rate, a shortage of high‐quality donor tissue is a considerable limitation. Therefore, bioeng...

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Veröffentlicht in:Journal of biophotonics 2019-11, Vol.12 (11), p.e201900098-n/a
Hauptverfasser: Park, Jaeseok, Lee, Kyoung‐Pil, Kim, Hyeonji, Park, Sungjo, Wijesinghe, Ruchire E., Lee, Jaeyul, Han, Sangyeob, Lee, Sangbong, Kim, Pilun, Cho, Dong‐Woo, Jang, Jinah, Kim, Hong K., Jeon, Mansik, Kim, Jeehyun
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container_issue 11
container_start_page e201900098
container_title Journal of biophotonics
container_volume 12
creator Park, Jaeseok
Lee, Kyoung‐Pil
Kim, Hyeonji
Park, Sungjo
Wijesinghe, Ruchire E.
Lee, Jaeyul
Han, Sangyeob
Lee, Sangbong
Kim, Pilun
Cho, Dong‐Woo
Jang, Jinah
Kim, Hong K.
Jeon, Mansik
Kim, Jeehyun
description Corneal transplantation by full‐thickness penetrating keratoplasty with human donor tissue is a widely accepted treatment for damaged or diseased corneas. Although corneal transplantation has a high success rate, a shortage of high‐quality donor tissue is a considerable limitation. Therefore, bioengineered corneas could be an effective solution for this limitation, and a decellularized extracellular matrix comprises a promising scaffold for their fabrication. In this study, three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. We performed in vivo noninvasive monitoring of the rabbit corneas using swept‐source optical coherence tomography (OCT) after implanting the collagen sheets. Anterior segment OCT images and averaged amplitude‐scans were acquired biweekly to monitor corneal thickness after implantation for 1 month. The averaged cornea thickness in the control images was 430.3 ± 5.9 μm, while the averaged thickness after corneal implantation was 598.5 ± 11.8 μm and 564.5 ± 12.5 μm at 2 and 4 weeks, respectively. The corneal thickness reduction of 34 μm confirmed the biocompatibility through the image analysis of the depth‐intensity profile base. Moreover, hematoxylin and eosin staining supported the biocompatibility evaluation of the bioprinted decellularized collagen sheet implantation. Hence, the developed bioprinted decellularized collagen sheets could become an alternative solution to human corneal donor tissue, and the proposed image analysis procedure could be beneficial to confirm the success of the surgery. Three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. After implanting the collagen sheets, the rabbit corneas were monitored biweekly in vivo with a swept‐source optical coherence tomography system to assess the biocompatibility of the bioprinted implantation for 1 month through corneal thickness measurements. The small variation in the averaged corneal thickness along with evidence from hematoxylin and eosin‐stained histology images shows the potential use of the biocompatible collagen sheet.
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Although corneal transplantation has a high success rate, a shortage of high‐quality donor tissue is a considerable limitation. Therefore, bioengineered corneas could be an effective solution for this limitation, and a decellularized extracellular matrix comprises a promising scaffold for their fabrication. In this study, three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. We performed in vivo noninvasive monitoring of the rabbit corneas using swept‐source optical coherence tomography (OCT) after implanting the collagen sheets. Anterior segment OCT images and averaged amplitude‐scans were acquired biweekly to monitor corneal thickness after implantation for 1 month. The averaged cornea thickness in the control images was 430.3 ± 5.9 μm, while the averaged thickness after corneal implantation was 598.5 ± 11.8 μm and 564.5 ± 12.5 μm at 2 and 4 weeks, respectively. The corneal thickness reduction of 34 μm confirmed the biocompatibility through the image analysis of the depth‐intensity profile base. Moreover, hematoxylin and eosin staining supported the biocompatibility evaluation of the bioprinted decellularized collagen sheet implantation. Hence, the developed bioprinted decellularized collagen sheets could become an alternative solution to human corneal donor tissue, and the proposed image analysis procedure could be beneficial to confirm the success of the surgery. Three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. After implanting the collagen sheets, the rabbit corneas were monitored biweekly in vivo with a swept‐source optical coherence tomography system to assess the biocompatibility of the bioprinted implantation for 1 month through corneal thickness measurements. 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KGaA</publisher><subject>Animals ; Biocompatibility ; Bioengineering ; bioprinted collagen sheet ; Bioprinting ; Collagen ; Cornea ; Cornea - cytology ; Cornea - diagnostic imaging ; corneal implant ; Corneal transplantation ; Extracellular matrix ; Eye diseases ; Fabrication ; Full ; Image acquisition ; Image analysis ; Image processing ; Implantation ; Materials Testing ; Medical treatment ; noninvasive monitoring ; Optical Coherence Tomography ; Prostheses and Implants ; Rabbits ; Sheets ; Surgery ; Surgical implants ; Thickness ; Three dimensional printing ; Tissue Engineering ; Tissue Scaffolds - chemistry ; Tissues ; Tomography ; Tomography, Optical Coherence ; Transplantation</subject><ispartof>Journal of biophotonics, 2019-11, Vol.12 (11), p.e201900098-n/a</ispartof><rights>2019 The Authors. published by WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2019 The Authors. Journal of Biophotonics published by WILEY-VCH Verlag GmbH &amp; Co. 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KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4688-d640e36a99ede16e2a344cbe00efd24e03f520178fd62efb1107ac738387eec73</citedby><cites>FETCH-LOGICAL-c4688-d640e36a99ede16e2a344cbe00efd24e03f520178fd62efb1107ac738387eec73</cites><orcidid>0000-0002-0630-9039</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjbio.201900098$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbio.201900098$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31240872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Jaeseok</creatorcontrib><creatorcontrib>Lee, Kyoung‐Pil</creatorcontrib><creatorcontrib>Kim, Hyeonji</creatorcontrib><creatorcontrib>Park, Sungjo</creatorcontrib><creatorcontrib>Wijesinghe, Ruchire E.</creatorcontrib><creatorcontrib>Lee, Jaeyul</creatorcontrib><creatorcontrib>Han, Sangyeob</creatorcontrib><creatorcontrib>Lee, Sangbong</creatorcontrib><creatorcontrib>Kim, Pilun</creatorcontrib><creatorcontrib>Cho, Dong‐Woo</creatorcontrib><creatorcontrib>Jang, Jinah</creatorcontrib><creatorcontrib>Kim, Hong K.</creatorcontrib><creatorcontrib>Jeon, Mansik</creatorcontrib><creatorcontrib>Kim, Jeehyun</creatorcontrib><title>Biocompatibility evaluation of bioprinted decellularized collagen sheet implanted in vivo cornea using swept‐source optical coherence tomography</title><title>Journal of biophotonics</title><addtitle>J Biophotonics</addtitle><description>Corneal transplantation by full‐thickness penetrating keratoplasty with human donor tissue is a widely accepted treatment for damaged or diseased corneas. Although corneal transplantation has a high success rate, a shortage of high‐quality donor tissue is a considerable limitation. Therefore, bioengineered corneas could be an effective solution for this limitation, and a decellularized extracellular matrix comprises a promising scaffold for their fabrication. In this study, three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. We performed in vivo noninvasive monitoring of the rabbit corneas using swept‐source optical coherence tomography (OCT) after implanting the collagen sheets. Anterior segment OCT images and averaged amplitude‐scans were acquired biweekly to monitor corneal thickness after implantation for 1 month. The averaged cornea thickness in the control images was 430.3 ± 5.9 μm, while the averaged thickness after corneal implantation was 598.5 ± 11.8 μm and 564.5 ± 12.5 μm at 2 and 4 weeks, respectively. The corneal thickness reduction of 34 μm confirmed the biocompatibility through the image analysis of the depth‐intensity profile base. Moreover, hematoxylin and eosin staining supported the biocompatibility evaluation of the bioprinted decellularized collagen sheet implantation. Hence, the developed bioprinted decellularized collagen sheets could become an alternative solution to human corneal donor tissue, and the proposed image analysis procedure could be beneficial to confirm the success of the surgery. Three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. After implanting the collagen sheets, the rabbit corneas were monitored biweekly in vivo with a swept‐source optical coherence tomography system to assess the biocompatibility of the bioprinted implantation for 1 month through corneal thickness measurements. The small variation in the averaged corneal thickness along with evidence from hematoxylin and eosin‐stained histology images shows the potential use of the biocompatible collagen sheet.</description><subject>Animals</subject><subject>Biocompatibility</subject><subject>Bioengineering</subject><subject>bioprinted collagen sheet</subject><subject>Bioprinting</subject><subject>Collagen</subject><subject>Cornea</subject><subject>Cornea - cytology</subject><subject>Cornea - diagnostic imaging</subject><subject>corneal implant</subject><subject>Corneal transplantation</subject><subject>Extracellular matrix</subject><subject>Eye diseases</subject><subject>Fabrication</subject><subject>Full</subject><subject>Image acquisition</subject><subject>Image analysis</subject><subject>Image processing</subject><subject>Implantation</subject><subject>Materials Testing</subject><subject>Medical treatment</subject><subject>noninvasive monitoring</subject><subject>Optical Coherence Tomography</subject><subject>Prostheses and Implants</subject><subject>Rabbits</subject><subject>Sheets</subject><subject>Surgery</subject><subject>Surgical implants</subject><subject>Thickness</subject><subject>Three dimensional printing</subject><subject>Tissue Engineering</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Tissues</subject><subject>Tomography</subject><subject>Tomography, Optical Coherence</subject><subject>Transplantation</subject><issn>1864-063X</issn><issn>1864-0648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQxiMEoqVw5YgsceGyy9jOOs4FiVZAW1XqBSRuluNMdr1y7GAnWy0nHgHxiDxJvd2y_Llw8oz986eZ7yuK5xTmFIC9Xjc2zBnQGgBq-aA4plKUMxClfHio-eej4klKawABfMEfF0ecshJkxY6LH6c2mNAPerSNdXbcEtxoN-U2eBI6kuWHaP2ILWnRoHOT09F-za0JzuklepJWiCOx_eD0HWc92dhNyED0qMmUrF-SdIPD-PPb9xSmaJCEYbRGu8ysMKLPN2PowzLqYbV9WjzqtEv47P48KT69f_fx7Hx2df3h4uzt1cyUQspZK0pALnRdY4tUINO8LE2DANi1rETg3SIbU8muFQy7hlKotKm45LJCzMVJ8WavO0xNj61BP0btVF6313Grgrbq7xdvV2oZNqoCsRC8zAKv7gVi-DJhGlVv084j7TFMSTEmOGfZapnRl_-g62yEz-splsMQgjK5m2i-p0wMKUXsDsNQULu41S5udYg7f3jx5woH_Fe-Gaj3wI11uP2PnLo8vbj-LX4Lb5i9rA</recordid><startdate>201911</startdate><enddate>201911</enddate><creator>Park, Jaeseok</creator><creator>Lee, Kyoung‐Pil</creator><creator>Kim, Hyeonji</creator><creator>Park, Sungjo</creator><creator>Wijesinghe, Ruchire E.</creator><creator>Lee, Jaeyul</creator><creator>Han, Sangyeob</creator><creator>Lee, Sangbong</creator><creator>Kim, Pilun</creator><creator>Cho, Dong‐Woo</creator><creator>Jang, Jinah</creator><creator>Kim, Hong K.</creator><creator>Jeon, Mansik</creator><creator>Kim, Jeehyun</creator><general>WILEY‐VCH Verlag GmbH &amp; Co. KGaA</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><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>7QO</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>K9.</scope><scope>L7M</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0630-9039</orcidid></search><sort><creationdate>201911</creationdate><title>Biocompatibility evaluation of bioprinted decellularized collagen sheet implanted in vivo cornea using swept‐source optical coherence tomography</title><author>Park, Jaeseok ; Lee, Kyoung‐Pil ; Kim, Hyeonji ; Park, Sungjo ; Wijesinghe, Ruchire E. ; Lee, Jaeyul ; Han, Sangyeob ; Lee, Sangbong ; Kim, Pilun ; Cho, Dong‐Woo ; Jang, Jinah ; Kim, Hong K. ; Jeon, Mansik ; Kim, Jeehyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4688-d640e36a99ede16e2a344cbe00efd24e03f520178fd62efb1107ac738387eec73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Biocompatibility</topic><topic>Bioengineering</topic><topic>bioprinted collagen sheet</topic><topic>Bioprinting</topic><topic>Collagen</topic><topic>Cornea</topic><topic>Cornea - cytology</topic><topic>Cornea - diagnostic imaging</topic><topic>corneal implant</topic><topic>Corneal transplantation</topic><topic>Extracellular matrix</topic><topic>Eye diseases</topic><topic>Fabrication</topic><topic>Full</topic><topic>Image acquisition</topic><topic>Image analysis</topic><topic>Image processing</topic><topic>Implantation</topic><topic>Materials Testing</topic><topic>Medical treatment</topic><topic>noninvasive monitoring</topic><topic>Optical Coherence Tomography</topic><topic>Prostheses and Implants</topic><topic>Rabbits</topic><topic>Sheets</topic><topic>Surgery</topic><topic>Surgical implants</topic><topic>Thickness</topic><topic>Three dimensional printing</topic><topic>Tissue Engineering</topic><topic>Tissue Scaffolds - chemistry</topic><topic>Tissues</topic><topic>Tomography</topic><topic>Tomography, Optical Coherence</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Jaeseok</creatorcontrib><creatorcontrib>Lee, Kyoung‐Pil</creatorcontrib><creatorcontrib>Kim, Hyeonji</creatorcontrib><creatorcontrib>Park, Sungjo</creatorcontrib><creatorcontrib>Wijesinghe, Ruchire E.</creatorcontrib><creatorcontrib>Lee, Jaeyul</creatorcontrib><creatorcontrib>Han, Sangyeob</creatorcontrib><creatorcontrib>Lee, Sangbong</creatorcontrib><creatorcontrib>Kim, Pilun</creatorcontrib><creatorcontrib>Cho, Dong‐Woo</creatorcontrib><creatorcontrib>Jang, Jinah</creatorcontrib><creatorcontrib>Kim, Hong K.</creatorcontrib><creatorcontrib>Jeon, Mansik</creatorcontrib><creatorcontrib>Kim, Jeehyun</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Electronics &amp; 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The corneal thickness reduction of 34 μm confirmed the biocompatibility through the image analysis of the depth‐intensity profile base. Moreover, hematoxylin and eosin staining supported the biocompatibility evaluation of the bioprinted decellularized collagen sheet implantation. Hence, the developed bioprinted decellularized collagen sheets could become an alternative solution to human corneal donor tissue, and the proposed image analysis procedure could be beneficial to confirm the success of the surgery. Three‐dimensional bioprinted decellularized collagen sheets were implanted into the stromal layer of the cornea of five rabbits. After implanting the collagen sheets, the rabbit corneas were monitored biweekly in vivo with a swept‐source optical coherence tomography system to assess the biocompatibility of the bioprinted implantation for 1 month through corneal thickness measurements. The small variation in the averaged corneal thickness along with evidence from hematoxylin and eosin‐stained histology images shows the potential use of the biocompatible collagen sheet.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH &amp; Co. KGaA</pub><pmid>31240872</pmid><doi>10.1002/jbio.201900098</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-0630-9039</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Biocompatibility
Bioengineering
bioprinted collagen sheet
Bioprinting
Collagen
Cornea
Cornea - cytology
Cornea - diagnostic imaging
corneal implant
Corneal transplantation
Extracellular matrix
Eye diseases
Fabrication
Full
Image acquisition
Image analysis
Image processing
Implantation
Materials Testing
Medical treatment
noninvasive monitoring
Optical Coherence Tomography
Prostheses and Implants
Rabbits
Sheets
Surgery
Surgical implants
Thickness
Three dimensional printing
Tissue Engineering
Tissue Scaffolds - chemistry
Tissues
Tomography
Tomography, Optical Coherence
Transplantation
title Biocompatibility evaluation of bioprinted decellularized collagen sheet implanted in vivo cornea using swept‐source optical coherence tomography
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