Yihui Song , Sheng Hua , Sepidar Sayyar , Zhi Chen , Johnson Chung , Xiao Liu , Zhilian Yue , Cameron Angus , Benjamin Filippi , Stephen Beirne , Gordon Wallace , Gerard Sutton , Jingjing You
{"title":"角膜生物打印采用高浓度纯胶原I透明生物墨水","authors":"Yihui Song , Sheng Hua , Sepidar Sayyar , Zhi Chen , Johnson Chung , Xiao Liu , Zhilian Yue , Cameron Angus , Benjamin Filippi , Stephen Beirne , Gordon Wallace , Gerard Sutton , Jingjing You","doi":"10.1016/j.bprint.2022.e00235","DOIUrl":null,"url":null,"abstract":"<div><p><span><span><span>The use of 3D printing to produce a bioengineered cornea is emerging as an approach to help alleviate the global shortage of donor corneas. </span>Collagen Type 1 (Col-1) is the most abundant collagen in the human cornea. However, Col-I presents challenges as a bioink. It can self-assemble at neutral pH, making phase transitions as required for 3D printing difficult to control. Furthermore, low concentration solutions required for the transparency of printed Col-I lead to weak </span>mechanical properties<span> in its printed structures. In this study, Col-I at high concentrations, was tested with 15 different solutions to identify the composition preventing Col-I self-assembly. A stable Col-I bioink was then developed using riboflavin as a </span></span>photoinitiator<span> and UV irradiation-induced crosslinking. The mechanical properties and transparency, of the structures produced, were evaluated. The optimised Col-I bioink with corneal stromal cells was tested using a spiral printing method. The printed structure was transparent, and the encapsulated corneal stromal cells had over 90% viability after three weeks of culturing.</span></p></div>","PeriodicalId":37770,"journal":{"name":"Bioprinting","volume":"28 ","pages":"Article e00235"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Corneal bioprinting using a high concentration pure collagen I transparent bioink\",\"authors\":\"Yihui Song , Sheng Hua , Sepidar Sayyar , Zhi Chen , Johnson Chung , Xiao Liu , Zhilian Yue , Cameron Angus , Benjamin Filippi , Stephen Beirne , Gordon Wallace , Gerard Sutton , Jingjing You\",\"doi\":\"10.1016/j.bprint.2022.e00235\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span><span>The use of 3D printing to produce a bioengineered cornea is emerging as an approach to help alleviate the global shortage of donor corneas. </span>Collagen Type 1 (Col-1) is the most abundant collagen in the human cornea. However, Col-I presents challenges as a bioink. It can self-assemble at neutral pH, making phase transitions as required for 3D printing difficult to control. Furthermore, low concentration solutions required for the transparency of printed Col-I lead to weak </span>mechanical properties<span> in its printed structures. In this study, Col-I at high concentrations, was tested with 15 different solutions to identify the composition preventing Col-I self-assembly. A stable Col-I bioink was then developed using riboflavin as a </span></span>photoinitiator<span> and UV irradiation-induced crosslinking. The mechanical properties and transparency, of the structures produced, were evaluated. The optimised Col-I bioink with corneal stromal cells was tested using a spiral printing method. The printed structure was transparent, and the encapsulated corneal stromal cells had over 90% viability after three weeks of culturing.</span></p></div>\",\"PeriodicalId\":37770,\"journal\":{\"name\":\"Bioprinting\",\"volume\":\"28 \",\"pages\":\"Article e00235\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioprinting\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2405886622000458\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Computer Science\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioprinting","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405886622000458","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Computer Science","Score":null,"Total":0}
Corneal bioprinting using a high concentration pure collagen I transparent bioink
The use of 3D printing to produce a bioengineered cornea is emerging as an approach to help alleviate the global shortage of donor corneas. Collagen Type 1 (Col-1) is the most abundant collagen in the human cornea. However, Col-I presents challenges as a bioink. It can self-assemble at neutral pH, making phase transitions as required for 3D printing difficult to control. Furthermore, low concentration solutions required for the transparency of printed Col-I lead to weak mechanical properties in its printed structures. In this study, Col-I at high concentrations, was tested with 15 different solutions to identify the composition preventing Col-I self-assembly. A stable Col-I bioink was then developed using riboflavin as a photoinitiator and UV irradiation-induced crosslinking. The mechanical properties and transparency, of the structures produced, were evaluated. The optimised Col-I bioink with corneal stromal cells was tested using a spiral printing method. The printed structure was transparent, and the encapsulated corneal stromal cells had over 90% viability after three weeks of culturing.
期刊介绍:
Bioprinting is a broad-spectrum, multidisciplinary journal that covers all aspects of 3D fabrication technology involving biological tissues, organs and cells for medical and biotechnology applications. Topics covered include nanomaterials, biomaterials, scaffolds, 3D printing technology, imaging and CAD/CAM software and hardware, post-printing bioreactor maturation, cell and biological factor patterning, biofabrication, tissue engineering and other applications of 3D bioprinting technology. Bioprinting publishes research reports describing novel results with high clinical significance in all areas of 3D bioprinting research. Bioprinting issues contain a wide variety of review and analysis articles covering topics relevant to 3D bioprinting ranging from basic biological, material and technical advances to pre-clinical and clinical applications of 3D bioprinting.