Swelling compensation of engineered vasculature fabricated by additive manufacturing and sacrifice-based technique using thermoresponsive hydrogel.

IF 6.8 3区 医学 Q1 ENGINEERING, BIOMEDICAL International Journal of Bioprinting Pub Date : 2023-05-10 eCollection Date: 2023-01-01 DOI:10.18063/ijb.749
Xue Yang, Shuai Li, Xin Sun, Ya Ren, Lei Qiang, Yihao Liu, Jinwu Wang, Kerong Dai
{"title":"Swelling compensation of engineered vasculature fabricated by additive manufacturing and sacrifice-based technique using thermoresponsive hydrogel.","authors":"Xue Yang, Shuai Li, Xin Sun, Ya Ren, Lei Qiang, Yihao Liu, Jinwu Wang, Kerong Dai","doi":"10.18063/ijb.749","DOIUrl":null,"url":null,"abstract":"<p><p>Engineered vasculature is widely employed to maintain the cell viability within <i>in vitro</i> tissues. A variety of fabrication techniques for engineered vasculature have been explored, with combination of additive manufacturing with a sacrifice-based technique being the most common approach. However, the size deformation of vasculature caused by the swelling of sacrificial materials remains unaddressed. In this study, Pluronic F-127 (PF-127), the most widely used sacrificial material, was employed to study the deformation of the vasculature. Then, a thermoresponsive hydrogel comprising poly(N-isopropylacrylamide) (PNIPAM) and gelatin methacrylate (GelMA) was used to induce volume shrinkage at 37°C to compensate for the deformation of vasculature caused by the swelling of a three-dimensional (3D)-printed sacrificial template, and to generate vasculature of a smaller size than that after deformation. Our results showed that the vasculature diameter increased after the sacrificial template was removed, whereas it decreased to the designed diameter after the volume shrinkage. Human umbilical vein endothelial cells (HUVECs) formed an endothelial monolayer in the engineered vasculature. Osteosarcoma cells (OCs) were loaded into a hierarchical vasculature within the thermoresponsive hydrogel to investigate the interaction between HUVECs and OCs. New blood vessel infiltration was observed within the lumen of the engineered vasculature after <i>in vivo</i> subcutaneous implantation for 4 weeks. In addition, engineered vasculature was implanted in a rat ischemia model to further study the function of engineered vasculature for blood vessel infiltration. This study presents a small method aiming to accurately create engineered vasculature by additive manufacturing and a sacrificebased technique.</p>","PeriodicalId":48522,"journal":{"name":"International Journal of Bioprinting","volume":"9 5","pages":"749"},"PeriodicalIF":6.8000,"publicationDate":"2023-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/33/7a/IJB-9-5-749.PMC10339422.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Bioprinting","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.18063/ijb.749","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Engineered vasculature is widely employed to maintain the cell viability within in vitro tissues. A variety of fabrication techniques for engineered vasculature have been explored, with combination of additive manufacturing with a sacrifice-based technique being the most common approach. However, the size deformation of vasculature caused by the swelling of sacrificial materials remains unaddressed. In this study, Pluronic F-127 (PF-127), the most widely used sacrificial material, was employed to study the deformation of the vasculature. Then, a thermoresponsive hydrogel comprising poly(N-isopropylacrylamide) (PNIPAM) and gelatin methacrylate (GelMA) was used to induce volume shrinkage at 37°C to compensate for the deformation of vasculature caused by the swelling of a three-dimensional (3D)-printed sacrificial template, and to generate vasculature of a smaller size than that after deformation. Our results showed that the vasculature diameter increased after the sacrificial template was removed, whereas it decreased to the designed diameter after the volume shrinkage. Human umbilical vein endothelial cells (HUVECs) formed an endothelial monolayer in the engineered vasculature. Osteosarcoma cells (OCs) were loaded into a hierarchical vasculature within the thermoresponsive hydrogel to investigate the interaction between HUVECs and OCs. New blood vessel infiltration was observed within the lumen of the engineered vasculature after in vivo subcutaneous implantation for 4 weeks. In addition, engineered vasculature was implanted in a rat ischemia model to further study the function of engineered vasculature for blood vessel infiltration. This study presents a small method aiming to accurately create engineered vasculature by additive manufacturing and a sacrificebased technique.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
使用热致伸缩性水凝胶的增材制造和牺牲型技术制造的工程血管的膨胀补偿。
为了保持体外组织中细胞的活力,人们广泛采用了工程血管。人们探索了多种工程血管的制造技术,其中最常见的方法是将增材制造技术与牺牲材料技术相结合。然而,牺牲材料膨胀导致的血管尺寸变形问题仍未得到解决。在本研究中,我们采用了最广泛使用的牺牲材料 Pluronic F-127(PF-127)来研究血管的变形。然后,使用由聚(N-异丙基丙烯酰胺)(PNIPAM)和甲基丙烯酸明胶(GelMA)组成的热致伸缩性水凝胶在 37°C 下诱导体积收缩,以补偿三维(3D)打印牺牲模板膨胀引起的脉管变形,并生成比变形后更小的脉管。我们的结果表明,去除牺牲模板后,血管直径增大,而体积收缩后,血管直径减小到设计直径。人脐静脉内皮细胞(HUVECs)在工程血管中形成了内皮单层。骨肉瘤细胞(OCs)被载入热致伸缩水凝胶中的分层血管,以研究 HUVECs 和 OCs 之间的相互作用。在体内皮下植入 4 周后,在工程血管的管腔内观察到了新的血管浸润。此外,还在大鼠缺血模型中植入了工程血管,以进一步研究工程血管的血管浸润功能。本研究提出了一种小方法,旨在通过增材制造和基于牺牲的技术精确创建工程血管。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.90
自引率
4.80%
发文量
81
期刊介绍: The International Journal of Bioprinting is a globally recognized publication that focuses on the advancements, scientific discoveries, and practical implementations of Bioprinting. Bioprinting, in simple terms, involves the utilization of 3D printing technology and materials that contain living cells or biological components to fabricate tissues or other biotechnological products. Our journal encompasses interdisciplinary research that spans across technology, science, and clinical applications within the expansive realm of Bioprinting.
期刊最新文献
Additive-manufactured synthetic bone model with biomimicking tunable mechanical properties for evaluation of medical implants Designing a 3D-printed medical implant with mechanically macrostructural topology and microbionic lattices: A novel wedge-shaped spacer for high tibial osteotomy and biomechanical study PBF-LB fabrication of microgrooves for induction of osteogenic differentiation of human mesenchymal stem cells Building a degradable scaffold with 3D printing using Masquelet technique to promote osteoblast differentiation and angiogenesis in chronic tibial osteomyelitis with bone defects Design of biomedical gradient porous scaffold via a minimal surface dual-unit continuous transition connection strategy
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1