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一种用于在发育中的鸡胚绒毛尿囊膜上进行直接细胞生物学植入测试的聚(乙二醇)二丙烯酸酯3D打印微生物反应器。

A Poly-(ethylene glycol)-diacrylate 3D-Printed Micro-Bioreactor for Direct Cell Biological Implant-Testing on the Developing Chicken Chorioallantois Membrane.

作者信息

Lutsch Eric, Struber Andreas, Auer Georg, Fessmann Thomas, Lepperdinger Günter

机构信息

System-Precision-on-Chip-SPOC Laboratories, Department of Biosciences and Medical Biology, University Salzburg, Hellbrunnerstrasse 34, A-5020 Salzburg, Austria.

出版信息

Micromachines (Basel). 2022 Jul 31;13(8):1230. doi: 10.3390/mi13081230.

Abstract

Advancements in biomaterial manufacturing technologies calls for improved standards of fabrication and testing. Currently 3D-printable resins are being formulated which exhibit the potential to rapidly prototype biocompatible devices. For validation purposes, 3D-printed materials were subjected to a hierarchical validation onto the chorioallantoic membrane of the developing chicken, better known as the HET CAM assay. Working along these lines, prints made from poly-(ethylene glycol)-diacrylate (PEGDA), which had undergone appropriate post-print processing, outperformed other commercial resins. This material passed all tests without displaying adverse effects, as experienced with other resin types. Based on this finding, the micro bioreactors (MBR) design, first made of PDMS and that also passed with cell tests on the HET-CAM, was finally printed in PEGDA, and applied in vivo. Following this workflow shows the applicability of 3D-printable resins for biomedical device manufacturing, consents to adherence to the present standards of the 3R criteria in material research and development, and provides flexibility and fast iteration of design and test cycles for MBR adaptation and optimization.

摘要

生物材料制造技术的进步要求提高制造和测试标准。目前正在研发3D可打印树脂,它们具有快速制造生物相容性设备原型的潜力。为了进行验证,对3D打印材料在发育中的鸡的绒毛尿囊膜上进行了分级验证,即著名的鸡胚绒毛尿囊膜试验(HET CAM试验)。按照这些思路,由聚(乙二醇)二丙烯酸酯(PEGDA)制成并经过适当后处理的打印材料,其性能优于其他商用树脂。这种材料通过了所有测试,未显示出其他树脂类型所出现的不良反应。基于这一发现,最初由聚二甲基硅氧烷(PDMS)制成且也通过了HET-CAM细胞测试的微生物反应器(MBR)设计,最终用PEGDA打印并应用于体内。遵循此工作流程表明了3D可打印树脂在生物医学设备制造中的适用性,符合材料研发中现行的3R标准,并为MBR的适配和优化提供了设计和测试周期的灵活性和快速迭代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6024/9414255/0c1fe8eaaa9d/micromachines-13-01230-g001.jpg

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