4.6 Article Proceedings Paper

A Non-Cytotoxic Resin for Micro-Stereolithography for Cell Cultures of HUVECs

期刊

MICROMACHINES
卷 11, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/mi11030246

关键词

micro-stereolithography; cytotoxicity; resin development; microfluidics; cell culture; human umbilical vein endothelial cells (HUVECs); biocompatibility; 3D printing; additive manufacturing

资金

  1. Federal Ministry of Education and Research (BMBF
  2. Biotechnology2020+: Leibniz Research Cluster) [031A360C]
  3. Volkswagen Foundation (Experiment!)
  4. German Research Foundation (DFG, Research Training Group 1865: Hydrogel-based Microsystems)

向作者/读者索取更多资源

Three-dimensional (3D) printing of microfluidic devices continuously replaces conventional fabrication methods. A versatile tool for achieving microscopic feature sizes and short process times is micro-stereolithography (mu SL). However, common resins for mu SL lack biocompatibility and are cytotoxic. This work focuses on developing new photo-curable resins as a basis for mu SL fabrication of polymer materials and surfaces for cell culture. Different acrylate- and methacrylate-based compositions are screened for material characteristics including wettability, surface roughness, and swelling behavior. For further understanding, the impact of photo-absorber and photo-initiator on the cytotoxicity of 3D-printed substrates is studied. Cell culture experiments with human umbilical vein endothelial cells (HUVECs) in standard polystyrene vessels are compared to 3D-printed parts made from our library of homemade resins. Among these, after optimizing material composition and post-processing, we identify selected mixtures of poly(ethylene glycol) diacrylate (PEGDA) and poly(ethylene glycol) methyl ethyl methacrylate (PEGMEMA) as most suitable to allow for fabricating cell culture platforms that retain both the viability and proliferation of HUVECs. Next, our PEGDA/PEGMEMA resins will be further optimized regarding minimal feature size and cell adhesion to fabricate microscopic (microfluidic) cell culture platforms, e.g., for studying vascularization of HUVECs in vitro.

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