High Magnetic Field Laboratory, Key Laboratory of High Magnetic Field and Ion Beam Physical Biology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, Anhui, PR China; University of Science and Technology of China, Hefei 230036, Anhui, PR China.
Department of Precision Machinery and Precision Instrumentation, University of Science and Technology of China, Hefei 230026, Anhui, PR China.
Int J Biol Macromol. 2024 Oct;277(Pt 2):134338. doi: 10.1016/j.ijbiomac.2024.134338. Epub 2024 Jul 30.
Sodium alginate (SA) has gained widespread acclaim as a carrier medium for three-dimensional (3D) bioprinting of cells and a diverse array of bioactive substances, attributed to its remarkable biocompatibility and affordability. The conventional approach for fabricating alginate-based tissue engineering constructs entails a post-treatment phase employing a calcium ion solution. However, this method proves ineffectual in addressing the predicament of low precision during the 3D printing procedure and is unable to prevent issues such as non-uniform alginate gelation and substantial distortions. In this study, we introduced borate bioactive glass (BBG) into the SA matrix, capitalizing on the calcium ions released from the degradation of BBG to incite the cross-linking reaction within SA, resulting in the formation of BBG-SA hydrogels. Building upon this fundamental concept, it unveiled that BBG-SA hydrogels greatly enhance the precision of SA in extrusion-based 3D printing and significantly reduce volumetric contraction shrinkage post-printing, while also displaying certain adhesive properties and electrical conductivity. Furthermore, in vitro cellular experiments have unequivocally established the excellent biocompatibility of BBG-SA hydrogel and its capacity to actively stimulate osteogenic differentiation. Consequently, BBG-SA hydrogel emerges as a promising platform for 3D bioprinting, laying the foundation for the development of flexible, biocompatible electronic devices.
海藻酸钠(SA)作为细胞三维(3D)生物打印的载体介质和多种生物活性物质的载体得到了广泛的认可,这归因于其出色的生物相容性和可负担性。制造基于海藻酸盐的组织工程构建体的传统方法需要采用钙离子溶液进行后处理阶段。然而,这种方法在解决 3D 打印过程中精度低的问题时效果不佳,并且无法防止海藻酸盐凝胶不均匀和大量变形等问题。在本研究中,我们将硼酸盐生物活性玻璃(BBG)引入 SA 基质中,利用 BBG 降解释放的钙离子引发 SA 中的交联反应,形成 BBG-SA 水凝胶。基于这一基本概念,我们揭示了 BBG-SA 水凝胶极大地提高了 SA 在基于挤出的 3D 打印中的精度,并显著降低了打印后的体积收缩收缩,同时还显示出一定的粘附性能和导电性。此外,体外细胞实验明确证实了 BBG-SA 水凝胶的优异生物相容性及其主动刺激成骨分化的能力。因此,BBG-SA 水凝胶作为 3D 生物打印的有前途的平台,为开发灵活、生物相容的电子设备奠定了基础。