{"title":"Enhancing visible light-induced 3D bioprinting: alternating extruded support materials for bioink gelation.","authors":"Takashi Kotani, Takehito Hananouchi, Shinji Sakai","doi":"10.1088/1748-605X/adc0d6","DOIUrl":null,"url":null,"abstract":"<p><p>In 3D bioprinting, two promising approaches have gained significant attention: the use of support materials during printing and the utilization of bioinks gelled through ruthenium(II) tris-bipyridyl dication ([Ru(bpy)<sub>3</sub>]<sup>2+</sup>)-catalyzed photocrosslinking consuming sodium persulfate (SPS). Integrating these approaches while ensuring simplicity and printability remains a challenge. To address this challenge, we propose a technique in which the support material containing SPS is alternately extruded with the bioink containing polymer having phenolic hydroxyl moieties (polymer-Ph) and [Ru(bpy)<sub>3</sub>]<sup>2+</sup>under visible light irradiation. This method eliminates the problems of light shading and deformation caused by the support material, as the contact between the alternately extruded ink and the support material initiates the gelation of the ink via photocrosslinking. Using an ink containing 0.5 w/v% hyaluronic acid with phenolic hydroxyl moieties (HA-Ph) and 2.0 mM [Ru(bpy)<sub>3</sub>]<sup>2+</sup>alongside a support material containing 10 mM SPS, various constructs were successfully printed under 450 nm visible light. The human hepatoblastoma cells embedded in the printed construct showed approximately 95% viability after printing and proliferation over 14 d of culture. These results highlight the potential of this method to advance 3D bioprinting for tissue engineering applications.</p>","PeriodicalId":72389,"journal":{"name":"Biomedical materials (Bristol, England)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedical materials (Bristol, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1088/1748-605X/adc0d6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In 3D bioprinting, two promising approaches have gained significant attention: the use of support materials during printing and the utilization of bioinks gelled through ruthenium(II) tris-bipyridyl dication ([Ru(bpy)3]2+)-catalyzed photocrosslinking consuming sodium persulfate (SPS). Integrating these approaches while ensuring simplicity and printability remains a challenge. To address this challenge, we propose a technique in which the support material containing SPS is alternately extruded with the bioink containing polymer having phenolic hydroxyl moieties (polymer-Ph) and [Ru(bpy)3]2+under visible light irradiation. This method eliminates the problems of light shading and deformation caused by the support material, as the contact between the alternately extruded ink and the support material initiates the gelation of the ink via photocrosslinking. Using an ink containing 0.5 w/v% hyaluronic acid with phenolic hydroxyl moieties (HA-Ph) and 2.0 mM [Ru(bpy)3]2+alongside a support material containing 10 mM SPS, various constructs were successfully printed under 450 nm visible light. The human hepatoblastoma cells embedded in the printed construct showed approximately 95% viability after printing and proliferation over 14 d of culture. These results highlight the potential of this method to advance 3D bioprinting for tissue engineering applications.
在3D生物打印中,两种有前景的方法得到了极大的关注:在打印过程中使用支撑材料和利用通过钌(II)三联吡啶化([Ru(bpy)3]2+)催化光交联消耗过硫酸钠(SPS)凝胶化的生物墨水。在确保简单性和可打印性的同时集成这些方法仍然是一个挑战。为了解决这一挑战,我们提出了一种技术,在可见光照射下,将含有SPS的支撑材料与含有酚羟基基团(聚合物- ph)和[Ru(bpy)3]2+的生物链接聚合物交替挤压。这种方法消除了由支撑材料引起的遮光和变形问题,因为交替挤出的油墨和支撑材料之间的接触通过光交联启动了油墨的凝胶化。使用含有0.5 w/v%酚醛羟基透明质酸(HA-Ph)和2.0 mM [Ru(bpy)3]2+的墨水以及含有10 mM SPS的支撑材料,在450 nm可见光下成功打印了各种结构。人肝母细胞瘤细胞包埋在打印的构建物中,经过14天的打印和增殖,其存活率约为95%。这些结果突出了这种方法在组织工程应用中推进3D生物打印的潜力。