Christchurch Regenerative Medicine and Tissue Engineering (CReaTE), Group and Medical Technologies Centre of Research Excellence (MedTech CoRE), Department of Orthopaedic Surgery and Musculoskeletal Medicine, University of Otago Christchurch, 2 Riccarton Ave, Christchurch, 8140, New Zealand.
Department of Orthopaedics and Regenerative Medicine Center, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, Utrecht, 3584 CX, The Netherlands.
Adv Healthc Mater. 2020 Aug;9(15):e1901792. doi: 10.1002/adhm.201901792. Epub 2020 Apr 23.
Cartilage defects can result in pain, disability, and osteoarthritis. Hydrogels providing a chondroregeneration-permissive environment are often mechanically weak and display poor lateral integration into the surrounding cartilage. This study develops a visible-light responsive gelatin ink with enhanced interactions with the native tissue, and potential for intraoperative bioprinting. A dual-functionalized tyramine and methacryloyl gelatin (GelMA-Tyr) is synthesized. Photo-crosslinking of both groups is triggered in a single photoexposure by cell-compatible visible light in presence of tris(2,2'-bipyridyl)dichlororuthenium(II) and sodium persulfate as initiators. Neo-cartilage formation from embedded chondroprogenitor cells is demonstrated in vitro, and the hydrogel is successfully applied as bioink for extrusion-printing. Visible light in situ crosslinking in cartilage defects results in no damage to the surrounding tissue, in contrast to the native chondrocyte death caused by UV light (365-400 nm range), commonly used in biofabrication. Tyramine-binding to proteins in native cartilage leads to a 15-fold increment in the adhesive strength of the bioglue compared to pristine GelMA. Enhanced adhesion is observed also when the ink is extruded as printable filaments into the defect. Visible-light reactive GelMA-Tyr bioinks can act as orthobiologic carriers for in situ cartilage repair, providing a permissive environment for chondrogenesis, and establishing safe lateral integration into chondral defects.
软骨缺损可导致疼痛、残疾和骨关节炎。提供软骨再生允许环境的水凝胶通常机械强度较弱,并且与周围软骨的横向整合性差。本研究开发了一种可见光响应的明胶墨水,具有增强与天然组织相互作用的能力,并且具有术中生物打印的潜力。合成了双官能化的酪胺和甲基丙烯酰化明胶(GelMA-Tyr)。在存在三(2,2'-联吡啶)二氯化钌(II)和过硫酸钠作为引发剂的情况下,通过细胞相容的可见光在单个光暴露下触发两组的光交联。体外证明了嵌入软骨祖细胞的新软骨形成,并且成功地将水凝胶用作挤出打印的生物墨水。与通常用于生物制造的 365-400nm 范围内的紫外光(UV 光)相比,可见光原位交联不会对周围组织造成损伤,而 UV 光会导致周围组织中的天然软骨细胞死亡。与原始 GelMA 相比,天然软骨中的酪胺与蛋白质结合导致生物胶的粘附强度增加了 15 倍。当墨水以可打印的细丝挤出到缺陷中时,也观察到增强的粘附性。可见光反应性 GelMA-Tyr 生物墨水可用作原位软骨修复的组织工程载体,为软骨生成提供允许的环境,并安全地横向整合到软骨缺陷中。