Kim Min Suk, Choi Yuri, Lee Keel Yong
Department of Integrative Bioscience and Biotechnology, Sejong University, Seoul 05006, Republic of Korea.
Institute of Bioscience and Biotechnology, Sejong University, Seoul 05006, Republic of Korea.
Polymers (Basel). 2025 Aug 28;17(17):2337. doi: 10.3390/polym17172337.
Advancements in bioinks and three-dimensional (3D) printing and bioprinting have significantly advanced cardiovascular tissue engineering by enabling the fabrication of biomimetic cardiac and vascular constructs. Traditional 3D printing has contributed to the development of acellular scaffolds, vascular grafts, and patient-specific cardiovascular models that support surgical planning and biomedical applications. In contrast, 3D bioprinting has emerged as a transformative biofabrication technology that allows for the spatially controlled deposition of living cells and biomaterials to construct functional tissues in vitro. Bioinks-derived from natural biomaterials such as collagen and decellularized matrix, synthetic polymers such as polyethylene glycol (PEG) and polycaprolactone (PCL), or hybrid combinations-have been engineered to replicate extracellular environments while offering tunable mechanical properties. These formulations ensure biocompatibility, appropriate mechanical strength, and high printing fidelity, thereby maintaining cell viability, structural integrity, and precise architectural resolution in the printed constructs. Advanced bioprinting modalities, including extrusion-based bioprinting (such as the FRESH technique), droplet/inkjet bioprinting, digital light processing (DLP), two-photon polymerization (TPP), and melt electrowriting (MEW), enable the fabrication of complex cardiovascular structures such as vascular patches, ventricle-like heart pumps, and perfusable vascular networks, demonstrating the feasibility of constructing functional cardiac tissues in vitro. This review highlights the respective strengths of these technologies-for example, extrusion's ability to print high-cell-density bioinks and MEW's ultrafine fiber resolution-as well as their limitations, including shear-induced cell stress in extrusion and limited throughput in TPP. The integration of optimized bioink formulations with appropriate printing and bioprinting platforms has significantly enhanced the replication of native cardiac and vascular architectures, thereby advancing the functional maturation of engineered cardiovascular constructs.
生物墨水、三维(3D)打印和生物打印技术的进步,通过制造仿生心脏和血管构建体,极大地推动了心血管组织工程的发展。传统3D打印为无细胞支架、血管移植物以及支持手术规划和生物医学应用的患者特异性心血管模型的开发做出了贡献。相比之下,3D生物打印已成为一种变革性的生物制造技术,它允许在空间上控制活细胞和生物材料的沉积,以在体外构建功能性组织。源自天然生物材料(如胶原蛋白和脱细胞基质)、合成聚合物(如聚乙二醇(PEG)和聚己内酯(PCL))或混合组合的生物墨水,经过设计可复制细胞外环境,同时提供可调节的机械性能。这些配方确保了生物相容性、适当的机械强度和高打印保真度,从而在打印构建体中维持细胞活力、结构完整性和精确的结构分辨率。先进的生物打印方式,包括基于挤出的生物打印(如FRESH技术)、液滴/喷墨生物打印、数字光处理(DLP)、双光子聚合(TPP)和熔体静电纺丝(MEW),能够制造复杂的心血管结构,如血管补片、心室样心脏泵和可灌注的血管网络,证明了在体外构建功能性心脏组织的可行性。本综述强调了这些技术各自的优势,例如挤出技术打印高细胞密度生物墨水的能力和MEW的超细纤维分辨率,以及它们的局限性,包括挤出过程中剪切诱导的细胞应力和TPP的有限通量。将优化的生物墨水配方与合适的打印和生物打印平台相结合,显著增强了天然心脏和血管结构的复制,从而推动了工程化心血管构建体的功能成熟。