Nguyen Christopher D, Chen Ying, Kaplan David L, Mallidi Srivalleesha
Department of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA.
Ann Biomed Eng. 2025 Feb;53(2):371-382. doi: 10.1007/s10439-024-03617-7. Epub 2024 Sep 18.
Tissue engineering is a dynamic field focusing on the creation of advanced scaffolds for tissue and organ regeneration. These scaffolds are customized to their specific applications and are often designed to be complex, large structures to mimic tissues and organs. This study addresses the critical challenge of effectively characterizing these thick, optically opaque scaffolds that traditional imaging methods fail to fully image due to their optical limitations. We introduce a novel multi-modal imaging approach combining ultrasound, photoacoustic, and acoustic radiation force impulse imaging. This combination leverages its acoustic-based detection to overcome the limitations posed by optical imaging techniques. Ultrasound imaging is employed to monitor the scaffold structure, photoacoustic imaging is employed to monitor cell proliferation, and acoustic radiation force impulse imaging is employed to evaluate the homogeneity of scaffold stiffness. We applied this integrated imaging system to analyze melanoma cell growth within silk fibroin protein scaffolds with varying pore sizes and therefore stiffness over different cell incubation periods. Among various materials, silk fibroin was chosen for its unique combination of features including biocompatibility, tunable mechanical properties, and structural porosity which supports extensive cell proliferation. The results provide a detailed mesoscale view of the scaffolds' internal structure, including cell penetration depth and biomechanical properties. Our findings demonstrate that the developed multimodal imaging technique offers comprehensive insights into the physical and biological dynamics of tissue-engineered scaffolds. As the field of tissue engineering continues to advance, the importance of non-ionizing and non-invasive imaging systems becomes increasingly evident, and by facilitating a deeper understanding and better characterization of scaffold architectures, such imaging systems are pivotal in driving the success of future tissue-engineering solutions.
组织工程是一个充满活力的领域,专注于创建用于组织和器官再生的先进支架。这些支架是根据其特定应用定制的,通常设计为复杂的大型结构,以模拟组织和器官。本研究解决了一个关键挑战,即有效表征这些厚实、光学不透明的支架,传统成像方法由于其光学限制而无法对其进行完整成像。我们引入了一种新颖的多模态成像方法,将超声、光声和声学辐射力脉冲成像相结合。这种组合利用基于声学的检测来克服光学成像技术带来的限制。超声成像用于监测支架结构,光声成像用于监测细胞增殖,声学辐射力脉冲成像用于评估支架刚度的均匀性。我们应用这个集成成像系统来分析黑色素瘤细胞在不同孔径、因而在不同细胞培养期具有不同刚度的丝素蛋白支架内的生长情况。在各种材料中,选择丝素蛋白是因为它具有独特的特性组合,包括生物相容性、可调节的机械性能以及支持广泛细胞增殖的结构孔隙率。结果提供了支架内部结构的详细中尺度视图,包括细胞穿透深度和生物力学性能。我们的研究结果表明,所开发的多模态成像技术能够全面洞察组织工程支架的物理和生物学动态。随着组织工程领域的不断发展,非电离和非侵入性成像系统的重要性日益明显,通过促进对支架结构的更深入理解和更好表征,此类成像系统对于推动未来组织工程解决方案的成功至关重要。