Arishima Mareni, Haraguchi Ryota, Kawakita Hidetaka, Aoki Shigehisa, Oishi Yushi, Narita Takayuki
Department of Chemistry and Applied Chemistry, Saga University, Saga 840-8502, Japan.
Department of Pathology and Microbiology, Saga University, Saga 840-8501, Japan.
Polymers (Basel). 2025 Jan 23;17(3):287. doi: 10.3390/polym17030287.
The development of scaffold materials that effectively mimic the extracellular matrix while enabling controlled nutrient delivery remains a critical challenge in tissue engineering. Multi-channel collagen gels (MCCGs), which form through the competition between gelation and phase separation, have emerged as promising scaffolds due to their self-organized vessel-like structures. However, a systematic understanding of the relationship between the gelation conditions and functional properties is limited. In this study, MCCGs were developed as controllable perfusion culture scaffolds by investigating the effects of carbonate buffer concentration on channel formation, permeation behavior, and cell proliferation. MCCGs were prepared using different carbonate buffer concentrations (12.5, 25, and 50 mM), with 25 mM producing optimal channel formation, characterized by an approximately 60% channel area fraction and uniform distribution. Permeation studies revealed that fluid transport through MCCGs is governed by a complex interplay between capillary phenomena and hydraulic pressure, whose relative dominance shifts with flow rate: capillary action dominates at low flow rates (2.5 mL/h), whereas hydraulic pressure becomes the primary driver at higher rates (5.0-10.0 mL/h). Cell proliferation assessments demonstrated that MCCGs prepared with 25 mM carbonate buffer provided the most favorable microenvironment, achieving superior cell growth over 168 h through balanced media supply and cell adhesion area. This optimization approach through buffer concentration adjustment offers a cost-effective and scalable method for developing perfusion culture scaffolds, advancing both the fundamental understanding of functional gel systems and practical applications in tissue engineering and regenerative medicine.
开发能够有效模拟细胞外基质并实现可控营养物质输送的支架材料,仍然是组织工程中的一项关键挑战。多通道胶原蛋白凝胶(MCCGs)通过凝胶化和相分离之间的竞争形成,由于其自组织的血管样结构,已成为有前景的支架材料。然而,对凝胶化条件与功能特性之间关系的系统理解仍然有限。在本研究中,通过研究碳酸盐缓冲液浓度对通道形成、渗透行为和细胞增殖的影响,将MCCGs开发为可控灌注培养支架。使用不同的碳酸盐缓冲液浓度(12.5、25和50 mM)制备MCCGs,其中25 mM产生最佳的通道形成,其特征是通道面积分数约为60%且分布均匀。渗透研究表明,通过MCCGs的流体传输受毛细管现象和液压之间复杂相互作用的控制,其相对主导地位随流速而变化:在低流速(2.5 mL/h)下毛细管作用占主导,而在较高流速(5.0 - 10.0 mL/h)下液压成为主要驱动力。细胞增殖评估表明,用25 mM碳酸盐缓冲液制备的MCCGs提供了最有利的微环境,通过平衡的培养基供应和细胞粘附面积在168小时内实现了优异的细胞生长。这种通过缓冲液浓度调整的优化方法为开发灌注培养支架提供了一种经济高效且可扩展的方法,既推进了对功能性凝胶系统的基础理解,也促进了在组织工程和再生医学中的实际应用。