Haki Mahyar, Shafaei Nadia, Moeini Mohammad
Department of Biomedical Engineering, Amirkabir University of Technology (Tehran Polytechnic), Tehran, Iran.
J Biomed Mater Res A. 2025 Jan;113(1):e37837. doi: 10.1002/jbm.a.37837.
In situ gelling, cell-laden hydrogels hold promise for regenerating tissue lesions with irregular shapes located in complex and hard-to-reach anatomical sites. A notable example is the regeneration of neural tissue lost due to cerebral cavitation. However, hypoxia-induced cell necrosis during the vascularization period imposes a significant challenge to the success of this approach. Oxygen-releasing hydrogels have been developed to address this issue, but they suffer from fast oxygen release over a short period, limiting their efficacy. This study develops an in situ gelling hydrogel system based on silk fibroin (SF) and decellularized brain extracellular matrix (dECM) with sustained oxygen release and tunable gelation time. Calcium peroxide nanoparticles (CPO NPs) served as the oxygen generating material, which were encapsulated within SF microparticles before incorporation into the SF-dECM hydrogel, aiming to regulate the oxygen release rate. The total CPO content of the hydrogels was only 2%-4% w/w. Characterization of hydrogels containing various SF concentrations (2%, 4% or 6% w/v) and microparticle loadings (10%, 15% or 20% w/w) demonstrated that SF concentration in the hydrogel matrix significantly affects the swelling, resorption rate and mechanical properties, while microparticle loading has a milder effect. On the other hand, microparticle loading strongly affected the oxygen release profile. High SF concentration in the hydrogel matrix (6% w/v) led to slow resorption rate and high stiffness, likely unsuitable for intended application. Low SF concentration (2% w/v), on the other hand, led to a high swelling ratio and a less sustained oxygen release. Among 4% w/v SF hydrogels, increased microparticle loading led to a slower resorption rate, increased stiffness and enhanced oxygen release. However, cell viability was reduced at 20% w/w microparticle loading, likely due to decreased cell attachment. The 4% w/v SF hydrogels containing 10% w/w SF-CPO microparticles exhibited relatively low swelling ratio (12.8% ± 2.4%), appropriate resorption rate (70.16% ± 10.75% remaining weight after 28 days) and compressive modulus (36.9 ± 1.7 kPa) and sustained oxygen release for over 2 weeks. This sample also showed the highest viability under hypoxic conditions among tested hydrogel samples (87.6% ± 15.9%). Overall, the developed hydrogels in this study showed promise for potential application in brain tissue engineering.
原位凝胶化、负载细胞的水凝胶有望用于再生位于复杂且难以触及的解剖部位的不规则形状的组织损伤。一个显著的例子是因脑空洞形成而损失的神经组织的再生。然而,血管化期间缺氧诱导的细胞坏死对这种方法的成功构成了重大挑战。已开发出释氧水凝胶来解决这个问题,但它们存在短期内氧气快速释放的问题,限制了其功效。本研究开发了一种基于丝素蛋白(SF)和脱细胞脑细胞外基质(dECM)的原位凝胶化水凝胶系统,具有持续的氧气释放和可调的凝胶化时间。过氧化钙纳米颗粒(CPO NPs)作为产氧材料,在掺入SF - dECM水凝胶之前被封装在SF微粒中,旨在调节氧气释放速率。水凝胶中CPO的总含量仅为2% - 4% w/w。对含有不同SF浓度(2%、4%或6% w/v)和微粒负载量(10%、15%或20% w/w)的水凝胶的表征表明,水凝胶基质中的SF浓度显著影响溶胀、吸收速率和机械性能,而微粒负载量的影响较小。另一方面,微粒负载量对氧气释放曲线有强烈影响。水凝胶基质中高SF浓度(6% w/v)导致吸收速率缓慢和硬度高,可能不适合预期应用。另一方面,低SF浓度(2% w/v)导致高溶胀率和氧气释放持续性较差。在4% w/v SF水凝胶中,微粒负载量增加导致吸收速率减慢、硬度增加和氧气释放增强。然而,在20% w/w微粒负载量下细胞活力降低,可能是由于细胞附着减少。含有10% w/w SF - CPO微粒的4% w/v SF水凝胶表现出相对较低的溶胀率(12.8% ± 2.4%)、合适的吸收速率(28天后剩余重量的70.16% ± 10.75%)和压缩模量(36.9 ± 1.7 kPa),并持续释放氧气超过2周。该样品在测试的水凝胶样品中在缺氧条件下也显示出最高的活力(87.6% ± 15.9%)。总体而言,本研究中开发的水凝胶在脑组织工程中显示出潜在应用的前景。