In Situ Gelling Silk Fibroin/ECM Hydrogel With Sustained Oxygen Release for Neural Tissue Engineering Applications

IF 3.9 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Mahyar Haki, Nadia Shafaei, Mohammad Moeini
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引用次数: 0

Abstract

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.

原位胶凝丝素/ECM水凝胶与持续氧释放神经组织工程应用。
在原位凝胶中,充满细胞的水凝胶有望再生位于复杂和难以到达的解剖部位的不规则形状的组织病变。一个显著的例子是由于脑空化而丢失的神经组织的再生。然而,在血管形成期间缺氧诱导的细胞坏死对这种方法的成功提出了重大挑战。为了解决这个问题,已经开发出了释氧水凝胶,但它们在短时间内快速释放氧气,限制了它们的功效。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)的原位凝胶体系,该体系具有持续的氧释放和可调的凝胶时间。过氧化钙纳米颗粒(CPO NPs)作为生氧材料,被包裹在SF微颗粒中,然后掺入SF- decm水凝胶中,目的是调节氧气的释放速度。水凝胶的总CPO含量仅为2% ~ 4% w/w。对不同SF浓度(2%、4%或6% w/v)和微颗粒负载(10%、15%或20% w/w)的水凝胶进行表征表明,SF浓度对水凝胶基质的溶胀、吸收率和力学性能有显著影响,而微颗粒负载的影响较温和。另一方面,微粒负载强烈影响氧释放剖面。水凝胶基质中高SF浓度(6% w/v)导致吸收速度慢,硬度高,可能不适合预期的应用。另一方面,低SF浓度(2% w/v)导致高溶胀率和较短的持续氧释放。在4% w/v SF的水凝胶中,增加微粒负载导致吸收速率减慢,刚度增加和氧气释放增强。然而,在20% w/w的微粒负荷下,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水凝胶具有相对较低的溶胀率(12.8%±2.4%),适当的吸收率(28天后剩余重量70.16%±10.75%)和压缩模量(36.9±1.7 kPa)和持续2周以上的氧气释放。该样品在缺氧条件下也显示出最高的活力(87.6%±15.9%)。总的来说,本研究开发的水凝胶在脑组织工程中具有潜在的应用前景。
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来源期刊
Journal of biomedical materials research. Part A
Journal of biomedical materials research. Part A 工程技术-材料科学:生物材料
CiteScore
10.40
自引率
2.00%
发文量
135
审稿时长
3.6 months
期刊介绍: The Journal of Biomedical Materials Research Part A is an international, interdisciplinary, English-language publication of original contributions concerning studies of the preparation, performance, and evaluation of biomaterials; the chemical, physical, toxicological, and mechanical behavior of materials in physiological environments; and the response of blood and tissues to biomaterials. The Journal publishes peer-reviewed articles on all relevant biomaterial topics including the science and technology of alloys,polymers, ceramics, and reprocessed animal and human tissues in surgery,dentistry, artificial organs, and other medical devices. The Journal also publishes articles in interdisciplinary areas such as tissue engineering and controlled release technology where biomaterials play a significant role in the performance of the medical device. The Journal of Biomedical Materials Research is the official journal of the Society for Biomaterials (USA), the Japanese Society for Biomaterials, the Australasian Society for Biomaterials, and the Korean Society for Biomaterials. Articles are welcomed from all scientists. Membership in the Society for Biomaterials is not a prerequisite for submission.
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