Rodriguez Isaac, Saxena Gunjan, Sell Scott, Bowlin Gary
Department of Biomedical Engineering, The University of Memphis and Joint University of Memphis-UTHSC-Memphis Biomedical Engineering Program, 119D Engineering Technology, Memphis, TN 38152, USA.
Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Grosvenor Hall, Athens, OH 45701, USA.
Bioengineering (Basel). 2014 Jan 8;1(1):62-84. doi: 10.3390/bioengineering1010062.
The application of freeze-dried gelatin sponges as alternative bone grafting substitutes has many advantages, including the ability to swell, high porosity, tailorable degradation, and versatility to incorporate multiple components such as growth factors and nanofillers. The purpose of this study was to mineralize (M) and further characterize 1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC) cross-linked gelatin sponges enhanced with preparations rich in growth factors, hydroxyapatite, and chitin whiskers (PHCE). Sponges were characterized for their swelling and mineralization potential, surface characteristics, protein release, mechanical properties, and MG-63 cell attachment and infiltration. All sponges swelled up to 50% of their original volume upon hydration. Scanning electron microscopy showed sparse mineral deposition for gelatin-M scaffolds while PHCE-M scaffolds exhibited more uniform mineral nucleation. Over 21 days, PHCE-M scaffolds cumulatively released significantly more (30%) of its initial protein content than all other scaffolds. PHCE-M scaffolds reported lower modulus values (1.3-1.6 MPa) when compared to gelatin control scaffolds (1.6-3.2 MPa). Increased cell attachment and infiltration was noticed on PHCE and PHCE-M scaffolds. The results of the study demonstrate the enhanced performance of PHCE and PHCE-M scaffolds to serve as bone healing scaffolds. Their potential to release incorporated factors, comparable composition/mechanical properties to tissues developed in the early stages of bone healing, and enhanced initial cellular response make them suitable for further studies evaluating more complex cellular interactions.
冻干明胶海绵作为替代骨移植替代品的应用具有许多优点,包括膨胀能力、高孔隙率、可定制降解以及能够容纳多种成分(如生长因子和纳米填料)的多功能性。本研究的目的是对1-乙基-3-[3-二甲基氨基丙基]碳二亚胺盐酸盐(EDC)交联的明胶海绵进行矿化(M)处理,并进一步表征其性能,该海绵用富含生长因子、羟基磷灰石和甲壳素晶须(PHCE)的制剂增强。对海绵的膨胀和矿化潜力、表面特性、蛋白质释放、力学性能以及MG-63细胞附着和浸润情况进行了表征。所有海绵在水化后体积膨胀至原始体积的50%。扫描电子显微镜显示,明胶-M支架的矿物沉积稀疏,而PHCE-M支架表现出更均匀的矿物成核。在21天内,PHCE-M支架累计释放的初始蛋白质含量比所有其他支架显著多(30%)。与明胶对照支架(1.6-3.2 MPa)相比,PHCE-M支架的模量值较低(1.3-1.6 MPa)。在PHCE和PHCE-M支架上观察到细胞附着和浸润增加。研究结果表明,PHCE和PHCE-M支架作为骨愈合支架的性能得到了增强。它们释放所含因子的潜力、与骨愈合早期形成的组织相当的组成/力学性能以及增强的初始细胞反应使其适合于进一步研究评估更复杂的细胞相互作用。