自愈水凝胶
矿化(土壤科学)
生物医学工程
傅里叶变换红外光谱
化学
模拟体液
体内
材料科学
磷灰石
化学工程
矿物学
高分子化学
有机化学
生物技术
工程类
生物
医学
氮气
作者
Xinchen Wu,Tengfei Zhang,Brianna L. Hoff,Sanika Suvarnapathaki,Darlin Lantigua,Colleen McCarthy,Bin Wu,Gulden Camci‐Unal
标识
DOI:10.1002/adhm.202001101
摘要
Abstract Sequential mineralization enables the integration of minerals within the 3D structure of hydrogels. Hydrolyzed collagen‐based hydrogels are sequentially mineralized over 10 cycles. One cycle is defined as an incubation period in calcium chloride dihydrate followed by incubation in sodium phosphate dibasic dihydrate. Separate cycles are completed at 30‐minute and 24‐hour intervals. For the gels mineralized for 30 min and 24 h, the compressive moduli increases from 4.25 to 87.57 kPa and from 4.25 to 125.47 kPa, respectively, as the cycle number increases from 0 to 10. As indicated by X‐ray diffraction (XRD) and Fourier transform infrared analysis (FTIR) analyses, the minerals in the scaffolds are mainly hydroxyapatite. In vitro experiments, which measure mechanical properties, porous structure, mineral content, and gene expression are performed to evaluate the physical properties and osteoinductivity of the scaffolds. Real time‐quantitative polymerase chain reaction (RT‐qPCR) demonstrates 4–10 fold increase in the expression of BMP‐7 and osteocalcin. The in vivo subcutaneous implantation demonstrates that the scaffolds are biocompatible and 90% biodegradable. The critical size cranial defects in vivo exhibit nearly complete bone regeneration. Cycle 10 hydrogels mineralized for 24 h have a volume of 59.86 mm 3 and a density of 1946.45 HU. These results demonstrate the suitability of sequentially mineralized hydrogel scaffolds for bone repair and regeneration.
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