Nong Lu-Ming, Jiang Yu-Qing, Zhou Si-Yuan, Gao Gong-Ming, Ma Yong, Jiang Xi-Jia, Han Long
Department of Orthopedics, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou City, Jiangsu Province, China.
Department of Laboratory, The Affiliated Changzhou No. 2 People's Hospital of Nanjing Medical University, Changzhou City, Jiangsu Province, China.
Cell Tissue Bank. 2023 Mar;24(1):181-190. doi: 10.1007/s10561-022-10020-w. Epub 2022 Jul 6.
The process of generating type I/II collagen scaffolds is fraught with bubble formation, which can interfere with the three-dimensional structure of the scaffold. Herein, we applied low-temperature vacuum freeze-drying to remove mixed air bubbles under negative pressure. Type I and II rubber sponges were acid-solubilized via acid lysis and enzymolysis. Thereafter, vacuum negative pressure was applied to remove bubbles, and the cover glass press method was applied to shape the type I/II original scaffold. Vacuum negative pressure was applied for a second time to remove any residual bubbles. Subsequent application of carbamide/N-hydroxysuccinimide cross-linked the scaffold. The traditional method was used as the control group. The structure and number of residual bubbles and pore sizes of the two scaffolds were compared. Based on the relationship between the pressure and the number of residual bubbles, a curve was created, and the time of ice formation was calculated. The bubble content of the experimental group was significantly lower than that of the control group (P < 0.05). The pore diameter of the type I/II collagen scaffold was higher in the experimental group than in the control group. The time of icing effect of type I and II collagen solution was 136.54 ± 5.26 and 144.40 ± 6.45 s, respectively. The experimental scaffold had a more regular structure with actively proliferating chondrocytes that possessed adherent pseudopodia. The findings indicated that the vacuum negative pressure method did not affect the physical or chemical properties of collagen, and these scaffolds exhibited good biocompatibility with chondrocytes.
生成I/II型胶原蛋白支架的过程充满气泡形成问题,这会干扰支架的三维结构。在此,我们应用低温真空冷冻干燥在负压下去除混合气泡。I型和II型橡胶海绵通过酸解和酶解进行酸溶解。此后,施加真空负压以去除气泡,并采用盖玻片压制法对I/II型原始支架进行塑形。再次施加真空负压以去除任何残留气泡。随后应用尿素/N-羟基琥珀酰亚胺对支架进行交联。传统方法作为对照组。比较了两种支架的残留气泡结构和数量以及孔径。基于压力与残留气泡数量之间的关系绘制曲线,并计算结冰时间。实验组的气泡含量显著低于对照组(P < 0.05)。实验组I/II型胶原蛋白支架的孔径高于对照组。I型和II型胶原蛋白溶液的结冰效果时间分别为136.54 ± 5.26秒和144.40 ± 6.45秒。实验支架具有更规则的结构,其中增殖活跃的软骨细胞具有附着伪足。研究结果表明,真空负压法不影响胶原蛋白的物理或化学性质,并且这些支架与软骨细胞表现出良好的生物相容性。