Deng Y, Zhang Y, Li B W, Wang M, Tang L, Liu Y H
Department of Prosthodontics, Peking University School and Hospital of Stomatology & National Center of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology & NHC Research Center of Engineering and Technology for Computerized Dentistry & NMPA Key Laboratory for Dental Materials, Beijing 100081, China.
Department of General Dentistry Ⅱ, Peking University School and Hospital of Stomatology & National Center of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology & NHC Research Center of Engineering and Technology for Computerized Dentistry & NMPA Key Laboratory for Dental Materials, Beijing 100081, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2022 Jun 18;54(3):557-564. doi: 10.19723/j.issn.1671-167X.2022.03.024.
To compare the effects of three different crosslinkers on the biocompatibility, physical and chemical properties of decellularized small intestinal submucosa (SIS) porous scaffolds.
The SIS porous scaffolds were prepared by freeze-drying method and randomly divided into three groups, then crosslinked by glutaraldehyde (GA), 1-ethyl-3-(3-dimethylaminopropyl) carbodi-imide (EDC) and procyanidine (PA) respectively. To evaluate the physicochemical property of each sample in different groups, the following experiments were conducted. Macroscopic morphologies were observed and recorded. Microscopic morphologies of the scaffolds were observed using field emission scanning electron microscope (FESEM) and representative images were selected. Computer software (ImageJ) was used to calculate the pore size and porosity. The degree of crosslinking was determined by ninhydrin experiment. Collagenase degradation experiment was performed to assess the resistance of SIS scaffolds to enzyme degradation. To evaluate the mechanical properties, universal mechanical testing machine was used to determine the stress-strain curve and compression strength was calculated. Human bone marrow mesenchymal cells (hBMSCs) were cultured on the scaffolds after which cytotoxicity and cell proliferation were assessed.
All the scaffolds remained intact after different crosslinking treatments. The FESEM images showed uniformed interconnected micro structures of scaffolds in different groups. The pore size of EDC group[(161.90±13.44) μm] was significantly higher than GA group [(149.50±14.65) μm] and PA group[(140.10±12.06) μm] ( < 0.05). The porosity of PA group (79.62%±1.14%) was significantly lower than EDC group (85.11%±1.71%) and GA group (84.83%±1.89%) ( < 0.05). PA group showed the highest degree of crosslinking whereas the lowest swelling ratio. There was a significant difference in the swelling ratio of the three groups ( < 0.05). Regarding to the collagenase degradation experiment, the scaffolds in PA group showed a significantly lower weight loss rate than the other groups after 7 days degradation. The weight loss rates of GA group were significantly higher than those of the other groups on day 15, whereas the PA group had the lowest rate after 10 days and 15 days degradation. PA group showed better mechanical properties than the other two groups. More living cells could be seen in PA and EDC groups after live/dead cell staining. Additionally, the proliferation rate of hBMCSs was faster in PA and EDC groups than in GA group.
The scaffolds gained satisfying degree of crosslinking after three different crosslinking treatments. The samples after PA and EDC treatment had better physicochemical properties and biocompatibility compared with GA treatment. Crosslinking can be used as a promising and applicable method in the modification of SIS scaffolds.
比较三种不同交联剂对去细胞小肠黏膜下层(SIS)多孔支架生物相容性、物理和化学性质的影响。
采用冷冻干燥法制备SIS多孔支架,随机分为三组,分别用戊二醛(GA)、1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)和原花青素(PA)进行交联。为评估不同组各样本的理化性质,进行了以下实验。观察并记录宏观形态。使用场发射扫描电子显微镜(FESEM)观察支架的微观形态并选取代表性图像。利用计算机软件(ImageJ)计算孔径和孔隙率。通过茚三酮实验确定交联程度。进行胶原酶降解实验以评估SIS支架对酶降解的抗性。为评估力学性能,使用万能材料试验机测定应力-应变曲线并计算抗压强度。将人骨髓间充质细胞(hBMSCs)接种于支架上,之后评估细胞毒性和细胞增殖情况。
不同交联处理后所有支架均保持完整。FESEM图像显示不同组支架具有均匀互连的微观结构。EDC组的孔径[(161.90±13.44)μm]显著高于GA组[(149.50±14.65)μm]和PA组[(140.10±12.06)μm](P<0.05)。PA组的孔隙率(79.62%±1.14%)显著低于EDC组(85.11%±1.71%)和GA组(84.83%±1.89%)(P<0.05)。PA组显示出最高的交联程度和最低的溶胀率。三组的溶胀率存在显著差异(P<0.05)。关于胶原酶降解实验,PA组的支架在降解7天后失重率显著低于其他组。GA组在第15天的失重率显著高于其他组,而PA组在降解10天和15天后失重率最低。PA组的力学性能优于其他两组。活/死细胞染色后,PA组和EDC组可见更多活细胞。此外,PA组和EDC组中hBMCSs的增殖速率比GA组更快。
三种不同交联处理后支架获得了满意的交联程度。与GA处理相比,PA和EDC处理后的样本具有更好的理化性质和生物相容性。交联可作为一种有前景且适用的SIS支架改性方法。