Cao C L, Yang C C, Qu X Z, Han B, Wang X Y
Department of Cariology and Endodontology, Peking University School and Hospital of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Laboratory for Digital and Material Technology of Stomatology & Beijing Key Laboratory of Digital Stomatology, Beijing 100081, China.
College of Materials Science and Optoelectronic Technology, University of Chinese Academy of Sciences, Beijing 100049, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2020 Feb 18;52(1):10-17. doi: 10.19723/j.issn.1671-167X.2020.01.002.
To prepare glycol-chitosan (GC)-based single/dual-network hydrogels with different composition ratios (GC31, DN3131 and DN6262) and to investigate the effects of hydrogel scaffolds on biological behavior of human dental pulp cell (hDPC) encapsulated.
GC-based single-network hydrogels (GC31) and GC-based dual-network hydrogels (DN3131, DN6262) with different composition ratios were prepared. The injectability was defined as the average time needed to expel a certain volume of hydrogel under a constant force. The degradation of the hydrogel was determined by the weight loss with time. The fracture stress was measured using a universal testing machine. The proliferation of hDPCs in hydrogels was detected using the cell counting kit-8 (CCK-8) method and CalceinAM/PI Live/Dead assay. After 14 days of odontoblastic induction, the expression of alkaline phosphatase (ALP), dentin sialophosphoprotein (DSPP) and dentin matrix protein-1 (DMP-1) was detected by real-time quantitative reverse transcription PCR (real-time RT-PCR) and the mineralized nodules was observed by Von Kossa staining.
The injectability of all three groups of hydrogels was acceptable. The time of injection of GC31 was the shortest, and that of DN6262 was longer than DN3131 (P<0.05). The degradation rate of GC31 hydrogel in vitro was significantly faster than that of the dual-network hydrogel groups (P<0.05). There was no significant difference between DN3131 and DN6262 (P>0.05). The compressive resistance failure point of GC31 group was 1.10 kPa, while it was 7.33 kPa and 43.30 kPa for DN3131 and DN6262. The compressive strength of dual-network hydrogel was significantly enhanced compared with single-network hydrogel. hDPCs were in continuous proliferation in all the three groups, and the GC31 group showed a higher proliferation rate (P<0.05). The expression levels of DSPP, DMP-1 and ALP in the dual-network hydrogel groups (DN3131, DN6262) were significantly higher than that of GC31 after culturing for 14 days (P<0.05), there was no difference in the expression levels of DMP-1 and ALP between DN3131 and DN6262 (P>0.05); Von Kossa staining showed that more mineralization deposition and mass-shaped mineralized nodules formed in DN3131 and DN6262, while only light brown calcium deposition staining was observed in GC31 group, which was scattered in granular forms.
GC-based single/dual network hydrogels with different composition ratios met the injectable requirements. GC31 group had a lower mechanical properties, in which hDPCs exhibited a higher proliferation rate. dual-network hydrogels had slower degradation rate and higher mechanical properties, in which hDPCs exhibited better odontoblastic differentiation potential and mineralization potential.
制备具有不同组成比例的基于乙二醇壳聚糖(GC)的单/双网络水凝胶(GC31、DN3131和DN6262),并研究水凝胶支架对包封的人牙髓细胞(hDPC)生物学行为的影响。
制备具有不同组成比例的基于GC的单网络水凝胶(GC31)和基于GC的双网络水凝胶(DN3131、DN6262)。将可注射性定义为在恒定力下排出一定体积水凝胶所需的平均时间。通过随时间的重量损失来测定水凝胶的降解情况。使用万能试验机测量断裂应力。使用细胞计数试剂盒-8(CCK-8)法和钙黄绿素-AM/PI活/死检测法检测hDPC在水凝胶中的增殖情况。在成牙本质细胞诱导14天后,通过实时定量逆转录PCR(实时RT-PCR)检测碱性磷酸酶(ALP)、牙本质涎磷蛋白(DSPP)和牙本质基质蛋白-1(DMP-1)的表达,并通过冯科萨染色观察矿化结节。
三组水凝胶的可注射性均良好。GC31的注射时间最短,DN6262的注射时间长于DN3131(P<0.05)。GC31水凝胶在体外的降解速率明显快于双网络水凝胶组(P<0.05)。DN3131和DN6262之间无显著差异(P>0.05)。GC31组的抗压强度破坏点为1.10 kPa,而DN3131和DN6262分别为7.33 kPa和43.30 kPa。双网络水凝胶的抗压强度明显高于单网络水凝胶。hDPC在所有三组中均持续增殖,GC31组的增殖率更高(P<0.05)。培养14天后,双网络水凝胶组(DN3131、DN6262)中DSPP、DMP-1和ALP的表达水平明显高于GC31组(P<0.05),DN3131和DN6262之间DMP-1和ALP的表达水平无差异(P>0.05);冯科萨染色显示,DN3131和DN6262中形成了更多的矿化沉积和块状矿化结节,而GC31组仅观察到浅棕色钙沉积染色,呈颗粒状散在分布。
具有不同组成比例的基于GC的单/双网络水凝胶满足可注射要求。GC31组的力学性能较低,其中hDPC表现出较高的增殖率。双网络水凝胶的降解速率较慢且力学性能较高,其中hDPC表现出更好的成牙本质细胞分化潜能和矿化潜能。