Wang Xiangyao, Li Qilin, Lu Haibo, Liu Zhuo, Wu Yaxin, Mao Jing, Gong Shiqiang
Department of Stomatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
School of Stomatology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Polymers (Basel). 2022 Aug 3;14(15):3166. doi: 10.3390/polym14153166.
The structural integrity of a dentin matrix that has been demineralized by the clinical use of etchants or calcium-depleting endodontic irrigants, such as endodontic ethylenediaminetetraacetic acid (EDTA), is often deteriorated due to the collagenolytic activities of reactivated endogenous enzymes as well as the infiltration of extrinsic bacteria. Therefore, the biomodification of dentin collagen with improved stability and antibacterial activity holds great promise in conservative dentistry. The purpose of this study was to evaluate the effects of the combined application of trimethylated chitosan (TMC) and 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC) on the biostability and antibacterial activity of the demineralized dentin collagen matrix. The morphological changes in the collagen matrix were observed by scanning electron microscopy (SEM), the amount of TMC adsorbed on the collagen surface was detected by X-ray photoelectron spectroscopy, and the elastic modulus was measured by a three-point bending device. Dry weight loss and amino acid release were detected to evaluate its anti-collagenase degradation performance. The antibacterial performance was detected by confocal microscopy. The TMC-treated group had less collagen space and a more compact collagen arrangement, while the untreated group had a looser collagen arrangement. The combined application of TMC and EDC can increase the elastic modulus, reduce the loss of elastic modulus, and result in good antibacterial performance. The current study proved that a dentin collagen matrix biomodified by TMC and EDC showed improved biodegradation resistance and antibacterial activities.
在临床使用蚀刻剂或诸如牙髓乙二胺四乙酸(EDTA)等耗钙牙髓冲洗剂后,牙本质基质会发生脱矿,其结构完整性常因内源性酶的重新激活以及外源性细菌的侵入而受到破坏。因此,对牙本质胶原蛋白进行生物改性以提高其稳定性和抗菌活性,在保守牙科领域具有广阔前景。本研究旨在评估三甲基化壳聚糖(TMC)与盐酸1-乙基-3-[3-二甲基氨基丙基]碳二亚胺(EDC)联合应用对脱矿牙本质胶原蛋白基质的生物稳定性和抗菌活性的影响。通过扫描电子显微镜(SEM)观察胶原蛋白基质的形态变化,采用X射线光电子能谱检测吸附在胶原蛋白表面的TMC量,并用三点弯曲装置测量弹性模量。通过检测干重损失和氨基酸释放来评估其抗胶原酶降解性能。通过共聚焦显微镜检测抗菌性能。TMC处理组的胶原间隙较小,胶原排列更紧密,而未处理组的胶原排列较松散。TMC与EDC联合应用可提高弹性模量,减少弹性模量损失,并具有良好的抗菌性能。本研究证明,经TMC和EDC生物改性的牙本质胶原蛋白基质具有更好的抗生物降解性和抗菌活性。