Department of Dental Materials, Dental Medical Devices Testing Center, Peking University School and Hospital of Stomatology, No. 22, Zhongguancun South Avenue, Haidian District, Beijing, 100081, People's Republic of China.
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 & Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health & NMPA Key Laboratory for Dental Materials, Beijing, People's Republic of China.
BMC Oral Health. 2022 Sep 10;22(1):391. doi: 10.1186/s12903-022-02424-7.
When evaluating the efficacy and safety of various desensitizing products in vitro, their mechanism of action and clinical utility should be considered during test model selection. This study aimed to evaluate the effects of two desensitizers, an in-office use material and an at-home use material, on dentin specimen permeability, and their dentin barrier cytotoxicity with appropriate test models.
Two materials, GLUMA desensitizer (GLU) containing glutaraldehyde and remineralizing and desensitizing gel (RD) containing sodium fluoride and fumed silica, were selected. Human dentin specimens were divided into three groups (n = 6): in groups 1 and 2, GLU was applied, and in group 3, RD was applied and immersed in artificial saliva (AS) for 24 h. Dentin specimen permeability before and after each treatment/post-treatment was measured using a hydraulic device under a pressure of 20 cm HO. The perfusion fluid was deionized water, except in group 2 where 2% bovine serum albumin (BSA) was used. The representative specimens before and after treatment from each group were investigated using scanning electron microscopy. To measure cytotoxicity, test materials were applied to the occlusal surfaces of human dentin disks under which three-dimensional cell scaffolds were placed. After 24-h contact within the test device, cell viability was measured via 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays.
GLU significantly reduced the dentin permeability and occluded the dentinal tubules when 2% BSA was used as perfusion fluid. RD significantly reduced dentin permeability and occluded the tubules, but permeability rebounded after AS immersion. GLU significantly decreased cell viability, but RD was non-cytotoxic.
In vitro GLU application induced effective dentinal tubule occlusion only following the introduction of simulated dentinal fluid. RD provided effective tubule occlusion, but its full remineralization potential was not realized after a short period of immersion in AS. GLU may harm the pulp, whereas RD is sufficiently biocompatible.
在评估各种脱敏产品的疗效和安全性时,在选择测试模型时应考虑其作用机制和临床实用性。本研究旨在评估两种脱敏剂(含有戊二醛的 GLUMA 脱敏剂和含有氟化钠和气相法二氧化硅的再矿化和脱敏凝胶)对牙本质标本通透性的影响,并使用适当的测试模型评估其对牙本质屏障的细胞毒性。
选择 GLUMA 脱敏剂(GLU)和再矿化脱敏凝胶(RD)两种材料。将人牙本质标本分为三组(n=6):在第 1 组和第 2 组中,应用 GLU,在第 3 组中,应用 RD 并在人工唾液(AS)中浸泡 24 小时。在 20cmHO 的压力下使用液压装置测量每次处理/后处理前后牙本质标本的通透性。灌注液为去离子水,第 2 组除外,使用 2%牛血清白蛋白(BSA)。每组治疗前后的代表性标本均使用扫描电子显微镜进行研究。为了测量细胞毒性,将测试材料应用于人牙本质圆盘的咬合面,在该牙本质圆盘下放置三维细胞支架。在测试装置内接触 24 小时后,通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法测量细胞活力。
当使用 2%BSA 作为灌注液时,GLU 显著降低牙本质的通透性并封闭牙本质小管。RD 显著降低牙本质的通透性并封闭小管,但在 AS 浸泡后通透性反弹。GLU 显著降低细胞活力,但 RD 无细胞毒性。
体外 GLU 应用仅在引入模拟牙本质液后诱导有效的牙本质小管闭塞。RD 提供了有效的小管闭塞,但在短时间浸泡于 AS 后,其完全再矿化潜力并未实现。GLU 可能会伤害牙髓,而 RD 则具有足够的生物相容性。