Sharma Kashma, Sharma Shreya, Thapa Sonia, Bhagat Madhulika, Kumar Vijay, Sharma Vishal
Institute of Forensic Science & Criminology, Panjab University, Chandigarh 160014, India.
Cancer Pharmacology Division, CSIR-IIIM, Canal Road, Jammu 180001, Jammu and Kashmir, India.
ACS Omega. 2020 Oct 22;5(43):27886-27895. doi: 10.1021/acsomega.0c03125. eCollection 2020 Nov 3.
The aim of this study was to prepare a novel dental restorative material (NDRM) and to understand its cell viability behavior. The hydroxyapatite (HA) nanopowder was synthesized using a wet chemical precipitation method using calcium hydroxide and orthophosphoric acid as precursors. The as-prepared HA nanopowder was annealed at different temperatures to get a pure compound with a Ca/P ratio close to 1.67. The optimal temperature was found to be 600 °C, whereas at a higher temperature, HA starts decomposing into CaO. The preparation of NDRM was conducted in two steps. The first step comprises the preparation of HA nanopowder- and gelatin (G)-based film using microwave heating. In the second step, the homogenized mixture of the HA-G film was mixed with different amounts of acrylic acid to form a self-flowable NDRM paste. Further, both these materials (HA nanopowder and NDRM) were characterized using FTIR, XRD, and SEM-EDX analyses. The FTIR and XRD results show the peaks corresponding to natural bone apatite and therefore confirm the formation of HA. EDX results showed the presence of Ca and P in HA nanopowder and NDRM with Ca/P ratios of 1.79 and 1.63, respectively. Synthesized NDRM was also analyzed for its cytotoxic and reproductive viability potential against normal cells using MTT and clonogenic assay. The analysis showed significantly higher cellular viability on the treatment with NDRM when compared to HA nanopowder as well as no colony suppression by both materials was observed on the normal cell line (fR2) even after exposure for 24 h, indicating its nontoxicity. The synthesized NDRM therefore can be considered as a promising candidate for dental caries restoration applications.
本研究的目的是制备一种新型牙科修复材料(NDRM)并了解其细胞活力行为。以氢氧化钙和正磷酸为前驱体,采用湿化学沉淀法合成了羟基磷灰石(HA)纳米粉末。将制备好的HA纳米粉末在不同温度下退火,以得到钙磷比接近1.67的纯化合物。发现最佳温度为600℃,而在较高温度下,HA开始分解为CaO。NDRM的制备分两步进行。第一步包括使用微波加热制备基于HA纳米粉末和明胶(G)的薄膜。第二步,将HA-G薄膜的均匀混合物与不同量的丙烯酸混合,形成自流动的NDRM糊剂。此外,使用傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)和扫描电子显微镜-能谱分析(SEM-EDX)对这两种材料(HA纳米粉末和NDRM)进行了表征。FTIR和XRD结果显示了与天然骨磷灰石相对应的峰,因此证实了HA的形成。EDX结果表明,HA纳米粉末和NDRM中存在Ca和P,Ca/P比分别为1.79和1.63。还使用MTT和克隆形成试验分析了合成的NDRM对正常细胞的细胞毒性和增殖活力潜力。分析表明,与HA纳米粉末相比,用NDRM处理时细胞活力显著更高,并且即使在暴露24小时后,在正常细胞系(fR2)上也未观察到这两种材料对菌落的抑制作用,表明其无毒性。因此,合成的NDRM可被认为是龋齿修复应用的有前途的候选材料。