Abdillah Ridhofar Akbar Khusnul, Amalia Nadya Rafika, Budhy Theresia Indah, Luthfi Muhammad, Ridwan Rini Devijanti, Rianti Devi, Bramantoro Taufan, Ramadhani Nastiti Faradilla, Narmada Ida Bagus, Situmorang Putri Cahaya, Shariff Khairul Anuar, Noor Tengku Natasha Eleena Binti Tengku Ahmad, Nugraha Alexander Patera
Dental Health Science Study Program, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, Indonesia.
Department of Oral and Maxillofacial Pathology, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, Indonesia.
Eur J Dent. 2025 May 1. doi: 10.1055/s-0045-1806950.
The roselle flower () has shown potential as an alternative therapy for bone regeneration. This flower extract can induce osteoblast maturation, which is crucial for forming new bone. The study aim was to evaluate the viability of the 7F2 preosteoblast cell line following the application of a roselle flower nanoemulsion extract (RNE).This study utilized the 7F2 preosteoblast cell line to assess cell viability (%). The RNE was oven-dried at 35 to 40°C for 6 hours, resulting in a solid extract. The extract was then diluted into different concentrations. The preparation of 1% RNE was stirred at 1,400 rpm at 50°C for 90 minutes. Primary cultures of preosteoblast cell lines (7F2 cells) were distributed across 10 wells. Well 1 served as the positive control, representing 100% cell viability. Well 2 acted as the media control, containing only culture media without cells, representing 0% cell viability. Wells 3 to 10 were exposed to 1% RNE at serial concentrations of 100, 50, 25, 12.5, 6.25, 3.125, 1.56, and 0.78%. The viability of the 7F2 preosteoblast cell line was assessed using the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide or microtetrazolium assay. The treatment was conducted on days 1, 3, and 7 for observation.The findings indicated that the highest cell viability was observed on day 7, averaging 89.27% at a 0.78% concentration, while the lowest viability was 2.60% at a 100% concentration.These results suggest that RNE is nontoxic to the 7F2 preosteoblast cell line.
玫瑰茄花已显示出作为骨再生替代疗法的潜力。这种花提取物可诱导成骨细胞成熟,这对形成新骨至关重要。该研究的目的是评估应用玫瑰茄花纳米乳液提取物(RNE)后7F2前成骨细胞系的活力。本研究利用7F2前成骨细胞系评估细胞活力(%)。将RNE在35至40°C下烘干6小时,得到固体提取物。然后将提取物稀释成不同浓度。1%RNE的制剂在50°C下以1400转/分钟搅拌90分钟。前成骨细胞系(7F2细胞)的原代培养物分布在10个孔中。孔1作为阳性对照,代表100%的细胞活力。孔2作为培养基对照,仅含有无细胞的培养基,代表0%的细胞活力。孔3至10暴露于浓度分别为100%、50%、25%、12.5%、6.25%、3.125%、1.56%和0.78%的1%RNE中。使用3-[4,5-二甲基噻唑-2-基]-2,5-二苯基四氮唑溴盐或微量四氮唑测定法评估7F2前成骨细胞系的活力。在第1天、第3天和第7天进行处理以进行观察。研究结果表明,在第7天观察到最高细胞活力,在0.78%浓度下平均为89.27%,而在100%浓度下最低活力为2.60%。这些结果表明RNE对7F2前成骨细胞系无毒。