Ranjani Muthukrishnan Sudharshana, Kavitha Mahendran, Venkatesh Srinivasan
Department of Conservative Dentistry and Endodontics, The Tamil Nadu Dr. M.G.R. Medical University, Chennai below Tamil Nadu Government Dental College and Hospital, Chennai, Tamil Nadu, India.
Contemp Clin Dent. 2021 Jan-Mar;12(1):32-36. doi: 10.4103/ccd.ccd_474_19. Epub 2021 Mar 20.
The aim of this study was to compare the osteogenic potential of conventional glass-ionomer cement (GIC) with chitosan-modified GIC (CH-GIC) and bioactive glass-modified GIC (BAG-GIC) as a function of time in varying proportions.
CH-GIC was prepared by adding 10 v/v% (Group II) and 50 v/v% (Group III) CH to the commercial liquid of GIC. BAG-GIC was prepared by the addition of 10 wt% (Group IV) and 30 wt% (Group V) of BAG to the GIC powder. Conventional GIC was kept as Group I. Nine round-shaped samples measuring 2 mm thick and 5 mm in diameter were prepared for every experimental material. Human osteosarcoma cells were cultured and cell proliferation was assessed at 24, 48, and 72 h using 3-(4,5-dimethylthiazol-2-yl)- 2,5-diphenyltetrazolium bromide (MTT) assay, and cell differentiation was assessed at 7,14, and 21 days using alkaline phosphatase (ALP) assay. All experiments were done in triplicate. The data obtained were analyzed using one-way analysis of variance and Tukey honestly significant difference multiple comparisons at 0.05 level significance.
Cell culture studies showed a significant increase in proliferative activity and ALP activity in Group II, III, IV, and V than Group I at all-time intervals ( < 0.05). There was no statistically significant difference in osteogenic potential between CH-GIC and BAG-GIC groups.
The osteogenic potential was significantly higher in CH-GIC and BAG-GIC compared to conventional GIC.
本研究旨在比较传统玻璃离子水门汀(GIC)、壳聚糖改性玻璃离子水门汀(CH-GIC)和生物活性玻璃改性玻璃离子水门汀(BAG-GIC)在不同比例下随时间变化的成骨潜力。
通过向GIC的商业液体中添加10 v/v%(第二组)和50 v/v%(第三组)的壳聚糖来制备CH-GIC。通过向GIC粉末中添加10 wt%(第四组)和30 wt%(第五组)的生物活性玻璃来制备BAG-GIC。将传统GIC作为第一组。为每种实验材料制备9个厚度为2 mm、直径为5 mm的圆形样本。培养人骨肉瘤细胞,并使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法在24、48和72小时评估细胞增殖,使用碱性磷酸酶(ALP)法在7、14和21天评估细胞分化。所有实验均重复三次。使用单因素方差分析和Tukey真实显著性差异多重比较在0.05显著性水平分析获得的数据。
细胞培养研究表明,在所有时间间隔内,第二组、第三组、第四组和第五组的增殖活性和ALP活性均比第一组显著增加(P<0.05)。CH-GIC组和BAG-GIC组之间的成骨潜力没有统计学显著差异。
与传统GIC相比,CH-GIC和BAG-GIC的成骨潜力显著更高。