University of Gazi, Faculty of Dentistry, Department of Pediatric Dentistry, Ankara, Turkey.
Med Oral Patol Oral Cir Bucal. 2011 Jul 1;16(4):e584-7.
The objective of this study was to evaluate the cytotoxicity of the plant extract ankaferd blood stopper (ABS) in vitro.
ABS was eluted with fresh Dulbecco's Modified Eagle's Medium (DMEM) without serum for 72 h, at 37 °C. The cells treated with various dilutions of ABS were seeded into 96-well microplate at 10⁴/well in triplicates. Cells without treatment served as a control group. The number of viable cells after 48 h incubation was determined by a modified 3-(4, 5-dimethyl-thiazol-2-yl)-2, 5-diphenyl-tetrazolium bromide (MTT) assay. The relative viability of pulp cells was expressed as color intensity of the number in the experimental wells relative to that of the control group. Absorbances were read at 570 nm on a microplate reader with a background subtraction at 620 nm.
The results showed that ABS was cytotoxic to human pulp fibroblasts by MTT assay.
The influence of cytotoxicity to human pulp fibroblasts depended on concentration of ABS. The more dilutions exhibited less cytotoxic characteristics compared to the more concentrated forms.
本研究旨在评估植物提取物 ankaferd 血液止血剂(ABS)的体外细胞毒性。
将 ABS 用新鲜的 Dulbecco 改良 Eagle 培养基(DMEM)洗脱,无血清,37°C 孵育 72 小时。将用不同稀释度 ABS 处理的细胞接种到 96 孔微孔板中,每孔 104 个细胞,一式三份。未处理的细胞作为对照组。孵育 48 小时后,通过改良的 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法测定活细胞数量。牙髓细胞的相对活力表示为实验孔中细胞数量的颜色强度相对于对照组的颜色强度。在 570nm 处用微板阅读器读取吸光度,在 620nm 处进行背景扣除。
MTT 测定法显示 ABS 对人牙髓成纤维细胞具有细胞毒性。
细胞毒性对人牙髓成纤维细胞的影响取决于 ABS 的浓度。与更浓缩的形式相比,稀释度越高,表现出的细胞毒性特征越弱。