Narvekar Pranjali S, Shivanand Sunita, Patil Sneha, Raikar Sarvesh, Mallick Amrita, Doddwad Preeti K
Department of Conservative Dentistry and Endodontics, KLE Academy of Higher Education and Research, KLE VK Institute of Dental Sciences, Belagavi, Karnataka, India.
J Conserv Dent Endod. 2025 Mar;28(3):231-236. doi: 10.4103/JCDE.JCDE_842_24. Epub 2025 Mar 3.
The removal of intracanal medicament is essential for sealer penetration and the success of endodontic therapy.
To evaluate and compare the dentinal tubule penetration of a silicone-based endodontic sealer following N-acetyl cysteine (NAC) intracanal medicament removal using ultrasonic agitation and laser-activated irrigation.
Eighty-one extracted single-rooted mandibular premolars were decoronated and prepared with ProTaper Universal rotary files up to MAF F3. To prepare medicament, NAC powder was mixed with propylene glycol in the ratio of 1:1, placed using a size #30 Lentulospiral, and specimens stored in an incubator for 14 days. The specimens were then instrumented with #30 Hedström and divided into three groups according to final irrigant activation techniques: Group I: Diode laser activation, Group II: Passive Ultrasonic agitation, Group III: No agitation (positive control). Canals were obturated with GuttaFlow bioseal sealer mixed with 0.1% Rhodamine B dye and gutta-percha cones and incubated for 7 days. The specimens were sectioned horizontally to obtain 1 mm thick sections from 2, 5, and 8 mm from the apex. Sections were examined under Confocal Laser Scanning Microscope to measure the depth of sealer penetration (in µm).
One-way analysis of variance and Tukeys multiple test.
The highest mean depth of penetration of 728.52 µm was seen with Group I, followed by Group II and least was seen in Group III.
Diode laser activation group was most effective in the removal of NAC intracanal medicament from all the three regions of the root canal.
去除根管内药物对于封闭剂渗透和根管治疗的成功至关重要。
评估并比较使用超声震荡和激光激活冲洗去除N - 乙酰半胱氨酸(NAC)根管内药物后,一种硅基根管封闭剂在牙本质小管中的渗透情况。
81颗拔除的单根下颌前磨牙去冠,用ProTaper Universal旋转锉预备至MAF F3。制备药物时,将NAC粉末与丙二醇按1:1比例混合,用30号输送螺旋输送,标本置于培养箱中14天。然后用30号Hedström锉对标本进行预备,并根据最终冲洗激活技术分为三组:第一组:二极管激光激活;第二组:被动超声震荡;第三组:无震荡(阳性对照)。根管用混合0.1%罗丹明B染料的GuttaFlow生物封闭剂和牙胶尖充填,并孵育7天。将标本水平切片,从根尖2、5和8 mm处获得1 mm厚的切片。在共聚焦激光扫描显微镜下检查切片,测量封闭剂渗透深度(单位:µm)。
单因素方差分析和Tukey多重检验。
第一组的平均最高渗透深度为728.52 µm,其次是第二组,第三组最低。
二极管激光激活组在从根管的所有三个区域去除NAC根管内药物方面最有效。