Fereidooni Rahim, Shahravan Arash, Manochehrifar Hamed, Pardakhty Abbas, Nosrati Fatemeh, Mollaie Hamid Reza
Endodontology Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.
Iran Endod J. 2024;19(1):39-45. doi: 10.22037/iej.v19i1.42608.
Mechanical root canal preparations and irrigation solutions are essential for reducing microbial counts in the root canal system. However, these methods do not completely eliminate microorganisms. Intracanal medicaments are used to further decrease microbial counts. This study aims to assess the cytotoxicity of various intracanal medicaments.
In this in vitro study, murine fibroblast cell lines (L929) were cultured in a controlled environment. The MTT assay was employed to evaluate the cytotoxicity of different medicament combinations, including calcium hydroxide and triamcinolone (D1), niosomal doxycycline and triamcinolone (D2), calcium hydroxide (D3), and a combination of doxycycline and triamcinolone (D4). Statistical analysis was performed using ANOVA and Dunnett's test.
The results indicated that D1 and D2 had lower cytotoxicity, while D4 exhibited the highest cytotoxicity. D1 was found to be non-cytotoxic up to a concentration of 500 µg/mL over a period of 72 hours. D2 and D3 showed similar effects up to concentrations of 250 µg/mL and 100 µg/mL, respectively, for 72 hours. In contrast, D4 exhibited cytotoxicity at concentrations above 75 µg/mL at 72 hours.
This study suggests that encapsulating doxycycline in niosomal structures (D2) reduces cytotoxicity in murine fibroblast cell lines (L929) for at least 24 and 48 hours. These findings offer promising implications for the development of endodontic medicaments with improved biocompatibility.
机械根管预备和冲洗液对于减少根管系统中的微生物数量至关重要。然而,这些方法并不能完全消除微生物。根管内药物用于进一步降低微生物数量。本研究旨在评估各种根管内药物的细胞毒性。
在这项体外研究中,小鼠成纤维细胞系(L929)在可控环境中培养。采用MTT法评估不同药物组合的细胞毒性,包括氢氧化钙和曲安奈德(D1)、脂质体多西环素和曲安奈德(D2)、氢氧化钙(D3)以及多西环素和曲安奈德的组合(D4)。使用方差分析和邓尼特检验进行统计分析。
结果表明,D1和D2的细胞毒性较低,而D4的细胞毒性最高。发现D1在72小时内浓度高达500μg/mL时无细胞毒性。D2和D3在72小时内分别在浓度高达250μg/mL和100μg/mL时表现出相似的效果。相比之下,D4在72小时时浓度高于75μg/mL时表现出细胞毒性。
本研究表明,将多西环素包裹在脂质体结构中(D2)可在至少24小时和48小时内降低对小鼠成纤维细胞系(L929)的细胞毒性。这些发现为开发具有改善生物相容性的牙髓药物提供了有希望的启示。