Anticaries Potential of Temu Kunci-Serai Ethyl Acetate Extract Combination: In Vitro and Molecular Studies Approach

Muhammad Priyadi, Rizki Rachmad Saputra
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Abstract

Dental caries is one of the problems in dental disorders suffered by many people. There have been many ways of handling such as using temu kunci and lemongrass plants. This study aims to determine the antibacterial activity of caries in vitro and predict the mechanism of action of the bacteria that cause caries Streptococcus mutans. Temu kunci and lemongrass were extracted using ethyl acetate solvent. antibacterial tests against Streptococcus mutans were carried out using diffusion tests with a combination treatment of temu kunci: serai extracts 5% b/v: 5% b/v, 5% b/v: 10% b/v, and 10% b/v: 5% b/v. The positive control used amoxicillin and DMSO as a negative control. Potency as an anticaries drug of drived compound from Temu Kunci and Serai were evaluated by molecular docking using glucosyltransferase (3AIC). The results showed that the combination of temu kunci and serai with concentration 10% b/v: 5% b/v has potential as anticaries against Streptococcus mutans. Molecular studies depicted that Panduratin A, Isopanduratin, and 1,3-O-di-p-coumaroylglycerol have great activity toward 3AIC, respectively. Especially for Panduratin A and Isopanduratin, those compound depicted great and similar binding affinity (-8.4 kcal mol-1) that lower than Acarbose as native ligand (-8.3 kcal mol-1). Furthermore, those compound binding similarity ilustrated activity mechanism similarly with native ligand toward receptor. Additionally, the profiling drug-target interaction suggested Temu Kunci’s derived compounds have great potential as anticaries treatment.
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铁木苦刺-赛莱乙酸乙酯联合提取物的体外及分子研究
龋齿是困扰许多人的牙齿疾病之一。有许多处理方法,如使用铁木昆布和柠檬草植物。本研究旨在测定龋齿的体外抑菌活性,预测引起龋齿的细菌变形链球菌的作用机制。采用乙酸乙酯溶剂提取铁木苦参和柠檬草。采用扩散试验方法,将铁骨骨:血清提取物5% b/v: 5% b/v、5% b/v: 10% b/v、10% b/v: 5% b/v联合处理,对变形链球菌进行抑菌试验。阳性对照以阿莫西林和二甲基亚砜为阴性对照。采用葡萄糖基转移酶(3AIC)分子对接的方法,对铁木、铁木两种植物驱动化合物的抗肿瘤活性进行了评价。结果表明,以10% b/v: 5% b/v的浓度,铁骨毒液与血清联合使用,具有一定的抗变形链球菌作用。分子研究表明,Panduratin A、Isopanduratin和1,3- o -di-p-coumaroylglycerol分别对3AIC具有很强的活性。特别是Panduratin A和Isopanduratin,它们具有相似的结合亲和力(-8.4 kcal mol-1),低于阿卡波糖作为天然配体(-8.3 kcal mol-1)。此外,这些化合物的结合相似性说明了它们对受体的活性机制与天然配体相似。此外,药物-靶标相互作用的分析表明,铁木孔菌衍生化合物具有很大的抗肿瘤治疗潜力。
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