In Vitro and in Silico Analysis of Phytochemicals from Asteraceae Plant Species Against Wound-Infecting Pathogens

K.S. Shanmugam, L. Ramkumar, R. Jagadeesan
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Abstract

The idea of polyherbal combinations has a strong foundation in modern medicine and has had amazing success, givingpatients new hope. Polyherbal mixtures have managed various conditions, from cancer to autoimmune disorders. Given that it hasalready been shown to be secure and efficient, this therapeutic approach is gaining popularity. In alternative, complementarytherapies, polyherbal formulations blend many herbs to provide an additive effect. Physicians are accepting this strategy, which hasbeen used for generations. Numerous research papers in the pharmaceutical field demonstrate the efficacy of combining plants andthe present study aimed to evaluate antibacterial phytochemicals from a polyherbal extract. Phytoconstituents extracted with ethanoland ethyl acetate by conventional soxhlet method and chemical constituents were analyzed by qualitative and GC-MS. Antibacterialactivity of extracts tested by disc diffusion method against wound infecting pathogens. MIC was done by Alamar blue assay. Inhibitionof ESBL enzyme predicted by in silico docking using Autodock. Extraction with ethanol shows less significant positive results thanethylacetate in qualitative and antibacterial studies. GC-MS analysis showed the presence of 35 bioactive compounds from ethylacetate and 45 compounds from ethanol. Cyclononasiloxane, Octodecane, hexadecanoic acid, and Benzenedicarboxylic werecommonly found in both extracts. The ethylacetate PHE exhibited strong antibacterial activity and was more effective than thestandard. From GCMS, three compounds were predicted to have good ADME characteristics with high gastrointestinal absorptionand metabolic activity. Compound 6-(3-fluorobenzylamino) purine has been selected and investigated by in silico method, showingthat it has a greater binding affinity with ESBL, ompC, and murA after being docked. The ethyl acetate extract demonstrated goodaction against certain pathogenic bacteria in the current experiment, while the ethanol extract exhibited no activity. Our findingsconclude that the polyherbal extracts have broad-spectrum activity against bacteria and depend on the solvent used.
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菊科植物抗创面病原菌化学物质的体外和硅内分析
多种草药组合的想法在现代医学中有着坚实的基础,并取得了惊人的成功,给病人带来了新的希望。多种草药混合物可以治疗各种疾病,从癌症到自身免疫性疾病。考虑到它已经被证明是安全和有效的,这种治疗方法越来越受欢迎。在替代,补充疗法,多草药配方混合许多草药,以提供一个附加的效果。医生们正在接受这种已经使用了几代人的策略。在制药领域的许多研究论文证明了植物组合的功效,本研究旨在评估从多草药提取物中提取的抗菌植物化学物质。采用常规索氏法提取乙醇和乙酸乙酯提取物,采用定性和气相色谱-质谱法分析化学成分。圆盘扩散法测定提取物对创面感染病原菌的抑菌活性。MIC采用Alamar蓝法测定。基于Autodock的硅对接预测ESBL酶抑制。乙醇提取在定性和抗菌研究中的阳性结果不如乙酸乙酯显著。GC-MS分析表明乙酸乙酯中含有35种活性物质,乙醇中含有45种活性物质。环壬硅氧烷、八癸烷、十六烷酸和苯二羧酸在两种提取物中都很常见。乙酸乙酯PHE具有较强的抑菌活性,抑菌效果优于标准品。从GCMS中预测3种化合物具有良好的ADME特性,具有较高的胃肠道吸收和代谢活性。化合物6-(3-氟基氨基)嘌呤经硅法筛选和研究,发现其对接后与ESBL、ompC和murA具有更大的结合亲和力。在本实验中,乙酸乙酯提取物对某些致病菌表现出良好的抑制作用,而乙醇提取物则表现出无活性。我们的研究结果表明,多草药提取物具有广谱的抑菌活性,并取决于所使用的溶剂。
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