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In-vitro antibacterial properties of clove and cinnamon and their principle chemical constituents eugenol and trans-cinnamaldehyde against aggregatibacter actinomycetemcomitans.

机译:丁香和肉桂及其主要化学成分丁子香酚和反式肉桂醛的体外抗菌特性对集合放线菌的聚合酶的抑制作用。

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摘要

The use of antibiotics for the cure of infectious diseases first started in 1940's when the first antibiotic was discovered. With the passing years burgeoning classes of antibiotics promised the cure of almost all the infectious diseases. However, within a few years, development of resistance against antibiotics by the microorganisms placed a new challenge for future medical advances in the treatment of infectious diseases. Only six decades later it looks like the miracle of antibiotics is over. More and more bacteria have developed resistance against more and more antibiotics. The crisis today is accentuated by the limited number of new antibiotics, less number of researches being done on the antibiotics and limited number of new compounds and new targets. The search of plant products as antimicrobial agents has been growing in the last few decades. Clove and cinnamon are the spices that are very commonly used for flavoring food and beverages. The antimicrobial properties of clove and cinnamon against different bacteria are well documented in the previous research literature. In this study we tested the in-vitro antibacterial properties of ethanolic extracts of clove and cinnamon and their principle chemical constituents, eugenol and trans-cinnamaldehyde against Aggregatibacter actinomycetemcomitans. A. actinomycetemcomitans is a gram negative, facultative, anaerobic bacterium and is associated with a variety of infectious diseases. A. actinomycetemcomitans is a major etiologic agent in localized aggressive periodontitis (LAP). Also, A. actinomycetemcomitans has been isolated from the patients with infective endocarditis, infections of urinary tract and brain. In this study, we found that ethanolic extracts of clove, cinnamon and their principle chemical constituents, eugenol and trans-cinnamaldehyde respectively exhibit excellent growth inhibitory activity against different serotypes of A. actinomycetemcomitans. Eugenol and trans-cinnamaldehyde exhibit killing times of less than 3 hours. Trans-cinnamaldehyde shows the inhibition of growth of A. actinomycetemcomitans at much lower concentrations when compared to eugenol. The results from these experiments suggest that clove and cinnamon can be useful in prevention of local and systemic infections caused by A. actinomycetemcomitans. However, further studies are needed to investigate efficacy and safety of these antibiotics when used in-vivo against A. actinomycetemcomitans.
机译:1940年代,当发现第一种抗生素时,就开始使用抗生素治疗传染病。随着时间的流逝,新兴的抗生素类别有望治愈几乎所有的传染病。然而,在短短几年内,微生物对抗生素的抗性发展为治疗传染病的未来医学进步提出了新的挑战。仅仅六年后,看来抗生素的奇迹就结束了。越来越多的细菌对越来越多的抗生素产生了抗药性。如今的危机因新抗生素数量有限,对抗生素的研究数量减少以及新化合物和新靶标数量有限而加剧。在过去的几十年中,对作为抗菌剂的植物产品的搜索一直在增长。丁香和肉桂是非常常用于食品和饮料调味的香料。丁香和肉桂对不同细菌的抗微生物特性已在以前的研究文献中得到了充分证明。在这项研究中,我们测试了丁香和肉桂的乙醇提取物及其主要化学成分丁香酚和反肉桂醛的体外抗菌特性,以对抗聚合菌放线菌。 A.放线菌是一种革兰氏阴性,兼性厌氧细菌,与多种传染病有关。放线放线杆菌是局部侵袭性牙周炎(LAP)的主要病因。另外,已经从患有感染性心内膜炎,尿路和脑部感染的患者中分离出放线放线杆菌。在这项研究中,我们发现丁香,肉桂的乙醇提取物及其主要化学成分丁香酚和反肉桂醛分别对不同血清型的放线放线杆菌表现出优异的生长抑制活性。丁香酚和反式肉桂醛的杀灭时间少于3小时。当与丁子香酚相比时,反式肉桂醛在低得多的浓度下显示出放线菌的生长抑制。这些实验的结果表明,丁香和肉桂可用于预防由放线放线杆菌引起的局部和全身感染。但是,需要进一步研究以研究这些抗生素在体内抗放线放线杆菌的有效性和安全性。

著录项

  • 作者

    Sharma, Ajay.;

  • 作者单位

    Long Island University, The Brooklyn Center.;

  • 授予单位 Long Island University, The Brooklyn Center.;
  • 学科 Health Sciences Toxicology.;Health Sciences Pharmacology.;Biology Microbiology.
  • 学位 M.S.
  • 年度 2011
  • 页码 67 p.
  • 总页数 67
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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