Padhan Diptikanta, Pattnaik Smaranika, Behera Ajaya Kumar
Laboratory of Medical Microbiology, School of Life Sciences, Sambalpur University, Sambalpur, Odisha, India.
School of Chemistry, Sambalpur University, Sambalpur, Odisha, India.
Pharmacogn Mag. 2017 Oct;13(Suppl 3):S555-S560. doi: 10.4103/pm.pm_65_17. Epub 2017 Oct 11.
is used as a remedy in toothache complaints by the tribal people of Western part of Odisha, India.
The objective of this study was to study the growth-arresting activity of an indigenous Acmella essential oil (EO) ( Murr, ) and its isolated component, d-limonene against (microbial type culture collection 296).
The EO was extracted from flowers of indigenous using Clevenger's apparatus and analyzed by gas chromatography-mass spectrometry (GC-MS). High pressure liquid chromatography (HPLC) was carried out to isolate the major constituent. The isolated fraction was subjected to fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR). The antidermatophytic activity was screened for using "disc diffusion" and "slant dilution" method followed by optical, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) studies. The molecular dockings were made between d-limonene with cell wall synthesis-related key enzymes (14 methyl deaminase and monooxygenase).
The GC-MS analysis EO had inferred the presence of 7 number of major (≥2%) components. The component with highest peak area (%) was found to be 41.02. The HPLC-isolated fraction was identified as d-limonene (1,8 p-Mentha-diene) by FTIR and NMR. Qualitative and quantitative assays had suggested the growth inhibitory activity of Acmella EO and its component. Shrinkage, evacuation, cell wall puncture, and leakage of cellular constituents by the activity of Acmella oil and d-limonene were evidenced from optical, SEM, and TEM studies. The computer simulation had predicted the binding strengths of d-limonene and fluconazole with dermatophyte cell wall enzymes.
There could have been synergistic action of all or some of compounds present in indigenous Acmella EO.
There was presence of seven number of (d-limonene, ocimene, β-myrcene, cyclohexene, 3-(1, 5-dimethyl-4-hexenyl)-6-methylene, β-caryophyllene, and β-sesquiphellandrene and β-phellandrene) major components in the indigenous Acmella essential oilThe d-limonene content was 41.02% in the indigenous oilThe antidermatophytic activity of Acmella essential oil could have been attributable to its chemotypes. °C: Degree centigrade; w/v: Weight/volume; TS: Transverse section; min: minute; Hz: hertz: h: Hr.
在印度奥里萨邦西部,当地部落居民将其用作治疗牙痛的药物。
本研究旨在研究一种本土金纽扣属植物精油(EO)(穆尔)及其分离成分d-柠檬烯对须发癣菌(微生物菌种保藏中心296)的生长抑制活性。
使用克莱文杰装置从本土金纽扣属植物的花中提取精油,并通过气相色谱-质谱联用仪(GC-MS)进行分析。采用高压液相色谱(HPLC)分离主要成分。对分离得到的馏分进行傅里叶变换红外光谱(FTIR)和核磁共振(NMR)分析。采用“纸片扩散法”和“斜面稀释法”筛选抗皮肤癣菌活性,随后进行光学显微镜、扫描电子显微镜(SEM)和透射电子显微镜(TEM)研究。将d-柠檬烯与细胞壁合成相关关键酶(14-甲基脱氨酶和单加氧酶)进行分子对接。
GC-MS分析表明EO中存在7种主要成分(≥2%)。发现峰面积百分比最高的成分是41.02%。通过FTIR和NMR将HPLC分离得到的馏分鉴定为d-柠檬烯(1,8-对薄荷二烯)。定性和定量分析表明金纽扣属植物精油及其成分具有生长抑制活性。光学显微镜、SEM和TEM研究证明,金纽扣属植物精油和d-柠檬烯的活性导致细胞收缩、排空、细胞壁穿孔和细胞成分泄漏。计算机模拟预测了d-柠檬烯和氟康唑与皮肤癣菌细胞壁酶的结合强度。
本土金纽扣属植物精油中存在的所有或某些化合物可能存在协同作用。
本土金纽扣属植物精油中存在7种主要成分(d-柠檬烯、罗勒烯、β-月桂烯、环己烯、3-(1,5-二甲基-4-己烯基)-6-亚甲基、β-石竹烯和β-倍半水芹烯以及β-水芹烯)。本土精油中d-柠檬烯含量为41.02%。金纽扣属植物精油的抗皮肤癣菌活性可能归因于其化学类型。°C:摄氏度;w/v:重量/体积;TS:横切面;min:分钟;Hz:赫兹;h:小时。