Title of article :
Properties of macerated herbal oil
Author/Authors :
Kantawong Fahsai Department of Medical Technology - Faculty of Associated Medical Sciences - Chiang Mai University - Chiang Mai 50200, Thailand , Singhatong Supawatchara Department of Medical Technology - Faculty of Associated Medical Sciences - Chiang Mai University - Chiang Mai 50200, Thailand , Srilamay Aomjai Department of Medical Technology - Faculty of Associated Medical Sciences - Chiang Mai University - Chiang Mai 50200, Thailand , Boonyuen Kantarose Department of Medical Technology - Faculty of Associated Medical Sciences - Chiang Mai University - Chiang Mai 50200, Thailand , Mooti Niroot Department of Medical Technology - Faculty of Associated Medical Sciences - Chiang Mai University - Chiang Mai 50200, Thailand , Wanachantararak Phenphichar The Dental Research Center - Faculty of Dentistry - Chiang Mai University - Chiang Mai 50200, Thailand , Kuboki Thasaneeya Laboratory of Biomedical and Biophysical Chemistry - Institute for Materials Chemistry and Engineering - Kyushu University - Fukuoka, Japan
Abstract :
The addition of herbs into hot sesame
oil could increase the oil-pulling efficiency of
sesame oil. The aim of present study was to modify
the proportion of herbs and sesame oil with the
addition of other ingredients including menthol,
camphor, and borneol and improve the medicinal
properties and the scent of the oil.
Methods: Macerated herbal oil was prepared by
heat extraction of five species of herbs (Zingiber
cassumunar, Zingiber zerumbet, Plantago major
Linn, Citrus hystrix, and Amomum biflorum) with
hot sesame oil. The study was performed to evaluate
the anti-oxidant, anti-inflammatory, and anti-bacterial properties of this macerated herbal oil.
Results: Macerated herbal oil was evaluated for antioxidant activity using DPPH and ABTS
assays. It was shown that at dilution 1:2 in DMSO, the macerated herbal oil had DPPH and ABTS
radical scavenging activities equal to 63% and 22%, respectively. Macerated herbal oil dilution
1:8 in DMSO demonstrated ferric reducing capacity equivalent to ascorbic acid (0.208 μM) and
had reducing power equivalent to butylated hydroxytoluene (BHT) 7.41 μg/mL. MTT assay was
performed using immortalized human mesenchymal stem cells (HMSCs) as a cell culture model.
The result indicated that the cytotoxic concentration of the macerated herbal oil was ≥ 2.5 μL/
mL in complete DMEM. Anti-inflammatory effects were evaluated using the nitrite assay and
RT-PCR. It was found that the macerated herbal oil could inhibit nitrite accumulation in culture
media. Change in the expression of COX-2, Nrf2, and NF-kB in RT-PCR confirmed the antiinflammatory
activity of the macerated herbal oil.
Conclusion: It could be concluded that the macerated herbal oil could inhibit nitrite accumulation
in culture media, which might be the inhibitory effect of the macerated herbal oil on COX-2 or
Nrf2, the downstream modulator of the COX-2 pathway. Further intensive studies are needed for
the optimization before bringing this macerated herbal oil into clinical application.
Keywords :
Antibacterial , Anti-inflammatory , Antioxidant , HMSCs , Macerated herbal oil
Journal title :
Bioimpacts