Application of cedarwood essential oil
A technology of cedarwood essential oil and cedarwood, which is applied in the field of biomedicine, can solve the problems of large side effects, high price, and low medical treatment rate for CNS system diseases, and achieve the effects of reducing toxicity, improving cognitive function and good pharmacokinetic parameters.
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[0039] The preparation method of cedarwood essential oil of the present invention comprises steam distillation extraction, carbon dioxide supercritical extraction.
[0040] Cedarwood essential oil of the present invention detects with gas chromatography-mass spectrometry instrument, and its main components are α-cuprenene (α-cuprenene) (>30%), α-cis-cedrene (α -cis-himachalene) (>5%), γ-cis-cedrene (γ-cis-himachalene) (>3%).
Embodiment 1
[0042] Get Himalayan cedar (Cedrus deodara (Roxb.) G.Don) fresh or dry bark, stem, branch, leaf or fruit 100Kg, place in a heap for 2 days, crush to 50 mesh coarse particles, soak the coarse particles in 8 mass Double the amount of pH value of 5.0 hydrochloric acid aqueous solution, leaching overnight. 0.8% cellulase and 0.3% pectinase were added to the extraction mixture by mass percentage, and enzymolysis was carried out at 37° C. for 2.5 hours. Put the above sample and its mixture into a steam distillation extraction apparatus, reflux extraction at 110°C for 7 hours, collect the distillate, cool it to room temperature, and place it in an oil-water separator for separation. The oil layer was dried with anhydrous sodium sulfate and separated to obtain cedarwood essential oil.
Embodiment 2
[0044] Get Atlantic cedar (Cedrus atlantica (Endl.) Manetti ex Carrière) fresh or dry bark, stems, branches, leaves or fruit 120Kg, place in a heap for 2 days, crush to 50 mesh coarse particles, soak the coarse particles in 8 mass Double the amount of pH value of 5.0 hydrochloric acid aqueous solution, leaching overnight. 0.8% cellulase and 0.3% pectinase were added to the extraction mixture by mass percentage, and enzymolysis was carried out at 37° C. for 2.5 hours. Put the above sample and its mixture into a steam distillation extraction apparatus, reflux extraction at 110°C for 7 hours, collect the distillate, cool it to room temperature, and place it in an oil-water separator for separation. The oil layer was dried with anhydrous sodium sulfate and separated to obtain cedarwood essential oil.
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