Preparation method of litsea cubeba fruit essential oil with antibacterial activity
A technology of antibacterial activity and Radix chinensis, applied in the field of plant essential oils, can solve the problems of complicated preparation steps, long preparation time, low extraction rate, etc., and achieve the effects of improving extraction efficiency, shortening extraction time, and excellent bacteriostatic effect.
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Embodiment 1
[0027] A preparation method of litsea cubeba essential oil with antibacterial activity, comprising the following steps:
[0028] (1) Processing of Litsea Cubeba Raw Material: Put 40 g of Litsea Cubeba after cleaning into a retort.
[0029] (2) Extraction of Litsea Cubeba Essential Oil: Take Litsea Cubeba obtained in step (1) as raw material, add 750 mL of distilled water, extract for 15 min under the condition of microwave power of 750 W, and stand still to take out the upper layer oil sample.
[0030] (3) Drying of Litsea Cubeba Essential Oil: The oil sample obtained in step (2) was dried with anhydrous sodium sulfate to obtain 2.81 g of Litsea Cubeba Essential Oil, with a yield of 7.03%.
Embodiment 2
[0032] A preparation method of litsea cubeba essential oil with antibacterial activity, comprising the following steps:
[0033] (1) Processing of Litsea Cubeba Raw Materials: Litsea cubeba fruit is optimized and washed, and 30 g of the pretreated Litsea Cubeba fruit is weighed and put into a retort.
[0034] (2) Extraction of Litsea Cubeba essential oil: take Litsea cubeba obtained in step (1) as raw material, add 800mL of distilled water, extract for 10min under the condition of microwave power of 800W, and stand still to take out the upper layer oil sample.
[0035] (3) Drying of Litsea Cubeba Essential Oil: The oil sample obtained in step (2) was dried with anhydrous sodium sulfate to obtain 2.09 g of Litsea Cubeba Essential Oil, with a yield of 6.97%.
experiment example 1
[0045] Antibacterial experiment of experimental example 1 litsea cubeba essential oil
[0046] The size of the inhibition zone to Escherichia coli, Aspergillus niger, and Saccharomyces cerevisiae was measured by the filter paper method, and the specific experimental method was as follows:
[0047] (1) Prepare a number of circular filter paper sheets with a diameter of 9mm, divide them into three groups according to the experimental group, positive control group and blank control group, put Litsea cubeba essential oil into them respectively after dry heat sterilization, and use supercritical CO 2 Soak the extracted litsea cubeba essential oil and distilled water for 2 hours;
[0048](2) The concentration of the bacterial cell suspension is 107-108cfu / mL, and the petri dish is divided into Escherichia coli group, Aspergillus niger group and Saccharomyces cerevisiae group, and 0.2mL of bacterial cell suspension is added to each petri dish, and the coating is uniform;
[0049] (3...
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