A kind of artificial cultivation method of Paecilomyces cicadae and the analgesic water extract cultivated therewith
A Paecilomyces cicadae, artificial cultivation technology, applied in the field of analgesic water extracts, can solve the problems of few research reports on analgesic activity, no analgesic effect on pain, etc., achieves great development and application prospects, and has no addiction. , the effect of obvious analgesic effect
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[0033] Preparation of Paecilomyces cicadae aqueous extract:
[0034] (1) Get the artificially cultivated Paecilomyces cicadae fermentation product, 4000r / min, centrifuge 10-20min, abandon the supernatant, get Paecilomyces cicadae mycelium;
[0035] (2) Broken Paecilomyces cicada mycelium cells with a glass homogenizer, according to the ratio of mycelium (kg) to ultrapure water (L) 1:4-1:10, at room temperature, add ultrapure water to extract 3-5 times;
[0036] (3) The above water extract is centrifuged at 4000r / min for 10-20min, and the supernatant is taken;
[0037] (4) the supernatant is subjected to SephadexG-25 gel column chromatography to obtain the active component;
[0038] (5) The water extract is formulated into an aqueous solution containing 0.1-1.0 mg / ml of the active component, which is the Paecilomyces cicadae analgesic aqueous solution of the present invention.
Embodiment 1
[0039] Embodiment 1 (best parameter):
[0040] (1) artificially cultivated Paecilomyces cicadae fermentation product, 4000r / min, centrifugal 10-20min, abandon supernatant, obtain Paecilomyces cicadae mycelia 10g;
[0041] (2) Broken Paecilomyces cicadae mycelia cells with a glass homogenizer, according to mycelium (kg) and pure water (L) ratio 1:8, add 80ml pure water, at room temperature, add ultrapure water leaching 5 Second-rate;
[0042] (3) The above-mentioned water extract is centrifuged at 4000r / min for 10min, and the supernatant is taken;
[0043] (4) The supernatant was subjected to SephadexG-25 gel column chromatography to obtain the active components; the active components were shown in the gel column chromatogram as shown in Figure 1.
[0044] (5) The aqueous extract is formulated into an aqueous solution containing 0.40 mg / ml ± 0.02 mg / ml of the active component. (The concentration is determined by the Folin phenol method specified in the Chinese Pharmacopoeia)...
Embodiment 2
[0046] (1) artificially cultivated Paecilomyces cicadae fermentation product, 4000r / min, centrifugal 10-20min, abandon supernatant, obtain Paecilomyces cicadae mycelia 10g;
[0047] (2) Broken Paecilomyces cicadae mycelial cells with a glass homogenizer, according to mycelium (kg) and pure water (L) ratio 1:4, add 40ml pure water, at room temperature, add ultrapure water leaching 3 Second-rate;
[0048] (3) The above-mentioned water extract is centrifuged at 4000r / min for 20min, and the supernatant is taken;
[0049] (4) The supernatant is subjected to SephadexG-25 gel column chromatography to obtain the active component; the gel column chromatogram is approximate as shown in Figure 1;
[0050](5) The aqueous extract is formulated into an aqueous solution containing 0.40 mg / ml ± 0.02 mg / ml of the active component.
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