Application of maca extract and maca polysaccharide in preparation of product for treating spermatogenesis dysfunction diseases
A technology of maca extract and dysfunction, applied in the field of biomedicine, can solve problems such as inapplicability to male children, increased risk of genetic defect transmission, harsh conditions for in vitro cultured organs, etc.
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Embodiment 1
[0028] Embodiment 1: the preparation of maca extract
[0029] Select Yunnan Lijiang maca rhizomes of uniform size, crush them and pass through a 60-mesh sieve. Weigh 1 kg of maca powder, extract three times under reflux with 70% industrial ethanol of 10 times the volume, combine the extracts, concentrate by rotary evaporation to obtain an extract, disperse the extract with double distilled water, and dissolve into a suspension.
Embodiment 2
[0030] Embodiment 2: the preparation of maca polysaccharide
[0031] Select Yunnan Lijiang maca rhizomes of uniform size, crush them and pass through a 60-mesh sieve. Weigh 1 kg of maca powder, heat and reflux extract three times with 60%-80% industrial ethanol, combine the extracts, concentrate to 1L by rotary evaporation, slowly add 50%-70% ethanol for gradient sedimentation, and the final ethanol concentration is 70%-80 %, placed at room temperature for 20-24 hours, filtered with suction, and the filtrate was rotary evaporated to 500 mL, continued alcohol precipitation, adjusted the ethanol concentration to 70-80%, placed at room temperature for 20-24 hours, and filtered with suction. Combine the two precipitates, dissolve them in double-distilled water, then spin-steam them until there is no alcohol smell, and dissolve them again to 1-2L to form a maca crude polysaccharide solution.
Embodiment 3
[0032] Example 3: Using a mouse model to detect the effect of maca and maca polysaccharides in improving spermatogenesis disorders.
[0033] Busulfan modeling principle:
[0034] (1) animals
[0035] ICR normal mice, male, weighing 20-25g, 7-8 weeks old, SPF grade
[0036] (2) Mouse feeding conditions
[0037] All mice were free to forage for food and drink water, and were reared at room temperature (25±2)°C and relative humidity of 40%-70%. The experiment was started after 12 hours of alternating light and dark, and the mice were fed adaptively for one week.
[0038] (3) Mouse grouping and model setting
[0039] After one week of adaptive feeding, ICR mice were randomly divided into four groups according to body weight: blank group (control), busulfan model group (Busulfan, Bu), and melatonin positive control group (MT, Melatonin). Melanin, L-carnitine and its derivatives have a certain protective effect on spermatogenic dysfunction caused by busulfan, but L-carnitine has ...
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