Application of inonotus obliquus alcohol extract to preparation of drug/health-protection product for treating/preventing hyperuricemia related disease
A technology of Inonotus obliquus and Inonotus obliquus is applied in the directions of skeletal diseases, drug combinations, pharmaceutical formulations, etc., and can solve the problems such as the lack of involvement in anti-hyperuricemia, and achieve a significant uric acid-lowering effect, less side effects, Improve the effect of large side effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0045] Guangdong Yuewei Edible Fungus Technology Co., Ltd. provided and identified Inonotus obliquus samples, and the voucher specimen (YW20170703-IO) was deposited in Guangdong Institute of Microbiology. After taking 100g of Inonotus obliquus to powder (particle size less than 5mm) using a powdering machine, use 2L ethanol to extract at 65°C for 3 hours for a total of three times. After the extracts were combined, concentrated by rotary evaporation and lyophilized to obtain an ethanol extract of Inonotus obliquus (yield: 4.87 g; yield: 4.8%).
Embodiment 2
[0047] Active substance analysis and component analysis of the ethanol extract of Example 1
[0048] The fingerprint of the extract was determined by HPLC ( figure 1 ), and betulin alcohol, a characteristic component of Inonotus obliquus, was used as a control (Figure 2). After comparison, the characteristic peak of betulin in the extract appeared at 52 min ( figure 1 ), and the retention time of the betulin alcohol control ( figure 2 ) Are consistent, and the results show that the extract is an Inonotus obliquus extract. Among them, the chromatographic conditions are: Agilent1200HPLC; Waters Atlantis T3RP-C18 column; 5μm, 250mm×4.6mm; 1.0ml / min flow rate; elution solvent is methanol (0.1% formic acid, A) and deionized water; elution procedure 0min(10%A)→50min(100%A)→70min (100%A)→71min(10%A)→83min(10%A); detection wavelength is 280nm; column temperature is 30℃; sample amount is 10μl. The result is figure 1 with figure 2 Shown.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


