Method of preparing extract of Mallotus apelta and uses for fighting hepatitis B virus
A technology of extract and white back leaf, which is applied in the field of preparation of white back leaf extract and anti-hepatitis B virus, to achieve the effects of significant anti-hepatitis B virus, wide distribution, and suitable for industrial production
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Embodiment 1
[0028] Embodiment 1: Extraction and purification of flavonoids in the white-backed leaf plant:
[0029] Take the dry plant leaves of the white-backed leaves, remove impurities, crush or shred them, and extract in boiling water. Add 1-20L of water per kilogram of dry plant leaves, heat and extract for 1-8 hours, filter while hot, and collect the filtrate. The filter residue was extracted again with boiling water for 1 to 3 times, filtered while hot and then combined with the obtained filtrates.
[0030] The obtained filtrate is passed through a macroporous adsorption resin column at a temperature of 20°C to 80°C, eluted with water, and then eluted with 10% to 80% ethanol, and the ethanol eluate that reacts positively with the hydrochloric acid-magnesium powder solution is collected , dried under reduced pressure, and recrystallized to obtain the final product.
[0031] The macroporous resin is D101 macroporous resin or AB-8 resin. Plug the bottom of the chromatographic column...
Embodiment 2
[0033] Example 2: Inhibition of the expression of HBsAg and HBeAg in HepG 2215 cells by the flavonoids of Alba dorsa leaves. 2.1 Reagents: Eagles MEM dry powder (product of Gibco, USA); fetal bovine serum (product of Hyclone Lab, USA); G-418 (product of Genticin); L-glutamine (Amresco subpackage); Kanamycin (Amresco subpackage) ; DMSO (product of Biotech); 0.25% trypsin (product of Hyclone Lab, USA); hepatitis B surface antigen test kit and hepatitis B e antigen test kit (enzyme-linked immunoassay, product of Shanghai Rongsheng Biotechnology Co., Ltd.).
[0034] 2.2 In vitro cell culture: 2215 cells were constructed by the Mount Sinai Medical Center in the United States and donated by the Institute of Pharmaceutical Biotechnology, Chinese Academy of Medical Sciences. MEM medium for cell culture contains 10% fetal bovine serum, glutamine 300μg / ml, G-418380μg / ml, kanamycin 750μg / ml, with 5% NaHCO 3 Adjust the pH value to 7.2-7.4. Cells were cultured in MEM medium containing 10...
Embodiment 3
[0052] Example 3: Inhibition of DHBV-DNA replication by the flavonoids of the white back leaf
[0053] 3.1 Reagents: Positive control drug lamivudine (lamivudine, 3TC, GlaxoSmithKline Pharmaceutical Company); DMSO (Guangzhou Xingang Chemical Co., Ltd.); α-32P-Dctp (Beijing Furui Biotechnology Engineering Company); gap translation Kit (Promega); SephadexG-50 (Ficoll); PVP (Pharmacia); SDS (Merck); 0.45 μm nitrocellulose membrane (Amersham); protist DNA and bovine serum albumin were purchased from China Institute of Biophysics, Academy of Sciences.
[0054] 3.2 Experimental animals and source of virus: 1-day-old Peking duck, weighing 60-100 g, purchased from Beijing Qianjin Duck Farm. DHBV-DNA strong positive serum collected from Nanjing shelduck and stored at -70°C.
[0055] 3.3 Experimental method: 1-day-old Peking ducks were injected with 0.2ml of DHBV-DNA positive serum through the tibial vein of the legs per duck. Ducklings were randomly divided into 4 groups on the 7th ...
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