Rabdosia rubescens stem aqueous extract powder as well as preparation, anti-osteoporosis effect and application thereof
A technology of rubescens and water extract, applied in the field of biomedicine, can solve the problem of unknown biological activity of all components and the like
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Embodiment 1
[0042] Embodiment 1 prepares the water extract powder of the stem of Radix radix L.
[0043] Take 300g of dried Radix japonicus stalks, wash them with tap water, and chop them up. The chopped stems were heated in 700-1200 mL of distilled water at 50 °C-100 °C for 0.5-4 h while stirring (200-400 rpm). Cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure to obtain 72 g of water extract powder of the stems of Radix sativa.
Embodiment 2
[0044] Embodiment 2 Measures the chromatogram and mass spectrometry ion current spectrum of Bossium radix stem aqueous extract powder
[0045] 2-1. Preparation of sample solution (10mg / mL)
[0046] Weigh 26.7mg of the water extract powder of the stems of Boswellia japonicus, and dissolve the powder in 2.67mL of ultrapure water. The resulting solution was ultrasonically shaken for 1 minute, and then centrifuged at 13000rpm for 10 minutes. Take the supernatant, pass through a 0.22μm filter membrane, and place it in a sample bottle for chromatography and mass spectrometry.
[0047] 2-2 Chromatographic conditions
[0048] Chromatographic column: Waters, Acquity HSS T3 column (2.1×100mm i.d., 1.7μm); injection volume: 2μL; PDA detector: 190-400nm; mobile phase: water (0.1% formic acid), acetonitrile; use this mobile phase and follow the gradient in Table 1 Wash the column.
[0049] Table 1 Mobile phase gradient table
[0050]
[0051] 2-3. Measurement chromatogram
[005...
Embodiment 3
[0057] Embodiment 3 specifies the structure of 28 kinds of components in the water extract powder of Rubescens sinensis stem
[0058] The UPLC chromatography of Example 2 was coupled with mass spectrometry, and the UPLC-mass spectrometry of the water extract powder of the stem of Radix Orbis lentils was determined. The mass spectrometry conditions are two modes of electrospray ionization, positive ion and negative ion. Ion mode parameters: capillary voltage is 1000V, desolvation gas flow rate is 800L / h, temperature is 450°C, source temperature is 120°C, cone gas flow rate is 50L / h, spray pressure is 6bar, fragmentation voltage is 20-45V, The sampling cone voltage is 6V, the acquisition mode is MSE continuum resolution mode, the data acquisition range of the mass number to charge number ratio (m / z) of charged particles is 100-1500, the low energy channel Trap fragmentation voltage is 6V, and the high energy channel The channel Trap fragmentation voltage selection gradient volt...
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