Application of magnoflorine in preparation of bone regulation drug synergist and pharmaceutical composition containing magnoflorine
A technology of magnolia base and composition, which is applied in the direction of drug combination, active ingredient of heterocyclic compound, pharmaceutical formula, etc., can solve the problem of difficult medicinal effect, and achieve the effect of promoting differentiation and mineralization
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Embodiment 1
[0051] Example 1 Effect of magnolanine with different test concentrations on MC3T3-E1 cell differentiation and mineralization activity
[0052] 1. Drug configuration to be tested
[0053] The purity of magnoflorine (CAS: 6681-18-1), psoralen (CAS: 66-97-7) and sweroside (CAS: 14215-86-2) is greater than 98% , purchased from Shanghai Ronghe Pharmaceutical Technology Development Co., Ltd., the structural formula is as follows figure 1 shown. In order to avoid the influence of the solvent on the cells, in this study, the drug was dissolved and administered according to one-thousandth of the volume of the administration medium, so all the drugs in this study were prepared at a concentration of 1000% of the final concentration of the drug-containing medium before administration For example, in the example, 10nM 17β-estradiol is used as a positive drug, and the dosing process is to add 1 μL of 10 μM 17β-estradiol to 1 mL of differentiation induction medium and mix to obtain a fina...
Embodiment 2
[0071] Example 2 Effects of magnolanine on the differentiation and mineralization of MC3T3-E1 cells induced by psoralen or glycosides
[0072] 1. Preparation of drug to be tested
[0073] Refer to Sections 1.1 to 1.8 in Example 1.
[0074] 2. Experimental method
[0075] 2.1. Cell differentiation activity
[0076] For the effect of magnolialine on the differentiation and mineralization activity of MC3T3-E1 cells induced by psoralen or psoralen, the experiment refers to part 2.1 in Example 1. The difference is that the specific dosing is: take 0.5 mL of Add 0.5 μL of the following solutions to the bone differentiation induction medium: blank solvent (absolute ethanol), 10 μM positive drug 17β-estradiol, different sample solutions to be tested (10 μM psoralen, 10 μM glycoside, 10 μM magnolialine, composition MP, and composition MS) were co-cultured for 7 days, and the drug-containing induction culture medium was replaced every 2 to 3 days. Experiments were repeated at least ...
Embodiment 3
[0081] Example 3 The effect of the composition MPS of magnolialine, psoralen and glucoside on the differentiation and mineralization activity of MC3T3-E1 cells
[0082] 1. Preparation of drug to be tested
[0083] Refer to Sections 1.1 to 1.8 in Example 1.
[0084] 2. Experimental method
[0085] 2.1. Cell differentiation activity
[0086] The influence experiment of the composition MPS of magnolialine, psoralen and glucoside on the differentiation and mineralization activity of MC3T3-E1 cells refers to part 2.1 in Example 1, the difference is that the specific dosing is as follows: Add 0.5 μL of the following solutions to 0.5 mL of osteogenic differentiation induction medium: blank solvent (absolute ethanol), 10 μM positive drug 17β-estradiol, different sample solutions to be tested (10 μM magnolialine, 10 mM psoralen, 1 mM When drug glycosides, composition PS and composition MPS) were co-cultured for 7 days, the drug-containing induction culture medium was replaced every ...
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