Fermentation product of lotus leaf-hawthorn extract and application of active ingredients of fermentation product to inhibition of fat formation
An active ingredient and fat-inhibiting technology, which is applied in the direction of organic active ingredients, medical preparations containing active ingredients, plant/algae/fungus/moss ingredients, etc., can solve problems such as difficulties in implementation, physical damage caused by exercise methods, and limited effects
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Embodiment 1
[0125] Example 1: The effect of the fermented product of lotus leaf hawthorn extract on reducing the fat content of adipocytes
[0126] Take the adipocytes provided in [Preparation Example C], divide them into three groups and culture them with the following medium respectively, at 37°C for 7 days, during which the medium is replaced every 3 days:
[0127] 1. Group I: adipocyte differentiation medium (500 microliters in total).
[0128] 2. Group II: adipocyte differentiation medium containing 5% (weight / weight) of the lotus leaf Hawthorn extract provided in [Preparation Example A-1] (500 microliters in total); and
[0129] 3. Group III: adipocyte differentiation medium containing 5% (weight / weight) of the fermented product of the lotus leaf hawthorn extract provided in [Preparation Example A-3] (500 microliters in total);
[0130] Afterwards, the cells provided by groups I to III were treated with staining and quantification steps as follows: medium was removed and cells were...
Embodiment 2
[0133] Example 2: The effect of different partitioning of the fermented product of lotus leaf hawthorn extract on reducing the fat content of adipocytes
[0134] Take the adipocytes provided in [Preparation Example C], divide them into four groups and culture them with the following medium respectively, at 37°C for 7 days, during which the medium is replaced every 3 days:
[0135] 1. Group i: adipocyte differentiation medium (500 microliters in total);
[0136] 2. Group ii: adipocyte differentiation medium containing 5% (weight / weight) of the fermented product of the lotus-leaf Hawthorn extract provided in [Preparation Example A-3] (500 microliters in total);
[0137] 3. Group iii: adipocyte differentiation medium containing 5% (weight / weight) of the n-butanol layer extract provided in [Preparation Example B-1] (500 microliters in total);
[0138] 4. Group iv: adipocyte differentiation medium containing 5% (weight / weight) of the aqueous layer extract provided in [Preparation ...
Embodiment 3
[0141] Embodiment 3: the effect of formula (I) to formula (III) compound in reducing the fat content of adipocytes
[0142] Take the adipocytes provided in [Preparation Example C], divide them into four groups and culture them with the following medium respectively, at 37°C for 7 days, during which the medium is replaced every 3 days:
[0143] 1. Group A: adipocyte differentiation medium (500 microliters in total);
[0144] 2. Group B: adipocyte differentiation medium containing 20 micrograms / ml [Preparation Example B-3] of the compound of formula (I) provided (500 microliters in total);
[0145] 3. Group C: the adipocyte differentiation medium (500 microliters in total) containing the compound of formula (II) provided by 20 micrograms / ml [Preparation Example B-3];
[0146] 4. Group D: adipocyte differentiation medium containing 20 μg / ml of the compound of formula (III) provided in [Preparation Example B-3] (500 μl in total).
[0147] Afterwards, the cells provided in Groups...
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