Application of black raspberry extract (BRBE) in preparation of drugs for treating gastric cancer
An extract, technology of black raspberry, applied in the field of medicine, can solve problems such as no report of black raspberry or its extract
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Embodiment 1
[0015] Embodiment 1: the preparation of BRBE
[0016] This example provides two methods for preparing BRBE.
[0017] (1) The black raspberry fruit is crushed by a masher, and then filtered through a 0.02-inch aperture sieve to remove seeds and make a puree. Strain the remaining fruit and repeat this operation a further three times to ensure adequate juice extraction. Juicing rate is 97%. The prepared puree was poured into a 1-inch freeze-drying dish coated with polyethylene film, and stored in a ventilated freezer. Further freeze-drying is carried out by a sublimator to obtain black raspberry fruit freeze-dried powder. The freeze-dried powder of black raspberry fruit was added to petroleum ether and then ultrasonically extracted twice. The ultrasonic extraction temperature was 25 ℃; the time was 30 min; the mass ratio of petroleum ether to black raspberry fruit freeze-dried powder was 4:1; The ultrasonic extracts were combined, and the solvent was recovered under reduced ...
Embodiment 2
[0019] Example 2: BRBE inhibits the growth of human gastric cancer cells in vitro
[0020] Using 5 kinds of human malignant gastric tumor (SGC7901, MNK45, BGC8223, HCG27, GC9811) cell lines, the in vitro anti-cancer activity of BRBE was determined by MTT method, the concentration range was 0-500 mg / ml, and the treatment time was 72 hours. Table 1.
[0021]
[0022] It can be seen from Table 1 that BRBE can inhibit the growth of human gastric cancer cells in vitro, and the sensitivity to BRBE is significantly different among different cell lines.
Embodiment 3
[0023] Example 3: BRBE combined with 5-FU inhibits the growth of human gastric cancer cells in vitro
[0024] Using 5 kinds of human malignant gastric tumor (SGC7901, MNK45, BGC8223, HCG27, GC9811) cell lines, the in vitro anticancer activity of BRBE alone and in combination with 5-FU was determined by MTT method, and the treatment time was 72 hours. The results are shown in the table 2.
[0025]
[0026] It can be seen from Table 2 that after combined administration, BRBE can significantly reduce the IC50 value of 5-FU in different cell lines.
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Abstract
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Application Information
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