Method for improving water solubility and small intestine digestion stability of curcumin
A technology of curcumin and stability is applied in the application field of curcumin to achieve the effects of improving solubility, improving digestive stability and having good market prospects
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Embodiment 1
[0025] The Protein Z protein samples were dissolved in 10mM Ops (pH7.0) buffer, and were respectively configured as Protein Z protein samples with concentration gradients of 0, 2, 4, 6, 8, and 10 μM. Take 1 mL of Protein Z samples with different concentrations, add excess curcumin samples respectively, and mix well in the dark for 24 hours, pass through a 0.45 μm filter membrane to obtain a protein Z protein solution dissolved in curcumin. Using an ultraviolet spectrophotometer to measure the absorbance value at 425nm to detect the content of curcumin dissolved in the sample, it was detected that the solubility of curcumin in aqueous solution increased from 0.43 μM to 10.59 μM, which was increased by about 24 times.
Embodiment 2
[0027] Use 10mMMops (pH 7.0) buffer to configure the Protein Z protein solution to make a 212μM protein sample; dissolve curcumin in absolute ethanol to make a 5mM homogeneous solution; dissolve trypsin in a 10mMMops (pH7.0) buffer to make a 50μM protease sample. According to the mixed volume of 5mL, Protein Z (8μM): curcumin (n / n) = 1:3, protein Z: trypsin (n / n) = 1:4 to mix the above solution, using 10mM Mops (pH7.0) The buffer was added to the 5mL reaction system, and no Protein Z was added as the control group. Put the sample at 37°C for reaction, take samples at 0, 30, 60, and 120 minutes, and boil for 5 minutes to terminate the reaction. Take 450 μL of the sample that terminated the reaction and add 450 μL of ethyl acetate to extract for 2 hours. The content of undegraded curcumin in the system was detected by HPLC. Compared with the curcumin content in the control system, the content of curcumin was 15.13 μM. The content was 24.76 μM, and the stability was increased b...
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