Delphinidin complex as an antiphlogistic or immunosuppressive active ingredient
A technology of delphinidin and immunosuppressant, applied in fields including, can solve problems such as heart rhythm disorder and high blood pressure
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preparation example Construction
[0088] Preparation of test solution:
[0089] To determine the delphinidin content of a solid prepared according to the invention (see below for the preparation method), approximately 50 mg of this composition was weighed into a 10 mL flask. Subsequent dissolution was performed using Diluent 2, and dilution was continued with the same Diluent 2 until a delphinidin concentration of approximately 0.1 mg / mL was reached.
[0090] The delphinidin content in the samples was calculated with the aid of Agilent ChemStation software and calibrated using the external standards mentioned above.
example 1
[0091] Example 1: Complexation of delphinidin with SBE-β-CD
[0092] This example investigates the complexation of delphinidin with different cyclodextrins and the solubility of said complexes in aqueous solutions.
[0093] Firstly, a neutral aqueous solution of each cyclodextrin with a weight percentage of 10% was prepared. For β-CD, due to its low solubility, the selected concentration is only 2% by weight.
[0094] 5 mL of each cyclodextrin aqueous solution was poured into a glass flask and pure water was added. An excess of delphinidin chloride was subsequently added. The required additional amount is 10 mg for α-, β- and γ-cyclodextrin solutions and 15 mg for HPBCD (2-hydroxypropyl-β-cyclodextrin) and SBE-β-CD solutions.
[0095] The suspension was stirred for 20 hours at 30°C in the dark. Filtration was then performed using a membrane filter with a pore size of 0.22 μm.
[0096] The achievable solubilities are listed in Table 1 below:
[0097] Cyclodextrin...
example 2
[0099] Example 2: Effect of pH
[0100] This example investigates the effect of pH on the solubility of delphinidin-SBE-β-CD. An aqueous solution of SBE-β-CD was prepared as described in Example 1, and the solution was adjusted to the acidic pH values described in Table 2 using 1 M HCL. Subsequently, delphinidin chloride was added and the operation continued as described in Example 1, with the only difference being that the shift time was reduced to 2.5 hours. The test results are listed in Table 2 below:
[0101] pH
[0102] It can be seen from the above table that when the pH value is between 4 and 5, the meridian-chelated delphinidin chloride is increased by about 2 times compared with that at neutral pH value.
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Abstract
Description
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Application Information
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