L-ornithine lipoic acid compound salt, and preparation method and application thereof
A technology of ornithine sulfur and compound salt is applied in the field of medicine and achieves the effects of low cost, high purity and simple and easy preparation method
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Embodiment 1
[0045] Embodiment 1: Preparation of L-ornithine lipoic acid compound salt
[0046] Step 1: Preparation of free L-ornithine
example 1
[0048] Dissolve 30g of L-ornithine hydrochloride in 1L of water, adjust its pH to 2.0 with hydrochloric acid, then flow the adjusted pH-adjusted L-ornithine hydrochloride solution through the filling chamber at a flow rate of 6ml / min The ion-exchange column of JK006 cation exchange resin, and then rinse the column with deionized water to wash away the chloride ions between the resins, and finally use 0.8mol / L ammonia water to flow through the column at a flow rate of 8ml / min to release the free L-ornithine Eluted from the resin, free L-ornithine aqueous solution was obtained.
example 2
[0050] According to the method disclosed in the patent document CN101955901, a fermented liquid containing L-ornithine is obtained, and after the fermented liquid is treated by removing bacteria and pigment, an aqueous solution containing free L-ornithine is obtained.
[0051] Step 2: preparing L-ornithine lipoic acid compound salt;
[0052] example 1:
[0053] Concentrate the free L-ornithine aqueous solution in Step 1 Example 1, and the concentration of free L-ornithine in the obtained concentrated solution is 54.7wt%. Dissolve 20g of lipoic acid in 400ml of absolute ethanol, add 22.5g of the above-mentioned free L-ornithine concentrate to it, and stir at a constant temperature of 20°C for 120min to complete the reaction and obtain an ethanol-insoluble precipitate, which is filtered to remove the solid-liquid mixture Ethanol, put the filtered solid into a blast drying oven, and dry at 40° C. for 6 to 8 hours to obtain 28.98 grams of light yellow solid powder. The above yel...
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