Preparing process of compound red skin blood-enriching oral liquid
A preparation process and technology for oral liquid, which is applied in the field of preparation of Fufang Hongyi Buxue Oral Liquid, can solve the problems of increasing raw material cost, loss of active ingredients of polysaccharides, etc., achieves the effects of simple and feasible preparation method, shortening extraction time, and avoiding waste of raw materials
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Embodiment 1
[0018] The preparation technology of compound red clothing blood-enhancing oral liquid, it comprises the steps:
[0019] 1) Take 20g of fungus, add 16 times the weight of water, soak for 30 minutes, heat to a slight boil for 2 hours, filter, add 10 times the weight of water to the dregs, heat and boil for 1 hour, filter, combine the filtrates, and concentrate to The density is 1.02g / ml, and the fungus extract is obtained;
[0020] 2) Take 100g of Lycium barbarum, crush it, add 5 times the weight of water, and cut it with a high-speed shearer for 60 minutes to obtain the soaking liquid. % ethanol, and the control pressure is 0.8Mpa, the temperature is 60°C, 300rpm is stirred and extracted for 120min, the filtrate is collected by filtration, then the filtrate is evaporated under reduced pressure to remove ethanol, the residual liquid is collected, dried for 6h, and the drying temperature is 70°C to obtain the wolfberry fruit extract 1.79g of the substance; adopting the content ...
Embodiment 2
[0029] Effect of extraction process on effective substances of polysaccharides:
[0030] Taking Comparative Example 1 as an example, the process of Lycium barbarum and Jujube were respectively used in Comparative Example 1, and the content of polysaccharide was determined by the phenol-sulfuric acid method, and the influence of different processes on the yield of polysaccharide was detected; see Table 1 for details:
[0031] Table 1
[0032] group
Embodiment 3
[0034] Toxicity test:
[0035] In this experiment, healthy SD rats were used, and the dosage gradient of compound Hongyi Buxue Oral Liquid prepared in Example 1 was administered orally. The dose gradients were 1ml / kg and 5ml / kg, and the administration was continued for 45 days. Within one week afterward, there was no significant effect on animal growth status, active diet, hematology, blood biochemistry, organ tissue structure, and urine routine, which indicated that the clinical medication was safe and reliable.
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