A traditional Chinese medicine for treating chronic atrophic gastritis and a preparation method thereof
A kind of atrophic gastritis, chronic technology, applied in the field of medicine, can solve the problem of inconsistency in the level of syndrome differentiation and treatment, affect the clinical curative effect, etc., achieve the effect of promoting gastric motility and highlighting the substantive characteristics
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Embodiment 1
[0049] Guizhi 50g Red Ginseng 50g Poria 50g
[0050] Amomum 50g Yizhiren 50g Paojiang 50g
[0051] Ginger 100g Cardamom 50g French pinellia 50g
[0052] Take all 9 medicinal materials, add water to extract twice, add 3000g of water for the first time, extract for 1 hour, add 3000g of water for the second time, extract for 1 hour; combine the extracts, concentrate to 80 ° C relative density of 1.20 ointment to obtain the active ingredient.
Embodiment 2
[0054] Guizhi 400g Red Ginseng 400g Poria 400g
[0055] Amomum 400g Yizhiren 400g Pao Jiang 400g
[0056] Ginger 500g Cardamom 400g French pinellia 400g.
[0057] Take all 9 medicinal materials, add water to extract twice, add 37000g of water for the first time, extract for 3 hours, add 37000g of water for the second time, extract for 3 hours; combine the extracts, concentrate to 80 °C when the relative density is 1.26 ointment to obtain the active ingredient.
[0058] The active ingredient is mixed with appropriate amount of starch and dextrin, granulated, dried and compressed to obtain the tablet of the present invention.
Embodiment 3
[0060] Guizhi 200g Red Ginseng 150g Poria 200g
[0061] Amomum 150g Yizhiren 150g Paojiang 200g
[0062] Ginger 300g White cardamom 150g French pinellia 150g
[0063] Take all 9 medicinal materials, add water to extract twice, add 13200g of water for the first time, extract for 2 hours, add 9900g of water for the second time, extract for 2 hours; combine the extracts, concentrate to 80 °C when the relative density is 1.25. ointment to obtain the active ingredient.
[0064] The active ingredient is mixed with an appropriate amount of sucrose and preservatives, and water is added to 1000g to obtain the oral liquid of the present invention.
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