Pharmaceutical composition for treating peptic ulcer and its preparation method and use
A technology for peptic ulcer and composition, applied in the field of medicine, can solve the problems of easy recurrence, large side effects of western medicine, long metabolism time, etc., and achieve the effect of small recurrence probability and significant curative effect.
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Embodiment 1
[0031] Embodiment 1 Preparation of cycloglycoside-prodipeptide of the present invention
[0032] The preparation method of cycloglycoside-prodipeptide of the present invention refers to the literature "Qin Xiancan, Yu Zhengpeng, etc., synthesis of cyclo(L-group-L-proline) dipeptide [J], Journal of Hainan Normal University: Natural Science Edition, 2008, 21 (2): 173-175 " the synthetic method of ring (L-group-L-pro) dipeptide is prepared the cycloglycoside-pro dipeptide of the present invention, and specific method is: L-proline methyl ester and N - tert-butoxycarbonyl-L-glycine as raw material, condensed by DCC to obtain a straight-chain dipeptide, and then de-Boc protected by HCl / Et2O, and formed into a ring under weak alkaline conditions to obtain a cyclic (glycine-proline) dipeptide.
Embodiment 2
[0034] Adenosine 5g, arginine 20g, dopamine 5g, tryptophan 5g, glutamine 10g, threonine 15g, methionine 10g, serine 10g, proline 15g, cycloglycoside-prodipeptide 5g (prepared by the method of Example 1), after mixing evenly, add 2.5g of potassium sorbate, mix evenly, add purified water to dissolve to 1000ml, stir and mix, filter, potting, sterilize at 115°C for 30min, Pack and serve.
Embodiment 3
[0036] Adenosine 5g, arginine 20g, dopamine 5g, tryptophan 5g, glutamine 10g, threonine 15g, methionine 10g, serine 10g, proline 15g, cycloglycoside-prodipeptide 5g (prepared by the method of Example 1), after mixing evenly, add 68g dextrin, 10g carboxymethyl starch sodium and mix, granulate, then add 2g of talcum powder, mix, compress, pack, to obtain .
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