Pharmaceutical composition of salviae miltiorrhizae extract for treating cardiovascular and cerebrovascular diseases and use thereof
A technology for cardiovascular and cerebrovascular diseases and a composition is applied in the field of pharmaceutical compositions, which can solve the problems of limitations, inability to reflect the compatibility and synergy of multi-component and multi-target points, and inability to exert the overall therapeutic effect of Salvia miltiorrhiza medicinal materials.
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Embodiment 1
[0110] Example 1: Lyophilized preparation of salvianolic acid B, salvianolic acid A and sodium tanshinone IIA sulfonate (5:2:1)
[0111] Get 20g of salvianolic acid B, 8g of salvianolic acid A and 4g of sodium tanshinone IIA sulfonate in Example 1, add 32g of sodium ascorbate and 12.5g of mannitol, dissolve in 350ml of distilled water, and set the volume to 400ml, filter and sterilize, aseptic conditions The next part is packed in 100 vials, freeze-dried, and sealed under nitrogen to obtain the final product.
Embodiment 2
[0112] Example 2: Lyophilized preparation of salvianolic acid B, salvianolic acid A and sodium tanshinone IIA sulfonate (3:1:1)
[0113] Get 21g of salvianolic acid B, 7g of salvianolic acid A and 7g of sodium tanshinone IIA sulfonate in Example 1, add 7.4g of magnesium hydrogen phosphate, 35g of sodium ascorbate, and 12.5g of mannitol, dissolve in 250ml of distilled water, stir for 20 minutes, and constant volume to 300ml, filter out the insoluble matter, sterilize by filtration, subpackage in 100 vials under aseptic conditions, freeze-dry, and seal under nitrogen to obtain the product.
Embodiment 3
[0114] Example 3: Salvianolic acid B, salvianolic acid A and sodium tanshinone IIA sulfonate (9:3:2) freeze-dried powder injection
[0115] Take 18g of salvianolic acid B, 6g of salvianolic acid and 4g of sodium tanshinone IIA sulfonate, add 6g of magnesium hydrogen phosphate, 27g of sodium ascorbate, and 12.5g of mannitol, dissolve them in 250ml of distilled water, stir for 20 minutes, filter out insolubles, filter out sterilized, freeze-dried under aseptic conditions, the newly prepared powdery pharmaceutical composition is divided into 100 vials, sealed under nitrogen, and the product is obtained.
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