Application of hyperosmotic fluid composition in preparing medicament for improving wound healing
A technology for anastomotic healing and composition, which is applied in the direction of drug combination, surgical drug, hydroxyl compound active ingredients, etc., and can solve the problems of not revealing the effect of hypertonic fluid composition, etc.
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Embodiment 1
[0021] Prepare according to the following ratio:
[0022] Hydroxyethyl starch 7.6 g
[0023] Sodium chloride 4.2 g
[0024] Add water for injection to 100ml
[0025] Dissolve 7.6 g of hydroxyethyl starch in 100 ml of water for injection, add 0.5 g of activated carbon, stir and heat at 90°C for 15 minutes, filter, add 4.2 g of sodium chloride (medical pure) and stir to dissolve, add 0.5 to 1.0 g of active The carbon is stirred and heated at 90°C for 10 minutes, then filtered, and passed through a 0.6-0.8 micron microporous membrane. Fill the obtained filtrate into 20ml, 50ml, 100ml, 250ml, 370ml or 500ml glass ampoules, large infusion glass bottles or plastic bottles (bags), and then pass the cap to 1.05kg / cm 2 , Sterilize at 121-123°C for 15-30 minutes to obtain a hypertonic liquid pharmaceutical composition.
Embodiment 2
[0027] Prepare according to the following ratio:
[0028] Hydroxyethyl starch 8g
[0029] Sodium chloride 4.1 g
[0030] Normal saline to 100ml
[0031] 8 grams of hydroxyethyl starch and 4.1 grams of sodium chloride were dissolved in 100 milliliters of physiological saline, and activated carbon was used for adsorption decolorization, filtration, filling and sterilization according to the method described in Example 1, to obtain a hypertonic liquid pharmaceutical composition.
Embodiment 3
[0033] Prepare according to the following ratio:
[0034] Sodium chloride 5.1 g
[0035] Carboxymethyl starch 18 g
[0036] Add water for injection to 100ml
[0037] Dissolve 18 g of carboxymethyl starch and 5.1 g of sodium chloride in 100 ml of water for injection, and use activated carbon to adsorb decolorization, filter, fill and sterilize according to the method described in Example 1 to obtain a hypertonic liquid pharmaceutical composition.
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