MOA lysozyme nasal spray preparation and preparation method thereof
A technology of lysozyme and nasal spray, applied in biochemical equipment and methods, local antibacterial agents, enzymes, etc., can solve the problems of poor use feeling and poor anti-inflammatory effect, and achieve the effect of improving nasal discharge symptoms and preventing inflammation
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Embodiment 1
[0028] The method for preparing MOA lysozyme nasal spray preparation comprises the steps:
[0029] Step 1: Mix 1 part of chlorhexidine acetate, 5 parts of MOA lysozyme, 1 part of glycerin, 1 part of witch hazel extract, 1 part of honeysuckle extract, 0.1 part of azelastine hydrochloride, and 1 part of recombinant human epidermal growth factor , 1 part of water-soluble chitosan, 1 part of glycerin, 1 part of sodium lactate, and 1 part of borneol were subjected to separation and sterilization treatment, ultrasonically extracted twice at 75 ° C, and put into raw material storage tanks respectively to obtain mixed raw materials.
[0030] Step 2: adding pure water to the mixed raw materials, dispersing and homogenizing, and using an ultrafiltration membrane with a molecular weight cut-off of 10000D to perform ultrafiltration separation to obtain a filtrate;
[0031] Step 3: sending the filtrate into an ion-exchange resin chromatography column for chromatography, and eluting with et...
Embodiment 2
[0035] Step 1: Mix 3 parts of chlorhexidine acetate, 20 parts of MOA lysozyme, 5 parts of glycerin, 5 parts of witch hazel extract, 5 parts of honeysuckle extract, 2 parts of azelastine hydrochloride, and 10 parts of recombinant human epidermal growth factor , 10 parts of water-soluble chitosan, 5 parts of glycerin, 4 parts of sodium lactate, and 4 parts of borneol were subjected to separation and sterilization treatment, ultrasonically extracted 3 times at 80° C., and put into raw material storage tanks respectively to obtain mixed raw materials.
[0036] Step 2: adding pure water to the mixed raw materials, dispersing and homogenizing, and using an ultrafiltration membrane with a molecular weight cut-off of 10000D to perform ultrafiltration separation to obtain a filtrate;
[0037] Step 3: sending the filtrate into an ion-exchange resin chromatography column for chromatography, and eluting with ethanol after chromatography, collecting and obtaining qualified eluted liquid;
...
Embodiment 3
[0041] Step 1: 2 parts of chlorhexidine acetate, 12 parts of MOA lysozyme, 3 parts of glycerin, 3 parts of witch hazel extract, 3 parts of honeysuckle extract, 1 part of azelastine hydrochloride, 5 parts of recombinant human epidermal growth factor, 5 parts of water-soluble chitosan, 3 parts of glycerin, 2 parts of sodium lactate, and 2 parts of borneol were separated and sterilized, ultrasonically extracted 3 times at 77°C, and put into raw material storage tanks respectively to obtain mixed raw materials.
[0042] Step 2: adding pure water to the mixed raw materials, dispersing and homogenizing, and using an ultrafiltration membrane with a molecular weight cut-off of 10000D to perform ultrafiltration separation to obtain a filtrate;
[0043] Step 3: sending the filtrate into an ion-exchange resin chromatography column for chromatography, and eluting with ethanol after chromatography, collecting and obtaining qualified eluted liquid;
[0044] Step 4: Filter the eluted solutio...
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