Pharmaceutical composition and composite burn cream for treating burns and scalds and preparation method thereof
A composition and drug technology, which can be used in drug combinations, medical raw materials derived from birds, and resistance to vector-borne diseases, etc., can solve the problem of promoting muscle growth without particularly obvious effects.
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Embodiment 1
[0047] Embodiment 1: Preparation of ultra-pure egg butter
[0048] Select fresh eggs, separate the egg yolk stock solution after breaking the shell; dry it at a temperature of 45-65°C; grind it into egg yolk powder with a particle size of 15-45 mesh; put the egg yolk powder into the extraction kettle, and pass in the extractant carbon dioxide The flow rate is 15-25kg / h, the extraction pressure is 30-50MPa, the extraction temperature is 35°C, and the extraction time is 4-10 hours; the extracted mixture is passed into a decompression separator, and the bottom is settled to separate the ultra-pure egg yolk Oil.
[0049] At present, the preparation process of ultra-pure egg yolk is relatively mature, and many methods similar to the above-mentioned embodiments can achieve the purpose of preparing ultra-pure egg yolk in the present invention. The present invention does not specifically limit the method for preparing ultra-pure egg yolk. A skilled person can select a suitable method...
Embodiment 2
[0050] Example 2: Preparation of bacterial protein antigen for immunization
[0051] (1) Culture of bacteria:
[0052] Staphylococcus aureus (ATCC26031) was activated by streaking on the solid plate of ordinary broth medium, and a single colony after activation was picked and inoculated in ordinary broth medium, and shaken at 37°C for 6-12 hours; Streak activation of Pseudomonas aeruginosa (ATCC27853) on the plate, pick the activated single colony and inoculate it in Sabouraud medium, shake and culture at 37°C for 6-12 hours; use serum broth medium solid plate streak activation Escherichia coli (ATCC25922 ), pick the activated single colony and inoculate it in the serum broth medium, shake culture at 37°C for 6-12 hours; use hexadecanetrimethylammonium bromide medium solid plate to streak and activate the beta-hemolytic streptococcus ( CMCC32210), pick the activated single colony and inoculate it in hexadecanetrimethylammonium bromide medium, and culture it with shaking at 37...
Embodiment 3
[0055] Embodiment 3: Immunization laying hen
[0056] (1) Preparation of mixed antigen:
[0057] Mix the bacterial protein antigens of the above-mentioned Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and hemolytic streptococcus at a concentration ratio of 1:1:1:1 to obtain a mixed antigen, and the final concentration of the mixed antigen is 50-500 μg / ml, stored at -80°C for future use.
[0058] It should be noted that in the present invention, any one or a combination of at least two of Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and hemolytic streptococcus can be used as an antigen to immunize laying poultry. However, in order to obtain a better bacteriostatic effect, it is preferable to use a mixture of the above four bacteria as a mixed antigen to immunize laying poultry. The mixing ratio of the above four bacteria can be determined empirically, but the present invention preferably mixes according to the concentration ratio of 1:1:1...
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