Bacillus pyocyaneus vaccine and preparation method thereof
A technology for Pseudomonas aeruginosa and vaccines, applied in the directions of antibacterial drugs, bacterial antigen components, etc., can solve the problems that antibiotics are difficult to cure Pseudomonas aeruginosa infection, and Pseudomonas aeruginosa vaccines cannot meet clinical immunity, etc., and achieve the effect of enhancing immune effect.
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specific Embodiment approach 1
[0010] Specific embodiment one: the present embodiment Pseudomonas aeruginosa vaccine is made of Pseudomonas aeruginosa P placed in normal saline 1 endotoxin, Pseudomonas aeruginosa P 2 endotoxin, Pseudomonas aeruginosa P 6 endotoxin and Pseudomonas aeruginosa P 103 The toxoid composition of Pseudomonas aeruginosa vaccine; Pseudomonas aeruginosa P 1 The concentration of endotoxin in protein is 1 / 6~1 / 3mg / mL, Pseudomonas aeruginosa P 2The concentration of endotoxin in protein is 1 / 6~1 / 3mg / mL, Pseudomonas aeruginosa P 6 The concentration of endotoxin in protein is 1 / 6~1 / 3mg / mL, Pseudomonas aeruginosa P 103 The concentration of the toxoid is 0.5-1 mg / mL in terms of protein mass; among them, Pseudomonas aeruginosa P 1 Preserved in the China Medical Microbiology Culture Collection Management Center, the preservation number is 10115; Pseudomonas aeruginosa P 2 Preserved in the China Medical Microbiology Culture Collection Management Center, the preservation number is 10116; Pse...
specific Embodiment approach 2
[0012] Specific embodiment two: the present embodiment Pseudomonas aeruginosa vaccine is prepared according to the following steps: 1. Pseudomonas aeruginosa P 1 ,P 2 and P 6 Inoculate in beef extract peptone medium respectively and culture at 37-42°C for 18-24 hours, then wash Pseudomonas aeruginosa into shake flasks with endotoxin liquid synthesis medium and then incubate at 37-42°C, 175-200r / min Under shaking culture for 24-30 hours, then adjust the pH value of the endotoxin liquid synthesis medium to 6.5-8.5, then add toluene and put it in the environment at 37-42°C for 48-72 hours, and then use a 1000K-3000K filter plate for ultra- Filter and collect the filtrate; 2. Add ZnCl with a concentration of 30~50g / mL in the filtrate respectively 2 solution, then stirred, precipitated, centrifuged at 4°C and 4000r / min for 20min, discarded the supernatant, and 2 HPO 4 Add saturated Na to the precipitate at a volume ratio of solution to precipitate 5:1 2 HPO 4 Solution, then e...
specific Embodiment approach 3
[0022] Embodiment 3: The difference between this embodiment and Embodiment 2 is that the air temperature of the electric fan in Step 3 is 25-50°C. Other steps and parameters are the same as those in Embodiment 2.
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