Rabies vaccine for human beings
A rabies vaccine and vaccine technology, which is applied in the direction of medical preparations containing active ingredients, antibody medical ingredients, peptides, etc., can solve the problems of increasing vaccine side effects, etc., and achieve the goal of overcoming immune limitations, good immune effect and safety Effect
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Embodiment 1
[0029] Embodiment 1 lysing and extraction and purification of whole rabies virus particles
[0030] The Vero cells were cultured at 37°C and passed through four consecutive passages. After the 4th passage cells are cultured for 3-5 days, they are rinsed with phosphate buffer, and the inoculation virus titer is not less than 7.5LgLD 50 / ml of rabies virus fixed virus CTN-1V strain. Then add cell maintenance solution and incubate at 35°C for 24 hours. Replace with fresh cell maintenance solution, and continue to culture for 2-4 days according to the above conditions. When the cytopathic CPE reaches ++~+++, harvest and combine the virus solution. Add β-propiolactone at a ratio of 1:4000 and place at 22°C for 8 days to inactivate the virus. After passing the inactivation test, it was concentrated by ultrafiltration with a 100KD filter membrane. 10 mg / ml protamine sulfate was added to the concentrated virus liquid to make the final concentration 0.1 mg / ml, centrifuged at 8000 r...
Embodiment 2
[0032] Get the human rabies virus particle cleavage protein (mainly containing the outer membrane fragment of the cleavage virus particle) and tetanus toxoid stock solution (Wuhan Institute of Biological Products) prepared above, and the mixing ratio according to the antigen content is: viral protein 10-150 μ g / dose ; The dosage of tetanus toxoid is 3Lf / dose-10Lf / dose; respectively combined to make liquid vaccine, then packaged, and finally tested and packaged.
Embodiment 3
[0034] Get human rabies purified stock solution (diploid cells) (National Institute for the Control of Pharmaceutical and Biological Products), rabies virus particle lysate protein and tetanus toxoid stock solution (Wuhan Institute of Biological Products) to make liquid vaccine according to the proportions in Table 1 . Human rabies vaccine was set as the control group, in which only 1% human serum albumin was added as the protective agent, and the specificity experiments of the four combined vaccines were carried out according to the method of the third part of the Chinese Pharmacopoeia. The experimental results are all qualified, indicating that the vaccine added with tetanus toxoid lysate protein of rabies virus particles is safe and effective.
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