Inactivation method of pathogenic microorganisms of chitosan
A technology of pathogenic microorganisms and chitosan, applied in the field of chitosan inactivation of pathogenic microorganisms and chitosan, can solve the problems of quality influence, molecular weight reduction, poor heat-resistant virus effect, etc., to avoid high-dose irradiation, The effect of maintaining quality and performance
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Embodiment 1
[0020] Take 1 part of chitosan sample, add about 10 7 cfu / g Bacillus pumilus spores (Spores of Bacillus pumilus), about 10 7 cfu / g Bacillus subtilis spores (Spores of Bacillus subtilis) and about 10 6 TCID 50 / g porcine parvovirus (PPV), 1g / bottle. Add 4.0% NaOH solution, the ratio of the amount of NaOH solution to chitosan is 20:1, keep warm at 80°C, and sterilize until the total number of colonies is less than 1000cfu / g. Filter, wash with water until neutral, subpackage in ampoules, freeze-dry, and the moisture content after drying is 9.6%. Fill with nitrogen gas and seal immediately. 50 kGy gamma-ray irradiation was carried out at -20°C. Reed-muench TCID after irradiation 50 The virus titer reduction (total reduction factor, TRF) was measured by the method, and the reduction of the number of colonies was measured.
[0021] The experimental results show that the residual titer of PPV is ≤0.5 lg TCID after initial inactivation by 4.0% NaOH solution at 80℃ and irradiate...
Embodiment 2
[0023] The preparation of chitosan is with embodiment 1.
[0024] The mass concentration of NaOH solution is 15%, the ratio of NaOH solution to chitosan is 30:1, and sterilized at 60°C until the total number of colonies is less than 1000cfu / g. Filter and wash with water until neutral. Dry under reduced pressure to a moisture content of 8.8%. The ampoules are subpackaged, filled with nitrogen, and sealed. A total dose of 25kGy γ-ray irradiation was carried out at room temperature, and the residual titer of PPV after irradiation was ≤0.5 lg TCID 50 , the number of colonies is reduced to ≤10cfu / g. The crystallinity of chitosan before and after irradiation was 36.4%, 36.7%, the degree of deacetylation were 84.2% and 84.6%, and the molecular weight decreased to 77.8% of the initial molecular weight.
Embodiment 3
[0026] The preparation of chitosan is with embodiment 1.
[0027] The mass concentration of NaOH solution is 40%, the ratio of NaOH solution to chitosan is 50:1, the temperature is room temperature, and the bacteria are sterilized until the total number of colonies is less than 1000cfu / g. Filter and wash with water until neutral. Drying under reduced pressure, the moisture content after drying is 8.9%. The ampoules are subpackaged, filled with nitrogen, and sealed. A total dose of 10kGy γ-ray irradiation was carried out at 30°C, and the residual titer of PPV after irradiation was ≤0.5 lg TCID 50 , the number of colonies is reduced to ≤10cfu / g. The crystallinity of chitosan was 36.4% and 36.2% before and after irradiation, the deacetylation degree was 84.2% and 85.0% respectively, and the molecular weight decreased to 80.1% of the initial molecular weight.
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