Method for quantification of 146S content in foot-and-mouth disease antigen by using liquid chromatography detection system
A liquid chromatography and detection system technology, applied in the field of biological detection, can solve the problems of insufficient removal of impurity proteins and nucleic acids, complex sample processing processes, and lack of detection patterns, and achieve accurate and fast detection, wide versatility, and quantitative results. accurate effect
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Embodiment 1
[0049] Quantitative detection of 146S antigen content in the sample of embodiment 1
[0050] 1. Materials
[0051] 1.1 Test samples: Bovine Asia I / JSL / GSZY / 06 virus, bovine O-type ONXC / 92 virus, and pig O-type O / ZK / 93-08 virus were purchased from Lanzhou Veterinary Research Institute.
[0052] 1.2 Instruments and reagents: Liquid chromatography detection system was purchased from Labtech, sucrose and protamine sulfate were purchased from sigma, and PEG6000 was purchased from AMRESCO.
[0053] The phase chromatography detection system is composed of a liquid chromatography detector, a chromatography workstation and a constant flow pump. The model of the liquid chromatography detector is UV600 ultraviolet-visible variable wavelength detector, and the model of the constant flow pump is P600 high pressure constant flow pump. The light source of the liquid chromatography detector is a deuterium lamp, the spectral bandwidth is 8nm, the wavelength accuracy is ±0.2nm, and the wavelen...
Embodiment 2
[0088] The 146S content recorded by the method of the present invention is based on the preparation of the vaccine, and the corresponding 146S content in the prepared bivalent vaccine is equal to the foot-and-mouth disease O type and the Asia I type antigen liquid. (Foot-and-mouth disease O type, Asia I type bivalent inactivated vaccine manufacture and inspection trial procedure " carry out, result is as shown in table 5, 146S content described in the table is foot-and-mouth disease O type or Asia I type antigen 146S content, the two are equal, For example: in bovine O type ONXC / 92-Asia I type bivalent inactivated antigen solution 3, the 146S content of FMD O type is 17.17 μg / ml, and the Asian I type 146S content is also 17.17 μg / ml, each half of the protection (PD 50 ) value is 15.59 for Asian I type and 12.51 for O type.
[0089] Table 5 The half protection value (PD) corresponding to the antigen solution with different 146S content (μg / ml) 50 )
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Embodiment 3
[0094] The optimization of embodiment 3 foot-and-mouth disease virus purification concentration conditions
[0095] 1 material
[0096] 1.1 Vaccine strain: Asia I / JSL / GSZY / 06 live virus was purchased from Lanzhou Veterinary Research Institute.
[0097] 1.2 Chemical reagents: protamine sulfate, a product of sigma; PEG6000 was purchased from AMRESCO.
[0098] 2 methods
[0099] According to the literature data and the results of preliminary experiments, the main factors affecting the purification and concentration of FMD were selected: the concentration, temperature and time of protamine sulfate, the concentration and stirring time of PEG6000 were optimized.
[0100] 2.1 Optimization of concentration of protamine sulfate
[0101] Take the Asia I / JSL / GSZY / 06 virus antigen of suspension culture in large-scale production, add protamine sulfate to different final concentrations, successively 0.5mg / ml, 1.0mg / ml, 1.5mg / ml, 2.0mg / ml and Five concentration gradients of 2.5mg / ml, aft...
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