Test evaluation method for sensitization of traditional Chinese medicine injection
An evaluation method and injection technology, applied in the field of detection, can solve the problems of ineffective detection of sensitization of traditional Chinese medicine injections, and achieve the effects of strong operational reliability, good experimental stability, and sensitive detection
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Embodiment 1
[0019] Example 1 Allergenicity Detection of Reduning Injection
[0020] 1. Method
[0021] 1. Sensitive parts of ultrafiltration enriched traditional Chinese medicine injection
[0022] Take respectively 100ml of Reduning injection (batch numbers: 100808, 111011, 101105, 101114) with known adverse reactions and Reduning injection (batch numbers: 110709, 120207, 120210, 120211) of the sample to be tested, and add Transfer to an ultrafiltration tube with a molecular weight cut-off of 3KD, centrifuge at 3500 rpm for 40 minutes, and after repeated ultrafiltration, the remaining 5ml solution is obtained from the 20-fold concentrated and enriched macromolecular allergenic sites of the above batch numbers, sterilized, and stored at 4 degrees.
[0023] 2. Co-culture of splenic mononuclear cell PBMC and stimulatory site
[0024] Take the ICR mouse and kill it by decapitation, soak it in 75% alcohol for 2 minutes, take it out, open the abdominal cavity, take out the spleen, put it in ...
Embodiment 2
[0038] Example 2 Sensitivity Detection of Salvia Miltiorrhiza, Radix Astragali, Shengmai, Puerarin, Xuesaitong Injection
[0039] 1. Method
[0040] 1. Sensitive parts of ultrafiltration enriched traditional Chinese medicine injection
[0041] Take 100ml each of Danshen, Astragalus, Shengmai, Puerarin, and Xuesaitong injections, add them to an ultrafiltration tube with a molecular weight cut-off of 3KD, and centrifuge at 3500 rpm for 40min. After repeated ultrafiltration, 20 and 60 times concentrated and enriched large Molecular sensitization parts, sterilized, stored at 4 degrees, and set aside.
[0042]2. Co-culture of splenic mononuclear cell PBMC and stimulatory site
[0043] Take the ICR mouse and kill it by decapitation, soak it in 75% alcohol for 2 minutes, take it out, open the abdominal cavity, take out the spleen, put it in a petri dish, cut it into pieces, squeeze it with a needle core to disperse it, and blow it with PBS (5ml) to disperse it into cells The suspe...
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