Preparation method of serum carbon dioxide determination reagent ball and reagent ball
A technology of carbon dioxide and reagents, which is applied in the preparation method of reagent balls for serum carbon dioxide determination and the field of reagent balls, can solve the problems of difficulty in applying instant diagnosis of patients, short validity period of liquid reagents, and use restrictions, and achieves guaranteed shape and reconstitution solubility, Good shape and effect of reconstitution solubility, high stability and precision
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[0033] The embodiment of the present invention provides a method for preparing a serum carbon dioxide measurement reagent ball, which can prepare a spherical serum carbon dioxide measurement reagent. Please refer to figure 1 , the method includes the following steps:
[0034] S10: Mix buffer, phosphoenolpyruvate, reduced coenzyme I, malate dehydrogenase, phosphoenolpyruvate carboxylase, magnesium salt, stabilizer, excipient and water to form a mixed solution, And adjust the pH value of the mixed solution to a preset value.
[0035] In this example, buffer, phosphoenolpyruvate, reduced coenzyme I, malate dehydrogenase, phosphoenolpyruvate carboxylase, magnesium salt, stabilizer, excipient and water (each component), and then thoroughly mix each component to obtain a mixed solution. The pH value of the mixed solution can be tested by methods such as pH test paper, and the pH value of the mixed solution can be adjusted to a preset value by adding sodium hydroxide. Wherein, the...
Embodiment 1
[0063] In this embodiment, the buffer includes Tris buffer, the stabilizer includes bovine serum albumin, the excipient includes mannitol, and the magnesium salt includes magnesium sulfate. The preparation method of serum carbon dioxide measurement reagent ball is as follows: a certain amount of Tris buffer, bovine serum albumin, mannitol, magnesium sulfate, phosphoenolpyruvate, reduced coenzyme Ⅰ, malate dehydrogenase, phosphoenol Formula pyruvate carboxylase and water are mixed to form a mixed solution, and the droplets of the mixed solution are dropped into liquid nitrogen to form ice balls with a volume of about 3.0ul, and the ice balls are freeze-dried to prepare reagent balls for measuring carbon dioxide in serum. And the microfluidic chip is prepared by using the serum carbon dioxide measuring reagent ball.
[0064] Specifically, in this embodiment, the mixed solution includes the following components: Tris buffer solution 5-150mmol / L, magnesium sulfate 0.1-10g / L, bovin...
Embodiment 2
[0066] In this embodiment, the buffer includes glycine-sodium hydroxide buffer, the magnesium salt includes magnesium acetate, the stabilizer includes sucrose, and the excipient includes dextran 10,000 and water-soluble starch. The preparation method of the serum carbon dioxide measurement reagent ball is as follows: a certain amount of glycine-sodium hydroxide buffer solution, magnesium acetate, sucrose, dextran 10,000, water-soluble starch, phosphoenolpyruvate, reduced coenzyme I, apple Acid dehydrogenase, phosphoenolpyruvate carboxylase and water are mixed to form a mixed solution, the droplets of the mixed solution are dropped in liquid nitrogen to form ice balls with a volume of about 2.5ul, and the ice balls are freeze-dried to obtain serum Carbon dioxide reagent balls. And the microfluidic chip is prepared by using the serum carbon dioxide measuring reagent ball.
[0067] Specifically, in this embodiment, the mixed solution includes the following components: glycine-so...
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