Spectrophotometry measuring method of content of gamma-cyclodextrin (gamma-CD) based on bromocresol green (BCG) developing method
A technology of bromocresol green and determination method, which is applied in the field of quantitative analysis of γ-cyclodextrin, can solve the problems affecting the accuracy and stability of the measurement results, insufficient estimation of the buffer capacity of the measurement solution, and affecting the accuracy of the measurement results, etc. Achieve the effects of avoiding experimental errors and fluctuations in data results, improving accuracy and repeatability, and avoiding errors
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Embodiment 1
[0036] Take 3mL of 0.35mmol / L BCG solution and add it to a 50mL brown colorimetric tube, then add 2mL of 5mmoL / L γ-CD solution, and then adjust the volume to 25mL with pH=4.4 acetic acid-sodium acetate buffer solution. ℃ in a constant temperature water bath for 25 minutes, and measure its absorbance at 625 nm with a buffer solution as a reference. In the blank experiment, 2 mL of distilled water was used to replace the γ-CD solution, and the rest of the experimental operations were the same.
[0037] Absorbance difference (ΔA) = sample solution absorbance (A) - blank solution absorbance (A')
Embodiment 2
[0039] Take 3mL of 0.35mmol / L BCG solution and add it to a 50mL brown colorimetric tube, then add 2mL of γ-CD solution, then adjust the volume to 25mL with pH=5.2 acetic acid-sodium acetate buffer solution, shake well, and place in a constant temperature water bath at 30°C Let it stand in the medium for 25min, and measure its absorbance at 625nm with the buffer solution as a reference. In the blank experiment, 2 mL of distilled water was used instead of the γ-CD solution, and the rest of the experimental operations were the same.
[0040] Absorbance difference (ΔA) = sample absorbance (A) - blank solution absorbance (A')
Embodiment 3
[0042] Take 3mL of 0.25mmol / L BCG solution and add it to a 50mL brown colorimetric tube, then add 2mL of γ-CD solution, then adjust the volume to 25mL with pH=4.4 acetic acid-sodium acetate buffer solution, shake well, and place in a constant temperature water bath at 30°C Let it stand in the medium for 25min, and measure its absorbance at 625nm with the buffer solution as a reference. In the blank experiment, 2 mL of distilled water was used instead of the γ-CD solution, and the rest of the experimental operations were the same.
[0043] Absorbance difference (ΔA) = sample absorbance (A) - blank solution absorbance (A')
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