Thin layer quantitative image recognition detection method for water-soluble natural product
A natural product and image recognition technology, which is applied in the field of natural products and food and medicine, achieves the effect of simple process, easy operation and wide application
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Embodiment 1
[0068](+)-Catechin ethanol solution, spotting 0.5 microliters with a capillary to thin-layer chromatography, after the solvent evaporates, use ethyl acetate / ethanol / water / acetic acid (5 / 2.85 / 0.15 / 0.12, v / v / v / v) developer plate to a distance of 20 mm, then allowed to dry, and then re-developed to 40 mm with chloroform / ethyl acetate / formic acid (1 / 1 / 0.03, v / v / v) developer length. Then take it out and wait for the solvent to evaporate to dry, and then stain it with p-methoxybenzaldehyde staining agent, place it on a heating platform at 250°C and heat it for 15 seconds to develop the color. After developing the color of the thin layer, scan it with a computer scanner, and set the resolution to 300dpi. The scanned images were denoised and smoothed with ImageJ, and then the background was removed, and finally quantitatively integrated, and the integrated value was compared with the standard value to obtain the measurement result. The actual value is 1.20 mg / mL of (+)-catechin sol...
Embodiment 2
[0071] The ethanol solution of quercetin was sampled with 0.5 microliters of capillary to thin-layer chromatography, and after the solvent was evaporated, it was washed with ethyl acetate / ethanol / water / acetic acid (5 / 2.85 / 0.15 / 0.12, v / v / v / v ) on the developer plate to a distance of 20 mm, then dried, and then re-developed to a length of 40 mm with chloroform / ethyl acetate / formic acid (1 / 1 / 0.03, v / v / v) developer. Then take it out and wait for the solvent to evaporate to dry, and then stain it with p-methoxybenzaldehyde staining agent, place it on a heating platform at 250°C and heat it for 15 seconds to develop the color. After developing the color of the thin layer, scan it with a computer scanner, and set the resolution to 300dpi. The scanned images were denoised and smoothed with ImageJ, and then the background was removed, and finally quantitatively integrated, and the integrated value was compared with the standard value to obtain the measurement result. The quercetin eth...
Embodiment 3
[0073] With the ethanol solution of tea saponin, spot 0.5 microliters to thin-layer chromatography with a capillary tube and wait for the solvent to evaporate, then use ethyl acetate / ethanol / water / acetic acid (5 / 2.85 / 0.15 / 0.12, v / v / v / v) The developer plate was developed to a distance of 20 mm, then allowed to dry, and then re-developed to a length of 40 mm with chloroform / ethyl acetate / formic acid (1 / 1 / 0.03, v / v / v) developer. Then take it out and wait for the solvent to evaporate to dry, and then stain it with p-methoxybenzaldehyde staining agent, place it on a heating platform at 250°C and heat it for 15 seconds to develop the color. After developing the color of the thin layer, scan it with a computer scanner, and set the resolution to 300dpi. The scanned images were denoised and smoothed with ImageJ, and then the background was removed, and finally quantitatively integrated, and the integrated value was compared with the standard value to obtain the measurement result. For...
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