An object of the present disclosure is to find a method in which a result of liquid chromatography can be predicted with high accuracy for a wide range of a mixing ratio of solvents by utilizing a result of thin-layer chromatography.

A liquid chromatography method for separating a mixture of two or more kinds of compounds, comprising the following steps: (1) performing thin-layer chromatography or column chromatography in a mixed solvent of two or more kinds of solvents having a different mixing ratio from each other or a single solvent; (2) creating a relational expression between a mixing ratio and an elution degree of a solvent for each compound in a sample based on a result of the step (1); and (3) determining an optimum condition based on the relational expression, and performing liquid chromatography.

An object of the present disclosure is to find a method in which a result of liquid chromatography can be predicted with high accuracy for a wide range of a mixing ratio of solvents by utilizing a result of thin-layer chromatography.

A liquid chromatography method for separating a mixture of two or more kinds of compounds, comprising the following steps: (1) performing thin-layer chromatography or column chromatography in a mixed solvent of two or more kinds of solvents having a different mixing ratio from each other or a single solvent; (2) creating a relational expression between a mixing ratio and an elution degree of a solvent for each compound in a sample based on a result of the step (1); and (3) determining an optimum condition based on the relational expression, and performing liquid chromatography.

A method for identification of characteristic components in a Kai-Xin-San by thin-layer chromatography (TLC) is provided, belonging to the technical field of pharmaceutical raw material detection and traditional Chinese medicine quality control. The method only needs to prepare two test solutions to simultaneously identify six characteristic components in the Kai-Xin-San, namely ginsenoside Rb1, ginsenoside Re, tenuifolin, -asarone, dehydrotumulosic acid, and pachymic acid. An automatic TLC spotting instrument can ensure even sampling and flat chromatographic bands and the silica gel G thin-layer plates after spotting are placed in the steam of the optimized developing solvent to allow pre-saturation.

A method for identification of characteristic components in a Kai-Xin-San by thin-layer chromatography (TLC) is provided, belonging to the technical field of pharmaceutical raw material detection and traditional Chinese medicine quality control. The method only needs to prepare two test solutions to simultaneously identify six characteristic components in the Kai-Xin-San, namely ginsenoside Rb1, ginsenoside Re, tenuifolin, -asarone, dehydrotumulosic acid, and pachymic acid. An automatic TLC spotting instrument can ensure even sampling and flat chromatographic bands and the silica gel G thin-layer plates after spotting are placed in the steam of the optimized developing solvent to allow pre-saturation.

A method is provided for preparing a sample of a specimen to be analysed from a thin-layer plate in thin-layer chromatography. The sample is removed from a surface of the thin-layer plate by means of a blade disposed at a receiving opening of a cannula and fed through the cannula to a specimen chamber connected to the cannula. A reduced pressure can be generated in the specimen chamber to suck the sample removed from the thin-layer plate by means of the cannula through the receiving opening into and through the cannula and into the specimen chamber. After removal and feed of the sample, the specimen chamber can be filled with a solvent to dissolve the sample. The cannula with the blade can be deflected against a spring force or the blade can be deflected against a spring force relative to the receiving opening of the cannula at the receiving opening of the cannula to prevent the blade from penetrating into the thin-layer plate with an excessive contact pressure during the removal of the sample from the thin-layer plate.

To develop the chromatogram, a prepared plate is placed in a chromatographic chamber where a tip, connected to multiple supply lines for different eluent components, enters from below. Each line includes a reservoir, pump, and tubing system. The tip is moved along a set path by a three-dimensional machine while the eluents are pumped with varying flow rates, controlled by a computer to produce a changing eluent composition over time. A digital camera tracks the position of the eluent front, and this data is used by the computer to adjust pump operations in real-time. Once the eluent front reaches its final position, pumping stops. The plate is then removed and dried, resulting in a developed chromatogram.

A method for rapidly detecting pesticides based on thin-layer chromatography (TLC) and enzyme inhibition principles. The method includes the following steps: cutting a TLC plate into a rectangle, and using one end of the rectangle to contact a sample extract to form a pesticide residue separation area; covering the other end of the rectangle with a small piece cut from filter paper or glass fiber and fixing on a piece of enzyme inhibition reaction test paper to form a pesticide enrichment area; pasting a side of the enzyme inhibition reaction test paper away from the pesticide residue separation area with a piece of filter paper immobilized with a chromogenic agent to form a substrate color development area; and performing color reaction.

A method for rapidly detecting pesticides based on thin-layer chromatography (TLC) and enzyme inhibition principles. The method includes the following steps: cutting a TLC plate into a rectangle, and using one end of the rectangle to contact a sample extract to form a pesticide residue separation area; covering the other end of the rectangle with a small piece cut from filter paper or glass fiber and fixing on a piece of enzyme inhibition reaction test paper to form a pesticide enrichment area; pasting a side of the enzyme inhibition reaction test paper away from the pesticide residue separation area with a piece of filter paper immobilized with a chromogenic agent to form a substrate color development area; and performing color reaction.