Two-dimensional highly effective liquid phase chromatographic system and its uses
A high-performance liquid chromatography and high-pressure liquid chromatography technology, applied in the field of two-dimensional high-performance liquid chromatography system, can solve problems such as difficult to fully utilize peak capacity, difficult to achieve column head focusing, complex flow path design, etc., to achieve simplified pretreatment Process, reduce accidental error, good separation effect
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Embodiment 1
[0039] Embodiment 1: Single column separation condition optimization
[0040] Prepare a mixed solution of standard samples containing 25 components, including 12 kinds of hydrophilic samples (uracil, uridine, pseudouridine, palmatine hydrochloride, nicotine, proparolol, atenolol, p-chlorobenzoic acid, p-hydroxybenzene Formic acid, hippuric acid, isonicotinic acid, Trp-Phe) and 13 kinds of hydrophobic samples (benzene, phenol, 2,6-dimethylphenol, toluene, o-chlorotoluene, 1,2,4-trimethylbenzene, biphenyl , 4-chlorobiphenyl, naphthalene, 2,3-dimethylnaphthalene, acenaphthene, pyrene, fluoranthene).
[0041] The mixture of standards was separated on a single column.
[0042] The HILIC column separation conditions are as follows: Atlantis TM HILIC Silica column (3μm, 2.1×150mm), phase A 100mM NH 4 Aqueous COOH, phase B acetonitrile. Gradient elution (93% B phase maintained for 8 min, then decreased to 85% B within 12 min, maintained for 5 min). The flow rate is 0.25mL / min, a...
Embodiment 2
[0045] The trapping capacity investigation of embodiment 2 component transfer column
[0046] Using the HILIC column as the first-dimensional analysis column, according to the single-column separation spectrum, it is determined that the switching time of the ten-way valve is 2.7 minutes. A C18 chromatographic column (column length 50mm) with the same inner diameter and packing material is used for the transfer of hydrophobic samples between two dimensions. In order to investigate the ability of the component transfer column to capture this part of the component, a detector is connected to the ⑤ position of the six-way valve to observe whether there is component outflow. The volume of the mixer connected to P5 in the flow path is 2.6mL, and the flow rate of P5 is set to 0.75mL / min. Therefore, starting from the switching of the ten-port valve, after 3.5min, all the residual components in the mixer will be flushed to the group. onto the transfer column. If the column cannot cap...
Embodiment 3
[0047] Example 3 The mixed standard sample was separated by a simultaneous separation flow platform.
[0048] According to the separation optimization results of a single column, the analysis conditions were set as follows. The flow path is shown in Figure 1. The first dimension uses a HILIC column, and the mobile phase conditions are the same as in Example 1. The second dimension uses RP column, mobile phase A is water, and other chromatographic conditions are the same as in Example 1, but compared with Example 1, the gradient is delayed by 6.2 min. The flow rate of the pump 5 was set at 0.75 mL / min, and the mobile phase was an aqueous solution containing 5% acetonitrile. The switching time of the ten-way valve is 2.7 minutes, and the switching time of the six-way valve is 6.2 minutes. The first-dimension detector adopts a semi-micro detection cell, the second-dimension detector adopts a conventional detection cell, and the detection wavelength is 254nm. as attached Fig...
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