Nano cuprous sulfide modified monolithic column material and preparation method thereof
A cuprous sulfide, monolithic column technology, applied in chemical instruments and methods, separation methods, other chemical processes, etc., can solve the problem of poor stability of oxides, inability to use target molecules for affinity enrichment, and limitations of metal oxide affinity chromatography and other problems, to achieve the effects of easy production, increased specific surface area, and strong adsorption
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Embodiment 1
[0029] Example 1: Preparation of monolithic column modified by nano-cuprous sulfide
[0030] Synthesis of the hybrid monolithic column skeleton: wash the quartz capillary with an inner diameter of 530 μm with HCl (0.1mol / L) for 2 hours, wash with water until neutral, wash with 1mol / L NaOH solution for 10 hours, and then wash with water and methanol respectively 0.5 hours, dry at 160°C under nitrogen for 5 hours, then fill the capillary with methanol / 3-(trimethoxysilyl)propyl methacrylate (1:1, v / v), keep at 50°C for 20 hours, washed with methanol for 1 hour, dried at 60°C under nitrogen for 1 hour, and sealed at both ends for use.
[0031] Add 120mg of methacryloyl-POSS cage mixture, 850μL of tetrahydrofuran, 120mg of Pluronic F127, 40μL of vinylimidazole in a centrifuge tube, dissolve it completely by ultrasonication, then add 2.5mg of azobisisobutyronitrile, and pour into the capillary after ultrasonication middle. Both ends were sealed with silica gel and reacted at 60°C ...
Embodiment 2
[0036] Example 2: Comparison of the adsorption effect of nano-cuprous sulfide modified monolithic column with commercial copper ion column and nickel ion column in the adsorption of kanamycin sulfate
[0037] Take 0.5mL nickel ion chelation column material (Ni Sepharose6Fast Flow, GE Healthcare), wash with buffer A (20mM PBS, 0.5M sodium chloride, 50mM EDTA, pH=7.4) three times, each time 1mL. Buffer B (20mM PBS, 0.5M sodium chloride, 5mM imidazole, pH=7.4) was washed three times, each time 1mL. Wash with ultrapure water three times, each time 1mL. The material was then copper ion chelated with 0.5 mL of copper chloride solution (0.1 M). Then wash three times with ultrapure water and buffer B respectively. After the supernatant was removed, 0.1 mL of ethanol was added for preservation, and the copper ion chelation column material was obtained.
[0038] The adsorption capacities of the synthesized nano-cuprous sulfide-modified monolithic columns and the commercialized copper...
Embodiment 3
[0045] Example 3: Nano cuprous sulfide modified monolithic column is used for the enrichment of kanamycin sulfate in milk
[0046] Add 10mL of fresh milk purchased from the supermarket, add kanamycin sulfate to make it 1μg / mL, and let it stand for 10 minutes to make it fully effective, add 1.25mL trichloroacetic acid (10%), vortex for 30s, ultrasonic for 15min, centrifuge Take 150 μL of supernatant for LC-MS detection, then take 6 mL of supernatant, add 350 μL of sodium hydroxide (1M) and 4.23 mL of acetonitrile, centrifuge and remove the supernatant for solid phase extraction.
[0047] Take a 3cm monolithic column modified with nano-cuprous sulfide, equilibrate with pH10 buffer, then load 1.5mL of sample, 0.1mL of 90% acetonitrile for weak washing, and then 100μL of eluent (80mM ammonium formate, 0.16% acetic acid, 20% acetonitrile) Eluted and used for LC-MS analysis. Figure 5 The MRM charts were detected for kanamycin sulfate before and after enrichment.
[0048] The mono...
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