Preparation method and application of porous silicon material for biological sample pretreatment
A biological sample and porous silicon technology, which is applied in the preparation of test samples, analysis of materials, and material analysis by electromagnetic means, etc., can solve the problems of difficult to achieve large-area ordered vertical pore preparation and small adjustable range of pore diameter. , to reduce degradation and non-specific molecular interference, reduce interference, and achieve a wide range of applications
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Embodiment 1
[0034] 1) Fix the P-type boron-doped crystal silicon wafer in the electrolytic cell, add 3ml of ethanol and 40% hydrofluoric acid with a volume ratio of 1:0.05-1:6 as the electrolyte, and use the silicon wafer as the Anode, platinum electrode as cathode, conduct DC electrolytic etching and stripping, set current intensity at 20-50mA cm2, etching time at 1-4min, rinse the porous silicon layer after etching with ethanol, ultrasonically pulverize for 5min, and vacuum dry Porous silicon microparticles with a pore diameter of 5-15 nm, a thickness of 1-10 μm, and a diameter of 10-50 μm are obtained.
[0035]2) Soak the porous silicon particles in 1) in a mixed solution of 10% mass fraction of 3-butenoic acid and toluene solvent, heat and reflux for 2 hours, then soak and wash with ethanol, and obtain 3-butenoic acid after vacuum drying Modified porous silicon materials.
[0036] 3) Soak the porous silicon particles in 1) in a mixed solution of N,N dimethylallylamine and toluene so...
Embodiment 2
[0043] In this example, a porous silicon material with a porosity of 50.4% modified by 3-butenoic acid is used as the enrichment material to remove the high peak protein in human serum, and the specific steps are as follows:
[0044] 1), sample adsorption
[0045] Human serum was diluted 10 times with deionized water as the test solution.
[0046] Adsorption: 10 mg of porous silicon material with a porosity of 50.4% modified by 3-butenoic acid was added to 30 μL of the solution to be tested, and incubated together for 1 h at room temperature with shaking. The above suspension was left to stand for 2 min, and after the porous silicon particles settled to the bottom of the centrifuge tube, the supernatant was removed with a pipette gun.
[0047] Washing: add 100 μL of washing buffer (PBS buffer at pH 7.4) to the centrifuge tube, vortex and shake, let the suspension stand for 2 min, and carefully remove the supernatant with a pipette gun. Add 100 μL of deionized water to the ce...
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