Application of polydopamine-modified silver nanoparticle in mass spectrometry detection
A silver nanoparticle and nanoparticle technology, applied in the field of mass spectrometry detection, to achieve the effect of enhancing desorption ionization ability, simple operation and broad application value
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Embodiment 1
[0043] Example 1. Preparation of AgNPs@PDA nanoparticles
[0044] Weigh 0.4g of dopamine and dissolve it in a round bottom flask containing 25mL of water, and adjust the pH to 7.8.
[0045] Prepare 0.01g / mL silver nitrate solution (the solvent is water), slowly drop 4mL into a round bottom flask, and collect samples after reacting at 60°C for 24 hours to obtain AgNPs@PDA nanoparticles. If the dripping method is not used, the obtained AgNPs are coral-like materials, such as figure 1 shown in a.
[0046] The TEM image of the prepared AgNPs@PDA nanoparticles is as follows figure 1 As shown in b, 1c, it can be seen from the figure that the AgNPs@PDA particles are spherical with a diameter between 85-110nm, the thickness of polydopamine is about 6.5nm, and the surface of polydopamine is attached with 3-5nm AgNPs, which can be clearly seen Lattice lines of silver.
[0047] AgNPs@PDA nanoparticles have good dispersibility in water, methanol, acetonitrile and other solvents, and can be evenl...
Embodiment 2
[0048] Example 2. Using AgNPs@PDA as the MALDI matrix to detect PA (18:0 / 18:0), the example uses AgNPs@PDA's own silver cluster peak calibration instrument.
[0049] Matrix dispersion: Weigh 2 mg of AgNPs@PDA particles prepared in Example 1 and dissolve in 1 mL of acetonitrile / water (80 / 20, v / v), and ultrasonically disperse for 20 minutes.
[0050] The preparation concentration is 10 -3 M phosphatidic acid PA (18:0 / 18:0) standard solution.
[0051] The matrix dispersion and the prepared standard solution were mixed according to the volume ratio of 1:1, and 2μL was spotted on the MALDI stainless steel target surface and dried at room temperature; sent to the mass spectrometer for analysis.
[0052] Mass spectrometry conditions are: equipped with a 9.4T superconducting magnet Bruker solariX mass spectrometer, laser wavelength 355nm, laser energy 75%, laser spot size 50μm, pulse frequency 150Hz, resolution 200m / z at 200m / z.
[0053] Test results such as figure 2 As shown, it can be seen f...
Embodiment 3
[0055] Example 3. Using AgNPs@PDA as a substrate to detect mouse brain lipid extract in positive ion mode
[0056] Refer to Example 2 for the preparation method of the matrix dispersion.
[0057] Lipid extraction: prepare mouse brain homogenate (200mg / mL), add 50μL of homogenate to 450μL of methanol, vortex for 1min, let stand for 5min, then vortex for 1min, and centrifuge for 10min in a centrifuge (1000g, 4℃) ). The supernatant was collected, dried with nitrogen, and re-dissolved in 200 μL of methanol.
[0058] The matrix solution and the re-dissolved lipid extract were mixed in a ratio of 1:1 (v / v), and then 2 μL was sampled on the MALDI stainless steel target surface with a pipette, dried at room temperature, and sent to the mass spectrometer for analysis.
[0059] Mass spectrometry conditions are: equipped with a 9.4T superconducting magnet Bruker solariX mass spectrometer, laser wavelength 355nm, laser energy 75%, laser spot size 50μm, pulse frequency 150Hz, resolution 200m / z at...
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