A nucleic acid detection method for food-borne pathogens based on hollow gold-silver core-shell nanoflower SERS nanoprobe HAU/AGSNFS-ATP
A gold-silver core-shell and nano-probe technology, which is applied in the field of photochemical analysis technology and biological detection, to meet the needs of on-site detection, high sensitivity and specificity detection, and achieve the effect of portability
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Embodiment 1
[0037] Example 1 Preparation of SERS nanoprobe HAu / AgSNFs-ATP and establishment of paper-based SERS sensing rapid detection method
[0038] Step 1, HAu / AgSNFs preparation: in 1mL H 3 NO solution (1×10 -2 -6×10 -2M) and 1mL NaOH solution (0.01-0.08M) mixed with 18mL AgNO 3 (0.1-1 M) solution was stirred for 5-20min, then 10mL of HAuCl was added 4 solution (2×10 -4 -10×10 -4 M) and 200 μL C 6 h 5 Na 3 o 7 The solution (0.5%-1.5%, w / v) was reacted at 80-110°C for 5 minutes to obtain HAu / AgSNFs.
[0039] Step 2, functional modification of HAu / AgSNFs: add 30 μL C to 10 mL HAu / AgSNFs aqueous solution 6 h 7 NS alcohol-water mixed solution (0.01-1M), centrifuged after stirring for 15 minutes, washed twice, and finally dispersed in aqueous solution to obtain SERS nanoprobe based on HAu / AgSNFs-ATP.
[0040] Different AgNO 3 The transmission electron microscope images of the HAu / AgSNFs nanoprobes prepared under the concentration figure 1 shown by figure 1 As can be seen, A...
Embodiment 2
[0046] Example 2 Application of Paper-based SERS Sensing Rapid Detection Method
[0047] 2.1 Application of paper-based SERS sensing rapid detection method in bacterial detection
[0048] 2.1.1 Take Staphylococcus aureus, Escherichia coli and Salmonella as examples to conduct qualitative and quantitative detection of bacteria
[0049] 2.1.1.1 Staphylococcus aureus
[0050] Heat the Staphylococcus aureus with a concentration of 0-7cfu / mL to extract the crude DNA, add the crude extract dropwise to the pretreatment area to adsorb the interfering substances in the reaction system, and then fold the device to combine the pretreatment area and the amplification The region overlaps, and the gene amplification is carried out; the total volume of the amplification reaction is 20 μL, which contains a pair of primers P1 and P2 with concentrations of 10 -6 M, the system also includes a concentration of 5 × 10 -4 M dNTPs, 1×Isothermopol Buffer, and Bst 2.0 WarmStart DNA polymerase; the ...
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