A microfluidic chip for Raman detection of methamphetamine in hair and its application method
A microfluidic chip, methamphetamine technology, applied in Raman scattering, chemical instruments and methods, laboratory containers, etc., can solve the problems of false positives, short detection time, etc., and achieve reliable detection results and less consumables. , Easy to carry and use
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Embodiment 1
[0039] see figure 1 , figure 2 , the device structure of the present invention is as follows:
[0040]The main body is in the shape of a cuboid (length X width: 31.5X 15.75mm), which is divided into upper and lower layers, including a base sheet A and a cover sheet B, and the two layers can realize sealed alignment bonding.
[0041] Substrate A includes: labeling solution pool 1 for immunogold sol, washing solution pool 2 for buffer solution, sample reaction and Raman detection area 4, waste solution pool 5 for stop solution , for the detection solution pool 6 of the immune magnetic antibody, for the detection solution pool 7 of the test solution for the hair extraction, wherein:
[0042] The waste liquid pool 5 is located at the rightmost end of the chip, and is connected to the detection area 4 on the left side through the fourth channel 4-1. A magnet is placed on the back of the detection area 4, and the washing liquid pool 2 is located at the leftmost end of the chip. ...
Embodiment 2
[0049] The nanoparticle preparation process of labeled immunogold is;
[0050] Take 49.5ml ultrapure water + 0.5ml HAuCl 3 Stir and disperse evenly, heat and condense to reflux, add 0.5ml Na at one time 3 Cit (trisodium citrate), the color first turns black, purple black, and finally purple red, and then condenses and refluxes for 15 minutes to obtain Au sol with a particle size of about 35nm; take 1ml Au sol + 2.5μl 1mM MBA and incubate for 1.5h, and then centrifugally disperse Add 2 μl 5 μg / ml methamphetamine antigen and incubate for 3.5 hours, disperse by centrifugation, and resuspend in 1 ml of phosphate buffer; add 10 μl of 10% BSA for incubation for 1 hour, and disperse by centrifugation in 1 ml of phosphate buffer.
[0051] The preparation process of the immunomagnetic nanoparticle solution is as follows:
[0052] Take 0.68g FeCl 3 +0.2g Na 3 Cit+20ml EG (ethylene glycol) ultrasonically dissolve, add 1.2g CH 3 COONa was stirred and mixed, and reacted with hydroth...
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