Method for detecting cocaine by using quartz crystal microbalance
A quartz crystal and microbalance technology, applied in the field of biosensors, can solve problems such as easy addiction, high toxicity, physical and psychological damage, and achieve the effects of saving manpower, realizing high automation, and reducing costs
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Embodiment 1
[0024] Step 1. Soak the cleaned gold-based QCM chip in 100 μL DNA assembly solution and incubate for 2 hours, then take out the QCM chip, rinse it with ethanol, and dry it with nitrogen to obtain a QCM chip with surface self-assembled DNA; the DNA assembly The solution is prepared by mixing DNA, NaCl and PBS buffer solution with a pH value of 7.2 at a concentration of 0.1M. The concentration of NaCl in the DNA assembly solution is 0.2M, and the concentration of DNA is 0.2 μM; the DNA is sulfhydryl-modified DNA, The DNA sequence (SEQ ID NO.1) is: 5'-TCA CAG ATG AGT AAA AAA AAA AAA-3';
[0025] Step 2. At room temperature, incubate the QCM chip of surface self-assembled DNA described in step 1 with an ethanol solution of 2 μM mercaptopolyethylene glycol for 2 h to seal the redundant sites on the chip surface, then take out the QCM chip and use Rinse with ethanol and blow dry with nitrogen;
[0026] Step 3. Dissolve 0.1mol (11.5g) of NHS in 250mL of dichloromethane, magnetically...
Embodiment 2
[0031] Step 1. Soak the cleaned gold-based QCM chip in 100 μL DNA assembly solution and incubate for 2 hours, then take out the QCM chip, rinse it with ethanol, and dry it with nitrogen to obtain a QCM chip with surface self-assembled DNA; the DNA assembly The solution is prepared by mixing DNA, NaCl and PBS buffer solution with a pH value of 7.2 at a concentration of 0.1M. The concentration of NaCl in the DNA assembly solution is 0.2M, and the concentration of DNA is 0.2 μM; the DNA is sulfhydryl-modified DNA, The DNA sequence (SEQ ID NO.1) is: 5'-TCA CAG ATG AGT AAA AAA AAA AAA-3';
[0032] Step 2. At room temperature, incubate the QCM chip of surface self-assembled DNA described in step 1 with an ethanol solution of 2 μM mercaptopolyethylene glycol for 2 h to seal the redundant sites on the chip surface, then take out the QCM chip and use Rinse with ethanol and blow dry with nitrogen;
[0033] Step 3. Dissolve 0.1mol (11.5g) of NHS in 250mL of dichloromethane, magnetically...
Embodiment 3
[0038] Step 1. Soak the cleaned gold-based QCM chip in 100 μL DNA assembly solution and incubate for 2 hours, then take out the QCM chip, rinse it with ethanol, and dry it with nitrogen to obtain a QCM chip with surface self-assembled DNA; the DNA assembly The solution is prepared by mixing DNA, NaCl and PBS buffer solution with a pH value of 7.2 at a concentration of 0.1M. The concentration of NaCl in the DNA assembly solution is 0.2M, and the concentration of DNA is 0.2 μM; the DNA is sulfhydryl-modified DNA, The DNA sequence (SEQ ID NO.1) is: 5'-TCA CAG ATG AGT AAA AAA AAA AAA-3';
[0039] Step 2. At room temperature, incubate the QCM chip of surface self-assembled DNA described in step 1 with an ethanol solution of 2 μM mercaptopolyethylene glycol for 2 h to seal the redundant sites on the chip surface, then take out the QCM chip and use Rinse with ethanol and blow dry with nitrogen;
[0040] Step 3. Dissolve 0.1mol (11.5g) of NHS in 250mL of dichloromethane, magnetically...
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