A kind of detection method of gum medicinal material
A technology of glue-like medicinal materials and detection methods, which is applied in the directions of measuring devices, material separation, and analytical materials, etc., can solve problems affecting the diet and drug safety of the masses, lack of technical support for identification, and difficulty in identifying the source of animal skins. Achieve the effect of high sensitivity, strong specificity and simple operation
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Embodiment 1
[0060] Take about 10 mg of deer, donkey, horse, cow and pig respectively, add 5 ml of phosphate buffer solution, dissolve the sample completely by ultrasonication, centrifuge at 12000 rpm for 20 min, take 150 μl of the supernatant, put it in a 2 ml centrifuge tube, and dissolve it with 1 ml of 50 mM PBS Dilute, add 1% trypsin (w / v), shake well, enzymolyze at 37°C for 12 hours, add 60μl of 10% TFA solution after enzymolysis, centrifuge at 12000rpm for 20min, and obtain deer, donkey, horse, cow and pig enzymes solution and stored at -20°C.
[0061] The deer, donkey, horse, cattle and pig enzymatic hydrolyzate were injected into the liquid chromatography-mass spectrometer in sequence, and the injection volume was 1 μg. μm×100mm), flow rate 0.3ml / min, mobile phase A (acetonitrile), mobile phase B (0.1% formic acid), 0~5min, 5~25%A linear gradient elution, 5~6min, 25~5%A Linear gradient elution, 6 ~ 7min, 5% A elution. The mass spectrometry conditions detected by the liquid mass ...
Embodiment 2
[0065] Embodiment 2 Deerskin Glue Authenticity Identification and Doping Situation
[0066] Take 4 batches of commercially available buckskin glue samples, about 10 mg for each batch, add 5 ml of phosphate buffer, ultrasonically dissolve the samples completely, centrifuge at 12000 rpm for 20 min, take 150 μl of the supernatant, and put it in a 2 ml centrifuge tube. Dilute with 1ml of 50mM PBS, add 1% trypsin (w / v), shake well, enzymatically hydrolyze at 37°C for 12 hours, add 60 μl of 10% TFA solution after enzymolysis to stop the reaction, centrifuge at 12000rpm for 20min, and obtain the deerskin glue medicinal enzyme The solution was stored at -20°C for later use.
[0067] The deerskin gum enzymatic hydrolysis solution was injected into the LC-MS instrument, the injection volume was 1 μg, and the liquid phase conditions detected by the LC-MS instrument were: the chromatographic column was a 1.7 μm C18 reverse-phase chromatographic column (2.1 μm×100 mm), and the flow rate wa...
Embodiment 3
[0085] Embodiment 3 donkey-hide gelatin authenticity identification and doping situation
[0086] Take 6 batches of commercially available donkey-hide gelatin samples, about 10 mg for each batch, add 5 ml of phosphate buffer, ultrasonically dissolve the samples completely, centrifuge at 12000 rpm for 20 min, take 150 μl of the supernatant, put it in a 2 ml centrifuge tube, and dilute it with 1 ml Dilute with 50mM PBS, add 1% trypsin (w / v), shake well, ultrasonically hydrolyze for 10min, add 60μl of 10% TFA solution after enzymolysis to stop the reaction, centrifuge at 12000rpm for 20min, and obtain the enzymatic hydrolyzate of donkey-hide gelatin, and place in- Store at 20°C for later use.
[0087] The donkey-hide gelatin enzymatic solution was injected into the LC-MS instrument, and the injection volume was 1 μg. The liquid phase conditions detected by the LC-MS instrument were: the chromatographic column was a 1.7 μm C18 reverse-phase chromatographic column (2.1 μm×100mm), a...
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