Residue testing method for levamisole hydrochloride in different tissues of aquatic product
A technology of levamisole hydrochloride and a detection method, which is applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of human health hazards, residues, and detection method system research that have not been reported, so as to reduce reagent waste, improve recovery rate, Detecting the effects of faster analysis
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2015-10-28
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
Figure 1 Figure 2 Figure 3
Abstract
Description
technical field
[0001] The invention belongs to the technical field of detection methods for levamisole hydrochloride, in particular to a detection method for detecting levamisole hydrochloride in aquatic product tissues by using ultra-high performance liquid chromatography. Background technique
[0002] Levamisole hydrochloride, English name: Levamisole Hydrochloride, molecular formula: C11H12N2S·ClH, molecular weight: 240.757, chemical structure as figure 1 shown. Chinese alias: (S)-6-phenyl-2,3,5,6-tetrahydro-imidazol[2,1-B]thiazole monohydrochloride; L-2,3,5,6-tetrahydro- 6-Phenylimidazol[2,1-6]thiazole hydrochloride; Anthelmintic speed; Levotetramisole; (S)-(-)-6-Phenyl-2,3,5,6-tetrahydroimidazo [2,1-b]thiazole hydrochloride; levamisole hydrochloride; L-2,3,5,6-tetrahydro-6-phenylimidazo(2,1-B)thiazole hydrochloride; hydrochloric acid Levamisole.
[0003] Levamisole hydrochloride is the L-isomer of tetramisole, and its activity is about 1 to 2 times that of tetramis...
Examples
Embodiment 1
[0055] Embodiment 1. Ultra-high performance liquid chromatography conditions--a comparative experiment of mobile phases with different ratios.
[0056] (1) Chromatographic conditions other than mobile phase
[0057] Instrument: Waters ACQUITY UPLC (with UV detector);
[0058] Chromatographic column: Waters BEH C18 (2.1mm×50mm, particle size 1.7μm);
[0059] Column temperature: 35°C;
[0060] Injection volume: 5 μL.
[0061] UV detection wavelength: 214nm.
[0062] Flow rate: 0.4mL / min;
[0063] (2) Different mobile phase composition
[0064] The ratios of phosphoric acid solution at pH 7.0 to acetonitrile were 90:10, 85:15, and 80:20, respectively.
[0065] (3) Results
[0066] Chromatographic analysis results such as image 3 , as shown in the figure, when the mobile phase changes, the chromatographic peak changes accordingly, and the pH=7.0 phosphoric acid solution is selected in this experiment. The ratio of phosphoric acid solution and acetonitrile in the mobile p...
Embodiment 2
[0067] Embodiment 2. Comparison of chromatographic behavior of levamisole hydrochloride on UPLC and traditional HPLC.
[0068] (1) UPLC chromatographic conditions
[0069] Instrument: Waters ACQUITY UPLC (with UV detector);
[0070] Chromatographic column: Waters BEH C18 (2.1mm×50mm, particle size 1.7μm);
[0071] Mobile phase: 0.05mol / L phosphoric acid (adjust pH to 7 with triethylamine): acetonitrile=85:15(V / V);
[0072] Column temperature: 35°C;
[0073] Injection volume: 5 μL.
[0074] UV detection wavelength: 214nm.
[0075] Flow rate: 0.4mL / min;
[0076] (2) HPLC chromatographic conditions
[0077] Instrument: Waters 1525 (with UV detector);
[0078] Chromatographic column: Waters symmetry C18 (4.6mm×150mm, particle size 5μm);
[0079] Mobile phase: 0.05mol / L phosphoric acid (adjust pH to 7 with triethylamine): acetonitrile=75:25(V / V);
[0080] Column temperature: 35°C;
[0081] Injection volume: 20 μL.
[0082]UV detection wavelength: 214nm.
[0083] Flow ra...
Embodiment 3
[0094] Embodiment three, the comparison of levamisole hydrochloride extractant in the aquatic product plasma.
[0095] (1) Chromatographic conditions
[0096] Instrument: Waters ACQUITY UPLC (with UV detector);
[0097] Chromatographic column: Waters BEH C18 (2.1mm×50mm, particle size 1.7μm);
[0098] Mobile phase: 0.05mol / L phosphoric acid (adjust pH to 7 with triethylamine): acetonitrile=85:15(V / V);
[0099] Column temperature: 35°C;
[0100] Injection volume: 5 μL.
[0101] UV detection wavelength: 214nm.
[0102] Flow rate: 0.4mL / min;
[0103] (2) Experimental steps
[0104] Accurately draw 1 mL of the plasma sample and place it in a 15 mL centrifuge tube, add 1 mL of borate buffer (pH=9) to the centrifuge tube, then add 10 mL of ethyl acetate / acetonitrile to the centrifuge tube, vortex for 2 minutes, Centrifuge in a centrifuge at 4000r / min for 5 minutes, transfer the supernatant in the centrifuge tube to a BUCHI 48-position parallel evaporator vacuum tube; add 5 mL...