Method for detecting insecticide resistance of schistosoma japonicum eggs to praziquantel in vitro
An in vitro detection, praziquantel technology, applied in biological testing, material inspection products, etc., can solve the problems of drug resistance, long time, missed inspection and missed treatment, etc., to achieve the effect of solving on-site detection and monitoring, and solving technical problems
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Embodiment 1
[0011] Embodiment 1: Sensitivity determination of eggs of Schistosoma japonicum praziquantel sensitive strains to praziquantel
[0012] Take two 50 mL flasks and transfer them into 5×10 -6 mol / L praziquantel normal saline and a single reference normal saline, add 1000~2000 eggs collected from feces of hosts infected with Schistosoma japonicum Sichuan sensitive strain, put them in a dark environment at 28°C for 24 h, and then place The eggs were transferred into fresh dechlorinated tap water, and the miracidia were hatched under the irradiation of incandescent lamp at 28 °C. Every 30 minutes after the hatching started, the tap water containing miracidia was collected with a 50 mL centrifuge tube, a few drops of Lugol's iodine solution was added and centrifuged, the collected miracidia were observed and counted under a microscope, and the egg hatching rate was calculated. The experiment was repeated three times. The results show that in warp 5×10 -6 After mol / L praziquantel...
Embodiment 2
[0013] Embodiment 2: Sensitivity determination of eggs of Schistosoma japonicum praziquantel sensitive strains to praziquantel
[0014] Take two 50 mL flasks and transfer them into 5×10 -6 mol / L praziquantel normal saline and a single reference normal saline, 1000-2000 eggs collected from the feces of hosts infected with Schistosoma japonicum Anhui sensitive strains were added to the flask, placed in a dark environment at 28°C for 24 h, and then placed The eggs were moved into fresh dechlorinated tap water, and the miracidia were hatched under the irradiation of incandescent lamp at 28°C. After the hatching started, the tap water containing miracidia was collected once every 30 min with a 50 mL centrifuge tube, after adding a few drops of Lugol's iodine solution, centrifuged, the collected miracidia were observed and counted under a microscope, and the egg hatching rate was calculated. The experiment was repeated three times. The results show that in warp 5×10 -6 After mo...
Embodiment 3
[0015] Embodiment 3: Sensitivity determination of eggs of Schistosoma japonicum praziquantel sensitive strain to praziquantel
[0016] Take two 50 mL flasks and transfer them into 5×10 -6 mol / L praziquantel normal saline and a single reference normal saline, 1000-2000 eggs collected from the feces of hosts infected with Schistosoma japonicum Hunan sensitive strains were added to the flask, placed in a dark environment at 28 ℃ for 24 h, and then placed The eggs were moved into fresh dechlorinated tap water, and the miracidia were hatched under the irradiation of incandescent lamp at 28°C. After the hatching started, the tap water containing miracidia was collected once every 30 min with a 50 mL centrifuge tube, after adding a few drops of Lugol's iodine solution, centrifuged, the collected miracidia were observed and counted under a microscope, and the egg hatching rate was calculated. The experiment was repeated three times. The results show that in warp 5×10 -6 After bei...
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