Sampling filtering bag for cryptospsridium and giardia detection in water
A technology of filter capsules and filter cups, which is applied in the field of filter capsules for detection and sampling of two insects in water, can solve the problems that the detection recovery rate is less than 40%, the recovery rate and detection efficiency are not up to the ideal state, and the detection process is cumbersome, etc. The effect of detection recovery, low detection cost, and less eluent volume
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[0021] as attached figure 1 , 2 As shown, the filter capsule for detection and sampling of two insects in water of the present invention is mainly composed of an upper filter cup 1 , a lower filter cup 2 , a sealing rubber ring 3 , a filter paper 4 and a mesh filter bed 5 .
[0022] The open end of the upper filter cup 1 is docked with the open end of the lower filter cup 2, and is sealed and connected by a sealing rubber ring 3.
[0023] The top of the upper filter cup 1 is the water inlet 6, and the bottom of the lower filter cup 2 is the water outlet 7.
[0024] The filter paper 4 and the mesh filter bed 5 are arranged on the open end of the lower filter cup 2 from top to bottom. Between the open end of cup 1 and the open end of lower filter cup 2. The diameter of the filter paper 4 is slightly larger than the diameter of the inner circle of the open end of the upper filter cup 1, and the diameters of the two are 10cm and 9.8cm respectively.
[0025] The filter paper 4 ...
experiment example
[0034] Take 1 part of 100L deionized water and add the standard samples of two worms (Giardia and Cryptosporidium) respectively. There are 100 Giardia and Cryptosporidium in the water sample, for example image 3 As shown, connect the two worm sampling devices, adjust the flow rate to 2000 mL / min, start the peristaltic pump for sampling and filtration, so that the water samples flow out through the filter paper 4, and wait until all the water samples pass through the filter paper 4. After rinsing the upper filter cup with about 1L of pure water, remove the filter paper 4 into a 1000 mL glass stoppered Erlenmeyer flask, add 150 mL of the prepared eluent, cover the sealing plug, and ultrasonically shake for 15 minutes at a temperature of 40 °C . After the ultrasonic vibration stops, open the sealing plug, pour out the eluate into the centrifuge tube, start centrifugal concentration, and finally use the immunomagnetic separation method to stain and prepare slices, count with a fl...
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