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Envirochek® Sampling Capsule Protocol

This bulletin describes the recommended method of use of the Envirochek capsule for the concentration and recovery of Giardia sp. cysts and Cryptosporidium sp. oocysts from water.

CAUTION: This method does not address all of the safety concerns that are associated with pathogen concentrating and testing. It is the responsibility of the user of this device and method to determine and employ all applicable safety measures to ensure the safety of themselves and others. Check for regulatory limitations that may apply prior to using this device.

1.0 Sample Collection Materials

1.1 Envirochek sampling capsule, one filter per sample. The filters are not reusable.

1.2 Hose-type tubing 12.7 mm (0.5 in.) I.D. Tygon® formula R-3603 (clear laboratory tubing) or equivalent.

1.3 Clamps

1.4 Water Meter (flow totalizer)

1.5 Flow control valve, 2L/min (0.5 gal/min)

1.6 Pump, electric or gasoline powered

1.7 Laboratory shaker (See Figure 2) with arms or equivalent agitation apparatus (Pall Life Sciences Part No. 4821 or 4822.)

1.8 Ice chest or cooler with cold packs

1.9 250 mL conical centrifuge tube

1.10 50 mL polypropylene tubes

1.11 Elution Buffer

  • 1 g Laureth-12 (Pall Life Sciences Part No. 4820)
  • 10 mL 1 M Tris, pH 7.4 (See 1.11.1)
  • 2 mL 0.5 M EDTA, 2 Na, pH 8.0 (See 1.11.2)
  • 150 µL Antifoam A
  • 1 L Deionized (DI) Water

1.11.1 Preparation of 1 M Tris, pH 7.4: Dissolve 121.1 g Tris in 700 mL DI water and adjust pH to 7.4 using 1 N HCL or NaOH. Filter-sterilize the sample through a 0.2 µm membrane (Pall Life Sciences Part Number 4632) into a sterile plastic container and store at room temperature.

1.11.2 Preparation of 0.5 M EDTA, 2 Na, pH 8.0: Dissolve 186.1 g ethylenediamine tetraacetic acid, disodium salt dihydrate in 800 mL and adjust to pH 8.0 with 1 N HCL or NaOH.

Preparation of buffer solution: Weigh 1 g Laureth-12 in a glass beaker and add 100 mL of DI water. Heat the beaker to melt the Laureth-12 using a hot plate or microwave and transfer the solution to a 1000 mL volumetric flask. Rinse the beaker several times to ensure the transfer of the detergent to the cylinder. Add 10 mL of Tris solution, pH 7.4; 2 mL of EDTA solution, pH 8.0; and 150 µL Antifoam A. Bring solution to a final volume of 1000 mL with DI water. The buffer will have an opaque appearance.


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2.0 Sample Collection

2.1 Retain the green vinyl caps provided with the Envirochek capsule for sample shipping and the elution process.

2.2 The exact installation is dependent on whether the water is from a pressurized water source. If the source is not pressurized, a pump is required. If a pump is required, the system will appear as in Figure 1a. If a pump is not required, the system will appear as in Figure 1b.

2.3 Before connecting the sampling system to the pressurized system or sample source, turn the pressurized system or pump on, allowing water to purge residual debris from the water lines for 2-3 minutes, or until the turbidity becomes uniform.

2.4 Turn off the pressurized source or pump and connect the sampling system without the Envirochek capsule.

2.5 Turn on the pressurized source or pump and adjust the flow rate to 2 L/min.

2.6 Allow approximately 76 L (20 gal) to flush the system.

2.7 Install the Envirochek capsule in line, securing the inlet and outlet ends with the appropriate fittings/clamps.

2.8 With a water-resistant marking pen, record the sampling location, name of the person performing the sampling, date, meter reading and turbidity of the sample on the label provided on the filter housing.

2.9 Initiate water flow.

2.10 Vent the residual air using the bleed valve by turning it in a counter clockwise direction. When the filter housing is full of water, close the bleed valve.


Figure 1a: Assembly of Envirochek sampling system with pump.

 


Figure 1b: Assembly of Envirochek sampling system without pump.

 

2.11 After you have collected your sample through the Envirochek capsule, shut off your water source. Allow the pressure to decay until flow stops.

2.12 Record the stop time and final meter reading in the appropriate spaces on the label on the filter.

2.13 Disconnect the inlet end of the Envirochek capsule, making sure not to spill any of the water remaining in the capsule. This water is part of your sample.

2.14 Seal the inlet of the capsule with the green vinyl end cap that was saved from step 2.1.

2.15 Loosen the outlet end and allow water to drain as much as possible. Water drainage from the capsule through the outlet is acceptable as the sample has passed through the membrane.

2.16 Seal the outlet of the capsule with the green vinyl end cap that was saved from step 2.1.

2.17 The Envirochek capsule should be placed on cold packs for storage or transport to the testing facility.

NOTE:Sample should be stored at 0°C - 8°C from time of filtration. Sample testing must be completed within 36 hours of sample collection.


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3.0 Elution Method

3.1 Assemble the laboratory shaker with the arms at full extension and the clamps aligned in a vertical position so that the capsules will be aligned horizontally as demonstrated in Figure 2.


Figure 2: Proper assembly of laboratory shaker.

3.2 Prepare sufficient elution buffer so all the samples to be eluted that day can be eluted with the same stock elution buffer solution. (See 1.11.)


Diagram 1: Elution buffer level.

3.3 Designate a 250 mL conical centrifuge tube for each sample and label with the sample number.

3.4 If the upper chamber of the capsule has water remaining in it, carefully decant this water into an appropriately labeled conical centrifuge tube to be used in section 4.0.

3.5 Hold the capsule in a vertical position with the inlet end up by using a ring stand or other means. Remove the end cap.

3.6 Add elution buffer to the inlet end of the capsule and allow the elution solution level to stabilize. Sufficient elution buffer should be added to the capsule to ensure the covering of the pleated white filter module by 12.7 mm (0.5 in.) (See Diagram 1.) Replace the green vinyl end cap to the inlet end of the capsule.

3.7 Securely clamp the capsule in one of the clamps on the shaker such that the bleed valve is facing toward you. Make sure the bleed valve is in the 12 o'clock position (See Figure 3.)

3.8 Turn on the shaker and set the speed at approximately 600 rpm and agitate for 5 minutes.

3.9 Remove the capsules from the shaker. Carefully remove the inlet end cap and decant the contents of the capsule into a 250 mL conical centrifuge tube.

3.10 Add elution buffer to the inlet end of the capsule and allow the elution solution level to stabilize. Sufficient elution buffer should be added to the capsule to ensure the covering of the pleated white filter module by 12.7 mm (0.5 in.) (See Diagram 1.) Replace the green vinyl end cap to the inlet end of the capsule.

 


Figure 3: Proper orientation of Envirochek capsule during the first cycle of the elution procedure.

3.11 Again secure the capsule in one of the clamps on the shaker such that the bleed valve is facing toward you. This time, make sure the bleed valve is in either the 3 or 9 o'clock position (See Figure 4.).

3.12 Turn on the shaker and set the speed at approximately 600 rpm and agitate for 5 minutes.

3.13 As before, remove the capsules from the shaker, carefully remove the inlet end cap, and decant the contents of the capsule into the same 250 mL conical centrifuge tube used for that sample.


Figure 4: Proper alignment of Envirochek capsule during the second cycle of the elution process.


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4.0 Concentration: Adjustment of pellet volume

4.1 Spin the sample at 1000-1100 x G for 10-15 minutes. Allow the centrifuge to coast to a stop. DO NOT USE THE BRAKE!

4.2 Record the volume of the pellet with date and the time that the concentration was completed. Use a Pasteur pipette to carefully remove the supernatant to just above the pellet.

4.2.1 If the pellet volume (volume of solid) is 0.5 mL or less, add reagent water to the centrifuge tube to bring the volume up to 10 mL. To resuspend the pellet, vortex the tube for 10-15 seconds. Proceed to step 5.0.

4.2.2 If the pellet volume is greater than 0.5 mL, use the equation below to determine how much reagent water needs to be added to the centrifuge tube to adjust the pellet to 0.5 mL:

Total Volume (mL) Required = Pellet Volume X 10 mL

0.5 mL

Add reagent water to the centrifuge tube to the calculated volume above. Vortex the centrifuge tube for 10-15 seconds to resuspend the pellet. Record the volume. Using a Pasteur pipette, reduce the resuspended volume to 10 mL (which will contain 0.5 mL of solids). Proceed to step 5.0.


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5.0 Detection

5.1 The sample is now ready for the detection stage of the process. Refer to the current approved detection method for your region.

Reference EPA Method 1622: Cryptosporidium in Water by Filtration/IMS/FA

WARNING: Employment of the products in applications not specified, or failure to follow all instructions contained in this technical bulletin, may result in improper functioning of the product, personal injury, or damage to property or the product. See Statement of Warranty in our most recent catalog.


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