The intended use for the IsoFlux™ Enhanced CTC Enrichment Kit is as a general-purpose laboratory reagent for dilution of blood samples to enrich for circulating tumor cells (CTCs). The kit is used with the IsoFlux System, a bench-top instrument for semiautomated cell isolation. The kit contains an immunomagnetic bead reagent targeted towards cells of epithelial origin. The Enhanced CTC kit is for Research Use Only.
SUMMARY AND EXPLANATION
Circulating tumor cells (CTCs) are cancer cells that shed from a primary or metastatic tumor and enter the peripheral circulation. Carcinomas are cancers of epithelial origin and include breast, prostate, lung, and colorectal cancers. These tumors shed CTCs that are of epithelial origin. CTCs are distinct from other blood cells since cells of epithelial origin are not normally found in the circulation.
The IsoFlux Enhanced CTC Enrichment Kit is designed to standardize and automate the enrichment of CTCs from biological samples using the IsoFlux System. CTCs are enriched from the sample using an immunomagnetic capture reagent while the sample flows through a microfluidic cartridge designed for cellular isolation. The kit produces an enriched cell pellet that can subsequently be used for further testing.
PRINCIPLES OF THE PROCEDURE
The IsoFlux Enhanced CTC Kit contains immunomagnetic capture beads (CTC beads), microfluidic cartridges, and additional reagents required for performing CTC enrichments. The CTC beads consist of two types micro-scale particles with a magnetic core surrounded by a polymeric layer; they are coated with antibodies targeting the EpCAM antigen and a second bead type with a linker chemistry that allows them to also be conjugated to EGFR antibodies. CTCs can be isolated from mononuclear cell suspensions of whole blood or other similar cell samples. CTC beads are then mixed with the cell sample to bind to the target cells during a period of incubation.
The cell sample and beads mixture is loaded onto the microfluidic cartridge and processed with the IsoFlux instrument, where the cells pass through the fluidic channel of the cartridge. Midway through the fluidic channel is a cell isolation zone that is exposed to an external magnetic field inside the instrument. The target cells having CTC beads attached are attracted towards the magnetic field. The target cells are collected on a removable disk that forms the roof of the isolation zone. After the sample is processed, the enriched cells are transferred inside the instrument to low volume recovery holder or a microfuge tube. The enriched CTCs are ready for further analysis.
- Instructions for Use
- 8 sterile microfluidic cartridges (includes 8 low-volume recovery holders, 8 microfuge tubes for cell recovery)
- 1 tube of 500μL CTC beads* (EpCAM pre-conjugated)
- 1 tube of 500μL RCE (pan mouse IgG) beads* (un-conjugated)
- 1 tube of 500μL Fc blocker reagent*
- 1 tube of 70μL EGFR antibody (EGFR Ab)
- 4 tubes of 12mL sterile preservative free Binding Buffer
*Contains 0.02% sodium azide as a preservative.
REAGENT STORAGE AND HANDLING
- EGFR Ab should be used immediately or store at 4°C.
- CTC, RCE beads and Fc blocker reagents should be stored at 2° to 8°C and used within 60 days after opening.
- Binding Buffer should be stored unopened at 2° to 8°C. After opening, unused buffer may be stored frozen at -20°C, thawed once, and used within 60 days.
- When properly stored, reagents are stable until the expiration date printed on the reagent container, kit box, or otherwise specified above. Do not use expired reagents.
- Protect reagents from heat in excess of 35°C. Do not freeze.
- Protect reagents from exposure to light.
- Microfluidic cartridges should be stored unopened at room temperature.
- Do not mix and match reagents from different kits.
MATERIALS REQUIRED, NOT PROVIDED
- IsoFlux Instrument (Catalog No. 950-0100)
- Permanent magnets (accessory parts included with IsoFlux instrument: large round and small cylindrical magnets)
- Swing bucket centrifuge capable of 1500xg (with brake settings)
- Test tube racks
- Calibrated micropipettes and tips Serological pipettes and pipettor
- 5 or 2mL low retention microfuge tubes (e.g. Protein LoBind tubes Eppendorf Cat. No. 022431081)
- Microfuge tube rotator
- 50mL Leucosep® tubes (with frit/separator) (Greiner, Catalog No. 227290)
- Phosphate Buffer Saline without Ca2+ Mg2+ (PBS-CMF)
- 50mL conical tubes
- Ficoll-Paque™ Plus (GE Healthcare, Catalog No. 17-1440-02)
- Optional: CTL-Wash™ Supplement (CTL, Catalog No. CTLW-010)
- Optional: Benzonase® Nuclease (Sigma, Catalog No. E8263)
- Optional: Nylon Mesh Cell Strainer, 40 Micron (BD, Catalog No. 352340)
WARNINGS AND PRECAUTIONS
- For Research Use Only
- Please read the entire contents of the Instructions for Use before processing samples.
- Caution: Care should be taken to collect and transfer blood samples before processing. Cells are fragile and can be damaged or lost if not handled properly.
- Caution: All personnel should follow universal precautions for biological sample handling and use personal protective equipment (i.e., safety glasses, laboratory coat, gloves, etc.).
- Caution: Microbial contamination of reagents can cause erroneous results and should be avoided.
- Warning: All biological specimens, cartridges and other materials coming into contact with the specimen(s) are considered bio-hazardous. Handle as if capable of transmitting infection. Treat and dispose of waste using proper precautions and in accordance with local, state, and federal regulations. Never pipette by mouth.
- Warning: Some of the reagents contain sodium azide as a preservative. If swallowed, seek medical advice immediately. Keep out of reach of children. Keep away from food and drink. Wear suitable protective clothing. Contact with acids liberates very toxic gas. Azide compounds should be flushed with large volumes of water during disposal to avoid deposits in lead or copper plumbing where explosive conditions can develop.
- Operator training is required to perform the test procedure.
Specimen collection and preparation
- Collect biological samples aseptically into an appropriate sample collection tube.
- If samples are being shipped or transported, pack the samples accordingly to control exposure to excessive temperatures or agitation. Typically, samples can be shipped in an insulated Styrofoam shipping container with cold (not frozen) gel packs as a buffer to temperature fluctuations.
- Depending on the sample type, a pre-processing step might be required such as density centrifugation or red blood cell lysis.
- A typical pre-processing procedure for human whole blood collected in 10mL K2EDTA tube (mononuclear cell fraction preparation) is provided in Section 3. Please consult the manufacturer’s instructions for pre-processing procedure for other cell sample types.
Antibody to Beads Coupling reaction: coating RCE beads with EGFR antibody and CTC beads preparation
This preparation suffices for 8 samples. Antibody-coupled beads are stable at 4°C and should be used within 4 weeks. This preparation is to be used in conjunction with the CTC (EpCAM) beads prepared below. Scale up or down as appropriate.
- Add 60μl of EGFR antibody (EGFR Ab) to the entire tube of RCE (pan mouse IgG) beads (500μL of bead solution). Close the tube.
- Briefly vortex for five seconds. Place the round magnet on one side of the tube so that the beads accumulate. Remove the tube from the magnet and invert several times to resuspend the beads. Repeat this process 10 times. This is referred as ACTIVE MIXING.
- Incubate for 60 minutes at room temp (or overnight at 4°C) with gentle tilting and rotation. The antibody conjugated beads are now referred as EGFR beads. Beads are now ready to be washed and used. Use 30µL of beads suspension per sample. Prepare 40µL per sample to allow room for pipetting. The preparation below suffices for 8 samples. Unused (unwashed) beads may be stored at 4°C and should be used within 4 weeks.
- Resuspend the RCE (EGFR-conjugated) beads stock to a uniform suspension with a micropipette. Dispense 400L of beads stock into a microfuge tube. Place the tube on the round magnet for 15 seconds until all the beads accumulate. With the magnet in place, remove and discard the buffer. Remove the tube from the magnet. Add 800L of Binding Buffer. Place the tube on the magnet for 15 seconds and discard the supernatant. Remove the tube from the magnet. Repeat the wash one more time. Place the tube on the magnet for 15 seconds and discard the supernatant. Resuspend the washed beads in 400L Binding Buffer. Keep on ice until use.
Wash CTC (EpCAM) BeadsµThis preparation suffices for 8 samples to be used in conjunction with the RCE EGFR conjugated beads prepared above. Scale up or down as appropriate.
- Re-suspend the CTC (EpCAM) beads stock to a uniform suspension with a micropipette.
- Dispense 400µL of beads stock into a 1.5mL microfuge tube.
- Place the tube on the round magnet for 15 seconds until all the beads accumulate.
- With the magnet in place, remove and discard the buffer. Remove the tube from the magnet. Add 800μL of Binding Buffer.
- Place the tube on the magnet for 15 seconds and discard the supernatant.
- Remove the tube from the magnet.
- Repeat the wash one more time. Place the tube on the magnet for 15 seconds and discard the supernatant.
- Re-suspend the washed beads in 400µL Binding Buffer. Keep on ice until use.
Pre-processing of whole blood sample (mononuclear cell (MNC) fraction preparation)
- For each sample to be processed coat a microfuge tube with 1mL of Binding Buffer and rotate at 4oC (or room temp) until use.
This is to minimize non-specific binding of cells to the tube. Alternatively if using Protein LoBind tubes (Eppendorf Cat. No. 022431081), coating is not required.
Prepare the 50mL Leucosep® tube by adding 15.2mL of Ficoll-Paque™ PLUS and centrifuging the tube at 1000xg for 30 seconds.
- Only when ready to process the blood sample, gently add 5mL of PBS-CMF to the Leucosep® tube.
- Immediately decant the blood from the blood collection tube into the Leucosep® tube. Gently rinse down the wall of the blood collection tube with 10mL of PBS-CMF. Re-cap and gently invert the blood collection tube several times to mix. Add the rinse to the same Leucosep® tube. Repeat the rinse once more.
- Immediately centrifuge the tubes at 800xg for 15 minutes with the brake setting to OFF. Alternatively centrifugation at 1000xg for 10 minutes may be used.
- Decant the supernatant from Leucosep® tube into a new 50mL conical tube, leaving about 5 to 10mL remaining. Gently swirl the remaining supernatant to dislodge any cells that may be stuck to the wall of the Leucosep® tube and then decant it into the same conical tube. Rinse the wall of the Leucosep® tube with 10mL of PBS-CMF and add that to the same 50mL conical tube. Be mindful not to suction the Ficoll-Paque™ PLUS through the frit; avoid pressing the pipette against the frit. Optional: CTL-Wash™ Supplement may be added to improve cell viability.
- Centrifuge at 280xg for 10 minutes with the brake setting to ON.
- Use a 25 or 50mL serological pipette to gently aspirate off the supernatant as much as possible without disturbing the pellet. Use a smaller pipette to remove the remaining supernatant closer to the bottom of the tube with up to 500l buffer may be left remaining. Alternatively, a vacuum set-up may be used to suction off the supernatant. Keep the pellet on ice. This is considered MNC. We recommend that you do not decant the supernatant, because the pellets might be very loose in clinical samples. Optional: Benzonase® Nuclease (up to 1000 Units per sample) may be added. Addition of nucleases is required for sample that have been stored for ≥24 hours or severely lysed to minimize cell aggregation due to cell lysis.
- Add 50µL of Fc Blocking Reagent to the PBMC sample in the 50mL conical tube above.
- Gently tap the tube on the bench a few times to loosen pellet. Tap patiently until the pellet is completely resuspended. If necessary, add up to 300µL of Binding Buffer to the tube. All cell clumps must be dispersed as they may clog the micro-channel during isolation. Incubate for 5 minutes on ice.
- Remove and discard the Binding from the microfuge tube prepared in Step 3.1. Gently resuspend the cell in the 50mL conical tube with a micropipette setting to no more than 300µL. Transfer the cell suspension into the microfuge tube. Rinse the residual cells in the 50mL conical tube with Binding Buffer and transfer to the same microfuge tube. The final volume should be no more than 1mL.
**IMPORTANT: maximum sample volume is 1mL when loading onto the cartridge. Try to prepare the sample at this step so that the volume is about 800L to allow for additional rinsing when loading onto the cartridge. We recommend using a 200L micropipette with wide-bored tip when transferring to minimize shear force, and allow for estimating the sample volume.
Coupling reaction of beads and cell sample:
- Resuspend the washed CTC beads with a micropipette. Add 30μL of washed CTC beads to the cell suspension.
- Resuspend the washed EGFR beads with a micropipette. Add 30μL of washed EGFR beads to the cell suspension.
- Invert the tube to mix. ACTIVE MIX: Place the round magnet on one side of the tube so that the beads accumulate. Remove the tube from the magnet and invert several times to resuspend the beads. Repeat this process 10 times.
- Incubate for 1 to 2 hours at 4°C with gentle tilting and rotation. The cell sample is now ready for CTC enrichment with the IsoFlux System. Optimum
incubation time is 2 hours. At 1 to 1.5 hours after incubation, the preparation for enrichment (section 5 below) may begin.
CTC enrichment with IsoFlux System
- Refer to the IsoFlux System Instructions for Use and on-screen commands for full instructions to process samples for cell enrichment.
- Power on the IsoFlux instrument. The touch screen panel will light up; the instrument will initialize and perform automatic routine system check. The touch screen will display “Run Protocol” and “Select Protocol” icons when the instrument is ready for use.
- Press “Run Protocol” to run the most recent protocol used (shown at the bottom of the touch screen). Press “Select Protocol” to select the appropriate protocol and then press “Run Protocol”.
- Select the Number of Samples to Run. Cartridge loading carriage(s) will slide out automatically. A total 4 samples can be processed simultaneously. Positions No. 1 and 2 are on the left carriage. Positions No. 3 and 4 are on the right carriage. Samples should be loaded from left to right sequentially from Position No. 1 to 4.
- Remove the microfluidic cartridge from the pouch and position it upright on a flat surface (see drawing below). The plastic retainer helps to keep the removable CellSpot (well No. 4) and sample retrieval Microfuge Tube (well No. 5) in place. The Low-Volume Recovery Holder is attached to the retainer. Hold the base of the cartridge down and carefully remove the retainer (taking care to keep the CellSpot and Microfuge Tube in place). Remove and keep the Low-Volume Recovery Holder to be used in next step.
- Decide if the enriched cells will be recovered with Low-Volume Recovery Holder or in the Microfuge Tube.
- If the enriched cells will be recovered with Low-Volume Recovery Holder, remove the Microfuge Tube in well No. 5 and insert the Low Volume Recovery Holder as shown below:
- If using the Microfuge tube, add 300µL of Binding Buffer to the Microfuge tube in the sample retrieval position on the cartridge (well No. 5) as showing below.
- Carefully open the cartridge lid and add 2.5 to 3mL Binding Buffer to the buffer reservoir (well No. 2) of each cartridge. Close the cartridge lid.
- Load cartridge(s) onto the carriage(s). Press Prime. Cartridge loading carriage(s) will slide in automatically. Machine will prime for about 6 minutes.
- After priming is completed, touch screen will show Ready to Load Sample. Press Ready to Load Sample. Left carriage will slide out automatically. Carefully open cartridge lids. Gently add the beads-coupled cell samples from Step 3.5 to the Sample well (well No. 1) and avoid forming bubbles. Carefully snap close the cartridge lid and load onto the carriage.
- After all cell samples are loaded for the left carriage, press Load. Left carriage will slide in automatically. If running one or two samples, cell isolation will start at this point. If running more than two samples, right carriage will slide out automatically. Load the rest of samples and press Load, right carriage will slide in automatically. Cell isolation will start.
- Cell isolation typically takes about 45 minutes but it may vary for different samples.
- After cell isolation is completed, touch screen will show Extract Sample. Press Extract Sample. Carriage(s) will slide out automatically.
- Immediately recover cells (well No. 5) from the Low Volume Recovery Holder. Remove and invert the holders such that the enriched cells are facing up. Immediately add 20L (a drop) of Binding Buffer to all the CellSpots to prevent cells from drying.
- If necessary, place the CellSpot over the small cylindrical magnet for 5 seconds to center the cells/beads pellet. Remove the CellSpot from the magnet.
- Rinse the micropipette tip with Binding buffer to minimize cell sticking to the tip. Gently aspirate the cells/beads into the pipette tip. Dispense the collected cells/beads into a new microfuge tube (not provided).
We recommend doing the liquid-to-liquid transfer (i.e. the microfuge tube should also contain a small volume of Binding Buffer).
- Place the microfuge tube on the large magnet. Aspirate most of the supernatant and rinse the CellSpot to collect any residual cells/beads. Repeat the previous two steps until no visible cells/beads are observed on the CellSpot.
- If using the Microfuge Tube, gently invert the tube 2-3 times until all the cells/beads are suspended in the Binding Buffer at the bottom of the tube.
- Centrifuge the microfuge tubes briefly to bring down any cells/beads from the edge of the tube. Enriched CTCs are now ready for further testing.