Neural Spheroids on SpheroHD Protocol

Preparing the SpheroHD Chip

1. Pipette 10 μl of 0.1% PEI in borate buffer (or neural coating of choice) into each of the four chambers of the Ibidi insert on the SpheroHD chip.
2. Incubate the PEI-coated SpheroHD chip in a cell culture incubator at 37°C, 5% CO₂ for at least 60 minutes.
3. Aspirate PEI from the chambers and rinse with 10 µl of sterile DI water 4 times, then allow the SpheroHD chip to air dry in a biosafety cabinet overnight at room temperature.

Culturing and Plating Neural Spheroids

1. Add 10 µl of neural spheroid media to each chamber of the Ibidi insert on the SpheroHD chip.

   Tip: More information on proper handling of the Ibidi 4 well FulTrac mico insert can be found on Ibidi’s website (Cat. No: 80486).

2. Using the provided single-well centrifuge holder and a balance, centrifuge at 1500 x
   g for 1 minute to remove bubbles.
3. Using a 200 µl wide-bore pipette tip, add one neural spheroid from culture to each chamber of the Ibidi insert on the SpheroHD.  To transfer, pipette up the spheroid, allow it to fall to the bottom of the wide bore tip, and touch the tip to the media in the chamber. This will pull the spheroid from the pipette tip into the chamber.
4. Centrifuge at 100 x g for 1 minute using the provided single-well centrifuge holder to bring the spheroids to the bottom of the chambers. Check under the microscope to ensure that all spheroids are positioned over the electrodes at the bottom of the well. Repeat or increase speed if necessary.
5. Once the spheroids are in place, incubate the SpheroHD MEA chip in a cell culture incubator at 37°C, 5% CO₂ for 1 hour.
6. Add enough neural spheroid media (about 1.75 mL) to cover the top surface of the Ibidi insert. Maximum volume for the SpheroHD chip is 2 mL.
7. Take recordings using the MEA Creator Kit on the Maestro Pro, Edge, or Volt as desired.

Required Materials

Consumables

Equipment