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When one scales up production using a classic magnetic separation system, one finds that the separation time increases quickly with an increase in production volume. An increase in separation time means that material losses are higher and aggregation problems become a serious problem. By using homogenous separation time, one finds that the magnetic separation process is shorter and the separation time can be easily estimated. In homogeneous systems material loss and bead aggregation is minimized.

This post is about biomagnetic separation in the production of magnetic beads for IVD kits. If you want to know its most important elements, download our free ebook The basic guide to use biomagnetic separation in production processes:

Standard magnetic separators generate inhomogeneous magnetic forces and fields. When production is scaled up, the inhomogeneity increases even further. Magnetic beads far from the magnet move much more slowly than those closer to the magnet. If you increase the force and/or separation time in order to capture the beads far from the magnet, you will increase the risk of irreversible bead aggregation in the beads that start near the magnet wall.

### Advantages of homogenous biomagnetic separation systems

In contrast, homogenous biomagnetic separation systems can generate the same force regardless of the scale of production or model of device. Since forces can be kept constant when moving from R&D to production (i.e. development using a SEPMAG A in the lab to production using a SEPMAG Q), the beads are in the same state and experience the same forces in each device. When we maintain the same force on the beads, the beads will move at a constant speed in both the R&D lab and the production line.

Since the beads are moving at a constant speed, we can calculate the correct separation time for a production process (based on maintaining losses as low as those experienced in the R&D lab while not increasing the risk for bead aggregation). The calculation is straightforward:

Therefore one can, for example, use a 50 ml centrifuge tube with a diameter of 30 mm in a SEPMAG A125 ml device. The optimal separation time (with losses below 1% and no resuspension problems) is determined in the lab to be 65 seconds.

If one moves the same process to a SEPMAG Q1L device using 1 Liter bottles with a radius of 55.5 mm and the same concentration of beads, the estimated separation time will be 65 * 55.5/30 = 109 seconds.

Therefore, homogenous biomagnetic separation conditions guarantee consistency regardless of volume and enable developers to easily determine the optimal separation time for their product (i.e. no material loss and no irreversible aggregation) at each volume.

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