EMS Poly III

Which solvents can be evacuated with the EMS Poly III?

The instrument handles any of the solvents currently used in embedding protocols. In principle any solvent can be safely and gradually evaporated as long as the proper settings for pressure vs temperature are observed. The one important rule is that the pressure should initially NEVER be lower than the saturated vapour pressure at that temperature. Values can be calculated with the Antoine Equation or taken from a graph. For the bulk removal of solvent it is advised to work at a pressure that is approximately 10% higher than the saturated vapour pressure. Failing to do so may lead to sudden boiling of the solvent and spilling of mixture and specimens from the vials. The risk of sudden spilling is higher with more volatile solvents such as propylene oxide and instrument settings need to be accurate.

Important: at no stage should solutions be allowed to bubble. Gas bubble formation needs to be avoided to prevent splashing and damage to the specimens when bubbles should form inside the specimen.

Although extensive testing has been carried out, specific combinations of solvent and resin need to be tested for their suitability for embedding and polymerisation in the EMS Poly III on an individual basis.

The EMS Poly III instrument is capable of effectively removing any of the solvents commonly used in embedding as long as the following rules are observed:

• Use small tissue pieces, smaller volume of cell pellets
• Use separate programs for embedding and polymerisation
• Use the smallest amount of resin in the embedding step
• During polymerisation do NOT lower the pressure to a level equal to or lower than the saturated vapour pressure as any trace amount of sol-vent will result in the formation of holes in the specimen

Small specimens are more easily embedded because of their favourable surface/volume ratio. Likewise, solvents are more easily extracted.

Along those lines it is obvious that solvent is more easily removed if the specimens are covered (or even just merely contained) in a minimum amount of resin. For instance, when using BEEM capsules it is typically sufficient to end up with 30-50 µI of resin at the end of the embedding run.

Using a dilute resin/solvent mixture, or a small volume of mixture in the embedding program leaves the specimens covered in a thin layer of resin by the end of the embedding run, just enough to cover or contain the specimen.

A procedure that has been tested for embedding yeast cells is described below and may serve as a starting point.

Yeast cells were fixed with glutaraldehyde in cacodylate buffer, washed in distilled water and postfixed with 1% KMn04 in distilled water.

After washing in distilled water the cells were dehydrated in a graded series of solvent/water mixtures: 50% - 70% - 80% - 90% -100% - 2xl00% absolute. Each step lasted 10min.

Cells are then resuspended in resin/solvent 1:10 (v/v) and after 10 min. pelleted. The pellet is resuspended in fresh mix (appr 1Ox the volume of the pellet) and then transferred into one or more BEEM capsules.

It is strongly recommended to transfer the suspension into BEEM vials OUTSIDE the EMS Poly III vacuum recipient to avoid spilling of resin inside the recipient. Any spilled resin on the vials should also be removed before inserting the BEEM vials into the recipient recessions.

Once all the BEEM vials have been transferred, the embedding program can start. The embedding program is followed by the polymerisation program, after the BEEM vials have been topped off with pure resin.

Alternately, silicone moulds can be used in the polymerisation program.