From: Perfusion fixation in brain banking: a systematic review
Study | Overall method | Study type | Tissue | Preservative agent(s) | Temperature | Storage duration |
---|---|---|---|---|---|---|
Alvernia 2010 [3] | Immersion in fixative | Surgical training | Separated head | 10% Formalin and 10% ethyl alcohol | 4 °C | Up to 4 years |
Benet 2014 [9] | Immersion in fixative | Surgical training | Separated head | 10% formaldehyde or 10% custom solution (ethanol 62.4%, glycerol 17%, phenol 10.2%, formaldehyde 2.3%, and water 8.1%) | 5 °C | Up to a year |
Insausti 1995 [42] | Cryoprotection and freezing | Histology | 1 cm-thick coronal tissue blocks | Solutions of 10 and 20% glycerol in 0.1 M phosphate buffer and 2% dimethylsulfoxide | −80 °C | NR |
Lyck 2008 [58] | Immersion in fixative | Histology | Whole brain | 0.1% paraformaldehyde in 0.15 M Sørensens phosphate buffer (pH 7.4) | 4 °C | Up to 4 years |
Sutoo 1994 [85] | Cryoprotection and freezing | Histology | 1 cm-thick coronal tissue blocks | Buffered 5% sucrose | −80 °C | NR |
Waldgovel 2006 [96] | Cryoprotection and freezing | Histology | Tissue blocks (many 1 cm-thick) | 20–30% sucrose in 0.1 M phosphate buffer with 0.1% sodium azide | −80 °C | NR |
Welikovitch 2018 [99] | Cryoprotection and freezing | Histology | Brain sections | 1.1 M sucrose, 37.5% ethylene glycol in PBS | −20 °C | NR |