This page is meant to be a collection of notes on Fomblin with regard to the LCN's standard operating protocol for ex vivo samples.

Background: Fomblin is the name brand of a fluoropolymer produced by Solvay Specialty Polymers S.p.A. that has been used since 1998 (Huang, G. Y., et al., 1998) as an immersion solution to improve MR-imaging SNR in tissue samples. The fluoropolymer uniquely lack's any MR-signal but has magnetic susceptibility similar to that of tissue, which results in MR-images with high SNR & CNR between the Fomblin and any suspended tissue. Since the use of Fomblin in MR-imaging is still quite young, the impact of the solution on tissue properties is unknown. We are maintaining this wiki page to document the following 5 levels of ex vivo processing with Fomblin to record any personal and literature-based experiences with the solution.

5 levels of the ex vivo procedure where Fomblin can impact tissue:

  1. Packing
  2. Scanning
  3. Post-Processing
  4. Histology
  5. Tissue storage



From email correspondence with Scott Brady from Lesker (12/22/14): He suggests we use Galden HT270 (Part #: HT270-7KG) which they provide to several facilities involved in the similar applications. He attached the this informational document on Galden products.

From email correspondence with Brain Edlow (03/28/17): We were initially using Fomblin LC08 from Solvay Solexis. Solvay Solexis stopped selling Fomblin LC08 a few years ago, so we transitioned to using Kurt J. Lesker products. Initially we used Fomblin 06/6 from Kurt J. Lesker. However, the specific gravity of Fomblin 06/6 was slightly higher than that of LC08, and as a result it was more technically challenging to pack whole brains in this fluid within an air-tight plastic bag for ex vivo MRI. We therefore transitioned to Galden HT200 (Galden is just a brand name of a Fomblin product) because of its lower specific gravity, which has made the brain packing process go more smoothly. I don't believe that anyone in our lab has noticed any differences in the quality of the imaging data acquired with these three slightly different fomblin solutions.




Hyare et al., 2008

Hyare et al., 2008 found that storing tissue in Fomblin for 2 days prior to MRI had no effect on scan or histology results when compared to matched samples stored in 10% formol-saline.

Synopsis: Formalin-fixed mouse brain tissue placed in Fomblin for 2 days prior to T1, T2, DWI, and MTR scans @ 9.4T produced the same results as formalin-fixed controls placed in 10% formol-saline solution 2 days prior to scanning. Both were scanned in Fomblin. They compared ROI-based quantitative MR measures, anatomical & cellular histology, and immunohistochemical staining.


The effects of Fomblin on histology were discussed in an email conversation between Nancy Kanwisher, Bruce Fischl, Allison Stevens, and Jean Augustinack (Bram Diamond was also cc'ed) on July 10th, 2018 with regard to Nancy's very important I54 brain.

Jean has found that Fomblin is okay for Nissl and basic histochemistry (myelin, thioflavines, etc). She also mentioned that it works for tau immunohistochemistry but may not work if one's antigen is covered or difficult to get to. That said, washing with a mild detergent (Dawn) after removing the majority of Fomblin has worked well to fix this issue in the past.

To clarify, Jean said that although Fomblin can be helpful for "pretty imaging", sticking with the fixative, typically Formalin, all the way would make less variables.

With regard to Clarity, Kwanghun noted that their lab had not yet investigated "how fomblin incubation affects tissue clearing and other downstream histological analysis" and added that he thinks "it'd be safe to not expose the brain to fomblin considering the importance of the brain".

Tissue Storage