Asymmetrical Oxide Experiment
With this new understanding of pore size and porosity control, I think we have a lot more flexibility on picking more optimal film conditions.
With this new understanding of pore size and porosity control, I think we have a lot more flexibility on picking more optimal film conditions.
Introduction Sphingosine-1-phosphate (S1P) is a bioactive sphingolipid with known paradoxical effects on endothelial cell (EC) barrier regulation. S1P binds 5 GPCRs: S1PR1 (Endothelial differentiation gene (EDG)-1), S1PR2 (EDG-5), S1PR3 (EDG-3), S1PR4 (EDG-6), and S1PR5 (EDG-8). Despite the aliases, endothelial cells predominantly express S1PR1&3. S1PR1 has been shown to have barrier protective or enhancing effects on…
As the title states, these are images from the monolithically fabricated devices used by Kyle and Vincent in Ottawa. These devices were fractured with tweezers, then tilted and metallized with 5 nm of Pt, mounted on carbon tape.
This week I tried to run a few “eq-tests” with some samples from wafer 187 to get some hydraulic permeability value for our membranes to see how they compare to the polymer filters used in the microcon and nanosep systems. Unfortunately I have no results to report, of the two samples I tested one broke…
As a proof-of-principle, Henry and I have been working on a microfluidic device for flowing blood cells/particles across cultured cells on pnc-Si. More on why this is important later. We’ve come up with a prototype and I’ve been testing it out. I will include schematics later but here are the first couple of movies I’ve…
In my previous blog, I alluded to the issues I was facing in achieving successful migration of neutrophils through the basement membrane into the collagen gels. I am successfully able to achieve transendothelial migration, but migration beyond the endothelial basement membrane is still not achievable. After a lot of thinking, I realized that this, in…
Originally, I created the following figure to visualize the relationship between sieving coefficient and molecular weight: (originally from this post) I can now take the protein dimensions that I obtained from crystal structures (posted here) and replot this figure: In this version of the figure the sigmoidal shape of the curve is even more obvious…
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very interesting- this really suggests we should do a series with increasingly thinner top oxide layers- eventually going to the agglomeration regime Joe has seen. Can we do this quickly, with say 20, 15, 10, and 5 nm oxide?
could you also email me the figure as I am having a hard time trying to import it. Thanks,
P. Fauchet
Sure, I also updated the post so the figure can be loaded as bigger image. I haven’t posted in so long on the blog I forgot how to get the images set right.
Charles
I am puzzled as to why 719 falls between the two other samples – or perhaps why 720 shows a higher porosity and average pore size than the 2 others. If one goal is to make high porosity samples that have very small pores, your results suggest that we should increase the thickness of both oxide layers- can someone try this?
I’m not sure why 720 shows a higher porosity and average pore size. I suspect that the thicker bottom oxide might promote pore size and porosity.
Increasing both top and bottom oxide has usually shown a decrease in pore size and porosity.