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#1 |
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Wanna be Gas-passer
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1) Does the size of the molecule cause a difference in diffusion, resulting in the lower ratio? 2) Could the fat:blood partition coefficient play any part in this? I know the coefficient is ~10 x more for desflurane. Can the difference be explained by the fact that there is so much more des being taken up into adipose? Wouldn't you eventually exhaust that adipose 'sink' and see the ratio approach 1? Thanks in advance for any help!
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#2 | |
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Senior Member
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#3 |
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Wanna be Gas-passer
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Thank you for the reply.
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#4 |
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和魂洋才
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I think that the tissue:blood solubility is not a significant factor compared to the "concentration effect," especially early on that curve. I don't have the strength to explain the concentration effect this morning, but I found a paper and a few links:
http://www.pharmacology2000.com/phys.../physics10.htm http://web.squ.edu.om/med-Lib/MED_CD.../020065r00.htm It's definitely not diffusion limitation, the uptake of both N2O and Desflurane is perfusion-limited at pretty much any physiologic level of cardiac output. |
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#5 |
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Wanna be Gas-passer
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Thanks for the links to that paper/sites. I checked them out, this is what I am taking away from this discussion:
It seems that the difference between the curves can be explained by the concentration effect, which is based on the fact that the inhaled concentrations of nitrous oxide are so much higher than desflurane (or any others, for that matter). The tissue:blood solubility might play some role in this process, but not nearly as significant as the concentration effect, and my idea about diffusion differences is pretty much wrong. ![]() I hope I'm getting that right. I guess it's back to studying things that are less interesting, but more relevant for my tests next week.
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