Well, I’ve come up with some ideas, yes. First, is it possible to, try and duplicate uM levels of the in vitro studies? That appears difficult, but with intestinal and hepatic reductions for R so great, it seems best to bypass them as much as possible, and focus mostly on methods that do not include P450 enzyme degradation..
That's where I hope alternative R formulations brings some relief. Sublingual/Buccal, liposomal, and micronized offer different routes to bio-availability, but after reading way too many studies and papers recently, what stands out to me each version is only somewhat useful to overcome the bio-availability issue. So an idea might be to combine modalities to obtain some serum R from each.
Here's a draft for a 30 hr regimen with five cycles. Optional - I’m taking: AC-11 350 mg 7am/7pm/7am.
Sources --------------------------------
S-B for Sublingual/Buccal - trans-resveratrol 75mg tablet in flavored base
L for Liposomal - Resveratrol/Curcumin 75 mg/200 mg mix per 6 ml
O-M for Oral Micronized* - +15% assimilated, 2-3x Cmax & AUC 500mg capsule
U for UltraCUR - Curcumin bound to Whey protein isolate 25 mg C per 1000mg whey
Schedule ------------------------------
7am 1pm 7pm 1am 7am Total Free-R**
S-B 75 mg S-B 75 mg S-B 75 mg S-B 75 mg S-B 75 mg 375 112 mg
L 37.5 mg L 37.5 mg L 37.5 mg L 37.5 mg L 37.5 mg 188 94 mg
---> ----> ----> Curcumin 500 250 mg
O-M 250mg O-M 250mg O-M 250mg O-M 250mg O-M 250 mg 1250 50 mg
U 500 mg U 250 mg U 500 mg U 250 mg U 250 mg (1750) (44) mg
estimated total free R** 256mg
estimated total free C** 294mg
*Can be taken with Lecithins, palm oils, rapeseed oils, soybean oils, sunflower oils, whey protein isolate shake. ** Estimated bioavailable free R, C
Another way to look at the free R issue and the schedule above is on a time continuum with each modality creating a rising/falling curve with variable length and AUC. Then each curve overlaps and sums within the six hour period, to give the total bioavailable concentration once you add the C. Finally, the addition of C increases bioavailability a bit further for maximal dose.
Nothing below is real or based on any studies, simply an illustration.....
Edited by Oakman, 26 December 2017 - 05:18 PM.