
I'm not concerned of any *commonly* used compound, completely nuking resv. Anyone?
BTW, besides LEF's resv product, Doctor's Best also carries a 100mg trans-resv pill (also including the beneficial polyphenols).
Posted 12 February 2007 - 09:26 PM
Posted 12 February 2007 - 10:01 PM
Yes, if you could translate I would really appreciate it.
Posted 12 February 2007 - 10:09 PM
Posted 12 February 2007 - 10:10 PM
Yes, if you could translate I would really appreciate it.
okies, crude :-) but as a service:
"
Stability
Resveratrol distinguishes itself through stability. In oposition to this marketing driven statements allege Resveratrol to be a unstable molecule susceptible to evaporation and oxidation. This is chemically speaking untrue.
Transresveratrol's boilingpoint is at 260°C and it's meltingpoint lies at 489°C. One speaks of Low volatile compounds from vapor pressure smaller then 0.1 Pascal, substances greater then 70 Pascal are considered lightly volatile. With a vapor preassure of 4.5x10 to the power of 8 Resveratrol lies considerably below this treshold. With increasing molecular weight (dimere and oligomere resveratrols) vapor pressure further decreases. (boy the guy uses some odd german :-) )
Moreover after heating redwine for 24 hours the ammount of trans-reveratrol in residue is identical to starting conditions demonstrating that even after prolonged cooking and oxidation resveratrol stays stable and low volatile.
"
Ups, translating (especially before going to bed) in a field where you don't know technical language is no walk in the park. Sorry if it's unintelligible.
Posted 12 February 2007 - 10:41 PM
When they came out with their BS about it having to be processed under nitrogen or it would degrade, I pointed out that the evidence showed it to be very stable just based on what we already knew. I called it a marketing ***** even though many jumped on the Longevex bandwagon based on the scare tactics.
Posted 13 February 2007 - 01:04 AM
Edited by shadowrun, 13 February 2007 - 01:20 AM.
Posted 13 February 2007 - 04:23 AM
<snip>
- Oil or Lecithin is a great addition as Resveratrol is soluble in fat
<snip>
Posted 13 February 2007 - 04:59 AM
Stability
Transresveratrol's boilingpoint is at 260°C and it's meltingpoint lies at 489°C.
Posted 13 February 2007 - 07:25 PM
It doesn't appear to be nearly as lipid soluble as has been represented, at least in a "kitchen setting".
I have played around with Orchid sourced ResV in various "dietary solvents"
It does not dissolve to a great degree in EVOO or Carleson's Fish oil even when warmed to 130F
Trying to dissolve 100mg of ResV into 15ml of either oil results in the majority settling out. Rough guesstimate is that no more than a few mg/ml solubility in common dietary oils even with warming and prolonged agitation.
As a comparison, CoQ10 powder will fairly easily dissolve 100mg into 15ml of fish oil. CoQ10 is known - or at least hyped - to have absorb-ability problems if not mixed in oil, yet is much more soluble in oil than ResV.
Just as a point of comparison, from eyeballing in the kitchen
ResV is insoluble in warm water
ResV is insoluble in warm distilled vinegar
ResV is moderately soluble in straight vodka = 40% EtOH
I did my kitchen tests out of curiosity and I am the first to state that they demonstrate nothing towards any ResV dosing methods or recommendations. Just from playing around though, I am somewhat intrigued by the association of the "French Paradox" with wine and the lack of easy solubility of ResV in any common consumable solvent except alcohol.
OBW
Posted 13 February 2007 - 10:57 PM
Posted 13 February 2007 - 11:37 PM
Why does solubility make a difference in terms of how bioavailable it is?
Posted 14 February 2007 - 03:32 AM
I haven't seen any evidence that it makes any difference. I don't know why people are obsessing over the solubility.
Clin Biochem. 2003 Feb;36(1):79-87. Links
Absorption of three wine-related polyphenols in three different matrices by healthy subjects.Goldberg DM, Yan J, Soleas GJ.
Department of Laboratory Medicine and Pathobiology, University of Toronto, ON, Canada M5G 1L5. david.goldberg@utoronto.ca
BACKGROUND: Despite their powerful biologic activities conducive to protection against atherosclerosis, cancer and inflammatory diseases demonstrated in vitro, there is considerable doubt whether the polyphenolic constituents present in red wine and other dietary components are effective in vivo. OBJECTIVE: We have tested the absorptive efficiency of three of these constituents (trans-resveratrol, [+]-catechin and quercetin) when given orally to healthy human subjects in three different media. DESIGN: Twelve healthy males aged 25 to 45 were randomly assigned to three different groups consuming orally one of the following polyphenols: trans-resveratrol, 25 mg/70 kg; [+]-catechin 25 mg/70 kg; quercetin 10 mg/70 kg. Each polyphenol was randomly administered at 4-week intervals in three different matrices: white wine (11.5% ethanol), grape juice, and vegetable juice/homogenate. Blood was collected at zero time and at four intervals over the first four hours after consumption; urine was collected at zero time and for the following 24-h. The sums of free and conjugated polyphenols were measured in blood serum and urine by a gas-chromatographic method. RESULTS: All three polyphenols were present in serum and urine predominantly as glucuronide and sulfate conjugates, reaching peak concentrations in the former around 30-min after consumption. The free polyphenols accounted for 1.7 to 1.9% (trans-resveratrol), 1.1 to 6.5% ([+]-catechin) and 17.2 to 26.9% (quercetin) of the peak serum concentrations. The absorption of trans-resveratrol was the most efficient as judged by peak serum concentration, area-under-the curve (4 h) and urinary 24-h excretion (16-17% of dose consumed). [+]-Catechin was the poorest by these criteria (urine 24-h excretion 1.2%-3.0% of dose consumed), with quercetin being intermediate (urine 24-h excretion 2.9%-7.0% of dose consumed). Some significant matrix effects were observed for the serum polyphenol concentrations, but in the case of urine no matrix promoted significantly higher excretion than the other two. CONCLUSIONS: The absorption of these three polyphenols is broadly equivalent in aqueous and alcoholic matrices but, at peak concentrations of 10 to 40 nmol/L, is inadequate to permit circulating concentrations of 5 to 100 micromol/L consistent with in vitro biologic activity. The voluminous literature reporting powerful in vitro anticancer and antiinflammatory effects of the free polyphenols is irrelevant, given that they are absorbed as conjugates.
PMID: 12554065 [PubMed - indexed for MEDLINE]
Posted 14 February 2007 - 03:51 AM
Posted 14 February 2007 - 05:07 PM
Posted 15 February 2007 - 02:48 AM
It occurs to me that being phenolic, resveratrol is a weak acid. In neutral or acidic solutions, it will remain protonated, (electrostatically neutral) and thus be insoluble. However, in a basic environment, it will deprotonate and take on a negative charge, which will quickly pull it into solution. I don't know the pKa of resveratrol offhand, but my guess is that it ionizes once it gets into the gut
Posted 15 February 2007 - 07:03 AM
Fearfrost indicated in another post that consuming the Resveratrol with an Alkaline substance (green tea) could increase its solubility...
I assume this might increase its bioavailability?
Posted 10 March 2007 - 01:16 AM
Also, don't take green tea. Green tea's EGCG has shown to inhibit the SIRT1 longevity gene that Trans-Resveratrol activates.
Posted 10 March 2007 - 01:51 AM
Mirian, do you have a cite for this? I hope this isn't so. I drink green tea all the time.
Posted 10 March 2007 - 02:04 AM
There is a Journal saying that Resveratrol is preserved better if it's with Grape Seed Extract.
There is a Journal saying that Quercetin helps Resveratrol absorb:
Don't take fish oil. Reserch oil shows it helps with people who already have heart disease but encourage atrial fibrillation in healthy people.
A French study has associated high ALA (type of fat from Flaxseed & Walnuts) intake to a one third lower risk of heart attacks.
Also, don't take green tea. Green tea's EGCG has shown to inhibit the SIRT1 longevity gene that Trans-Resveratrol activates.
Posted 06 April 2007 - 10:35 PM
Edited by mirian, 13 June 2007 - 08:01 AM.
Posted 06 April 2007 - 10:41 PM
Posted 07 April 2007 - 12:32 AM
Everything is about balance. This is a link showing how Longevinex is a scam:
Posted 07 April 2007 - 08:32 PM
Posted 18 April 2007 - 12:44 AM
My interest in supplements is recent, since I was diagnosed with prostate cancer(biopsy) July 2006, and don't remember any mention of timing between dosages of any supplements to prevent negative or neutralized results.
Edited by moodyblue, 05 August 2007 - 09:37 PM.
Posted 01 June 2007 - 07:53 AM
Posted 01 June 2007 - 05:07 PM
Posted 04 June 2007 - 01:12 AM
Posted 04 June 2007 - 02:55 AM
Posted 04 June 2007 - 05:18 AM
I'd settle for 80% extract product. Just enough to get the emodin down to reasonable levels while not breaking the bank.
Posted 07 June 2007 - 01:09 PM
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