Is DMSO safe to use as a solvent?
Has anyone tried to dissolve resveratrol with DMSO?
Edited by Wolf-Eye, 24 April 2009 - 11:01 AM.
Posted 24 April 2009 - 11:00 AM
Edited by Wolf-Eye, 24 April 2009 - 11:01 AM.
Posted 24 April 2009 - 11:47 AM
DMSO is suppose to be a very effective solvent.
Is DMSO safe to use as a solvent?
Has anyone tried to dissolve resveratrol with DMSO?
Edited by maxwatt, 24 April 2009 - 11:48 AM.
Posted 24 April 2009 - 03:38 PM
Edited by Wolf-Eye, 24 April 2009 - 03:39 PM.
Posted 24 April 2009 - 03:50 PM
Posted 24 April 2009 - 03:54 PM
Posted 25 April 2009 - 12:36 PM
- Luetolin =30-60mg
- Resveratrol Glucoside = 200mg
- Piperine = 2-5mg
- Resveratrol CIS/TRANS 50:50 = 300mg Trans (want big particle size)
- HPMC = a few pinches
- Cyclodextrin = 400mgs
- Mix and stir in grape fruit juice (sulfanation inhibitor).....
Posted 27 April 2009 - 10:34 AM
Posted 29 April 2009 - 12:52 AM
- Luetolin =30-60mg
- Resveratrol Glucoside = 200mg
- Piperine = 2-5mg
- Resveratrol CIS/TRANS 50:50 = 300mg Trans (want big particle size)
- HPMC = a few pinches
- Cyclodextrin = 400mgs
- Mix and stir in grape fruit juice (sulfanation inhibitor).....
Is this what your are currently taking? Have you measured your blood serum levels with it?
Considering that luteolin is such an effective sulfonation inhibitor, I would think the requirement for grapefruit juice is redundant; any juice or even water would do.
The main metabolic pathway for resveratrol is sulfonation; I would think the piperine is not really needed, has lttle effect. You could use freshly ground black pepper instead, though, if you didn't have any piperine lying around.
Isn't considerable stirring necessary to get the resveratrol molecules to be enveloped by the cyclodextrine molecules? I've read half an hour or more with a magnetic stirrer. In any case, your formulation is not something that could be just put in a capsule for that reason. It would go nicely in Tween80 though. Even without a surfactant, I'd think you'd get enhanced serum levels with resveratrol, polydatin and lutelin in a pill.
Posted 29 April 2009 - 12:54 AM
- Luetolin =30-60mg
- Resveratrol Glucoside = 200mg
- Piperine = 2-5mg
- Resveratrol CIS/TRANS 50:50 = 300mg Trans (want big particle size)
- HPMC = a few pinches
- Cyclodextrin = 400mgs
- Mix and stir in grape fruit juice (sulfanation inhibitor).....
Is this what your are currently taking? Have you measured your blood serum levels with it?
Considering that luteolin is such an effective sulfonation inhibitor, I would think the requirement for grapefruit juice is redundant; any juice or even water would do.
The main metabolic pathway for resveratrol is sulfonation; I would think the piperine is not really needed, has lttle effect. You could use freshly ground black pepper instead, though, if you didn't have any piperine lying around.
Isn't considerable stirring necessary to get the resveratrol molecules to be enveloped by the cyclodextrine molecules? I've read half an hour or more with a magnetic stirrer. In any case, your formulation is not something that could be just put in a capsule for that reason. It would go nicely in Tween80 though. Even without a surfactant, I'd think you'd get enhanced serum levels with resveratrol, polydatin and lutelin in a pill.
Posted 29 April 2009 - 03:35 AM
- Luetolin =30-60mg
- Resveratrol Glucoside = 200mg
- Piperine = 2-5mg
- Resveratrol CIS/TRANS 50:50 = 300mg Trans (want big particle size)
- HPMC = a few pinches
- Cyclodextrin = 400mgs
- Mix and stir in grape fruit juice (sulfanation inhibitor).....
Is this what your are currently taking? Have you measured your blood serum levels with it?
Considering that luteolin is such an effective sulfonation inhibitor, I would think the requirement for grapefruit juice is redundant; any juice or even water would do.
The main metabolic pathway for resveratrol is sulfonation; I would think the piperine is not really needed, has lttle effect. You could use freshly ground black pepper instead, though, if you didn't have any piperine lying around.
Isn't considerable stirring necessary to get the resveratrol molecules to be enveloped by the cyclodextrine molecules? I've read half an hour or more with a magnetic stirrer. In any case, your formulation is not something that could be just put in a capsule for that reason. It would go nicely in Tween80 though. Even without a surfactant, I'd think you'd get enhanced serum levels with resveratrol, polydatin and lutelin in a pill.
Currently I take 50:50 cis trans resveratrol, sometimes I pop a 200mg polydatin pill. Also I sometimes put a very large amount of pure resveratrol powder into my morning coffee.
My cycling endurance is currently outstanding....
Posted 29 April 2009 - 11:32 PM
- Luetolin =30-60mg
- Resveratrol Glucoside = 200mg
- Piperine = 2-5mg
- Resveratrol CIS/TRANS 50:50 = 300mg Trans (want big particle size)
- HPMC = a few pinches
- Cyclodextrin = 400mgs
- Mix and stir in grape fruit juice (sulfanation inhibitor).....
Is this what your are currently taking? Have you measured your blood serum levels with it?
Considering that luteolin is such an effective sulfonation inhibitor, I would think the requirement for grapefruit juice is redundant; any juice or even water would do.
The main metabolic pathway for resveratrol is sulfonation; I would think the piperine is not really needed, has lttle effect. You could use freshly ground black pepper instead, though, if you didn't have any piperine lying around.
Isn't considerable stirring necessary to get the resveratrol molecules to be enveloped by the cyclodextrine molecules? I've read half an hour or more with a magnetic stirrer. In any case, your formulation is not something that could be just put in a capsule for that reason. It would go nicely in Tween80 though. Even without a surfactant, I'd think you'd get enhanced serum levels with resveratrol, polydatin and lutelin in a pill.
Currently I take 50:50 cis trans resveratrol, sometimes I pop a 200mg polydatin pill. Also I sometimes put a very large amount of pure resveratrol powder into my morning coffee.
My cycling endurance is currently outstanding....
Why 50:50 cis:trans ?
Posted 30 April 2009 - 03:33 AM
I bet it's something else; maybe a 50% extract. I'm not even sure that it's possible to maintain a 50/50 cis/trans resveratrol for long. Doesn't the cis isomer spontaneously convert to trans at a reasonable rate? Trans is more stable than cis, FWIW. It doesn't make sense that someone would go to the trouble to create an unnatural isomer when it doesn't even have the activity that we want.I like the emodin (spelling?) ! =)Why 50:50 cis:trans ?
It was something that provided to me... (Dunno maybe it helps with clogging phase I metabolism)
Posted 30 April 2009 - 10:05 AM
I bet it's something else; maybe a 50% extract. I'm not even sure that it's possible to maintain a 50/50 cis/trans resveratrol for long. Doesn't the cis isomer spontaneously convert to trans at a reasonable rate? Trans is more stable than cis, FWIW. It doesn't make sense that someone would go to the trouble to create an unnatural isomer when it doesn't even have the activity that we want.I like the emodin (spelling?) ! =)Why 50:50 cis:trans ?
It was something that provided to me... (Dunno maybe it helps with clogging phase I metabolism)
PMID: 17065200Fang J, Zhou Q, Shi XL, Jiang BH.
The Institute for Nutritional Sciences, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences, Graduate School of Chinese Academy of Sciences, Shanghai 200031, China. jfang@sibs.ac.cn
Insulin-like growth factor 1 receptor (IGF-1R) activation is required for prostate cell proliferation. Prostate cancer is one of the most commonly diagnosed malignant tumors in Western countries. Overexpression of IGF-1R in prostate cancer is associated with tumor growth. These suggest that IGF-1R inhibitory agents may be of preventive and/or therapeutic value. With evidence accumulating for a chemopreventive role of flavonoids, the effects of luteolin, a bioactive flavonoid, on IGF-1R signaling in prostate cancer cells were examined. Luteolin inhibited insulin-like growth factor 1 (IGF-1) induced activation of IGF-1R and AKT in prostate cancer PC-3 and DU145 cells. Inhibition of AKT by luteolin resulted in decreased phosphorylation of its downstream targets, including p70S6K1, GSK-3beta and FKHR/FKHRL1. Luteolin also inhibited the IGF-1-induced activation of EGFR and MAPK/ERK signaling. Luteolin inhibited expression of cyclin D1 and increased expression of p21. As a result, luteolin suppressed proliferation and induced apoptosis of prostate cancer cells. Knockdown of IGF-1R by siRNA led to inhibition of proliferation of prostate cancer cells. Results of in vivo tumor growth assay indicated that luteolin inhibited PC-3 tumor growth. Immunoblotting of the extracts of tumor tissues showed that luteolin inhibited IGF-1R/AKT signaling. Our results provide a new insight into the mechanisms that luteolin is against cancer cells.
Edited by maxwatt, 30 April 2009 - 06:21 PM.
Posted 30 April 2009 - 10:56 AM
Posted 30 April 2009 - 02:12 PM
send me an email if you cannot PMv. interesting. i'm sold on trying the luteolin.
Posted 30 April 2009 - 03:21 PM
<br />
<br />send me an email if you cannot PM<br /><br /><br />v. interesting. i'm sold on trying the luteolin.
<br /><br /><br />
i can't get any msgs through on the personal controls area. drop me an email at my spam account ***. i'll reply from my real email address.
Edited by prophets, 17 November 2016 - 02:46 PM.
Posted 03 May 2009 - 01:09 AM
Posted 08 May 2009 - 02:34 PM
Luteolin reduces IL-6 production in microglia by inhibiting JNK phosphorylation and activation of AP-1.
Luteolin, a flavonoid found in high concentrations in celery and green pepper, has been shown to reduce production of proinflammatory mediators in LPS-stimulated macrophages, fibroblasts, and intestinal epithelial cells. Because excessive production of proinflammatory cytokines by activated brain microglia can cause behavioral pathology and neurodegeneration, we sought to determine whether luteolin also regulates microglial cell production of a prototypic inflammatory cytokine, IL-6. Pretreatment of primary murine microlgia and BV-2 microglial cells with luteolin inhibited LPS-stimulated IL-6 production at both the mRNA and protein levels. To determine how luteolin inhibited IL-6 production in microglia, EMSAs were performed to establish the effects of luteolin on LPS-induced binding of transcription factors to the NF-kappaB and activator protein-1 (AP-1) sites on the IL-6 promoter. Whereas luteolin had no effect on the LPS-induced increase in NF-kappaB DNA binding activity, it markedly reduced AP-1 transcription factor binding activity. Consistent with this finding, luteolin did not inhibit LPS-induced degradation of IkappaB-alpha but inhibited JNK phosphorylation. To determine whether luteolin might have similar effects in vivo, mice were provided drinking water supplemented with luteolin for 21 days and then they were injected i.p. with LPS. Luteolin consumption reduced LPS-induced IL-6 in plasma 4 h after injection. Furthermore, luteolin decreased the induction of IL-6 mRNA by LPS in hippocampus but not in the cortex or cerebellum. Taken together, these data suggest luteolin inhibits LPS-induced IL-6 production in the brain by inhibiting the JNK signaling pathway and activation of AP-1 in microglia. Thus, luteolin may be useful for mitigating neuroinflammation.
Edited by Wolf-Eye, 08 May 2009 - 02:51 PM.
Posted 18 May 2009 - 05:22 AM
Posted 18 May 2009 - 10:51 AM
I have been 99% trans-res (Mega-Res) dissolved in coconut oil and applied transdermally. I use 250mg dissolved in 1/2 teaspoon of coconut oil. The res seems to dissolve quite well but I have no idea if it's being absorbed adequately. Does anyone have any experience using coconut oil as a delivery system?
Edited by maxwatt, 18 May 2009 - 10:52 AM.
Posted 22 May 2009 - 04:22 PM
I have been 99% trans-res (Mega-Res) dissolved in coconut oil and applied transdermally. I use 250mg dissolved in 1/2 teaspoon of coconut oil. The res seems to dissolve quite well but I have no idea if it's being absorbed adequately. Does anyone have any experience using coconut oil as a delivery system?
Likely it penetrates the first few layers of the dermis with the coconut oil, and local tissue concentrations may be helpful, but you will not achieve significant systemic levels this way.
Posted 30 May 2009 - 03:34 PM
Posted 30 May 2009 - 07:45 PM
Edited by Anthony_Loera, 30 May 2009 - 08:35 PM.
Posted 31 May 2009 - 11:21 AM
Interesting. I am more interested in seeing if just taking a capsule is a good means of delivery or is it better to mix the res with something?250% more bioavailable...?
In comparison to what, to their 50% resveratrol product?
You know, the one that is supposed to be pure resveratrol with 500mg, of which only 250mg is trans-resveratrol?
http://www.imminst.o...o...st&p=188484 [...]
Now after the micronized resveratrol was created as a consumer product, using the public Sirtris data. A silly marketing method is used to continue to sell the product created in 2007 instead of creating a better product.
Edited by Michael, 27 July 2009 - 01:02 PM.
Trim quotes
Posted 31 May 2009 - 08:41 PM
Interesting. I am more interested in seeing if just taking a capsule is a good means of delivery or is it better to mix the res with something?
Posted 08 June 2009 - 01:00 AM
Interesting. I am more interested in seeing if just taking a capsule is a good means of delivery or is it better to mix the res with something?
Please read this thread, and the charts in Sirtris patent application.
You will see an increase in absorption using micronized resveratrol with HPMC/DOSS and tween 80.
Cheers
A
Posted 08 June 2009 - 03:19 AM
Resveratrol's transdermal flux has been measured, and it is very low. The problem is not the size of the molecule, resveratrol being fairly small, but the hydrophilicity of it. Small hydrophobic molecules are likely to be reasonable (though not assured) candidates for transdermal delivery, but hydrophiles are not.how certain are you that resveratrol can pass the first layers of skin?
I'm not very well versed with skin absorbability..could it be that res is too large of a molecule to even pass the 1st few layers?
Posted 08 June 2009 - 01:05 PM
Resveratrol's transdermal flux has been measured, and it is very low. The problem is not the size of the molecule, resveratrol being fairly small, but the hydrophilicity of it. Small hydrophobic molecules are likely to be reasonable (though not assured) candidates for transdermal delivery, but hydrophiles are not.how certain are you that resveratrol can pass the first layers of skin?
I'm not very well versed with skin absorbability..could it be that res is too large of a molecule to even pass the 1st few layers?
Can you even get resveratrol dissolved in coconut oil? In other words, do you get a clear solution? If it's pasty looking, then it isn't dissolved. My experience dissolving resveratrol in very hydrophobic solvents has been poor.
Posted 10 June 2009 - 11:36 AM
Posted 10 June 2009 - 12:21 PM
I've read most of this forum please help. What is the most efficient and effective way of taking resveratrol?
w/ lecithin, PEG3350. Everclear, vodka, Tween 20-80?
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