Edited by tregar, 04 January 2022 - 04:39 PM.

HPBCD DMT sublingually active under tongue
#21
Posted 04 January 2022 - 03:24 PM
#22
Posted 05 January 2022 - 08:52 AM
#23
Posted 08 January 2022 - 12:50 PM
Cyclodextrins at high doses can increase drug permeability by direct action on mucosal membranes and enhance drug absorption and/or bioavailability. These effects are possibly caused by solubilisation of membrane lipids through inclusion complexation with cyclodextrins and the ability of cyclodextrins to cause perturbation of membrane integrity. However, unlike detergents, cyclodextrins solubilize membrane components without entering into the membrane, therefore the perturbing effects of cyclodextrins are mild and reversible [7].Cyclodextrins are absorbed poorly via mucosal membranes.
The oral bioavailability of cyclodextrins is very low in adult animals and humans (0.1–3%), except for RM-β-CD, which has a bioavailability of 12% in rats. Because of their bulky and hydrophilic nature only insignificant amounts of cyclodextrins are absorbed from the gastrointestinal tract by passive diffusion [33, 27].
Sublingual mucosa as a route for systemic drug delivery.pdf 240.7KB
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Thermodynamic properties of hydroxypropyl Beta cyclodextrin and guest interaction, a survey of recent studies, 2021.pdf 854.1KB
76 downloads
questions-answers-cyclodextrins-used-excipients-medicinal-products-human-use_en.pdf 273.35KB
1602 downloads
HPBCD solubility enhancement table for 68 drugs.pdf 61.76KB
309 downloads
Edited by tregar, 08 January 2022 - 06:28 PM.
#24
Posted 14 January 2022 - 11:16 AM
For storage, I remove the plunger from a 3ml syringe (100 in a box for dirt cheap on-line) and backfill or pour the contents of the HPBCD complexed DMT spoon down the syringe for storage in a freezer long-term, to defrost, pull plunger out of syringe again (so pressure does not build up) and place syringe in a mug of hot water, contents will flow easily again. Shoot contents under tongue when cools down. Syringe tips lock onto the end of the syringe to prevent spillage or loss of contents. This is how I pre-pare the 2 additional doses for use at each 1.5 hour point for the evening and store at room temp. I like to trip strongly for 4.5 hours, so 3 doses total...but the afterglow continues way beyond this.
"Cyclodextrins used as excipients" pdf, European Medicines Agency, Oct 9, 2017: Page 11 of 16:
According to the data in section 2 one can conclude that below 20 mg/kg/day no serious adverse effects are to be expected for all routes of administration and no statement is deemed necessary.
Above 20 mg/kg/day, cyclodextrins may show some activity, and because there are insufficient safety data in children below two years old, it is advisable to inform about the quantity of cyclodextrin in the product and that for use in children below two years old, a doctor’s recommendation is needed.
Above 200 mg/kg/day cyclodextrins may theoretically cause problems in the digestive system when given orally, and cause mild renal toxicity when given parenteral, which information can be given. Depending on the amount, cyclodextrins may influence the Cyclodextrins used as excipients permeability of tissues and therefore the bioavailability of active substances given topically (nasal, rectal, dermal, ocular).
This is exactly the way I use the HPBCD sublingually, when I complex 90mg DMT to (x7) or 630mg of HPBCD, and I re-dose two more times every 1.5 hour, I am using 1890mg of HPBCD for the evening. I weigh 95kg, so I am using less than 20mg/kg/day or less than 1900mg per day. This always gives me a 4.5 hour long +5 Shulgin level strength experience with super-long afterglow. Very similar to 600mg plus of mescaline.
pic 1: 300mg of pure THH for oral use taken 45 minutes before, not shown: 35mg of freebase harmine for sublingual use taken at exact same under tongue as the 0.5ml (10 drop) 90mg DMT complexed to 630mg HPBCD stored in a 3ml syringe if desired.
Pic 2: Ibogaine and tetrahydroaharmine are in the same beta-carboline family. Alex Garant's artwork will have you seeing double.
#25
Posted 15 January 2022 - 08:02 AM
Re-wrote above post as could not edit:
For storage, I remove the plunger from a 3ml syringe (100 in a box for dirt cheap on-line) and backfill or pour the contents of the HPBCD complexed DMT spoon down the syringe for storage in a freezer long-term, to defrost, pull plunger out of syringe again (so pressure does not build up) and place syringe in a mug of hot water, contents will flow easily again. Shoot contents under tongue when cools down. Syringe tips lock onto the end of the syringe to prevent spillage or loss of contents. This is how I pre-pare the 2 additional doses for use at each 1.5 hour point for the evening and store at room temp. I like to trip strongly for 4.5 hours, so 3 doses total...but the afterglow continues way beyond this.
"Cyclodextrins used as excipients" pdf, European Medicines Agency, Oct 9, 2017: Page 11 of 16:
According to the data in section 2 one can conclude that below 20 mg/kg/day no serious adverse effects are to be expected for all routes of administration and no statement is deemed necessary.
Above 20 mg/kg/day, cyclodextrins may show some activity, and because there are insufficient safety data in children below two years old, it is advisable to inform about the quantity of cyclodextrin in the product and that for use in children below two years old, a doctor’s recommendation is needed.
Above 200 mg/kg/day cyclodextrins may theoretically cause problems in the digestive system when given orally, and cause mild renal toxicity when given parenteral, which information can be given. Depending on the amount, cyclodextrins may influence the Cyclodextrins used as excipients permeability of tissues and therefore the bioavailability of active substances given topically (nasal, rectal, dermal, ocular).
This is exactly the way I use the HPBCD sublingually, when I complex 90mg DMT to (x7) or 630mg of HPBCD, and I re-dose two more times every 1.5 hour, I am using 1890mg of HPBCD for the evening. I weigh 95kg, so I am using less than 20mg/kg/day or less than 1900mg per day. This always gives me a 4.5 hour long +5 Shulgin level strength experience with super-long afterglow. Very similar to 600mg of mescaline.
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Read lots of questions concerning tetrahydroharmine or THH, so will add this in closing:
As a long time chemist, have years of experience with home-made pure THH, it does not convert back to harmaline, and I've had THH remain 100% stable for many years in a closet, that still glowed pale blue under blacklight, and worked just as well as the day it was made.
See post #13 of this thread for how to make it yourself with pictures in 1.5 hour using harmaline which you can often find on-line if don't want to start from scratch. All you need is a cheap stir mantel from *mazon, vinegar, 10% janitorial ammonia from hardware store, zinc dust, cotton ball in a funnel. I always encourage everyone to learn chemistry.
The liftmode THH paperwork indicates it is made in China, if it truly is over 99% pure, then by all means it should only glow pale blue. Any green in the glow means it has un-converted harmaline, how much is anyone's guess. Harmaline is sedating and causes nausea and dizziness at high doses.
pic 1: 300mg of pure THH for oral use taken 45 minutes before, not shown: 35mg of freebase harmine for sublingual use taken at exact same time under tongue as the 0.5ml (10 drop) 90mg DMT complexed to 630mg HPBCD stored in a 3ml syringe if desired.
Pic 2: Pure tetrahydroharmine glows pale blue under blacklight like LSD or psilocin, harmaline reduces to tetrahydroharmine by gaining a hydrogen atom. Tetrahydroharmine is in the same beta-carboline family as ibogaine, remarkable way beyond 4k monochrome (blue or green for me) closed eye teaching visions at 300mg for hours. No sedation, pleasant stimulation. Adding even small amounts of sublingual or oral HPBCD DMT adds color to the visions.
Edited by tregar, 15 January 2022 - 09:15 AM.
#26
Posted 16 January 2022 - 10:05 AM
I tried the sublingual 2HPBCD / DMT combination last night (60mg n,n + 480mg 2HPBCD), along with 175mg oral Liftmode brand 'THH' and 25mg sublingual harmine. (I'm 150lbs, so I dropped the harmine dosage from Ava's recommended 35mg.)I was very sensitive to the burn - it was almost intolerable and I will not be retrying this ROA. And it is still annoying the next day under my tongue.I did it twice last night as the first time it did not work as I probably did not complex the mixture properly and also did not get the mixture off the spoon very well. So after an hour, I mixed a second batch, using the same amounts of 2HPBCD, dmt, and harmine. (I did not mix the harmine in, just placed it under my tongue for a minute before inserting the complexed mixture.)The second batch of dmt DID work Very happy After about 10 minutes it started to come on, and it quickly became very strong with a few-minute rush, similar to a decent vaped dose.However, it wore off about 10-15 minutes after it started.I did not notice anything extra from the alleged THH. And I did not notice any lengthening of the experience from either the harmine nor the THH.Before giving up on this liftmode THH, I'll try it again and up the dose to closer to 300mg in hopes that there is at least *some* THH in there. And I will use the oral method of complexing the dmt then melting it into hot water to drink along with the THH and maybe ~170mg harmine. Alternatively, I may try complexing the harmine and using it sublingually, upping the dose to 35mg.
Cyclodextrins can be used to reduce or prevent gastrointestinal and ocular irritation, reduce or eliminate unpleasant smells or tastes.The oral bioavailability of cyclodextrins is very low in adult animals and humans (0.1–3%), except for RM-β-CD, which has a bioavailability of 12% in rats. Because of their bulky and hydrophilic nature only insignificant amounts of cyclodextrins are absorbed from the gastrointestinal tract by passive diffusion [33, 27].
Thus, tetrahydroharmine may prolong the half-life of DMT by blocking it's intraneuronal uptake, and hence, its inactivation by MAO, localized in mitochondria within the neuron.
Tetrahydroharmine (THH) has the ability to raise your vibration in a most powerful, yet subtle way. It brings a crystalline prismy texture to spice and adds a super clear watery dimension to Aya, like looking down through 10meters of shimmering Caribbean Sea on clear blue day. It brings a dimension of pure light to the entheogenic experience and encourages entities & intelligences of only the Highest Order. If one is not accustomed to perceiving these experiences with a spiritual perspective most of the nuances & subtleties THH brings on are overlooked and remain unseen and one would better enjoy Harmaline as a house painter chooses a roller over a brush, its about preference & choice.
As to how the THH altered the experience -> I find rue extract+DMT to be very similar to mushrooms. I found the THH added to the rue+DMT to shift the experience to a state much closer to that provided by LSD. It was more clear, more energetic, more focused, and when confusion struck it was definitely more "acid-like".
The vine carries the content of the message, the teaching, and the insight. The purpose of drinking Ayahuasca is to receive the message the vine imparts.
For many people, Ayahuasca-a slowed-down low-res interface of the DMT flash-seems to convey strong messages from the natural world, of nature as sentient energy and spirit matter, of the need to protect the planet we have been given.Yage whispers that human beings are meant to be gardeners of this reality, journeyers, storytellers and singers, weavers of the sacred. DMT, on the other hand, conveys no overt human or humane message.
My experience with smoked DMT was qualitatively different from the realms and beings Ayahuasca introduced me to. For whereas the Ayahuasca worlds seemed rich, luxurious, and abundant in the transformations of organic and supernatural life, DMT brought me to a world--or to some aspect of a world--that appeared from the outset to be highly artificial, constructed, inorganic, and in essence technological.
In the western world, Ayahuasca acquired a new definition: It was now, by definition, the combination of Banisteriopsis caapi and a DMT-containing plant. Ayahuasca became, by definition “orally active DMT.” The first anthropologist to adopt the new definition seems to have been Luis Eduardo Luna in 1984. Luna spent time with Terence McKenna, absorbing his perspective, before beginning his fieldwork. Since then, anthropologists have increasingly adopted this definition and filtered their observations through it. The preeminence of the Ayahuasca vine in the indigenous Amazonian world became the elephant in the living room of Ayahuasca studies, with a tacit agreement to pretend it doesn’t exist.The leaves were Ayahuasca’s “helpers,” I was told, and their purpose was to “brighten and clarify” the visions. The vine is like a cave, and the leaf is like a torch you use to see what is inside the cave. The vine is like a book, and the leaf is like the candle you use to read the book.The vine is like a snowy television set, and the leaf helps to tune in the picture. There was a subtle attitude that the need for strong leaf was the sign of a beginner: An experienced ayahuasquero could see the visions even in low light.Ayahuasca vine is not visionary in the same way as DMT. Visions from vine-only brewsare shadowy, monochromatic, like silhouettes, or curling smoke, or clouds moving across the night sky. It is because their visions are usually monochromatic that vines are classified by the color of vision they produce: white, black, blue, red (in my experience, dark maroon).Snakes, the most common vision on Ayahuasca, are considered the manifest spirit of the vine. Vine visions can be hard to see; in fact, the “visions” may not be visual at all, but auditory or somatic or intuitive. But the vine carries the content of the message, the teaching, and the insight.The leaf helps illuminate the content, but the teachings are credited to the vine. Vine visions are “frequently associated with writing, to a code that is present in visions…or in the ‘books’ where the spirits keep the secrets of the forest.” (Calavia Saez 2011:135).The vine is The Teacher, The Healer, The Guide. The purpose of drinking Ayahuasca is to receive the message the vine imparts. This is why it is the vine, not the leaf, that is classified by the type of vision it gives. “For them the vine is, in truth, a living guide, a friend, a paternal authority” (Weiskopf 2005:104).Listening to the Vine:While I was living in the village, someone began the process of shamanic apprenticeship. There was a series of ceremonies with brews of special strength for that purpose; brews with enormous quantities of vine. About two to three pounds of fresh vine per person was used (about 25 to 35 times the amount needed for MAOI inhibition). Those were powerful experiences indeed.Although the apprenticeship began with crushingly vine-heavy brews, the more the apprentice progressed, the weaker the brew he would need. He would learn to see the dimmest of visions. If he spent a full two years “fasting,” then eventually even smelling or tasting the brew, even touching an Ayahuasca plant, would be enough to visit her realms. On the other hand, he would learn to navigate the strongest of brews with clear focus, and be undistracted by any amount of DMT fireworks.
A traditional saying among Ayahuasqueros is that the jungle vine brings powerful realistic visions, but that the chacruna brings light to these visions. According to the view of Western research, this is not the case; essentially the entire psycho-activity resides with the chacruna leaves DMT content.Ayahuasca researcher Luis Eduardo Luna recently observed that when surveying tribal lore praising the jungle vine, he could find no traces of similar mythology around the two most common plant admixtures; psychotria viridis or diplpterys cabrerana, even though these DMT plants to a Westerner would appear much more important than the harmala alkaloids of the B. caapi liana.
Thus, tetrahydroharmine may prolong the half-life of DMT by blocking it's intraneuronal uptake, and hence, its inactivation by MAO, localized in mitochondria within the neuron.
You can't compare sublingual or oral either..20-30mg sublingual harmine is enough to activate sublingual DMT and cause effects on it's own. 20mg sublingual is probably comparable to 200mg oral.
The absorption of drugs through the sublingual route is 3 to 10 times greater than oral route and is surpassed by hypodermic injection. Sublingual mucosa under tongue is only 100 to 200 microns thick.
Cyclodextrins at high doses can increase drug permeability by direct action on mucosal membranes and enhance drug absorption and/or bioavailability. These effects are possibly caused by solubilisation of membrane lipids through inclusion complexation with cyclodextrins and the ability of cyclodextrins to cause perturbation of membrane integrity. However, unlike detergents, cyclodextrins solubilize membrane components without entering into the membrane, therefore the perturbing effects of cyclodextrins are mild and reversible [7].Cyclodextrins are absorbed poorly via mucosal membranes.
Edited by tregar, 16 January 2022 - 10:56 AM.
#27
Posted 17 January 2022 - 08:09 AM
#28
Posted 19 January 2022 - 05:18 AM
#29
Posted 23 January 2022 - 11:53 AM
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The end: Multiple encounters with death and depression & 80mg DMT complexed to 560mg HPBCD oral Ayahuasca report
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The human race is careening toward extinction: rising acidity of the oceans threatens coral reefs, habitat destruction, non-native species (predatory fish, bullfrogs, fungus, pathogens), climate change (alters temperature and water levels), pollution and diseases (especially chytridiomycosis, caused from the chytrid fungus) all have been shown to contribute to worldwide amphibian declines.We clear forest that are full of trees even though we continue to pump CO2 into the air even though we know it's heating up the ozone and melting ice caps; we clear forests that are full of trees that could potentially help clean that co2 out of the air, the Amazon rainforest is the lungs of the planet, but miles of it are slashed & burned every week so that cattle can graize there instead to make hamburgers, and massive soybean cultivation. We throw away plastic water bottles, and worst of all, we feed into the corporate systems that keep this destruction going.
Experiments that involved several people found the leaf brew form superior to extracted actives, the leaf brews were very strong and powerful & clairavoyant (+5 Shulgin scale), while the extracted actives were mild (+3 Shulgin scale) at best, even up to 100mg. Again, this is poorly understood.
This combined with the HPBCD complexation results (which we really ought to replicate and confirm) makes me wonder whether there are saccharides in leaf brews which perform a similar effect to HPBCD. There is still so much scope for really interesting research here -thanks for posting.
I've seen anecdotal reports of quidded D. cabrerana leaf being active.
People are getting pleasant DMT effects from sublingual Virola calophylla resin. I don't think it has that much DMT in it. So why does the resin work so well when DMT is so hard to use sublingually?
Edited by tregar, 23 January 2022 - 06:33 PM.
#30
Posted 27 January 2022 - 07:57 AM
Igorcarajo said:
Instead of the harmine sublingual, have you tried orally ingested harmine, maybe at the same time as THH, 45 minutes before the sublingual HPBCD-complexed DMT?
Edited by tregar, 27 January 2022 - 01:51 PM.
#31
Posted 05 February 2022 - 09:17 AM
Making this thread so that I can post my thoughts on the dosing method described in this threadhxxps://www.dmt-nexus.me/forum/default.aspx?g=posts&t=96861My few experiences have consisted of about 60 mg of freebase DMT dissolved in 500 mg of HPBCD, with 250-300 mg of THH, and about 35 mg of sublingual harmala/harmalineFrom the start I want to say that sublingual DMT with oral THH is everything I wanted ayahuasca/pharmahuasca to be. And I think it is also the best way for someone to be introduced to DMTWhere do I start with the pros- no nausea at all, even if you take sublingual harmine/harmaline with it. It is such an odd and pleasant feeling to not have to fight constant nausea and vomit inducing dizziness. I literally don't have to worry about having a handy throwup bucket like I did with typical oral DMT.- just the right kind of duration, it never overstays it's welcome, in about an hour you will get whatever you had to receive. No need for a bedridden 2+ h long comedown- crisp, clear headspace. Previous oral DMT experiences have always given me this pinch of delirium and sleepiness to my mental state. But with this combo and I am fully present in it- no come-up anxiety, the transition is gradual and smooth- the DMT visuals are there, and in one experience they seemed even more glowing, or with actual real-life landscapes or persons assembling before my vision instead of the usual DMT geometry- your body will love to move to the music you are listening- let's say you accidental swallow the DMT solution or the saliva build-up becomes unbearable - you will still have a pharmahuasca experience with less if not any nausea. And also this form of oral DMT seems to absorb way better than a typical pharmahuasca- you need less DMT than the typical pharmahuasca- if you aborted the experience (saliva build-up that you spit out) you will now in about 25-30 minutes for sure, and then you can try again with the same DMT dosage, it won't stack like in pharmahuasca where it can sometimes take even 2 hours to enter fullyNow the cons:- the saliva build-up can abort your start or break it's knees. Now if you swallow the solution you will still get a top-tier pharmahuasca trip, I repeat again, with barely any nausea. I tried with some cotton rolls in my mouth to stop the saliva pooling around the DMT solution but it was useless. Next thing I want to try are some saliva pads dentists use: either I trap the solution between the pad and the mouth floor, or I infuse the pads with the DMT solution, put the pad to the cheek mucosa or sublingual mucosa, and enjoy the slow release of DMT (even your lips can absorb this stuff pretty well, one of these days I will use the solution as ointment only for the lips to test it)- and that is pretty much it, I can't think of any other cons of this way of taking DMTWith that in mind here are some questions that could be explored in the future- how to get consistently the neon-glowing visions, they feel like such an eye-candy that your eyes feel compelled to see in all their beauty; is it a certain THH treshhold? less harmine/harmaline or more sublingual harmine/harmaline?- do we really need the mouth floor? can I just smear this on my lips, inner cheek, upper gums or mouth top since with these there is not saliva problem?I still can't believe people aren't all over this method, especially beginners. It is so versatile and maybe even "comfortable". It is worth experimenting only on it for me, goodbye throw bucket and tissues next to my bed, goodbye retching and holding in the taste of earthy vomit, goodbye 5 hour long sedation and diziness that takes up your entire day.I predict in a short time sublingual DMT will have it's separate section on the Nexus.
#32
Posted 06 February 2022 - 10:19 AM
- how to get consistently the neon-glowing visions, they feel like such an eye-candy that your eyes feel compelled to see in all their beauty; is it a certain THH treshhold? less harmine/harmaline or more sublingual harmine/harmaline?
#33
Posted 06 February 2022 - 01:37 PM
- how to get consistently the neon-glowing visions, they feel like such an eye-candy that your eyes feel compelled to see in all their beauty; is it a certain THH treshhold? less harmine/harmaline or more sublingual harmine/harmaline?
#34
Posted 07 February 2022 - 08:15 AM
Always test any THH you may acquire elsewhere. For example, there is a THH many are using that is made in China, with several reports of it not glowing blue when a bit is rubbed on a wet q-tip and smeared on a paper palate, and the plate held under blacklight. Pure tetrahydroharmine glows light blue like LSD under UV light, any green in the glow indicates unconverted harmaline. Five reports so far from nexus people saying it glows green instead of blue like pure THH even though the paperwork indicates over 98% pure. THH never converts back to harmaline once made and remains stable indefintely, so this tells me the initial synthesis on those particular batches was incomplete.
The THH I have does not glow blue (it did not come with a purity certificate), but it definitely is not harmine or harmaline since it does not give nausea at all. Taking more than 300 mg of it makes me a bit dizzy and that's it. And post experience I do feel the typical calmness or composure I got from previous aya drinks.
#35
Posted 12 February 2022 - 05:02 AM
My preference is the sublingual HPBCD dmt, seems to always be some five times stronger than oral, like L-dreamer states: no delirium, very clear and crisp, zero dizziness, zero nausea, when combined with 35mg sublingual harmine and 300mg oral very pure tetrahydroharmine, perfect experience, intensely beautiful and clear just like mescaline. No words to describe. For music lovers like myself, it is a joy to listen to music for hours on end, sounds heavenly just like high dose cactus tea. Profound music enhancement, open eyed beauty infinite, abundant neon colors, the most beautiful teaching Ayahuasca visions, the divine spiritual insights gained are worth the admission alone.
Dirt cheap experience compared to the rare and expensive cactus which I also love dearly. 90mg HPBCD dmt sublingual + 35mg sublingual harmine + 300mg pure THH is like 600mg of mescaline. Intensely beautiful experience.
Taking 200mg of oral harmine + 300mg of oral THH + the sublingual HPBCD DMT taken 1 hour later is an experience so incredible and strong, still no nausea and dizziness for me:
In my trip diary that June night, I documented this oral harmine + oral THH + 90mg sublingual HPBCD dmt around 1 hour later as the most powerful sublingual experience of my life. Not only was there no dizziness or nausea but no anxiety as well, very impressed. For reasons posted by Dr. Narang on post #1, the sublingual HPBCD DMT was many factors more powerful than any dosage of oral HPBCD DMT. It was many factors stronger, around x5 times. It was so powerful that I saw curtains of neon-colored visuals in the open doorway when I looked to my right. Everything in all directions was surrounded by brilliant neon-colored rainbow reflections, the euphoria and music enhancement was very powerful.
Open-eyed beauty was beyond belief, divine and infinite. The tracers were so powerful, that they went on forever like a hall of mirrors into the distance, and instead of there just being multiples of my hands when I waved them, there were beautiful colored fractals inside the tracer smears. One hour after the sublingual HPBCD DMT started to work, it was still as strong visually & transcendence wise as when it started. Only at the 1.5 hour point did the DMT ween down in strength several levels.
The 200mg of harmine was so powerful, that I continued by taking a 2nd dose of sublingual HPBCD DMT again 2 hours later after the 1st dose, and it again worked just as strong as the first dose. With closed eyes were seen brightly colored Ayahuasca visions, in my diary I noted that I saw close to a hundred rapidly changing visions from Egyptian scenery to elaborate art carvings in stone, way beyond 4k in detail. This resulted in a +5 strength Shulgin level journey with life changing consequences.
The harmine having a half-life of from 1 to 3 hours, did not die off until around 5 hours later, so each time I took a re-dose of sublingual HPBCD DMT for the evening, it continued to work very strongly. I highly recommend this approach, and plan to use the oral harmine again with the oral THH many times again in the future, but only using the HPBCD DMT sublingually as noted above. Take care, all the best...peace, love and music.
Pic: 70 grams of pure tetrahydroharmine, will last me a lifetime, more valuable to me than any gold, never depart with. Refer to post #13 on how to make if interested. Pure THH glows blue under blacklight when a bit dabbed onto wet cue tip and smeared on plate under blacklight, serpents are the manifest Spirit of Ayahuasca.
Edited by tregar, 12 February 2022 - 09:57 AM.
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#36
Posted 16 February 2022 - 10:29 AM
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#37
Posted 21 February 2022 - 08:48 AM
Had another try today.Ava was not kidding with the images of beautiful women. Today I had a vision of a naked blonde with the body of a literal Goddess opening my mind's eye like you would a zipper at the beggining. The perfection of the female form in full display with a glistening astral skin. And it wasn't any libido increase, just a sense of witnessing beauty. This effect is so peculiar to me, ava mentioned about certain adrenergic receptors that THH touches like mescaline does, but I could not find a source on how these receptors are actually involved in "Aesthetic perception"
L-dreamer you can find a book that explains receptorome psychedelic theory in James Kent book "Psychedelic information theory." Your visions of naked blonde Goddess beauty is very common in my own sublingual Ayahuasca visions as well, many times I've witnessed naked female forms, a spiritual beauty quality like artwork or music in all her divine perfection.
You can't compare sublingual or oral either..20-30mg sublingual harmine is enough to activate sublingual DMT and cause effects on it's own. 20mg sublingual is probably comparable to 200mg oral.
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#38
Posted 03 March 2022 - 01:24 AM
You can't compare sublingual or oral either..20-30mg sublingual harmine is enough to activate sublingual DMT and cause effects on it's own. 20mg sublingual is probably comparable to 200mg oral.
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#39
Posted 05 March 2022 - 09:48 AM
In my trip diary this June night, I documented this oral 200mg harmine + oral 300mg THH + 90mg sublingual HPBCD dmt around 1 hour later as the most powerful sublingual experience of my life. Not only was there no dizziness or nausea or delirium, but no anxiety as well, very impressed. For reasons posted by Dr. Narang on post #1, the sublingual HPBCD DMT was many factors more powerful than any dosage of oral HPBCD DMT. It was many factors stronger, around x5 times.It was so powerful that I saw curtains of neon-colored visuals in the open doorway when I looked to my right. Everything in all directions was surrounded by brilliant neon-colored rainbow reflections, the euphoria and music enhancement was very powerful.Open-eyed beauty was beyond belief, divine and infinite. The tracers were so powerful, that they went on forever like a hall of mirrors into the distance, and instead of there just being multiples of my hands when I waved them, there were beautiful colored fractals inside the tracer smears. One hour after the sublingual HPBCD DMT started to work, it was still as strong visually & transcendence wise as when it started. Only at the 1.5 hour point did the DMT ween down in strength several levels.The 200mg of harmine was so powerful, that I continued by taking a 2nd dose of sublingual 90mg HPBCD DMT again 2 hours later after the 1st dose, and it again worked just as strong as the first dose. With closed eyes were seen brightly colored Ayahuasca visions, in my diary I note that I saw close to a hundred rapidly changing visions from incredibly beautiful women, birds, gardens, palaces, temples, inner decorations of these palaces, artwork of an entire culture, ancient pristine & perfect architecture to elaborate art carvings in stone, way beyond 4k in detail. The visions never repeat, of a beauty that defies comprehension. This resulted in a +5 strength Shulgin level journey with life changing consequences.The harmine having a half-life of from 1 to 3 hours, did not die off until around 5 hours later, so each time I took a re-dose of sublingual HPBCD DMT for the evening, it continued to work very strongly. I highly recommend this approach, and plan to use the oral harmine again with the oral THH many times again in the future, but only using the HPBCD DMT sublingually as noted above.
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#40
Posted 07 March 2022 - 09:44 AM
What this graph says--in short--is that if you trip some day then you would need to take almost 3 times as much (300%) the day after to achieve the same effect. At least 1-2 weeks of clean time/abstinence would be required for a good estimation. Making sense of your experience usually takes even longer than a week or so, you need time to fully integrate your last trip. Tripping hard definitely requires recovery time. Tetrahydroharmine is unusual in the psychedelic world, in that it "reverses the serotonin transporter" similar to ibogaine, instead of acting directly at 5-ht1a substrate (makes up over 80% of serotonin receptors in the brain) like LSD, mescaline, shrooms. I've done an experiment once in my lifetime taking 300mg of THH every 4 days, and it indeed becomes increasingly stronger and stronger for up to 2 weeks, before a point is reached where you have to stop to reset for a week. So in other words, THH has reverse tolerance, but only up to a point. She is a very special compound, best kept secret in the psychedelic world, 12 reasons why she is important on post #1.
Personal note: I may be a long term chemist, but I developed a method many years ago so that anyone can make tetrahydroharmine (THH) at home. See post #12. I actually fell into a trance state after a death and received the information from a divine source on how to do this, as I was stuck at one point for weeks on end with no solution. No fancy chemicals or equipment needed like TIHKAL THH Synthesis. Due to the hundreds of Spiritual centers in South America needing these plants, Caapi is increasingly being harder to find. You can do this with normal coffee filters and cotton ball stuffed in a funnel. Tetrahydroharmine (THH): she is as valuable as mescaline, can't do without her. Diamondlike shimmering in her beauty.
In brews analyzed by the UDV, Santo Daime and Shuar Indian, THH levels were at the same high levels of harmine in the plant. Somehow, over their day's long cooking process perhaps using vitamin C (hydrogen doner) in the cooking, the THH would attain levels found as harmine in the plants. Harmaline levels often found zero but always very low (0 to 30mg levels) in a typical brew. Just google tetrahydroharmine wikipedia and read the studies attached at bottom.