Activated Charcoal 100% 60’s

Activated Charcoal 100% pure Capsule 500mg.

Why Our Pure Activated Charcoal Capsule Works Quicker & Better

1. Higher binding power per capsule
   Other products often contain only 30% Activated Charcoal mixed with fillers such as brown rice flour. In a 500 mg capsule, that means just 150 mg is real charcoal, while the rest is inactive bulk. Our formula contains a full 500 mg of 100% pure Activated Charcoal, giving over three times more active binding sites per capsule. This means toxins are bound faster and more completely, with fewer capsules needed.
2. Faster onset of action
   Because every milligram of our capsule is active charcoal (and not filler), there is maximum surface area available immediately in the stomach and intestines. This ensures that mould toxins, Candida die-off by-products, and other harmful compounds are captured more quickly than in diluted formulas.
3. Greater efficiency
   With diluted products, clients may need to take 3–4 capsules to equal the binding power of just one of ours. That means more filler intake and less efficiency. Our pure capsules provide direct, fast, and powerful detox support.

 

Why Our Powder is More Difficult to Work With

We use a pharmaceutical-grade activated charcoal powder with a particle size of 0–100 microns.

• Ultra-fine particle size creates a very high surface area (thousands of square meters per gram), making it extremely effective at trapping toxins.
• However, this also makes it very light and fluffy, which means it is more difficult to handle in production. It tends to float, cling to equipment, and compress poorly compared to coarser powders.
• Even though it is harder to manufacture with, we choose this grade because it ensures maximum toxin-binding capacity and faster action for our clients.

 

Summary

• Our product is 100% pure Activated Charcoal — no fillers.
• Each capsule provides the full 500 mg active dose, unlike diluted formulas.
• It works faster and better, binding toxins efficiently and reducing the number of capsules needed.
• We use an ultra-fine pharmaceutical charcoal (0–100 μm) with superior surface area, even though it is harder to encapsulate, because it gives the best detox effect.

 

Comprehensive Explanation: Activated Charcoal

 

What it is:

Activated Charcoal (AC) is a highly processed, medical-grade form of carbon that has been treated at extremely high temperatures to create an enormous surface area filled with millions of microscopic pores. Just one gram of activated charcoal can have up to 3,000 m² of surface area, making it a natural adsorbent (binding surface) for toxins in the digestive tract.

It is completely inert and not absorbed into the bloodstream — meaning it works only in the gut, where it captures unwanted compounds such as mould toxins, Candida die-off aldehydes, gases, pesticides, and bile-bound chemicals, carrying them safely out in the stool.

 

How it works:

Unlike absorption (where a substance is taken inside), adsorption means toxins stick to the surface of charcoal. These toxins are held tightly in the pores and then carried safely out of the body through the stool. This makes AC a powerful gut-local detoxifier, preventing toxins from being reabsorbed into the bloodstream (interrupting enterohepatic recirculation).

 

How is Activated Charcoal Made?

1. Raw Material Selection
   • Activated Charcoal is usually made from natural carbon-rich sources such as coconut shells, hardwood, bamboo, or other plant materials.
   • These materials are chosen because they leave behind a pure carbon base when heated.

 

1. Carbonization
   • The raw material is heated to 600–900°C in an oxygen-limited environment.
   • This removes water and volatile compounds, leaving behind a black carbon structure (similar to normal charcoal, but not yet “activated”).

 

1. Activation
   • The carbonized material is then treated to open up pores and massively increase surface area. This can be done by:
     • Steam Activation: Exposing the carbon to hot steam at 800–1,100°C, which burns away internal channels and creates micropores.
     • Chemical Activation: Treating with natural activating agents (like phosphoric acid or zinc salts) before heating, which also produces a porous network.

 

1. Milling & Grading
   • After activation, the charcoal is ground into a fine powder (0–100 µm for pharmaceutical grade).
   • The fine size ensures the maximum binding capacity is available when taken as capsules or mixed in liquids.

 

Why it Works

• Pores act as binding sites: Toxins, gases, and small molecules “stick” to the surface of the pores through weak electrical and hydrophobic forces (adsorption).
• Size-specific action: Small, hydrophobic toxins (like aflatoxin, ochratoxin A, aldehydes) fit perfectly into these pores, while nutrients like vitamin C, minerals, and proteins are too polar or too large to bind significantly.
• Safe elimination: Because it is not absorbed into the bloodstream, everything bound to Activated Charcoal is excreted naturally in the stool within 12–24 hours.

 

What it binds:

AC is most effective for small, hydrophobic, and aromatic toxins — especially mycotoxins from mould (aflatoxins, ochratoxin A, zearalenone), aldehydes from Candida die-off, pesticides, drug residues, and bile-bound chemicals.

 

What it does not bind:
It is far less effective at binding large molecules (polysaccharides, proteins, whole Candida cells, parasites, worms, eggs) or very polar/ionic nutrients (vitamin C, B vitamins, amino acids, most minerals). These are too big or too water-soluble to fit into the charcoal pores, and they remain available for absorption.

 

Timing & action:
AC begins working immediately when it enters the gut. Because it is not absorbed into the bloodstream, its effect is 100% local. It remains active until excreted in the stool, usually within 12–24 hours.

 

What is retained vs excreted:

• Excreted with AC: Mycotoxins, aldehydes, pesticides, volatile oils, sterols, fat-soluble vitamins (if dose is large and taken close to meals/supplements).
• Retained (absorbed): Vitamin C, amino acids, ionic minerals, polysaccharides, fibers, and most water-soluble nutrients.

 

Excretion route:

Everything bound to AC is excreted in stool, which may turn dark or black. This is harmless and a normal sign that charcoal is carrying toxins out.

Comparison table of common essential oils (EOs) and how 100% pure Activated Charcoal (AC) capsules interact with them. Since essential oils are mostly small, lipophilic (fat-loving), volatile molecules (100–200 Da range), they are among the compounds most likely to be bound by AC. This explains why large doses of charcoal can reduce the effect of oils if taken together.

 

Comprehensive Table: What Activated Charcoal Binds vs Not

Category	Example Molecules	Approx Size (MW / Physical Size)	AC Affinity	What Happens with AC (500 mg capsule)	Excreted vs Retained
Mycotoxins	Aflatoxin B1 (312 Da), Ochratoxin A (403 Da), Zearalenone (318 Da), Sterigmatocystin (324 Da)	Small, planar, <2 nm	High	Strong adsorption into micropores	Excreted (80–100%)
Trichothecenes	DON (296 Da), T-2 toxin (466 Da)	Small, polar	Moderate	Variable adsorption, pH-dependent	Partial excretion; partial absorption
Fumonisins	Fumonisin B1 (721 Da)	Larger, polar	Moderate	Partial adsorption depending on AC pore size	Mixed outcome
Candida by-products	Acetaldehyde (44 Da), aromatic aldehydes	Very small	High	Easily adsorbed	Excreted
Whole Candida cells	Yeast: 4–6 µm; Hyphae up to 20–50 µm	Micrometer scale (too big)	None	Cannot fit pores	Remain (cleared by immune system & stool bulk)
Parasites & worms	Protozoa 5–50 µm; Worm eggs 50–150 µm	Micrometer scale	None	Too large to adsorb	Remain (excreted mechanically)
Proteins & polysaccharides	β-glucans, mucilage, inulin	Thousands of Da, large	Very low	Too large to fit	Remain
Volatile oils & terpenes	Thymol, carvacrol, citral, cinnamaldehyde	150–200 Da	High	Some adsorption	Partial excretion
Sterols	β-sitosterol (414 Da)	Small, lipophilic	High	Partially adsorbed	Partial excretion
Fat-soluble vitamins	A, D, E, K (328–472 Da)	Small, lipophilic	High	Can be adsorbed at higher doses	Partial excretion
Water-soluble vitamins	Vitamin C (176 Da), B vitamins (120–300 Da)	Small, polar, ionic	Low	Not adsorbed	Retained
Amino acids	Glutamine (146 Da), Taurine (125 Da), NAC (163 Da)	Small, polar	Low	Not adsorbed	Retained
Minerals (ionic)	Zinc gluconate, Se-glycinate, Mg²⁺, Na⁺	Ionic	Low	Not adsorbed	Retained
Fulvic acid (comparison)	Fulvic fractions 500–2000 Da	Small, polar	Moderate	Some adsorbed, many act as “shuttles”	Mixed: part retained, part excreted

 

Summary for Product Sheet

• Activated Charcoal is a pure toxin binder that works only in the gut.
• It binds small toxic molecules (mycotoxins, aldehydes, pesticides, volatile oils, fat-soluble toxins) and safely removes them in the stool.
• It does not bind whole organisms or large nutrients (Candida cells, parasites, proteins, vitamins like C, amino acids, minerals).
• It starts working immediately after ingestion, stays active until excreted, and turns stool dark as it carries toxins out.

 

Key Notes

• Essential oils are small, aromatic molecules → AC binds them strongly.
• When taking 100% Activated Charcoal capsules (500 mg), most essential oils taken at the same time will be adsorbed and carried out in stool instead of being absorbed.
• Timing matters: To get the benefits of essential oils (capsules, tinctures, aromatherapy internally), take them at least 2 hours apart from charcoal capsules.
• Retained: Water-soluble plant compounds (e.g., polyphenols, flavonoid glycosides) are not bound and remain active.

 

✨ In simple terms: Pure Activated Charcoal is excellent at binding essential oils—which is useful if the goal is detox, but it means that EO-based remedies should be spaced away from charcoal use.

 

General herbs we use in our products (not the essential oils, but the main herbal actives).

Because herbs are chemically diverse, I’ve grouped their representative actives (alkaloids, flavonoids, glycosides, terpenes, polysaccharides, etc.) and shown:

• Molecular weight (MW/size range)
• Affinity to Activated Charcoal (AC)
• % Retained vs % Excreted (for a 500 mg 100% AC capsule)
• Key comments

 

⚖️ Note: Percentages are approximate ranges based on polarity, molecular weight, and adsorption studies. They are useful for client education but not exact lab values.

 

General Herbs & Activated Charcoal 500mg Capsule

Herb (common)	Representative Actives	MW/Size	AC Affinity	% Retained	% Excreted	Comments
African Potato (Hypoxis)	β-sitosterol glycosides	400–600 Da	Moderate–High	80–90%	10–20%	Sterols partly bound; polysaccharides remain
Aloe	Aloin, aloe-emodin (anthraquinones)	~418 Da	Moderate	85–95%	5–15%	Polysaccharides not affected
Andrographis	Andrographolide (diterpene lactone)	~350 Da	Moderate	85–95%	5–15%	Glycosides absorbed normally
Barberry / Goldenseal	Berberine alkaloid	336 Da	Moderate	85–95%	5–15%	Small fraction bound
Bearberry (Uva Ursi)	Arbutin glycoside	272 Da	Low	95–100%	0–5%	Almost fully retained
Bilberry	Anthocyanins (glycosides)	430–950 Da	Low–Moderate	90–95%	5–10%	Pigments mostly retained
Black Jack (Bidens)	Flavonoids, phenylpropanoids	300–600 Da	Moderate	85–95%	5–15%	Minor flavonoid loss
Buchu	Pulegone, menthone (EOs)	152–170 Da	High	70–80%	20–30%	Volatile oils strongly bound
Burdock Root	Arctiin (lignan), inulin	534 Da; >1000 Da	Moderate	85–95%	5–15%	Inulin fiber fully retained
Calendula	Flavonoids, saponins	300–900 Da	Low–Moderate	90–98%	2–10%	Saponins largely unaffected
Cancerbush (Sutherlandia)	Canavanine, glycosides	176–700 Da	Low–Moderate	90–95%	5–10%	Small triterpene fraction bound
Cayenne (Capsicum)	Capsaicinoids	305–337 Da	High	70–85%	15–30%	Capsaicin partly bound
Chamomile	Apigenin, flavonoids	270–430 Da	Moderate–High	80–90%	10–20%	Apigenin aglycone partly bound
Cinnamon	Cinnamaldehyde (EO)	132 Da	High	70–80%	20–30%	EO strongly bound
Cordyceps	Cordycepin, β-glucans	251 Da; polymers	Low	95–100%	0–5%	Polysaccharides not bound
Cryptolepis	Cryptolepine alkaloid	232 Da	High	70–85%	15–30%	Lipophilic alkaloid partly bound
Cumin / Black Seed	Thymoquinone	164 Da	High	70–85%	15–30%	Strong EO binding
Dandelion	Caffeoylquinic acids	354–516 Da	Low–Moderate	90–95%	5–10%	Polar acids mostly safe
Echinacea	Alkylamides, caffeic acids	247–354 Da	High (alkylamides)	75–85%	15–25%	Alkylamides bound; phenolic acids remain
Garlic	Allicin, organosulfurs	162–250 Da	Moderate	85–90%	10–15%	Minor sulfur compound loss
Grape Seed Extract	Procyanidins (OPCs)	290–900 Da	Moderate–High	80–90%	10–20%	Larger oligomers bound
Grapefruit	Naringin glycoside	~580 Da	Low–Moderate	90–95%	5–10%	Polar flavonoids remain
Lavender	Linalool, linalyl acetate	154–196 Da	High	70–80%	20–30%	Volatile oils bound
Lemon Balm	Rosmarinic acid, EOs	360 Da; 152 Da	Low–High	85–95%	5–15%	Oils bound; phenolic acids retained
Milk Thistle	Silymarin flavonolignans	~482 Da	Moderate–High	80–90%	10–20%	Small fraction bound
Moringa	Quercetin, glucosinolates	302 Da	Moderate–High	80–90%	10–20%	Quercetin partly bound
Neem	Azadirachtin, limonoids	720–1000 Da	Moderate–High	80–90%	10–20%	Some limonoids bound
Olive Leaf	Oleuropein	540 Da	Low–Moderate	90–95%	5–10%	Mostly retained
Oregano	Carvacrol, thymol (EOs)	150 Da	High	70–80%	20–30%	Strong EO binding
Pau d’Arco	Lapachol	242 Da	High	70–85%	15–30%	Lipophilic napthoquinone bound
Plantain	Aucubin glycoside	346 Da	Low	95–100%	0–5%	Fully retained
Psyllium	Soluble fiber (polymers)	Very large	Indirect	—	—	Not bound; escorts toxins
Reishi	Triterpenes, β-glucans	400–500 Da; polymers	Moderate–High	80–90%	10–20%	β-glucans retained
Shiitake	Lentinan (β-glucan), eritadenine	Polysaccharide; 271 Da	Low	95–100%	0–5%	Retained
Slippery Elm	Mucilage polysaccharides	Very large	Indirect	—	—	Protective coating, not bound
Thyme	Thymol, carvacrol (EOs)	150 Da	High	70–80%	20–30%	EO strongly bound
Turmeric	Curcuminoids	368–400 Da	High	70–85%	15–30%	Partly bound if taken with AC
Wormwood	Thujone, lactones	152–248 Da	High	70–80%	20–30%	Volatile fraction bound
Yarrow	Flavonoids, azulenes	270–500 Da	Moderate–High	80–90%	10–20%	Mostly retained
Yellow Dock	Anthraquinone glycosides	~430 Da	Moderate	85–90%	10–15%	Glycosides partly bound

 

Key Takeaways

• Most water-soluble compounds (vitamin C, caffeic acids, polysaccharides, glycosides, fibers) → 95–100% retained.
• Lipophilic, volatile, and aromatic compounds (essential oils, sterols, alkylamides, curcuminoids, capsaicin) → only 70–85% retained, 15–30% excreted with 500 mg AC.
• Fibers (psyllium, slippery elm, inulin) → not bound at all; instead they escort toxins and protect the gut lining.
• Overall: charcoal removes toxins more than nutrients, but spacing from EO-rich herbs maximises retention.

 

We now go right into the science of how Activated Charcoal (AC) works.

Clients often think charcoal “absorbs” like a sponge, but the truth is it adsorbs toxins onto its surface. Here is a clear explanation:

 

1. What are the “receptors” in Activated Charcoal?

 

Activated Charcoal doesn’t have biological receptors like cells do. Instead, it has millions of tiny pores created by superheating carbon. These pores are of different sizes:

• Micropores (<2 nanometers) → catch very small molecules like aflatoxin, ochratoxin, aldehydes.
• Mesopores (2–50 nanometers) → trap medium-sized molecules like bile acids, sterols, volatile oils.
• Macropores (>50 nanometers) → serve as “entrances” or channels that guide molecules into the smaller binding pores.

 

Together, these pores create a surface area so vast that 1 gram of AC can expose up to 3,000 m² of binding surface.

 

2. How do toxins “stick” inside?

 

The walls of the pores act as the “catching sites” for toxins. Instead of chemical reactions, the mechanism is mostly:

• Van der Waals forces (weak electrical attractions)
• Hydrophobic interactions (fat-loving toxins are drawn to the carbon surface)
• π–π stacking (planar, aromatic molecules like mycotoxins stack flat against the carbon sheets)

 

These interactions hold the toxins tightly inside the pores, much like dust sticking to a static cloth. They are not absorbed into the charcoal, just stuck on the surface until excreted.

 

3. What gets caught vs what slips through?

 

• Caught (Excreted):
  • Hydrophobic, planar toxins (aflatoxin, ochratoxin A, zearalenone, sterigmatocystin)
  • Aromatic aldehydes (Candida die-off acetaldehyde)
  • Volatile oils (thymol, carvacrol, menthol)
  • Sterols, bile acids, pesticides

 

• Slip through (Remain):
  • Large molecules (proteins, polysaccharides, Candida or parasite cells, worm eggs) — too big for the pores
  • Very polar/ionic nutrients (vitamin C, amino acids, minerals) — too water-soluble to stick

 

4. What happens afterward?

 

Once toxins are caught, the AC–toxin complex cannot be broken down or absorbed by the gut. It simply passes through the intestines and is excreted in stool, usually within 12–24 hours.

 

✨ Summary:

Activated Charcoal works by using its millions of pores as “toxin traps”. These pore walls act like natural binding sites (receptors), catching small, fat-loving toxins through weak electrical and hydrophobic forces, and carrying them safely out of the body in stool.

 

What does it do to the Digestive System and organs? Where does it work, and is it safe?

Clients often ask if Activated Charcoal (AC) is safe and how it affects the digestive system and organs. Herewith comprehensive and clear explanation.

 

1. Where Activated Charcoal Works

 

• Stomach & Intestines: AC acts only inside the digestive tract. It does not enter the bloodstream because it cannot cross the intestinal lining.
• Primary action site: The gut lumen, where food, herbs, supplements, and toxins mix before absorption.
• Excretion: AC, along with everything it binds, is passed out in the stool within 12–24 hours.

 

👉 In short: it stays in the gut and never leaves it.

 

2. What it Does to the Digestive System

 

• Binding toxins: Catches mycotoxins, pesticides, bile acids, aldehydes, and some drugs before they can be absorbed.
• Reduces reabsorption: Stops toxins from being reabsorbed through the enterohepatic cycle (where the liver dumps toxins into bile and the gut tries to reabsorb them).
• Gas & bloating relief: Binds some intestinal gases and bacterial metabolites, reducing bloating.
• Protective effect: By reducing irritants, AC can calm gut inflammation and protect the intestinal lining.
• Side effects at high doses:
  • Constipation (most common) → because AC can slow gut motility and absorb water.
  • Black stools → harmless, but expected.
  • Rarely, if taken without enough water, can cause gut blockage in very high doses.

 

3. What it Does to Organs

 

• Liver: Indirect support — by catching toxins in the gut, AC prevents them from cycling back to the liver, reducing liver burden.
• Kidneys: No direct effect, because AC is not absorbed. Kidneys benefit indirectly, since fewer toxins enter the blood.
• Other organs: AC never reaches other tissues. Its role is purely gut-local.

 

4. Is it Safe?

 

• Yes, in recommended amounts.
• AC is considered biologically inert — the body does not digest or absorb it.
• Safe for short- or medium-term use in detox protocols or for binding acute toxins.
• Safety considerations:
  • Should be taken away from medications (at least 2 hours apart) to avoid interference.
  • Long-term, high-dose use can reduce absorption of fat-soluble vitamins (A, D, E, K) and some essential oils — this is why many formulas (like your 500 mg capsule) only use a small supportive dose.
  • Always drink plenty of water with AC to prevent constipation.

 

✨ Summary:

Activated Charcoal works only in the gut, where it safely binds toxins and carries them out in the stool. It does not enter the blood, so it has no direct effect on the liver, kidneys, or other organs — instead, it reduces their workload by preventing toxins from being absorbed. At proper doses it is safe, though higher intakes can cause constipation or bind nutrients if not spaced properly.

 

Safe Use Guide: 100% Pure Activated Charcoal

✓ Safe & Beneficial Effects	⚠️ Precautions & Considerations
Works only in the gut — never enters the bloodstream	Take 2 hours away from medications or supplements (AC may bind them)
Binds and removes mould toxins, Candida die-off aldehydes, pesticides, gases	In very high doses, may reduce absorption of fat-soluble vitamins (A, D, E, K)
Helps reduce gas, bloating, diarrhoea, food poisoning symptoms	May cause constipation if not enough water is taken
Relieves liver & kidney load by preventing toxin reabsorption	Causes black stools — harmless but expected
Inert and non-toxic — body does not digest or absorb it	Not a substitute for antifungal, antiparasitic, or medical treatments
Starts working immediately in stomach and intestines	Very rarely, excessive doses without water may cause gut blockage

 

Key Client Guidance

• Dosage: Follow label instructions (commonly 500 mg capsules, 2–4 caps up to 3× daily in detox programs).
• Hydration: Always take with a full glass of water.
• Timing: Keep 2 hours apart from medicines and supplements.
• Duration: Safe for short- or medium-term detox; for long-term use, combine with nutrient-rich diet and monitoring.
• Excretion: Leaves body in stool within 12–24 hrs — turning stool dark is normal and harmless.

 

✨ Summary:

Activated Charcoal is a safe, natural binder that works only in the gut, catching toxins before they are absorbed, supporting detox while protecting the body’s organs. With water and proper timing, it is an effective and well-tolerated detox aid.

 

Activated Charcoal in our 500 mg Mould & Mycotoxin Capsule

“Our capsule uses a very small amount of activated charcoal, so it focuses on binding mycotoxins while leaving 80–100% of most herb actives available; only a small fraction (often ≤10–20%) of the most lipophilic, volatile components may bind.”

Each 500 mg Mould & Mycotoxin Capsule contains only 6.435 mg of Activated Charcoal, a gentle amount that supports detox without depleting nutrients. At this level, charcoal selectively binds and removes harmful mycotoxins and die-off by-products from mould, Candida, and fungi, while leaving the beneficial herbs, amino acids, vitamins, and minerals in the formula fully available for absorption. This ensures safe and effective toxin removal with maximum therapeutic benefit.

 

Each of our 500 mg Mould & Mycotoxin capsules contains only 6.435 mg of Activated Charcoal. This is a very small supportive dose—just over 1% of the total capsule. At this level, the charcoal does not dominate the formula but plays a selective role as a gentle binder. Its purpose is to help catch the tiny toxic molecules that mould, fungi, and Candida can release, such as mycotoxins (aflatoxin, ochratoxin, zearalenone) and aldehydes. These toxins are all nano-sized compounds (measured in billionths of a meter), which fit into the pores of charcoal and are carried out of the body through the stool.

Because the charcoal content is low, it has minimal impact on the nutrients and herbs in the capsule. Most of the vitamins, amino acids, minerals, and polar herbal compounds (such as vitamin C, zinc, selenium, glutamine, NAC, caffeic acids, and polysaccharides) are not bound at all and remain fully available for absorption. Only a very small fraction of fat-soluble or lipophilic compounds—like essential oils, sterols, curcuminoids, or fat-soluble vitamins—may interact with the charcoal. Even then, at 6.435 mg, the charcoal has a limited capacity, so binding of beneficial compounds is minor.

The benefit of including this small amount of charcoal is that it supports detox without depleting nutrients. It acts like a mop in the gut, capturing the toxic by-products of mould and Candida die-off while leaving the rest of the formula to do its therapeutic job. In contrast to a full charcoal capsule (250–500 mg), which would bind nutrients much more aggressively, our low-dose inclusion ensures a balanced effect: binding and removing toxins while allowing the herbs, amino acids, and vitamins in the capsule to be absorbed and support the body’s recovery.

 

Overview

Activated charcoal (AC) is a porous adsorbent with an enormous surface area that captures molecules within its micropores (<2 nm) and mesopores (2–50 nm). Mycotoxins such as aflatoxins, ochratoxin A, and trichothecenes are small molecules (typically 300–750 Da; 0.8–1.8 nm) that fit easily into AC’s pore system.

In our capsule, AC is present at 6.435 mg, which is a very small amount compared with common stand-alone binder doses (250–1000 mg). At this level, AC functions as a gentle supportive binder: it helps to capture free mycotoxins and microbial by-products in the gut, while leaving the majority of our herbal actives bioavailable.

 

Why it removes “remnants” of killed mould/mycotoxins

When antifungal and immune-supporting herbs act against mould, candida, and other pathogens, fragments of cell walls and soluble toxins are released into the gut. AC adsorbs (Adsorption is the process where molecules of a substance, called the adsorbate, adhere to the surface of another substance, the adsorbent. This surface phenomenon can occur with gases or liquids and is driven by unsaturated forces on the adsorbent’s surface, which form bonds with the adsorbate) toxic debris and hydrophobic molecules so that they can be excreted, reducing toxic recirculation.

 

Selectivity and molecular size

Binding to AC depends on chemical nature, not just size:

• Hydrophobic and aromatic molecules are adsorbed most strongly.
• Polar and ionic compounds show little to no binding.
• Fulvic acid and mucilage from our formulation partially shield beneficial nutrients from AC.
• Psyllium fiber further escorts both toxins and AC-bound material out of the body.

 

Context in our formulation

• At 6.435 mg, AC’s effect is modest and not comparable to therapeutic binder protocols.
• Mycotoxin capture: directionally helpful but limited in volume.
• Herbal interference: minimal; only certain lipophilic actives (volatile oils, curcuminoids, sterols) are modestly affected.
• Polar vitamins, amino acids, and minerals remain fully bioavailable.

 

Supportive synergy in our capsule

• Fulvic acid competes with AC surfaces, protecting nutrients.
• Psyllium seed and slippery elm fibers reduce direct AC–herb interactions while enhancing toxin clearance.
• Mucilage creates a protective matrix, lowering adsorption of delicate phytochemicals.

 

Mycotoxin size reference

• Aflatoxin B1 (~312 Da; 0.9–1.1 nm): strong AC binding.
• Ochratoxin A (~403 Da; 1.1–1.3 nm): strong AC binding.
• Zearalenone (~318 Da; 1.1–1.3 nm): moderate–high AC binding.
• Deoxynivalenol (~296 Da; 0.9–1.1 nm): moderate binding.
• T-2 toxin (~466 Da; 1.2–1.6 nm): moderate–high binding.
• Fumonisin B1 (~721 Da; 1.5–2.0 nm): variable, binds better in mesoporous AC.

 

Our 500 mg Mould & Mycotoxin Capsule showing, for each ingredient: the key active compounds, their approx. MW/size, affinity to Activated Charcoal (AC), and the likely outcome in our ~6.44 mg AC context (what tends to Remain vs be Excreted/Bound).

• Remain: compounds that are not appreciably bound by AC → absorbed to act in the body.
• Excreted/Bound: compounds that do attach to AC in the gut → carried out in stool (together with toxins).

 

Activated Charcoal Interaction in our 500 mg Capsule (with estimated % retained vs excreted)

Ingredient	Representative Active(s)	Approx MW/size	AC Affinity	What Remains (Retained & Absorbed)	What is Excreted/Bound (with AC)	Estimated % Retained / Excreted
Activated Charcoal	—	—	—	—	Mycotoxins, bile-carried hydrophobics	—
Fulvic Acid	Fulvic acids	500–2000 Da	Moderate	Most organic acids, trace minerals	Small fraction of fulvic	85–95 / 5–15
African Potato (Hypoxis)	β-sitosterol glycosides	400–600 Da	Moderate–High	Polysaccharides, minerals	Small sterol fraction	80–92 / 8–20
Aloe marlothii	Aloin, aloe-emodin	~418 Da	Moderate	Polysaccharides/mucilage	Minor anthraquinones	85–95 / 5–15
Andrographis	Andrographolide	~350 Da	Moderate	Polar glycosides	Some lactone	85–95 / 5–15
Barberry / Berberine	Berberine	336 Da	Moderate	Ionized/polar salt forms	Small free berberine	85–95 / 5–15
Bearberry (Uva-ursi)	Arbutin	272 Da	Low	Arbutin	Negligible	95–100 / 0–5
Bilberry	Anthocyanins	430–950 Da	Low–Moderate	Most anthocyanins	Minimal	90–98 / 2–10
Black Jack (Bidens)	Flavonoids, phenylpropanoids	300–600 Da	Moderate	Glycosides	Some aglycones	85–95 / 5–15
Buchu	Pulegone, menthone (EOs)	152–170 Da	High	Flavonoids, tannins	Some volatile oils	80–90 / 10–20
Burdock Root	Arctiin; inulin	534 Da; polymers	Moderate	Inulin, minerals	Some lignans	85–95 / 5–15
Calendula	Flavonoids, triterpenes, saponins	300–900 Da	Low–Moderate	Saponins/glycosides	Minor aglycones	90–98 / 2–10
Cancerbush (Sutherlandia)	Canavanine; sutherlandiosides	176–700 Da	Low–Moderate	Canavanine, glycosides	Some triterpene glycosides	90–98 / 2–10
Cayenne	Capsaicinoids	305–337 Da	High	Vitamins/polars	Some capsaicinoids	80–90 / 10–20
Chamomile	Apigenin, flavonoids, azulenes	270–430 Da	Moderate–High	Glycosides/coumarins	Apigenin aglycone fraction	80–92 / 8–20
Christmas Bush	Polyphenols, diterpenes	300–500 Da	Moderate	Polar polyphenols	Some diterpenes	85–95 / 5–15
Cinnamon	Cinnamaldehyde (EO)	132 Da	High	Tannins/water-solubles	Volatile cinnamaldehyde	80–90 / 10–20
Cordyceps	Cordycepin; β-glucans	251 Da; polymers	Low	Cordycepin, β-glucans	Negligible	95–100 / 0–5
Coriander	Linalool (EO)	154 Da	High	Polar flavonoids	Some linalool	80–90 / 10–20
Cryptolepis	Cryptolepine	232 Da	High	Glycosidic/ionized forms	Some cryptolepine	80–90 / 10–20
Cumin (Black seed)	Thymoquinone	164 Da	High	Fatty acids/sterols	Some thymoquinone	80–90 / 10–20
Dandelion	Caffeoylquinic acids; STLs	354–516 Da	Low–Moderate	Chlorogenic/caffeic acids	Minor STLs	90–98 / 2–10
Echinacea	Alkylamides; caffeic acids	247–354 Da	High (alkylamides)	Phenolic acids	Some alkylamides	80–90 / 10–20
Garlic	Allicin; organosulfurs	162–250 Da	Moderate	Water-soluble S-compounds	Small allicin fraction	85–95 / 5–15
Goldenseal	Berberine	336 Da	Moderate	Majority as salts	Small free fraction	85–95 / 5–15
Grape Seed Extract	Procyanidins	290–900 Da	Moderate–High	Monomers/small oligomers	Larger oligomers	80–92 / 8–20
Grapefruit Extract	Naringin (glycoside)	~580 Da	Low–Moderate	Naringin/polar flavonoids	Minimal	90–98 / 2–10
Horseradish Root	Allyl isothiocyanate	99 Da	Moderate–High	Glucosinolates	Small volatile fraction	80–92 / 8–20
Lavender Leaf	Linalool, linalyl acetate	154–196 Da	High	Rosmarinic acid/phenolics	Small EO fraction	80–90 / 10–20
Lemon Balm	Rosmarinic acid; EOs	360 Da; volatiles	Low / High	Rosmarinic acid	Some volatile oils	90–98 / 2–10 (phenolics)
Lemongrass	Citral (EO)	152 Da	High	Polyphenols	Some citral	80–90 / 10–20
Licorice Root	Glycyrrhizin; flavonoids	822 Da	Moderate	Glycyrrhizin/polysaccharides	Minor aglycones	85–95 / 5–15
Lion’s Mane	β-glucans; erinacines	polymers; ~500–700 Da	Low–Moderate	β-glucans	Small erinacine fraction	90–98 / 2–10
Milk Thistle	Silymarin complex	~482 Da	Moderate–High	Majority of silymarin	Small fraction	80–92 / 8–20
Moringa	Quercetin; glucosinolates	302 Da; polar	Moderate–High (quercetin)	Glucosinolates	Some quercetin	80–92 / 8–20
Neem	Azadirachtin; limonoids	720–1000 Da	Moderate–High	Polar phenolics	Some limonoids	80–92 / 8–20
Olive Leaf	Oleuropein; hydroxytyrosol	540 Da; 154 Da	Low–Moderate	Oleuropein/hydroxytyrosol	Minimal	90–98 / 2–10
Oregano	Carvacrol, thymol (EOs)	~150 Da	High	Rosmarinic acid	Some volatile oils	80–90 / 10–20
Pau d’Arco	Lapachol	242 Da	High	Glycosides	Some lapachol	80–90 / 10–20
Plantain	Aucubin (glycoside)	346 Da	Low	Aucubin	Negligible	95–100 / 0–5
Psyllium Seed	Soluble fiber	Very high MW	Indirect	Fiber not absorbed; escorts toxins	—	— (escort effect)
Pumpkin Seed	Phytosterols; fatty acids	280–400 Da	High	Protein/minerals	Some sterols	80–90 / 10–20
Reishi	Triterpenes; β-glucans	400–500 Da; polymers	Moderate–High	β-glucans	Some triterpenes	80–92 / 8–20
Shiitake	Lentinan; eritadenine	Polymer; 271 Da	Low	Both retained	Negligible	95–100 / 0–5
Slippery Elm	Mucilage polysaccharides	Very high MW	Indirect	Protective mucilage	Escorts debris; limits binding	— (protective)
Tansy	Thujone (EO)	152 Da	High	Polar flavonoids	Some thujone	80–90 / 10–20
Thyme	Thymol, carvacrol (EOs)	~150 Da	High	Phenolic acids	Some volatile oils	80–90 / 10–20
Turmeric	Curcuminoids	368–400 Da	High	Majority of curcuminoids	Small fraction bound	80–90 / 10–20
Walnut Leaves & Shells	Juglone; tannins	174–1000 Da	Moderate–High	Ellagitannins/phenolic acids	Some juglone/tannins	80–92 / 8–20
Wormwood (African)	Thujone; STLs	152–248 Da	High	Flavonoids	Some volatiles/STLs	80–90 / 10–20
Yarrow	Flavonoids; azulenes	270–500 Da	Moderate–High	Glycosides	Some azulenes/aglycones	80–92 / 8–20
Yellow Dock	Anthraquinone glycosides	~430 Da	Moderate	Glycosidic forms	Some aglycones	85–95 / 5–15
Vitamin A acetate	Retinyl acetate	328 Da	High	Most vitamin A	Small fraction	80–90 / 10–20
Vitamin C	Ascorbic acid (ionic)	176 Da	Low	All retained	None	95–100 / 0–5
Vitamin D3	Cholecalciferol	384 Da	High	Most vitamin D3	Small fraction	80–90 / 10–20
Vitamin E acetate	α-Tocopheryl acetate	472 Da	High	Most vitamin E	Small fraction	80–90 / 10–20
L-Glutamine	Amino acid	146 Da	Low	All retained	None	95–100 / 0–5
N-Acetyl-L-Cysteine	NAC	163 Da	Low	All retained	None	95–100 / 0–5
Quercetin	Flavonol (aglycone)	302 Da	Moderate–High	Majority	Some bound	80–92 / 8–20
Selenium AAC (glycinate)	Chelated selenium	~200–300 Da	Low	Retained	None	95–100 / 0–5
Taurine	Sulfonic amino acid	125 Da	Low	Retained	None	95–100 / 0–5
Zinc Gluconate	Mineral salt/chelate	—	Low	Retained	None	95–100 / 0–5

 

MW = Molecular Weight

• Molecular weight (MW) is the “mass” of a single molecule, expressed in Daltons (Da) or grams per mole (g/mol).
• Small molecules have low MW (e.g., Vitamin C = 176 Da). Large molecules like polysaccharides have high MW (thousands of Da).
• MW gives an idea of whether a molecule is small enough to fit into the pores of activated charcoal.

 

Size

• In addition to MW, molecules have a physical size/shape (measured in nanometers, nm).
• Activated Charcoal has different types of pores:
  • Micropores (<2 nm)
  • Mesopores (2–50 nm)
• Most mycotoxins are small molecules (0.8–1.8 nm) → they easily fit into AC micropores.
• Large molecules (like polysaccharides, proteins, mucilage) are too bulky → they do not fit, so they are not bound.

 

Why it matters for our capsule

• Low MW, lipophilic, aromatic compounds (essential oils, sterols, small toxins) → more likely to bind.
• High MW or polar molecules (fibers, glycosides, vitamins, amino acids) → less likely to bind.
• That’s why in the table we show both MW/size and affinity: it explains scientifically why some compounds are retained while others may be excreted with charcoal.

 

👉 Example:

• Aflatoxin B1: 312 Da (~1.1 nm) → fits in micropores → strongly adsorbed.
• Vitamin C: 176 Da but very polar/ionic → doesn’t stick to charcoal → remains available.
• Polysaccharides (Slippery Elm mucilage, Psyllium fiber): very large (>10,000 Da) → can’t fit → remain in gut, not bound.

 

Adsorption is the process where molecules of a substance, called the adsorbate, adhere to the surface of another substance, the adsorbent. This surface phenomenon can occur with gases or liquids and is driven by unsaturated forces on the adsorbent’s surface, which form bonds with the adsorbate. Key examples include activated carbon purifying water by adsorbing organic molecules and activated alumina removing moisture from air.

 

Key Conclusions

1. At 6.435 mg per capsule, AC provides a supportive binder effect for mycotoxins without materially reducing absorption of most actives.
2. Volatile oils, sterols, curcuminoids, and lipophilic flavonoids are the most affected, but only minor fractions are bound at this level.
3. Polar compounds (vitamin C, NAC, taurine, glutamine, polyphenol glycosides) are unaffected and remain bioavailable.
4. Fulvic acid, psyllium, and slippery elm further reduce any interference and enhance elimination.
5. Clients do not need to separate dosing for this product from most supplements; a 1–2 hour gap is only advised for sensitive prescription medications.

 

Comparison table with our 6.435mg AC, compared to 50% in a capsule. Will the outcome still be the same?

The outcome would not be the same. Jumping from ~6.435 mg AC to ~50% of a 500 mg capsule (~250 mg AC) massively increases binding capacity and competition for actives, so a lot more of the lipophilic/aromatic compounds will end up bound & excreted instead of absorbed.

Below are clear, client-friendly comparisons.

1) Affinity-Tier Comparison (retained vs excreted)

These evidence-informed ranges assume one 500 mg capsule taken with food/fiber/fulvic. They’re educational estimates (not lab measurements).

Affinity tier to AC	Examples (chemistry)	6.435 mg AC Estimated Retained / Excreted	~250 mg AC (50%) Estimated Retained / Excreted
Low	Highly polar/ionic: vitamin C, amino acids (glutamine, NAC, taurine), mineral chelates (zinc gluconate, Se-glycinate)	95–100% / 0–5%	90–100% / 0–10%
Low–Moderate	Polar phenolics & glycosides: anthocyanins (bilberry), naringin (grapefruit), chlorogenic/rosmarinic acids	90–98% / 2–10%	75–95% / 5–25%
Moderate	Mid-polarity aromatics: berberine (partly ionized), lignans, many flavonoids	85–95% / 5–15%	50–85% / 15–50%
Moderate–High	Planar aromatics/terpenoids: silymarin (milk thistle), quercetin, larger OPCs, triterpenes	80–92% / 8–20%	30–70% / 30–70%
High	Volatile oils & very lipophilic: carvacrol/thymol (oregano/thyme), cinnamaldehyde, citral, thujone; sterols; curcuminoids; fat-soluble vitamins A/D/E	80–90% / 10–20%	20–60% / 40–80%

 

Takeaway: at 50% AC, many key lipophilic actives (EOs, sterols, curcuminoids, fat-soluble vitamins) can shift from “mostly retained” to substantially excreted.

 

2) What this means for typical actives in our formula

Ingredient/Active (example)	Affinity	6.435 mg AC (Retained → Excreted)	~250 mg AC (50%) (Retained → Excreted)	Comment for clients
Vitamin C (ascorbic acid)	Low	~98–100% → 0–2%	~95–100% → 0–5%	Polar/ionic → barely affected even at high AC.
Amino acids (Glutamine, NAC, Taurine)	Low	95–100% → 0–5%	90–100% → 0–10%	Still largely available.
Minerals (Zinc gluconate, Se-glycinate)	Low	95–100% → 0–5%	90–100% → 0–10%	Ionic/chelated → minimal loss.
Anthocyanins (Bilberry)	Low–Mod	90–98% → 2–10%	75–95% → 5–25%	Some extra loss at 50% AC.
Rosmarinic/Chlorogenic acids (Lemon balm, Dandelion)	Low–Mod	90–98% → 2–10%	75–95% → 5–25%	Still mostly retained.
Berberine (Barberry/Goldenseal)	Moderate	85–95% → 5–15%	50–85% → 15–50%	Much bigger hit at 50% AC (less systemic berberine).
Quercetin (Moringa/Quercetin)	Mod–High	80–92% → 8–20%	30–70% → 30–70%	Large planar aromatic → vulnerable at high AC.
Silymarin (Milk thistle)	Mod–High	80–92% → 8–20%	30–70% → 30–70%	Hepatic support could be blunted at 50% AC.
OPCs (Grape seed)	Mod–High	80–92% → 8–20%	30–70% → 30–70%	Larger oligomers bind more at high AC.
Curcuminoids (Turmeric)	High	80–90% → 10–20%	20–60% → 40–80%	Major loss at 50% AC unless separated.
Essential oils: Oregano/Thyme (carvacrol/thymol), Cinnamon (cinnamaldehyde), Lemongrass (citral), Lavender (linalool)	High	80–90% → 10–20%	20–60% → 40–80%	Volatile, lipophilic → strongly affected by high AC.
Sterols (Pumpkin seed, Hypoxis β-sitosterol)	High	80–90% → 10–20%	20–60% → 40–80%	Sterol uptake heavily reduced at 50% AC.
Fat-soluble vitamins A/D/E	High	80–90% → 10–20%	20–60% → 40–80%	Strongly impacted at 50% AC.
β-Glucans & Mucilage (Lion’s mane, Reishi, Slippery elm, Psyllium)	Indirect/Low	≈100% retained	≈100% retained	Big, hydrophilic polymers; they escort toxins and can even reduce AC–nutrient contact.
Fulvic acids	Moderate	85–95% → 5–15%	60–85% → 15–40%	At high AC, more fulvics will be taken up by charcoal; charcoal sites less “coated” by small dose competition.
Mycotoxins (aflatoxin, OTA, etc.)	High	Capture: modest	Capture: high	Detox improves with higher AC—but so does nutrient binding.

 

Practical guidance

• With 6.435 mg AC (our current formula):
  • Acts as a gentle binder while preserving most herb actives.
  • No strict separation from supplements needed (medications: consider 1–2 h spacing).
• With ~250 mg AC (50% capsule):
  • Mycotoxin capture improves, but lipophilic actives and fat-soluble vitamins would be substantially sequestered.
  • Strongly recommend separating that capsule from herbs/nutrients by ≥2 hours, ideally taking the high-AC binder away from meals/supplements/meds.
  • For best outcomes: make the high-AC binder a separate product and keep the multi-herb capsule’s AC low (as it is now).

 

Guide to what a 100% Activated Charcoal (AC) 500 mg capsule can bind from common mould/mycotoxin exposures, including a note on fungus & Candida.

 

What AC Binds: Major Mould & Mycotoxins

Legend (AC Affinity):
High = consistently strong binding in vitro; Moderate = variable/condition-dependent; Low = generally limited.
(“What remains” = fraction likely to escape binding and be absorbed; “What is adsorbed” = fraction likely to be bound to AC and excreted.)

Notes: Activated charcoal shows very strong binding for many planar, hydrophobic mycotoxins (e.g., aflatoxins, ochratoxin A, zearalenone) across studies, while binding is more variable for others (e.g., fumonisin B1, some trichothecenes like DON/T-2) and depends on AC pore structure, pH, and matrix. PubMedScienceDirectMDPI

Mycotoxin (family)	Main mold producers	MW (Da)	AC Affinity	What is adsorbed (excreted with AC)	What remains (absorbed)	Key evidence
Aflatoxins (B1, B2, G1, G2)	Aspergillus flavus, A. parasiticus	B1: 312.27	High	Majority at adequate AC dose	Minor fraction	Strong AC performance v. aflatoxins reported across binders; AFB1 MW confirmed. PubMedPubChemNIST WebBook
Ochratoxin A (OTA)	Aspergillus, Penicillium spp.	403.8	High	Very high (often >97% in vitro stomach-like conditions with AC)	Small fraction	Multiple studies/reviews; >97% at 1 ppm with activated coconut charcoal. PMCMDPIPubChem
Zearalenone (ZEA)	Fusarium spp.	318.36	High	High (planar, hydrophobic lactone)	Small–moderate	AC among best adsorbents for ZEA; MW confirmed. ScienceDirectMDPIUS EPA
Deoxynivalenol (DON / vomitoxin)	Fusarium graminearum	296.32	Moderate (variable)	Moderate; increases with optimized porous carbons	Notable fraction	Carbon materials can adsorb DON; performance varies by AC type/pH. PMC+1
T-2 toxin (trichothecene)	Fusarium spp.	466.5	Low–Moderate	Limited–moderate	Moderate–substantial	Systematic data show lower adsorption averages vs AFB1/ZEA. Nature
HT-2 toxin	Fusarium spp.	424.5	Low–Moderate	Limited–moderate	Moderate	Generalized from trichothecene behavior; lower than AFB1/OTA/ZEA. Nature
Nivalenol (NIV)	Fusarium spp.	312.3	Low–Moderate	Limited–moderate	Moderate	Polar trichothecene; variable adsorption. PMC
Fumonisin B1 (FB1)	Fusarium verticillioides	721.8	Moderate (pH-dependent)	Moderate with suitable AC/conditions	Variable	Adsorption to AC demonstrated; improved at mildly acidic pH; MW confirmed. ResearchGateMilliporeSigmaPMC
Sterigmatocystin	Aspergillus spp.	324.3	High	High (structurally akin to aflatoxins)	Small	Structural analog to AFB1; MW confirmed. WikipediaPubChem
Citrinin	Penicillium, Monascus spp.	250.25	Moderate–High	Moderate–high	Small–moderate	MW confirmed; planar aromatic polyketide → adsorbable. PubChemWikipedia
Patulin	Penicillium expansum	154.12	Moderate–High	Moderate–high	Small–moderate	AC used for patulin removal; MW confirmed. PubChemfermentek.com
Alternariol (AOH)	Alternaria spp.	258.23	Moderate–High	Moderate–high	Small–moderate	Polyphenolic, planar; MW confirmed. PubChemWikipedia
Alternariol monomethyl ether (AME)	Alternaria spp.	272.25	Moderate–High	Moderate–high	Small–moderate	Often behaves like AOH; MW confirmed. PubChem
Enniatin B (cyclo-depsipeptide)	Fusarium spp.	639.8	High	High (lipophilic cyclic peptide)	Small	Lipophilic; AC effective vs multiple mycotoxins. MW confirmed. PubChemMDPI
Beauvericin	Beauveria, Fusarium spp.	783.9	High	High (very lipophilic cyclic peptide)	Small	As above; MW confirmed. PubChem
Gliotoxin	Aspergillus fumigatus	326.4	High	High (hydrophobic ETP)	Small	Lipophilic fungal metabolite; MW confirmed. PubChemWikipedia
Mycophenolic acid	Penicillium spp.	320.3	Moderate–High	Moderate–high	Small–moderate	Lipophilic phenolic acid; MW confirmed. PubChem

 

Bottom line: With 500 mg of pure AC, binding is strongest for aflatoxins, OTA, ZEA, sterigmatocystin, enniatins/beauvericin, gliotoxin. It’s more variable for fumonisins and some trichothecenes (e.g., DON, T-2/HT-2), but still meaningful with the right AC and gut conditions (pH, contact time). PubMedScienceDirectMDPINature

 

What about “mould,” “fungus,” and “Candida” themselves?

• Whole fungal cells/spores (e.g., Aspergillus, Penicillium, Candida) are microscopic particles (µm-scale)—too large to “fit” AC’s micro/mesopores. AC doesn’t kill or trap whole organisms like an antimicrobial or antiparasitic drug would.
• AC can adsorb hydrophobic toxins and cell-wall breakdown by-products those organisms release (e.g., gliotoxin, small aromatic phenolics), which are the main symptom-driving molecules in the gut. (See table above for individual toxins.)

 

Dosing Questions (for 100% AC capsules, 500 mg each)

Your scenario: “Typically they take 2–4 capsules, 3× daily.” → That’s 3–6 g/day total.

 

Is it better to spread to 3× daily

Yes. Spacing doses (e.g., breakfast / mid-afternoon / bedtime) maintains continuous binding coverage as bile continuously delivers recirculating toxins to the gut. Frequent smaller doses reduce ‘gaps’ where toxins could reabsorb (enterohepatic recirculation). This matches how AC is used to interrupt toxin recirculation in clinical toxicology (repeated doses), though exact protocols vary by toxin and setting. PubMed

 

What if you take more at once vs less but more often?

• More at once: Higher instant capacity (good if a single meal/exposure is the issue) but more likely to grab co-ingested nutrients/meds.
• Less, more often: Steadier coverage with less nutrient competition per dose—often preferable for ongoing mycotoxin exposure.

 

Practical tip: Keep at least 2 hours away from medications and key supplements (longer for narrow-therapeutic-index drugs). AC is non-specific and can adsorb some drugs. PubMed

 

Does AC keep you awake at night

No direct stimulant effect. AC is inert and not absorbed; it shouldn’t affect sleep physiology. Some people prefer bedtime AC because it’s far from meds/food; others avoid it if they’re prone to constipation or reflux when lying down. (Hydration helps.)

 

How is everything excreted

Activated Charcoal stays in the gut; bound toxins leave via stool, often darkening it. This is the desired pathway—sequestration + fecal excretion reduces re-entry into the bloodstream. PubMed

 

Does pure Activated Charcoal excrete parasites & worms?

No. AC is not an antiparasitic and doesn’t kill or expel worms. It may adsorb toxins and irritants that parasites produce, which can reduce symptoms, but confirmed deworming requires antiparasitic medications or targeted botanicals under professional guidance. Use AC as a supportive binder, not as a stand-alone parasite treatment.

 

Safety & Practical Notes 

• Separate AC from medications by ≥2 hours (longer if critical meds).
• Expect black stools; watch for constipation—add water + fiber.
• For extended high-dose use (grams/day), check with a clinician—especially if on anticoagulants, thyroid meds, digoxin, anticonvulsants, etc.
• AC choice matters: pore size distribution and surface chemistry drive performance differences for harder toxins like fumonisins/DON. PMC+1

 

Quick reference: Molecular weights (Da)

AFB1 312.27, OTA 403.8, ZEA 318.36, DON 296.32, T-2 466.5, HT-2 424.5, FB1 721.8, Sterigmatocystin 324.3, Citrinin 250.25, Patulin 154.12, Alternariol 258.23, AME 272.25, Enniatin B 639.8, Beauvericin 783.9, Gliotoxin 326.4, Mycophenolic acid 320.3. PubChem+12PubChem+12PubChem+12US EPANatureMilliporeSigma

 

What happens to the die-off cells of parasites, worms, eggs, broken down candida? What are their sizes, and does AC help in any way?

This practical question comes up a lot when clients are doing detox or antifungal/antiparasitic protocols. Let’s break it down clearly.

1. What happens to die-off cells (parasites, worms, Candida)?

 

When antifungal, antibacterial, or antiparasitic herbs/medicines act, they damage or kill the organism. The results include:

• Whole or partial cells/fragments → pieces of cell wall, membranes, organelles.
• Intracellular contents → proteins, enzymes, metabolites, nucleic acids, endotoxins.
• Toxins and by-products → mycotoxins from fungi, acetaldehyde from Candida, inflammatory molecules, ammonia, etc.

 

The immune system + gut peristalsis then process and move these remnants:

• Large debris is phagocytosed (eaten) by immune cells or broken down enzymatically.
• Smaller fragments and soluble toxins spill into the gut lumen.
• From there, they can either be absorbed (and cause Herx/die-off symptoms) or bound & eliminated if adsorbents/fiber are present.

 

2. Approximate size ranges

 

Organism / debris	Typical size (live cell/egg)	Debris/fragment size after die-off	AC relevance
Parasites (protozoa)	5–50 µm	fragments <1 µm; soluble toxins	Too large intact, but soluble debris can be adsorbed
Helminths (worms)	cm–m long; eggs 50–150 µm	cell wall pieces, proteins, lipids, heme products	AC cannot bind intact worms/eggs (too big) but can bind breakdown toxins & some proteins
Candida yeast cells	4–6 µm (hyphae up to 20–50 µm)	cell wall fragments, mannans, β-glucans, acetaldehyde, aromatic toxins	Whole cells too large; AC binds acetaldehyde, aromatic aldehydes, phenolic by-products
Bacterial die-off (Herx)	0.5–2 µm	endotoxins, lipopolysaccharides (~10–20 kDa)	LPS is large/polar, AC has limited direct effect but can adsorb associated hydrophobic fragments
Mycotoxins (secondary metabolites of fungi)	0.8–2 nm	already small molecules	Ideal targets for AC binding

 

⚖️ Scale reminder: Activated Charcoal pores bind best to small molecules (<2 nm). Whole cells/eggs are thousands of times larger (microns) → far too big to enter AC pores.

3. Does Activated Charcoal help?

 

✅ Yes, for toxins & fragments:

• AC does not capture whole parasites, eggs, or intact yeast (too big).
• But it does capture many of the toxic breakdown products released during die-off (acetaldehyde, aromatic aldehydes, phenolic toxins, mycotoxins, bile-bound irritants).
• This reduces Herxheimer/die-off symptoms (fatigue, brain fog, inflammation).

 

❌ No, for whole organisms/eggs:

• These must be cleared by peristalsis, fiber, mucilage, bile, and the immune system.
• AC helps indirectly by reducing the irritant load from what those cells release when broken.

 

4. How die-off is excreted

 

• Large debris (parasite fragments, worm segments, fungal cell walls): moved by gut motility + stool bulk (fiber is critical).
• Smaller toxic molecules: can be adsorbed by AC or excreted with bile (then bound by AC).
• If not bound, toxins may re-absorb via enterohepatic recirculation → this is what AC helps interrupt.

 

5. Summary

 

• Whole parasites/worms/eggs: too big for charcoal → leave via stool if motility/fiber is good.
• Candida cells: too big, but their toxic by-products (acetaldehyde, phenolic aldehydes, mycotoxins) are ideal AC targets.
• Size difference: cells/eggs = micrometers (10⁻⁶ m), toxins = nanometers (10⁻⁹ m). AC pores only take the nano-sized toxins.
• Charcoal role: not a dewormer or antifungal, but a binder that reduces symptoms of die-off by catching what those organisms release.

 

Comparison table that shows the differences between Activated Charcoal (AC) and Fulvic Acid (FA), including:

• How each one works (mechanism)
• What they bind best
• What % is excreted vs absorbed
• Practical effect for detox and nutrients

 

Comparison Table: Activated Charcoal vs Fulvic Acid

Feature	Activated Charcoal (AC)	Fulvic Acid (FA)
What it is	Pure carbon, highly porous, inert substance	Complex mixture of very small organic acids, phenolics, and trace minerals
Absorption into body	0% absorbed (works only in the gut)	Partially absorbed (tiny molecules can cross membranes and enter cells)
Mechanism of action	Works like a sponge: tiny pores physically adsorb small hydrophobic molecules (toxins, mycotoxins, bile-bound chemicals) and carry them out in stool	Works like a shuttle/chelator: chemically binds metals, minerals, and charged toxins; also carries nutrients across membranes and into cells
Best binding targets	Mycotoxins (aflatoxins, ochratoxin, zearalenone), aldehydes (Candida die-off), aromatic toxins, pesticides, bile-bound toxins	Heavy metals (lead, mercury, cadmium, arsenic), radionuclides, pesticides, agrochemicals, some herbicides; enhances absorption of trace minerals
What happens to toxins	Bound in gut → excreted 100% via stool	Bound in gut (unabsorbed fraction) → excreted in stool; absorbed fraction can carry metals/toxins to kidneys for urinary excretion
Impact on nutrients	Can also bind fat-soluble vitamins (A, D, E, K), sterols, essential oils, some medications (if dose is high or close to timing) → small nutrient loss	Generally protective: fulvic acids can increase absorption of minerals (zinc, selenium, iron, magnesium) and vitamins; risk of nutrient loss is low
% Retained vs Excreted (nutrients)	Retained: ~80–95% (most nutrients escape binding at therapeutic doses) Excreted: ~5–20% of lipophilic compounds if timing is close	Retained: ~90–100% (nutrients often enhanced) Excreted: only bound heavy metals, excess minerals, and toxins
% Retained vs Excreted (toxins)	Retained: 0–20% (some mycotoxins/trichothecenes can slip past if charcoal dose is low) Excreted: ~80–100% of many mycotoxins and hydrophobic toxins	Retained: ~0–20% (some very large toxins not bound) Excreted: ~80–100% of metals, pesticides, and charged toxins
Where it works	Only in gut lumen (not absorbed)	Gut + systemic (tiny fraction absorbed into blood; works inside cells and kidneys too)
Time in body	Passes through gut in ~12–24 hours	Circulates systemically (absorbed fraction) for hours, unabsorbed part passes in stool
End effect	Reduces toxin reabsorption, relieves Herx/die-off symptoms, interrupts enterohepatic recirculation	Mobilizes and chelates metals/toxins, supports cellular energy, improves nutrient absorption

 

Summary for Clients

• Activated Charcoal is like a sponge that stays in the gut. It grabs mycotoxins, aldehydes, pesticides, bile toxins and carries them out in stool. But it can also grab a small fraction of vitamins, oils, and medicines if taken too close in time.
• Fulvic Acid is like a shuttle and chelator. It works both in the gut and inside the body, escorting metals and toxins out, while enhancing nutrient absorption. Unlike AC, it usually improves nutrient status rather than reducing it.
• Using them together is synergistic: AC binds hydrophobic mycotoxins in the gut; FA chelates metals and supports nutrient uptake.