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Liposomal Delivery Platform:Potency on the Certificate Is Not Potency in the Cell



Liposomal Ingredients | High Absorption Series | Demeter Biotech

 

Liposomal Delivery Platform

Potency on the Certificate Is Not Potency in the Cell

A COA tells you what is inside the powder. It does not tell you how much survives the stomach and reaches the bloodstream. Our liposomal series is engineered to close that gap — with specifications you can audit.

50–90%Active loading options
≥ 90–92%Encapsulation efficiency
80–300 nmRehydrated vesicle size
75+Liposomal SKUs

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The Absorption Problem

Three Obstacles Between Your Formula and the Bloodstream

Most high-value nutraceutical actives fail for the same reasons. Understanding which one applies to your ingredient is the first step in specifying the right delivery format.

  • 1

    Poor aqueous solubility

    Lipophilic molecules such as CoQ10, curcuminoids and resveratrol barely disperse in the gut, so only a fraction is available for absorption at all.

  • 2

    Chemical fragility in the stomach

    Glutathione oxidises, vitamin C degrades under heat and light, and some actives hydrolyse in gastric acid before they ever reach the intestine.

  • 3

    Transport saturation and first-pass clearance

    Vitamin C uptake is capped by sodium-dependent transporters; curcuminoids are rapidly conjugated and cleared. Raising the dose stops helping.

Reported Oral Bioavailability of Unformulated Actives

Curcuminoids

~1%
Resveratrol

~1%
Berberine

~1%
CoQ10

~2%
Silybin

~3%
Quercetin

~5%
Vitamin C (1 g dose)*

~16%

Representative values compiled from published literature on unformulated actives. Indicative only — not a product-specific claim. Liposomal encapsulation is one of several formulation strategies used to address low bioavailability.

How It Works

From Raw Active to Cellular Uptake in Five Steps

A phospholipid bilayer structured like a human cell membrane carries the payload through the barriers that stop a conventional powder.

1

High-Pressure Homogenisation

The active and food-grade phospholipids are processed into nanoscale bilayer vesicles.

2

Precision Spray Drying

The liquid dispersion becomes a free-flowing powder with controlled granule size (D50 ~12–18 μm).

3

Rehydration on Use

In aqueous media the granules release intact liposome spheres in the 80–300 nm range.

4

Protection in Transit

The bilayer shields the payload from gastric acid, oxidation and enzymatic breakdown.

5

Lymphatic Uptake

Vesicles are absorbed through lymphatic pathways, bypassing part of first-pass metabolism.

This section describes liposomal delivery science in general terms. It is not a claim of specific clinical outcomes for any individual ingredient.

Two Numbers Buyers Confuse

Loading and Encapsulation Are Not the Same Thing

Confusing them is the most common — and most expensive — mistake in liposomal procurement.

Active Loading

active weight ÷ total powder weight

How much real active sits in the powder; the rest is phospholipid carrier. Our standard grades are 50%, 70% and — for selected actives — 90%. Higher loading means less carrier per dose.

Encapsulation Efficiency

encapsulated active ÷ total active

Of the active present, how much is genuinely inside the vesicle rather than free on the outside. Our series verifies ≥ 90–92% by centrifugation and HPLC. Low EE% means you are paying for unencapsulated powder.

Raw Material Purity

purity before encapsulation

The purity of the active itself, prior to processing — for example NMN at ≥ 99.5%. This is a third figure, independent of the other two, and should appear separately on the COA.

Powder Required to Deliver 250 mg of Active

Standard powder · 99.5% purity — 251 mg total
250 mg active
Liposomal · 70% loading — 357 mg total
250 mg active
+107 mg carrier
Liposomal · 50% loading — 500 mg total
250 mg active
+250 mg carrier

Arithmetic example: powder required to deliver 250 mg of active ingredient. Higher loading reduces the carrier volume per effective dose — which is what determines cost-in-use, not price per kilogram.

Technical Specifications

Verified Parameters for the Flagship Grades

Every figure below is generated by batch testing and reported on the COA. Specifications for the wider portfolio are available on request.

Product Active Loading Encapsulation Efficiency Vesicle Size (rehydrated) Particle Distribution Phospholipid Source Shelf Life
Liposomal Coenzyme Q10 50% / 70% / 90% ≥ 92% 80–120 nm (DLS) PDI ≤ 0.25 Non-GMO sunflower 24 months
Liposomal Glutathione 50% / 70% / 90% ≥ 90% 100–300 nm Span 2.307 (D50 12.2 μm) Food-grade lecithin 24 months
Liposomal NMN 50% / 70% ≥ 92% 100–250 nm Span 1.450 (D50 16.9 μm) Food-grade lecithin 24 months
Liposomal Curcumin 50% / 70% ≥ 90% 100–300 nm Span 5.284 (D50 17.5 μm) Food-grade lecithin 24 months
Liposomal Vitamin C 50% / 70% ≥ 90% 100–300 nm (DLS) PDI ≤ 0.3 Non-GMO sunflower / soy 24 months

Maximum Active Loading by Grade

Coenzyme Q10

90%
Glutathione

90%
NMN

70%
Curcumin

70%
Vitamin C

70%

Hot Selling Products

Flagship Grades With Full Test Reports

These five carry complete particle-size and encapsulation documentation — Malvern Mastersizer granule analysis, DLS vesicle sizing, HPLC assay and EE% verification.

Liposomal NMN

Liposomal NMN

50% / 70% Loading

EE ≥ 92%D50 16.9 μm100–250 nm

NAD+ precursor shielded from gastric degradation. Substrate purity ≥ 99.5% verified by HPLC.

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Liposomal Glutathione (Reduced)

Liposomal Glutathione (Reduced)

50% / 70% / 90% Loading

EE ≥ 90%D50 12.2 μmOdor-Masking

Protects the active thiol group, preserves the reduced state and traps sulfurous aroma inside the vesicle.

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Liposomal Coenzyme Q10

Liposomal Coenzyme Q10

50% / 70% / 90% Loading

EE ≥ 92%80–120 nmZeta −25~−35 mV

Non-GMO sunflower lecithin, PDI ≤ 0.25. The tightest size distribution in the series.

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Liposomal Curcumin

Liposomal Curcumin

50% / 70% Loading

EE ≥ 90%D50 17.5 μm100–300 nm

Turns a hydrophobic pigment into a dispersible emulsion. No synthetic emulsifiers or surfactants.

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Liposomal Vitamin C

Liposomal Vitamin C

50% / 70% Loading

EE ≥ 90%PDI ≤ 0.3Gastro-Friendly

Non-acidic delivery that bypasses the saturation limit of sodium-dependent vitamin C transporters.

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Full Portfolio

The Series by Application Category

Fifteen representative grades across seven categories — from NAD+ precursors to botanical extracts and everyday micronutrients.

Longevity & NAD+ Support

NMN, NR, PQQ and senolytic actives for healthy-aging formulations.

Liposomal NR (Nicotinamide Riboside)
Liposomal NR (Nicotinamide Riboside)
50%
Liposomal PQQ
Liposomal PQQ
50%
Liposomal Urolithin A
Liposomal Urolithin A
98%
Liposomal Spermidine
Liposomal Spermidine
50% / 70%

Antioxidant & Detox

Master-antioxidant and glutathione-precursor actives.

Liposomal NAC
Liposomal NAC
Glutathione precursor
Liposomal Alpha Lipoic Acid
Liposomal Alpha Lipoic Acid
ALA
Liposomal Fisetin
Liposomal Fisetin
Senolytic

Cellular Energy & Cardiovascular

Mitochondrial and cardiometabolic support ingredients.

Liposomal Resveratrol
Liposomal Resveratrol
50% / 70%
Liposomal Pterostilbene
Liposomal Pterostilbene
Trans-pterostilbene

Anti-Inflammatory & Metabolic

Botanical actives for inflammatory balance and metabolic health.

Liposomal Apigenin
Liposomal Apigenin
Pure apigenin
Liposomal Berberine HCl
Liposomal Berberine HCl
Berberine
Liposomal TUDCA
Liposomal TUDCA
Tauroursodeoxycholic acid

Brain, Mood & Sleep

Nootropic and relaxation actives with improved handling.

Liposomal Alpha GPC
Liposomal Alpha GPC
Nootropic
Liposomal L-Theanine
Liposomal L-Theanine
Green tea extract
Liposomal Melatonin
Liposomal Melatonin
Sleep support
Liposomal GABA
Liposomal GABA
Gamma-aminobutyric acid

Vitamins & Minerals

Everyday nutrients reformulated for tolerance and uptake.

Liposomal Vitamin D3
Liposomal Vitamin D3
50%
Liposomal Magnesium Glycinate
Liposomal Magnesium Glycinate
High loading
Liposomal Vitamin B12
Liposomal Vitamin B12
Methylcobalamin

Botanical Extracts

Standardised plant extracts in liposomal form.

Liposomal Milk Thistle
Liposomal Milk Thistle
Silymarin / silybin
Liposomal Quercetin
Liposomal Quercetin
50% / 70%
Liposomal Rhodiola Rosea
Liposomal Rhodiola Rosea
Salidroside / rosavins
Liposomal Green Tea Extract
Liposomal Green Tea Extract
Plant-derived

Quality & Testing

What We Measure — and What You Receive

Malvern Mastersizer 2000

Dry powder granule size, D50 and Span for flowability and dosing consistency

Malvern Zetasizer (DLS)

Nano-scale vesicle size, PDI distribution and zeta potential stability

HPLC

Active assay, loading verification and encapsulation efficiency by centrifugation

TEM

Structural confirmation of spherical bilayer formation after rehydration

ICP-MS

Heavy metal compliance — Pb ≤ 2 ppm, As ≤ 1 ppm

Encapsulation Efficiency by Grade

Coenzyme Q10

≥ 92%
NMN

≥ 92%
Glutathione

≥ 90%
Curcumin

≥ 90%
Vitamin C

≥ 90%

Encapsulation efficiency by flagship grade, verified by centrifugation and HPLC.

ISOGMPHACCPHalalKosher

Applications

Where Liposomal Grades Earn Their Premium

Capsules & Tablets

High loading keeps serving sizes compact for space-restricted dosage forms.

Sachets & Drink Mixes

Water-dispersible powder re-forms a stable emulsion — no clumping, no sediment.

Functional Beverages

Nano-scale dispersion suits ready-to-drink and shot formats.

Beauty-from-Within

Actives such as glutathione and vitamin C for internal skin-brightening concepts.

Clinical & Professional

Batch-verified particle data for protocols that require documented specifications.

Gummies & Chewables

Odor masking and gastro-friendly profiles improve sensory acceptance.

FAQ

Questions Procurement Teams Actually Ask

What is the difference between Active Loading and Encapsulation Efficiency?

Active Loading (50% / 70% / 90%) is the share of actual active compound in the total weight of the powder. Encapsulation Efficiency (≥ 90–92%) is the share of that active which is genuinely trapped inside the liposome vesicle rather than sitting free on the outside. Both numbers appear on our COA.

Why is the powder particle size measured in micrometres when liposomes are nanometres?

The D50 value (typically 12–18 μm) describes the dry spray-dried granule, which is what matters for industrial flowability and dosing. Once rehydrated, those granules release the actual 80–300 nm liposome spheres that perform the delivery.

How much liposomal powder do I need for a target active dose?

Divide the target dose by the loading. For 250 mg of active: roughly 251 mg of a 99.5% pure powder, 357 mg of a 70% loading powder, or 500 mg of a 50% loading powder. Higher loading means less carrier per dose.

Which phospholipid source do you use?

Non-GMO sunflower lecithin as standard, with soy lecithin available on request. Both are food-grade and suitable for clean-label positioning.

Is the powder water-soluble or water-dispersible?

Water-dispersible. When added to water it re-forms a stable nano-scale emulsion that may appear slightly milky or opaque — that opacity is the physical signature of a true liposomal system, not a defect.

What testing documentation is provided?

Batch COA with assay and encapsulation efficiency, particle size analysis (Malvern Mastersizer / Zetasizer), TEM structural confirmation where applicable, and heavy metal testing by ICP-MS (Pb ≤ 2 ppm, As ≤ 1 ppm). Full COA and TDS are provided for quality audit.

What are the standard packing and supply terms?

1 kg aluminium foil bags and 25 kg fibre drums with internal PE lining. Samples are available; OEM and private-label formats — hard capsules, soft capsules, tablets, granules, sachets — can be produced to specification.

Can loading and carrier be customised?

Yes. Bespoke loading levels (for example 60%) and alternative phospholipid carriers can be developed for bulk industrial orders, subject to minimum quantity.

How should the powder be stored?

Store in a cool, dry place away from light and heat, in tightly sealed packaging. Shelf life is 24 months under recommended conditions.

Are your liposomal ingredients suitable for vegan formulations?

The delivery system is built from plant-derived phospholipids with no synthetic emulsifiers or surfactants. Suitability for a specific finished-product claim should be confirmed against your own formulation and certification scheme.

Request Specifications, Samples and Batch COA

Tell us the active, the target loading and the dosage form. We will return available grades, particle data and documentation for evaluation.

Note: Specifications listed are typical batch values for the flagship grades shown and are provided for evaluation purposes; confirm against the batch COA supplied with your order. Statements about delivery technology describe formulation science in general and have not been evaluated by any regulatory authority. This product range is not intended to diagnose, treat, cure or prevent any disease. Buyers are responsible for compliance with the labelling and health-claim regulations of their target market.

 


Post time: Sep-08-2026