ab:MAX™ LIPOSOMAL TECHNOLOGY

What’s inside
matters.
So does delivery.

From digestive exposure to absorption.
Explore why formulation matters.

Explore the technology ↓
KOREAN INNOVATION / A CLOSER LOOK
SMALL STRUCTURE. BIG QUESTIONS.Illustrative phospholipid bilayer around a vitamin C ingredient
Ingredient + phospholipid structureILLUSTRATIVE

01 / THE DIGESTIVE CHALLENGE

The amount you take
isn’t the whole story.

Before an ingredient can be absorbed, it must navigate a changing digestive environment. Its stability—and the way it’s formulated—can influence what becomes available for absorption.

  1. 01

    Ingredients meet the digestive environment.

    As a supplement releases its contents, ingredients encounter stomach acid and digestive enzymes. How they respond depends on their chemistry and formulation.

  2. 02

    Sensitive ingredients can change along the way.

    Changing pH and chemical reactions can alter susceptible ingredients before absorption. Some remain stable; others are more vulnerable to degradation.

  3. 03

    What’s available must still be absorbed.

    At the intestinal lining, stability is only part of the story. The ingredient must also be available in a form the body can absorb.

How we study digestive behavior ↗
FOLLOW THE INGREDIENT01 / STOMACH EXPOSURE
Supplement ingredients encountering a changing digestive environmentIllustrative ingredient particles encounter the stomach and small intestine. Some shapes change to represent possible chemical degradation. The view zooms into a highlighted point in the small intestine to reveal a circular cross-section with the intestinal lining surrounding the central space, distinguishing availability from absorption. No particle count represents a measured loss or absorption rate. EsophagusStomachSmallintestine
MAGNIFIED / ILLUSTRATIVE

Illustrative ingredient particles, before liposomal formulation.

Scroll to follow the journey ↓

As a supplement releases its contents, ingredients encounter stomach acid and digestive enzymes. How they respond depends on their chemistry and formulation.

Conceptual illustration, not a product result. Stability and absorption vary by ingredient and formulation. Particle counts, size and timing do not represent measured loss or uptake.

FORMULATING FOR THE JOURNEY

The ingredient matters.
So does its formulation.

Liposomal formulations can carry selected ingredients in a water-based interior or within a phospholipid membrane. The goal is to influence how an ingredient is carried and released. Performance depends on the specific formulation.

02 / THE LIPOSOMAL STRUCTURE

Meet the structure
around the ingredient.

Scroll to see a phospholipid bilayer assemble around an illustrative vitamin C ingredient.

  1. 01

    A place for the ingredient.

    Water-soluble ingredients can sit within the liposome’s aqueous interior; fat-soluble ingredients can associate with its lipid membrane.

  2. 02

    A barrier around sensitive ingredients.

    Encapsulation can help limit direct exposure to the surrounding environment. The degree of protection depends on the ingredient and membrane composition.

  3. 03

    Delivery includes release.

    Lipid structures can change during digestion and release their contents. The goal is to help make the ingredient available for absorption; human testing determines whether exposure improves.

  4. 04

    The lipids open. The ingredient is released.

    In the small intestine, bile and enzymes can reorganize or break down the lipid membrane, releasing its contents.

  5. 05

    At the surface of absorption.

    Released ingredients can become available for uptake across the intestinal lining. How much is absorbed depends on the ingredient and formulation.

Explore our liposomal standard ↗
A CLOSER LOOK03 / LIPOSOMAL STRUCTURE
A liposome surrounding an illustrated vitamin C ingredientAs you scroll, two layers of lipid molecules gather around a water-based interior containing the illustrated ingredient. The view then moves to a circular intestinal lining. Lipids separate and ingredient particles are released toward the lining; selective uptake is illustrated. This is a conceptual pathway, not evidence of a product’s absorption.INTESTINAL LINING · MAGNIFIED CROSS-SECTIONInside thesmall intestineCVITAMIN CLipid bilayerWater-based interiorLipid membrane opensReleased ingredientRELEASE → AVAILABILITY → UPTAKE
Scroll to animate, or press Play ↓

Conceptual cross-section; not to scale. Encapsulation is illustrated, not a manufacturing process or absorption result.

03 / LOOK BEYOND THE LABEL

Designed for delivery.
Evaluated through evidence.

A liposomal structure explains the approach. Testing shows how a specific formulation performs, from stability and ingredient release to measured exposure in people.

01 / STRUCTURE

Is the structure there?

Examine the structures in the sample.

02 / ENCAPSULATION

What’s associated
with the carrier?

Measure ingredient association.

03 / STABILITY

How does it
hold up?

Assess stability, release and digestive behavior under defined conditions.

04 / HUMAN RESEARCH

What happens
in people?

Measure human exposure for the identified preparation. Clinical benefits need their own evidence.

Cryo-TEM image from Haroutine’s validation page showing vesicular structures, with original 100 nanometer scale bar
Cryo-TEM image from Haroutine’s validation page.
Source asset: liposomal sodium hyaluronate. View context ↗

MAKE THE INVISIBLE VISIBLE

Look closer.
Ask for evidence.

Imaging lets us examine visible vesicles. It is one piece of a larger validation process.

01

See the structure.

Inspect visible shape and layers.

02

Understand its limits.

An image alone cannot prove encapsulation percentage or absorption.

03

Connect the evidence.

Read results with their sample and testing conditions.

Explore our validation standard ↗
Laboratory image from Haroutine’s Korean research platform pageKOREAN DEVELOPMENT PLATFORM

DEVELOPED THROUGH KOREAN INNOVATION

Thoughtful formulas.
A closer connection
to the science.

Haroutine is backed by Wooree’s Korean development and manufacturing platform, connecting formulation, production and structural imaging.

  1. 01 Formulate with purpose
  2. 02 Examine the details
  3. 03 Keep building the evidence
Inside our approach ↗

A LITTLE MORE CLARITY

Good questions.
Clear answers.

Does digestion destroy every supplement?+

No. Release and dissolution can help make ingredients available for absorption. Chemical degradation is different: it changes the ingredient itself. Sensitivity varies by ingredient and formulation.

Do liposomes remain intact throughout digestion?+

Not necessarily. Bile and digestive enzymes can alter lipid structures and release their contents. A formulation needs its own testing; a liposomal label alone does not establish protection or absorption.

What is a liposome?+

A microscopic vesicle with a phospholipid membrane. The formation illustration above uses a water-soluble ingredient inside its aqueous core.

Is everything in a formula liposomal?+

No. Look at the identified ingredients in each formula. For example, AMC combines marine collagen with selected liposomal supporting nutrients.

Does liposomal mean better absorbed?+

That requires evidence for the specific preparation. The animations explain concepts; they do not show a measured absorption result.

What can Cryo-TEM tell us?+

It shows visible structures. Other methods address ingredient association, stability and human exposure.

Where can I explore the research?+

Visit our validation standard ↗ for methods, research and the context behind each result.

GOOD SCIENCE BELONGS IN YOUR ROUTINE

Consider the ingredient.
Understand the formulation.

Find your formula ↑