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AUREVIA CD//CORE

Final combined fill volume [pending] · Pack imagery represents current concept and is subject to change.

AUREVIA CD · Foundational Formula

AUREVIA CD//CORE

The foundation of the AUREVIA cyclodextrin platform.

Development CollectionPlatform Prototype. Mechanistically informed. Finished-product validation pending. Ingredients, quantities, serving instructions and commercial claims remain subject to change.
Foundational FormulaDualPhase™ SystemSunflower phospholipids · cholesterol-free

AUREVIA CD//CORE is the cleanest and most focused formula in the AUREVIA CD collection. A dedicated aqueous phase carries α-cyclodextrin and HPβCD, paired with a separately stored cholesterol-free phospholipid phase. The two phases remain separated during storage and combine immediately before use — an architecture intended to reduce prolonged pre-use interaction between the cyclodextrins and the liposomal phospholipids.

$112$128Member price· 30 dual-chamber liquid-gel sachets

Not available for purchase until finished-product validation is complete.

DualPhase™ architecture
Separated during storage
Analytical validation programme
Transparent formulation
AUREVIA DualPhase™ System

Cyclodextrin intelligence. Liposomal precision.

Each daily unit contains two connected chambers — a purified aqueous cyclodextrin matrix and a separately manufactured phospholipid phase — combined only at the moment of use.

Phase One — Cyclodextrin Matrix

  • α-CyclodextrinFinal quantity pending regulatory approval
    • Principal gut-phase cyclodextrin component
    • Soluble-fibre-style formulation ingredient
    • Supports the digestive lipid-pathway positioning
    • Mechanistically distinct role from HPβCD

    Human evidence for α-CD is mixed. Not presented as a guaranteed cholesterol-lowering ingredient.

  • HPβCD (2-Hydroxypropyl-β-cyclodextrin)Pending regulatory, toxicological and safety review
    • Advanced cyclodextrin-research component
    • Supports cholesterol inclusion and exchange research
    • Creates a differentiated technical platform

    Preclinical mouse findings must not be presented as proof of oral plaque removal in humans.

  • Purified water
    • Primary aqueous carrier
  • Vegetable glycerin
    • Liquid-gel texture
    • Mouthfeel
    • Viscosity control
    • Palatability support
  • Buffering system
    • pH control
    • Ingredient stability
    • Taste management
    • Packaging compatibility
  • Natural flavour system
    • Restrained citrus or neutral flavour, pending sensory evaluation

Phase Two — Liposomal Support Matrix

  • Sunflower phosphatidylcholine
    • Cholesterol-free phospholipid source
    • Liposomal / phospholipid-vesicle formation
    • Carrier for lipid-compatible components
    • Separation from the cyclodextrin chamber during storage
  • Natural mixed tocopherols
    • Oxidative protection of the phospholipid phase
    • Shelf-life support
    • Stability of lipid-sensitive components

    Not promoted as a principal cardiovascular active unless separately substantiated.

DisclosureCyclodextrin inclusion is dynamic, reversible and concentration-dependent. The AUREVIA DualPhase™ System is designed to reduce prolonged cyclodextrin–phospholipid contact before use and to preserve a measurable free or exchangeable cyclodextrin fraction. This must be demonstrated through finished-product analytical testing.
Proposed consumer positioning

Designed to support.

Proposed structure/function positioning. Requires final formulation-specific substantiation and regional regulatory approval.

  • Healthy lipid-metabolism pathways
  • Digestive lipid handling
  • General cardiovascular wellness
  • A structured heart-health routine
  • Consumer access to a differentiated cyclodextrin formulation platform
Dual Cyclodextrin Architecture

Combines α-CD and HPβCD as two technically distinct cyclodextrin components.

Separated During Storage

The cyclodextrin and phospholipid phases remain separated until use.

Cholesterol-Free Phospholipid Phase

Sunflower-derived phosphatidylcholine — no cholesterol added to the liposomal matrix.

Built for Verification

Designed to support separate chamber testing and finished-product characterisation.

Complete ingredient explorer

Nothing hidden.

Final quantities are declared once formulation and regulatory review are complete.

IngredientRolePer servingEvidence
α-CyclodextrinGut-phase cyclodextrinTBCEmerging
HPβCDAdvanced cyclodextrin researchTBCMechanistic
Sunflower phosphatidylcholineCholesterol-free liposomal carrierTBCEstablished
Mixed tocopherolsLipid-phase antioxidantTBCEstablished
Vegetable glycerinTexture & palatabilityTBCEstablished
What makes AUREVIA CD//CORE different

The foundational AUREVIA DualPhase™ formula.

Two environments, one daily unit

Rather than storing cyclodextrins and phospholipids together for the entire shelf life, CD//CORE keeps them in two dedicated chambers until use.

Focused formulation

Avoids the large number of co-active ingredients used in more advanced products — the preferred formula for analytical validation, cyclodextrin-fraction testing and simulated digestion.

Research-led positioning

Not positioned as an artery-clearing treatment. A carefully designed dual-phase cyclodextrin and phospholipid system for adults building a modern cardiovascular-wellness routine.

Developed for
  • Adults interested in general cardiovascular wellness
  • Consumers focused on healthy lipid-metabolism pathways
  • Existing cyclodextrin users seeking a differentiated oral format
  • Early adopters interested in formulation technology
  • Practitioners assessing new supplement-delivery platforms
  • Consumers seeking a simpler introduction to the AUREVIA CD collection
Proposed use
Combine both chambers immediately before use. Use only according to the final approved product label. Final instructions will be established through formula validation, safety review, regulatory assessment, palatability testing, human tolerability evaluation and packaging validation.
Safety panel

Consult a qualified healthcare professional before use if you:

  • Are pregnant or breastfeeding
  • Take prescription medication
  • Have kidney or liver disease
  • Have diagnosed cardiovascular disease
  • Use lipid-lowering medication
  • Are receiving specialist medical care
  • Are preparing for surgery or another medical procedure
  • Have experienced sensitivity to cyclodextrins or formulation ingredients

Do not discontinue or replace prescribed treatment.

FAQ

Questions we get, answered honestly.

Does the phospholipid phase completely fill the HPβCD cavities?+

That should not be assumed. Cyclodextrin inclusion is dynamic and dependent on the complete formulation environment. CD//CORE is designed to reduce prolonged pre-use interaction by storing the phases separately. Actual free, exchangeable and complexed fractions must be measured in the finished product.

Does CD//CORE remove arterial plaque?+

No such claim is made. The finished product has not been shown to remove plaque, reverse atherosclerosis or replace medical treatment.

Why include both α-CD and HPβCD?+

They serve different proposed formulation purposes. α-CD is positioned primarily around the digestive lipid pathway; HPβCD provides the more advanced cholesterol-interaction research platform.

Is the finished product clinically tested?+

Not yet. Ingredient research cannot be treated as finished-product clinical evidence.