Our Technology - LipoEdge
Our Technology
Foundation Science

Lipoedge: Experts in Liposomes

Delivering highest quality liposomes & maintaining steadfast commitment to research excellence.

Phospholipids in Lecithin
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Phosphatidylcholine (PC)

Primary bilayer-forming lipid responsible for vesicle architecture.

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Phosphatidylethanolamine (PE)

Supports membrane flexibility and dynamic behaviour.

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Phosphatidylinositol (PI)

Aids membrane organisation and structural integrity.

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Phosphatidic Acid (PA)

Improves lipid packing stability within the bilayer.

Lecithin Quality Influences
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Liposome Formation

Uniform vesicles and optimal encapsulation across batches.

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Membrane Integrity

Structural stability maintained consistently over time.

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Encapsulation & Retention

Maintains the integrity and potency of the actives.

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Batch-to-Batch Reproducibility

Consistent and reliable quality in every manufactured batch.

Raw Materials

Natural Sources of Lecithin

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Sunflower Lecithin

Non-GMO, allergen-free profile with excellent nutraceutical scalability and regulatory comfort.

Preferred
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Soya Lecithin

High PC content but associated with GMO perceptions and allergen labelling requirements.

Use with Caution
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Egg Lecithin

Highest PC content naturally, but animal origin and egg-allergen status limit nutraceutical use.

Limited Use
Comparative Analysis

Phospholipid Profile

Composition ranges across the three major lecithin sources used in pharmaceutical and cosmeceutical liposomal formulations.

Phospholipid Sunflower Soybean Egg Yolk
Phosphatidylcholine (PC) 20 – 26% 20 – 22% 70 – 80%
Phosphatidylethanolamine (PE) 4 – 10% 16 – 22% 10 – 17%
Phosphatidylinositol (PI) 15 – 19% 13 – 16% –
Phosphatidic Acid (PA) 2 – 5% 5 – 10% –
Phosphatidylserine (PS) < 1% ~ 1% < 1%
LPC < 3% < 3% 2%
Selection Guide

Factors for Choosing Lecithin

FactorSunflowerSoyEgg
Plant-based suitability Yes Yes No
Allergen perception Lower Higher β€” FALCPA / EU Annex II Higher β€” FALCPA / EU Annex II
Clean-label positioning Strong; Non-GMO Sensitive; ~94% US soy is GE Limited (animal origin)
Global nutraceutical scalability Excellent Good (with label caveats) Limited
✦ Recommended

Why Sunflower Lecithin

Sunflower lecithin is widely preferred for modern nutraceutical liposomes because it balances performance, regulatory comfort, and consumer acceptance. Its non-GMO and allergen-free profile simplifies global compliance without sacrificing lipid quality.

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Why Not Soy or Egg Lecithin?

Soy lecithin: Widely used but associated with allergen labelling requirements and GMO-related perceptions in specific markets, limiting clean-label positioning.

Egg lecithin: Naturally rich in PC and effective for bilayer formation, but its animal origin and egg-allergen status restrict suitability for nutraceutical use.

Key Benefits

Advantages of Sunflower Lecithin

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Non-Allergen

Reduces allergen and labelling concerns, enabling broader market acceptance globally.

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Non-GMO

Supports GMO-sensitive markets and aligns with clean, non-GMO product positioning.

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Plant-based & Vegetarian

Compatible with global dietary, cultural, and vegan lifestyle preferences.

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Globally Scalable

Sourced from widely cultivated sunflower oil crops with reliable supply chains.

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Reliable Liposome Performance

Purified sunflower lecithin forms stable bilayers with consistent, predictable quality.

Upstream Processing

Purification of Lecithin

Liposomal excellence begins with phospholipid purity. Natural lecithin is a complex mixture of phospholipids, neutral lipids, and trace impurities. While suitable for general emulsification, raw lecithin is not optimal for high-performance liposomal systems.

Our liposomal technology focuses on purifying lecithin into high-purity phosphatidylcholine (PC) β€” the primary structural lipid responsible for stable liposome bilayer formation.

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High-Performance Liposomes
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High Quality Lipid
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Overcoming Lecithin Limitations
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Pure Phosphatidylcholine
Purification of Lecithin
Why Our Technology Stands Out - Lipoedge
Technical Excellence

Why Our Technology Stands Out

The level of purity ensures that liposomes formed using WBCIL phosphatidylcholine are more uniform, reproducible, and stable. This purified phosphatidylcholine is subsequently engineered into liposomes and evaluated through rigorous physicochemical, biological, and performance-based characterisation.

>90%
Phospholipid Purity
Robust
Bilayer Formation
↑ Eff.
Improved Encapsulation Efficiency
Stable
Enhanced Physical & Chemical Stability
Operational Standards

Quality and Compliance

Conduct internal inspections ensuring process control, content uniformity, and traceability in compliance with SOPs to maintain batch consistency and finished product quality.

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Process Control
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Content Uniformity
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Batch Consistency
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SOP Compliance
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Quality Traceability
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Internal Inspection
Scientific Validation

Liposomal Characterizations

Comprehensive physicochemical testing protocols to Characterize Liposomes.

01
Phospholipid composition of liposome:

HPLC-based mapping of the phospholipid composition of liposomes. A high concentration of Phosphatidylcholine (PC) translates into higher product purity and greater shelf life.

02
Poly Dispersity Index (PDI):

Indicates uniformity in the size distribution of liposomes. High uniformity guarantees batch-to-batch clinical consistency. Acceptance criteria: ≀ 0.5

03
Particle Size:

Nanoscale formulation allows for significantly increased cellular uptake. Acceptance criteria: 200 nm-300 nm

04
Zeta Potential:

An indicator of the liposome’s surface charge. High Zeta Potential creates a strong repulsion between particles, preventing clumping and ensuring stability. Acceptance criteria: Β± 30 mV

05
Fourier Transform Infrared Spectroscopy (FTIR):

It acts like a β€œmolecular fingerprint”. Every ingredient has a unique signal. FTIR confirms the chemical stability of the liposome.

06
Enery Dispersive X-Ray Spectroscopy (EDAX):

A surface scan using EDAX examines the liposome’s surface and confirms its chemical composition. The presence of only the core components of a liposome- Nitrogen, Carbon, Oxygen, and Phosphorus verifies the purity of the liposomal preparation.

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Scanning Electron Microscope (SEM):

A microscopic-based examination that confirms spherical, smooth-surfaced nanoscale vesicle morphology of liposomes