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Guide · Technical

Liposome particle size.

Why 50–200 nm matters, and how particle size, PDI and zeta potential are measured and read.

LIPOLOGICS

By the Lipologics technical team · Hoynoza Technologies Pvt Ltd · Updated 24 September 2026

Key facts
  • HNOVA™ liposomes are 50 nm to under 200 nm.
  • Under 200 nm keeps liquids clear, stable and sterile-filterable.
  • Size is measured by DLS alongside PDI (uniformity) and zeta potential (stability).
  • Ask for batch-specific values and the method used.

Why particle size matters

Particle size shapes almost everything about how a liposomal ingredient behaves:

  • Stability. Small, uniform vesicles resist settling and aggregation, so a liquid stays clear and consistent on the shelf.
  • Filterability. Vesicles well under 200 nm can pass a 0.2 µm sterile filter, which is a practical reason nano-liposomes are favoured for liquids.
  • Appearance. Smaller vesicles scatter less light, so dispersions look clearer.
  • Interaction with the body. Size influences how vesicles behave in the gut and how they are taken up; nanometre-scale vesicles are designed to make better use of these pathways.

How small is 50–200 nm?

From a glucose molecule to a human hair
1 nm10 nm100 nm1 µm10 µm100 µmGlucose≈1 nmAlbumin protein≈7 nmInfluenza virus≈100 nmBacterium (E. coli)≈1–2 µmRed blood cell≈7 µmHuman hair≈70 µmHNOVA™ liposomes50 to <200 nmLogarithmic scale — each step is ten times larger. Sizes are approximate.
Reference sizes are approximate and shown for orientation only.

The HNOVA™ range: 50 nm to under 200 nm

HNOVA™ liposomes are engineered into the 50 nm to under 200 nm band — small enough to remain dispersed and filterable, large enough to carry a useful payload. Exact size and distribution are confirmed per active and per batch and reported on the Certificate of Analysis.

How size and stability are measured

Size is usually measured by dynamic light scattering (DLS), which reports an average hydrodynamic diameter and the polydispersity index. Zeta potential is measured on the same instrument. Electron microscopy can confirm shape.

ParameterWhat it tells youCommon reading
Particle sizeAverage vesicle diameter (DLS, nm)Nano-liposomes are typically under 200 nm; HNOVA™ targets 50 to under 200 nm
PDIHow uniform the sizes are (0–1)Lower is more uniform; values below about 0.3 are commonly regarded as acceptable for lipid carriers, below 0.2 as narrow
Zeta potentialSurface charge (mV)Magnitudes above about 30 mV are a common rule of thumb for stable dispersions, though it depends on the system
Encapsulation efficiencyShare of the active inside the vesicles (%)Higher is better; confirmed per active and per batch

How to read a CoA

When you receive a Certificate of Analysis for a liposomal ingredient, check that it reports the method as well as the numbers, that size is given as both average and PDI, and that results are batch-specific rather than typical values. See what our CoA covers.

Questions

Frequently asked questions

What is the ideal liposome size?

There is no single ideal; it depends on the application. For ingredients, nano-liposomes under 200 nm are favoured because they stay dispersed and can be sterile-filtered.

What is PDI in liposomes?

The polydispersity index describes how uniform vesicle sizes are on a scale of 0 to 1. Lower values mean a narrower distribution.

What is zeta potential?

The electrical potential at the vesicle surface, measured in mV. Larger magnitudes generally mean the particles repel each other and stay dispersed.

How do you measure liposome size?

Most commonly by dynamic light scattering (DLS); electron microscopy can confirm size and shape.

What size are HNOVA™ liposomes?

50 nm to under 200 nm, confirmed per active and per batch.

Get in touch

Request a Certificate of Analysis.