The Exosome Group

Methods

An exosome claim is only as strong as the measurement behind it.

How we choose methods, match them to the source, and report what the data does and doesn’t show.

Methods

No single method answers every question.

Each study pairs methods so one covers what another can’t. This is the panel we draw from.

QuestionCommon methodsWhat it tells youWhat it can’t tell you alone
Concentration and sizeNanoparticle tracking analysis, tunable resistive pulse sensing or nano-flow cytometryHow many particles of what size are in the sampleWhich of those particles are vesicles
MorphologyTransmission electron microscopy or cryo-electron microscopyWhether intact, membrane-bound vesicles are presentA reliable count across the whole sample
IdentityProtein markers chosen for the source, by western blot, ELISA or single-vesicle methodsWhether the particles carry proteins expected for vesicles from that sourceEndosomal origin, so whether they are exosomes
PurityParticle-to-protein ratios and markers of what else came along, such as casein or lipoproteinsHow much of the preparation is something other than vesiclesWhether the vesicles are active
Recovery from your formatFeasibility work on your cream, serum or powderWhether vesicles can be recovered and measured in the finished productThat every format can be measured; some can’t
Stability and consistencyThe same panel across lots and storage timepointsWhether the numbers hold from lot to lot and over shelf lifePerformance on skin

Matched to the source

Each source brings its own lookalikes.

Plant, milk, microbial and human-derived vesicles each get the methods and markers that fit where they came from.

SourceWhat else looks like a vesicleIdentity evidence that fits
Human-derived and cell cultureProtein aggregates and lipoproteins of similar sizeTetraspanin markers such as CD63, CD9 and CD81, alongside a second, independent method
Milk and colostrumCasein micelles of similar size, in large numbersCasein removed before counting; markers tested with antibodies suited to the species
PlantDebris from broken cells, when tissue is blended, ground or pressedPlant markers (candidates include TET8 and PEN1), and a clear statement of plant EV or plant-derived nanovesicle
Microbial, including microalgaeCell debris and culture media componentsMammalian markers don’t apply; identity evidence is chosen for the organism

Independent laboratories

Every measurement runs at an independent laboratory that we name in the study plan, before work starts. You see which lab, which instruments and which methods before you approve the quote.

The Exosome Group sells no ingredients, instruments or manufacturing. We decline work where we would have a stake in the answer. Our founder’s other businesses are named in scope and disclosures.

Exact about words

The word on your label, used correctly.

“Exosome” leads our headlines because it is the word on your label and the word buyers search. Inside our reports, the science stays exact. MISEV2023 recommends “extracellular vesicle” and keeps “exosome” for vesicles whose endosomal origin has been shown, so a report never calls your particles exosomes without that evidence.

exosome

extracellular vesicle

Unless endosomal origin is shown. MISEV2023, Welsh et al. 2024

The word on the shelf, and the word in the report.

MISEV2023

MISEV2023 is a map.

MISEV2023 is guidance from the International Society for Extracellular Vesicles on how to produce, separate, characterize and report vesicle studies. It has no pass mark and no certificate, so a product can’t hold a MISEV2023 approval.

We design studies and write reports against each section that applies to your source, and never describe a product as “compliant.”

  • How many particles are there?
  • What else is in the sample?
  • What shows they are vesicles?
  • How do they hold up in storage?
Questions MISEV2023 helps a careful study answer, for a given source.

Source: Welsh JA et al. Minimal information for studies of extracellular vesicles (MISEV2023). J Extracell Vesicles. 2024;13(2):e12404.

On file

What belongs behind a label number.

  1. The method and instrument that produced it.
  2. Whether it was measured on the raw ingredient or the finished product.
  3. How many lots, with lot numbers and dates.
  4. A blank: the same formula without the vesicle ingredient, measured the same way.
  5. The unit, written out in full: per mL, per gram or per vial, at release or at expiry.
Keep these with the data behind the claim.

One lot shows what one sample measured on one day. We treat three lots as the floor behind a label claim. That is how we work, not a regulator’s rule.