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Particle Metrix · Nanoparticle Tracking Analysis

Watch each particle move, and read its size, charge, and markers.

ZetaView® Evolution tracks thousands of individual nanoparticles in real time — turning Brownian motion into hydrodynamic size, a whole-cell scan into absolute concentration, an applied field into zeta potential, and fluorescent labels into specificity. One instrument, six measurements, no calibration curves.

Measurement cell · live tracking Acquiring
Brownian trajectories → hydrodynamic diameter tracking…
10–1000
Particle size range (nm)
6
Measurements, one cell
4
Excitation lasers · up to 11 channels
0
Calibration curves
The instrument

One bench-top platform, every measurement.

Up to four excitation lasers, a high-sensitivity CMOS camera, and a quartz-glass measurement cell work together under ZetaSphere® software — so size, concentration, zeta potential, fluorescence, and colocalization all come from the same particles, in a single run.

ZetaView® Evolution · Quatt configurationMade in Germany
Particle Metrix ZetaView Evolution Quatt nanoparticle tracking analyzer, a navy and white bench-top instrument
Engineered by Particle Metrixbench-top NTA

Inside the platform

  • Up to four excitation lasers — selected from 405 / 488 / 520 / 640 / 660 nm, doubling as scatter and fluorescence sources.
  • High-sensitivity CMOS camera — records the light each particle scatters, and its fluorescence, particle by particle.
  • Quartz-glass measurement cell — zeta potential measured directly inside the cell, with no disposables.
  • ZetaSphere® software — one-click multiparameter acquisition, live statistics, and full sample reporting.
Configurations — Mono (1 laser) · Twin (2) · Quatt (4) · up to 11 fluorescence channels
ZetaView® Evolution Quatt · with ZetaSphere® softwareIn the lab
ZetaView Evolution Quatt on a laboratory bench beside a monitor running ZetaSphere software, with sample vials and buffer bottles
Size · concentration · zeta · fluorescence · colocalization — one cell, one runZetaSphere®
How each measurement works

Six measurements, one sample.

Nanoparticle tracking analysis follows particles one at a time rather than averaging the whole suspension. That single difference is what lets ZetaView resolve a polydisperse sample into its true size distribution, count particles in absolute terms, measure their surface charge, and separate a genuine subpopulation from background.

The panels below illustrate the measurement principle behind each capability. Adjusting a parameter shows how the instrument's read-out responds to a change in the sample, the label, or the settings — an aid to understanding the technology, not a stand-in for validated measurement data.

Capability 01

Particle size distribution

Brownian motion is faster for small particles and slower for large ones. The Stokes–Einstein relation converts each tracked path into a hydrodynamic diameter, and thousands of particles build a full distribution — not a single average.

Drag polydispersity and switch sample type. Watch D10 / D50 / D90 and the span respond — a monodisperse standard collapses to a sharp peak; a real EV prep spreads wide.

98
Mode (nm)
118 nm
D50 median
1.14
Span (D90−D10)/D50
Size distribution · particles/mL (rel.)NTA
50 100 150 200 300 400 hydrodynamic diameter (nm) → D10 D50 D90
Polydispersity moderate
Concentration scanning · whole-cell volumetric scanScanning
Sample concentration
Capability 02

Concentration Scanning Technology

ZetaView® Evolution sweeps the laser through the entire measurement cell, illuminating each plane in turn and capturing every particle it crosses. Counting the whole volume — not a single fixed field — yields an absolute, calibration-free concentration that stays comparable across sample types and across scatter and fluorescence channels.

Watch the illuminated plane scan the whole cell. Switch the laser: in scatter it captures every particle; in fluorescence only labelled particles light up. Because the full volume is scanned, the count doesn't depend on camera gain or laser intensity.

Concentration /mL
Particles captured
Capability 03

Zeta potential

Apply an electric field and charged particles migrate; their velocity reveals the zeta potential — the effective surface charge that governs colloidal stability. ZetaView measures this in the same cell, on the same particles it just sized.

Sweep the pH. Near the isoelectric point the charge collapses toward zero and particles aggregate; push pH away and |ζ| climbs past 30 mV into the stable regime.

-36.6
Zeta (mV)
Stable
Colloidal stability
Electrophoretic mobility · applied field± field
+ drift velocity ∝ |zeta| · direction shows particle charge sign 0 (IEP) −60 +30 mV
Suspension pH 7.0
F-NTA · scatter vs fluorescenceDetecting
light scatter · all particles 64 particles scatter — specificity unknown scatter sees everything · fluorescence isolates your marker
Marker-positive fraction 45%
Capability 04

Fluorescence detection

Light scatter sees every particle — vesicles, aggregates, and contaminants alike. Add a fluorescent label and ZetaView counts only what carries your marker, separating specific signal from a noisy background in the very same sample.

Toggle scatter and fluorescence, pick a tetraspanin channel, and set how many particles carry the marker. Specific count is always a subset of total scatter — that gap is your specificity.

64
Scatter (total)
29
Fluorescent (specific)
45%
% positive
Capability 05

Colocalization analysis

Two labels, two lasers. ZetaView detects each particle in both fluorescence channels and resolves the population into three groups — CD9-positive, CD63-positive, and the colocalized double-positive vesicles that carry both markers at once.

Raising the colocalization degree moves events into the double-positive bar — the co-expressed subpopulation a bulk assay averages away. Colocalization NTA (C-NTA) needs at least two lasers, available on the Twin and Quatt configurations.

372
Double-positive
477
CD9 only
391
CD63 only
Colocalization counts · CD9 / CD63 populationsCounting
0 223 446 669 892 477 CD9+ only 391 CD63+ only 372 colocalized CD9+ CD63+ particles counted
Colocalization degree moderate
Subpopulation gating · size × charge × fluorescenceGating
50 100 150 200 250 0 -20 -40 -60 size (nm) → zeta potential (mV) gated subpopulation marker+
Size gate ≥ 90 nm
Charge gate |ζ| ≥ 15 mV
Capability 06

Subpopulation analysis

Real preparations are mixtures — vesicles of different sizes and surface charge, labelled and unlabelled particles, and free-protein debris all overlap. Resolving a subpopulation by size, zeta potential, and fluorescence together isolates a genuine subset and reports its count, fraction, and characteristic size.

Set the size and charge gates to enclose a cluster, then switch to marker-positive to keep only fluorescently labelled particles. The instrument reports what falls inside — separating a true EV subset from background that any single parameter would blur together.

100
Gated events
40%
% of total
136 nm
Median size in gate
Where it's used

From EV discovery to lot release.

The same multiparameter read supports academic discovery and regulated manufacturing — characterising biological nanoparticles wherever size, count, charge, and markers all matter.

Extracellular vesicles

Size, concentration, and tetraspanin profiling with per-EV fluorescence.

Lipid nanoparticles

Size and zeta for LNP stability in mRNA and gene-delivery work.

Viruses & VLPs

Titre, integrity, and stability for diagnostics and vaccine development.

Biopharma QC

Lot-to-lot consistency and stability studies for GLP/GMP workflows.

ZetaSphere® · multiparameter reportLive
ZetaSphere software showing live nanoparticle tracking, instrument configuration, and multiparameter result plots
Size · concentration · zeta · fluorescence · colocalizationone report
Trusted by scientists worldwide

Adopted across EV, LNP, and virus research.

ZetaView® is used by research groups and biopharma teams worldwide for extracellular-vesicle, lipid-nanoparticle, and viral-vector characterisation — every parameter captured and reported in ZetaSphere®.

Medical University of Vienna Masaryk University Ludwig Boltzmann Institute for Traumatology Steinbeis
Why ZetaView Evolution

Reproducible data, calibration-free.

Proven

Widely cited platform

An NTA system established across peer-reviewed EV, virus, and nanomedicine literature.

Multiparameter

One cell, one workflow

Size, concentration, zeta, fluorescence, and colocalization on the same particles — no instrument-hopping.

Traceable

Data integrity built in

ZetaSphere® logs database events and predefined settings for reproducible, auditable multiparameter workflows.

Size range
10 – 1000 nm (sample and laser dependent)
Concentration
10⁵ – 10⁹ particles/mL · calibration-free Concentration Scanning Technology
Zeta potential
−500 to +500 mV · measured directly in the quartz-glass cell, no disposables · pH 1–13
Fluorescence
Up to four lasers (405 / 488 / 520 / 640 / 660 nm) · up to 11 channels · sensitivity < 20 AF488 molecules
Parameters
Size · concentration · zeta · fluorescence (F-NTA) · colocalization (C-NTA)
Software
ZetaSphere® — one-click multiparameter acquisition, live statistics, reporting
Configurations
Mono (1 laser) · Twin (2) · Quatt (4) · Made in Germany
Product photographs courtesy of Particle Metrix. Interactive panels are teaching models — representative behaviour, not instrument specifications or a substitute for method validation.

Bring multiparameter NTA to your biology.

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For Research Use Only. Not for use in diagnostic procedures.