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PICK. MEASURE. RELEASE. REPEAT.

EXCHANGEABLE COLLOIDAL PROBE

GAIN 10x THROUGHPUT AND MUCH MORE FREEDOM.

Colloids are ubiquitous in both industry and nature, being the key component in emulsions, foams, gels and aerosols.

The traditional colloidal probe technique allows to study single colloids by gluing them onto an atomic force (AFM) cantilever leading to valuable insights about colloid-colloid or colloid-substrate interactions. Yet the procedure is complex and throughput low. 

With FluidFM, colloidal probe measurements become orders of magnitude easier and faster.

 

Fast and easy. In this video, three micrometer colloids are attracted from suspension with a vacuum, held briefly, and then released again with a pressure pulse. 

Odoo • Text and Image
Odoo • Text and Image
Odoo • Text and Image
Odoo • Text and Image

Pick a colloid from solution or substrate with negative pressure. Measure. Release it with a pressure pulse. Repeat.

100

COLLOIDS A DAY 

10x EASIER

THAN STANDARD METHODS

0.5 to 100 µm

SUPPORTED PARTICLE SIZE

pN

FORCE RESOLUTION

A COLLOIDAL PROBE WHICH CAN BE EXCHANGED

By applying a negative pressure inside, FluidFM micropipettes and nanopipettes can be used to attract floating colloids - or pick them up directly from a surface.

The process takes less than a minute and results in a colloidal probe with very repeatable cantilever position as the FluidFM aperture automatically centers the colloid.

After the measurement it can be removed from the cantilever with a positive pressure pulse, before attaching a fresh colloid to the probe.

Fluorescent CRISPR-Cas9 complexes injected into mouse primary hepatocytes with the FluidFM Bio-CRISPR.

Colloid for cell measurements. A 20 micrometer colloid is picked up by a FluidFM micropipette. 1. Before pickup.

Fluorescent CRISPR-Cas9 complexes injected into mouse primary hepatocytes with the FluidFM Bio-CRISPR.

2. Colloid is attached and ready for measurements. 

Measure 100 colloidal probes in one day

The simple physical principle enables measurements of dozens of colloids in an hour if desired. All with the same FluidFM probe. It is common that one FluidFM probe can be used for several experiment days, given proper care and storage.

From sub-µm to 100 µm

FluidFM addresses the largest range of colloid dimensions. Our customers reported to work with colloid sizes from 500 nm up to 100 µm. Using focused ion beam the FluidFM probes can be further modified and even smaller or larger particles are potentially in reach.

Switch colloidal probe anytime

Whether the colloidal probe is degraded, has become contaminated or you simply want to change the probe geometry or chemistry – you can switch the colloidal probe at anytime.

Self-centering

The colloid position on the FluidFM cantilever is given by the FluidFM aperture. Thus, every colloidal probe will be centered automatically and at the same position – as long as the same FluidFM probe is used.

Measure in air or liquid

While most of our customer work with colloids in liquids, others have used FluidFM to pick up and measure particles and microorganisms in air.

Explore liquid and gaseous colloidal probes

The FluidFM colloidal probe works solely using physical microfluidic forces; no glue needed. This also means that the user can potentially hold microscopic droplets or bubbles in the same manner. There is much left to explore.

Fluorescent CRISPR-Cas9 complexes injected into mouse primary hepatocytes with the FluidFM Bio-CRISPR.

Three micrometer colloids are picked up by a FluidFM micropipette and are used as colloidal probe.  

Fluorescent CRISPR-Cas9 complexes injected into mouse primary hepatocytes with the FluidFM Bio-CRISPR.

This transparent colloid of 50 micrometer diameter acts as lense, magnifying the FluidFM micropipette opening as it is held tightly by it. 

In a few seconds, a 50 µm silica bead is targeted and immobilized with a FluidFM micropipette having 8 µm aperture size. Upon suction application, the bead is removed from the substrate and is ready to be used. 

Colloidal probe technique – easier than ever.  

Get in touch with us to find out how FluidFM can help your research.  



Contact us.

PUBLICATION HIGHLIGHTS.

FluidFM has a huge potential for colloidal probe experiments. Below, we present 3 highlight publications; many more can be found in our publications section.


Sub-micrometer colloids

Industry relevant colloids typically range from 1 nm to 1000 nm, yet the classical colloidal probe technique works with colloids of 1 µm or larger. Here, researchers from the University of Bayreuth and ETH Zurich present a new method using FluidFM which unlocks the use of colloidal probes below 1 µm.

N. Helfricht, A. Mark, L. Dorwling-Carter, T. Zambelli and G. Papastavrou.  Extending the Limits of Direct Force Measurements: Colloidal Probes from Sub – Micron Particles.  Nanoscale. doi: 10.1039/C7NR02226C.


Soft colloids

Often colloids can consist of soft biological material. In contrast, the established colloidal probe technique mainly works with hard colloids – mostly due to the high complexity of gluing soft colloids to the cantilever. Here, researchers from the University of Bayreuth describe a universal approach using FluidFM to measure soft colloids.

A. Mark, N. Helfricht, A. Rauh, M. Karg & G. Papastavrou. The Next Generation of Colloidal Probes: A Universal Approach for Soft and Ultra‐Small Particles. (2019) Small. Doi:10.1002/smll.201902976


Characterizing soft material

3D printing has become prevalent in many fields, especially in tissue engineering. Yet so far it was not possible to melt-electrowrite (MEW) hydrogels, limiting print architecture and resolution of this important material in biomedicine. Researchers from The Julius Maximilians University of Würzburg and the University Hospital Würzburg have discovered a way unlocking MEW with promising implications to directly print soft, yet resilient tissues. FluidFM helped to characterize the printed material with its fast colloidal probe technique.

D. Nahm, F. Weigl, N. Schaefer, A. Sancho, A. Frank, J. Groll, C. Villmann, H.W. Schmidt, P. Dalton, R. Luxenhofer. A versatile biomaterial ink platform for the melt electrowriting of chemically-crosslinked hydrogels. (2019) Materials Horizon. Doi:10.1039/C9MH01654F