Based on traditional optical microscopes, the
NanoSight LM10 employs a laser light source to light up nanoscale particles in a 0.3ml sample introduced to the viewing unit through a disposable syringe. In the presence of a perfect black background, particles appear as point-scatterers moving under Brownian motion.
NanoSight LM10 is perfect for use in research laboratories. Agglomerates, contaminants, and polydisperse and multimodal systems can be quickly identified and quantified. The instrument has a high-specification sCMOS camera, which enhances the sensitivity of the LM10 by a factor of x100. This means the detection limit for a certain particle type has been enhanced by a factor of 2 when compared to the traditional instrument.
Users can automatically track and size nanoparticles using the image analysis Nanoparticle Tracking Analysis (NTA) software suite. Additionally, video clips of images can be obtained and archived for future reference.
The main features of the
NanoSight LM10 are:
Compact and easy to use
High specification sCMOS camera
Real-time dynamic nano-particle visualization
Particle counting and sizing
Particle size distributions displayed as histograms
Data output to spreadsheet
Video clip capture
The applications of the
NanoSight LM10 are:
Pharmaceutical nanoparticles - liposomes
Ceramic and metallic nanoparticles
Colloidal suspensions and polymer nanoparticles
Carbon nanotubes (multi-walled)
Cosmetics and foodstuffs
Wear debris in lubricants
Chemical mechanical polishing slurries
Nanoparticles in fuels and oils (soot, catalyst, wax etc.)
The Malvern Panalytical NanoSight NTA system allows us to directly and reliably quantify extracellular vesicle yields from the cell lines under investigation, which is critical to this project. We are also using the system to study the fusion of extracellular vesicles with synthetic nanoparticles, for the purpose of engineering the properties of the nanoparticles. We use a combination of the light scattering and fluorescence tracking functions of the NanoSight system to determine the proportion of fluorescently labeled nanoparticles that have bound to the extracellular vesicles. Having determined that we can quantify binding, the next step will be to scale up and apply NTA as a QC and process evaluation technique.
Dr Paulaitis, Researcher, Department of Chemical and Biomolecular Engineering, Ohio State University