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Analytik Reports on Use of the CPS Disc Centrifuge System for Characterising Nanoparticles at the University of Liverpool and University College Dublin

publication date: May 1, 2014
 | 
author/source: Analytik Ltd

analytik CPS Disc Centrifuge

Analytik, leading suppliers of innovative analytical instrumentation, report on use of CPS Disc Centrifuges for high resolution nanoparticle size analysis at the University of Liverpool and University College Dublin. 

As a Postdoctoral Research Fellow and a member of Professor Mathias Brust’s group at the University of Liverpool, Dr Željka Krpetić developed gold nanoparticle systems for biological applications. In particular, her research was focused on preparative nanochemistry and functionalisation of nanoparticles aimed at sensing, targeting, delivery and cancer therapy. As a Postdoctoral researcher at Strathclyde University working in the group of Professor Duncan Graham she designed novel particle systems for use in multimodal nanoparticle-based sensing. Furthermore she developed gold nanoparticles capable of avoiding cellular uptake by endocytosis-dependent mechanisms, also while working with Professor Brust. Dr Krpetić is now a Senior Postdoctoral Research Fellow and a member of the Centre for BioNano Interactions directed by Professor Kenneth A. Dawson at University College Dublin. She is working on developing high quality, next-generation nanomaterials for biomedical applications in addition to new analytical approaches for the challenging characterisation of nanoparticles in situ in complex biological fluids. 

Functionalised nanoparticles consist of a relatively dense and hard inorganic core that is surrounded by a soft shell of comparatively low density (typically small organic molecules, peptides, proteins, DNA, etc). This description particularly applies to the case of monolayer protected clusters (MPCs) of gold that are the most widely studied example of such materials. Traditionally, the commonly used particle sizing techniques examine either the particle core alone (TEM) or the entire particle (DLS), while an explicit distinction between the core and the ligand shell is rarely made. This is of particular interest in the study of complex interactions of nanomaterials with biological fluids and for investigating subtle changes that may occur in the particle ligand shell post functionalisation or changes in particle stability that cannot be estimated using other techniques (e.g. UV-visible spectroscopy or DLS). Given the important roles the ligands play, not only as stabilisers but also to impart chemical functionality and other properties to the particles, the availability of a routinely applicable robust method for ligand shell thickness determination is highly desirable, and now provided by Differential Centrifugal Sedimentation. 

Describing her experiences with particle characterisation instrumentation, Dr Krpetić says “For routine particle characterisation, I have used UV-visible spectroscopy to determine the changes in the refractive index of gold nanoparticles post-functionalisation and to calculate their concentration in dispersions. I have used Dynamic Light Scattering (DLS) techniques but mostly Transmission Electron Microscopy as a routine tool to size the particles. To gain more information on the particle ligand shell, I have used ATR-FTIR and HR-NMR spectroscopies. These all have their limitations as these techniques require a lot of material for investigation which is not always feasible.” 

Continuing, Dr Krpetić described her choice to use the CPS system: “The benefits and opportunities using the CPS system are numerous. Differential Centrifugal Sedimentation (DCS) is an ultra-high resolution technique that reliably measures the size of nanoparticles in solution of almost any material, provided the density is known. Its accuracy is coming from the fact that the technique measures all the particles in the sample injected to the CPS disc. The reproducibility of measurements is extraordinary, thanks to the calibration by standards prior to each measurement. It can be used to determine minute aggregation patterns, i.e. presence of dimers and trimers in dispersion that other techniques cannot determine. This is of particular importance in applications for SERS spectroscopy for example, where it is very important to control the aggregation patterns of metal nanoparticles. It can be used to measure the ligand shell thickness of monolayer protected gold particles as recently demonstrated in our publication ‘High-Resolution Sizing of Monolayer-Protected Gold Clusters by Differential Centrifugal Sedimentation’ ACS Nano, 2013, 7 (10), pp 8881–8890. We found that unlike TEM, DCS is highly sensitive to small changes in the thickness of the organic ligand shell and can be applied to monitor shell thickness variations of as little as 0.1 nm on particles of a given core size. This is important as these variations cannot normally be visualised by Electron Microscopy or assessed with DLS techniques with such accuracy. It is also a good and reliable method for investigating the binding of individual macromolecules to nanoparticles, assessing the stability of colloidal dispersions post-functionalisation and particle monodispersity and evaluating the success of coupling reactions.” 

DCS represents a valid alternative to TEM, in particular for the rapid, routine analysis of monodisperse colloids dispersed in almost any solvent (aqueous or organic) and by extension, those with multimodal size distributions. The CPS instrument should be considered a ‘must have’ instrument for particle sizing and evaluation of dispersion quality in diverse media in all modern laboratories that are dealing with nanofabrication and reliable detailed particle characterisation for all applications in modern nanotechnology. 


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