Feasibility of asymmetric flow field-flow fractionation coupled to ICP-MS for the characterization of wear metal particles and metalloproteins in biofluids from hip replacement patients

2015 ◽  
Vol 407 (16) ◽  
pp. 4541-4554 ◽  
Author(s):  
Katrin Loeschner ◽  
Chris F. Harrington ◽  
Jacque-Lucca Kearney ◽  
David J. Langton ◽  
Erik H. Larsen
2013 ◽  
Vol 405 (25) ◽  
pp. 8185-8195 ◽  
Author(s):  
Katrin Loeschner ◽  
Jana Navratilova ◽  
Carsten Købler ◽  
Kristian Mølhave ◽  
Stephan Wagner ◽  
...  

2018 ◽  
Vol 7 (1) ◽  
pp. 216-223 ◽  
Author(s):  
Irina Sulaeva ◽  
Philipp Vejdovszky ◽  
Ute Henniges ◽  
Arnulf Kai Mahler ◽  
Thomas Rosenau ◽  
...  

Separations ◽  
2018 ◽  
Vol 5 (4) ◽  
pp. 56 ◽  
Author(s):  
Manuel Correia ◽  
Toni Uusimäki ◽  
Allan Philippe ◽  
Katrin Loeschner

According to the current European regulation on cosmetics, any ingredient present as a nanomaterial should be indicated in the ingredient list. There is a need for analytical methods capable of determining the size of the relevant ingredients and thus assessing if these are nanomaterials or not. An analytical method based on asymmetric flow field-flow fractionation (AF4) and inductively coupled plasma-mass spectrometry (ICP-MS) was developed to determine the size of particles present in a commercial toothpaste. Multi-angle light scattering (MALS) was used for on-line size determination. The number-based particle size distributions (PSDs) of the particles were retrieved upon mathematical conversion of the mass-based PSDs recovered from the AF4-ICP-MS fractograms. AF4-ICP-MS allowed to separate and detect Al2O3 and TiO2 particles in the toothpaste and to retrieve a correct TiO2 number-based PSD. The potential presence of particles in the lower size range of the Al2O3 mass-based PSD had a strong impact on sizing and nanomaterial classification upon conversion. AF4 coupled with ICP-MS and MALS was found to be a powerful approach for characterization of different particles in a multiple-particle system such as toothpaste. Confirmation of particle size by a secondary method such as single particle ICP-MS or hydrodynamic chromatography was crucial.


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