| Literature DB >> 25892833 |
Günter Allmaier1, Anne Maißer2, Christian Laschober3, Paul Messner4, Wladyslaw W Szymanski2.
Abstract
The electrophoretic mobility of charged, airborne nanoparticles (NPs) or macromolecules and their specific complexes opens new avenues for their analysis and handling. The newly developed parallel differential mobility analyzer in combination with an electrostatic particle sampler enables not only the characterization of bio-NPs, but even their sampling while preserving their bioactivity (e.g., the enzyme activity of galactosidase). Precondition for the applicability of this technique is a well-defined charging status of the NPs in question. This charge conditioning can be achieved by means of a radioactive source, Po-210, even if the yield in terms of charged particles is low for sub-20-nm particles and the aging of the source influences the size spectra measured. Nevertheless, this technique enables size-defined sampling and enrichment, combined with real-time measurement of the size of both NPs and viruses. Furthermore, it allows determination of the number of attached biospecific antibodies, thereby providing information about the surface coverage of viruses by antibodies.Entities:
Keywords: Antibody; Bio-NP; Differential mobility analyzer; Electrophoretic mobility; Electrostatic particle sampler; GEMMA; Gas-phase electrophoretic mobility molecular analyzer; Macromolecule; Nanoparticle; Parallel differential mobility analyzer; Virus
Year: 2011 PMID: 25892833 PMCID: PMC4397955 DOI: 10.1016/j.trac.2010.10.008
Source DB: PubMed Journal: Trends Analyt Chem ISSN: 0165-9936 Impact factor: 12.296