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Sizing nanomatter in biological fluids by fluorescence single particle tracking

Kevin Braeckmans (UGent) , Kevin Buyens (UGent) , Wim Bouquet-Geerardyn, Chris Vervaet (UGent) , Philippe Joye (UGent) , Filip De Vos (UGent) , Laurent Plawinski, Loic Doeuvre, Eduardo Angles-Cano, Niek Sanders (UGent) , et al.
(2010) NANO LETTERS. 10(11). p.4435-4442
Author
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Abstract
Accurate sizing of nanoparticles in biological media is important for drug delivery and biomedical imaging applications since size directly influences the nanoparticle processing and nanotoxicity in vivo. Using fluorescence single particle cracking we have succeeded for the first time in following the aggregation of drug delivery nanoparticles in real time in undiluted whole blood. We demonstrate that, by using a suitable surface functionalization, nanoparticle aggregation in the blood circulation is prevented to a large extent.
Keywords
MICROPARTICLES, DYNAMICS, LIPOSOMES, DELIVERY, POLY(ETHYLENE GLYCOL), CELLS, DRUG, SIZE, Nanobiophotonics, nanoparticles, drug delivery, nanomedicines, medical diagnostics

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Chicago
Braeckmans, Kevin, Kevin Buyens, Wim Bouquet-Geerardyn, Chris Vervaet, Philippe Joye, Filip De Vos, Laurent Plawinski, et al. 2010. “Sizing Nanomatter in Biological Fluids by Fluorescence Single Particle Tracking.” Nano Letters 10 (11): 4435–4442.
APA
Braeckmans, Kevin, Buyens, K., Bouquet-Geerardyn, W., Vervaet, C., Joye, P., De Vos, F., Plawinski, L., et al. (2010). Sizing nanomatter in biological fluids by fluorescence single particle tracking. NANO LETTERS, 10(11), 4435–4442.
Vancouver
1.
Braeckmans K, Buyens K, Bouquet-Geerardyn W, Vervaet C, Joye P, De Vos F, et al. Sizing nanomatter in biological fluids by fluorescence single particle tracking. NANO LETTERS. 2010;10(11):4435–42.
MLA
Braeckmans, Kevin, Kevin Buyens, Wim Bouquet-Geerardyn, et al. “Sizing Nanomatter in Biological Fluids by Fluorescence Single Particle Tracking.” NANO LETTERS 10.11 (2010): 4435–4442. Print.
@article{1850220,
  abstract     = {Accurate sizing of nanoparticles in biological media is important for drug delivery and biomedical imaging applications since size directly influences the nanoparticle processing and nanotoxicity in vivo. Using fluorescence single particle cracking we have succeeded for the first time in following the aggregation of drug delivery nanoparticles in real time in undiluted whole blood. We demonstrate that, by using a suitable surface functionalization, nanoparticle aggregation in the blood circulation is prevented to a large extent.},
  author       = {Braeckmans, Kevin and Buyens, Kevin and Bouquet-Geerardyn, Wim and Vervaet, Chris and Joye, Philippe and De Vos, Filip and Plawinski, Laurent and Doeuvre, Loic and Angles-Cano, Eduardo and Sanders, Niek and Demeester, Jo and De Smedt, Stefaan},
  issn         = {1530-6984},
  journal      = {NANO LETTERS},
  keyword      = {MICROPARTICLES,DYNAMICS,LIPOSOMES,DELIVERY,POLY(ETHYLENE GLYCOL),CELLS,DRUG,SIZE,Nanobiophotonics,nanoparticles,drug delivery,nanomedicines,medical diagnostics},
  language     = {eng},
  number       = {11},
  pages        = {4435--4442},
  title        = {Sizing nanomatter in biological fluids by fluorescence single particle tracking},
  url          = {http://dx.doi.org/10.1021/nl103264u},
  volume       = {10},
  year         = {2010},
}
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