Journal Article FZJ-2014-03389

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Margination of micro- and nano-particles in blood flow and its effect on drug delivery

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2014
Nature Publishing Group London

Scientific reports 4, 4871 () [10.1038/srep04871]

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Abstract: Drug delivery by micro- and nano-carriers enables controlled transport of pharmaceuticals to targeted sites. Even though carrier fabrication has made much progress recently, the delivery including controlled particle distribution and adhesion within the body remains a great challenge. The adhesion of carriers is strongly affected by their margination properties (migration toward walls) in the microvasculature. To investigate margination characteristics of carriers of different shapes and sizes and to elucidate the relevant physical mechanisms, we employ mesoscopic hydrodynamic simulations of blood flow. Particle margination is studied for a wide range of hematocrit values, vessel sizes, and flow rates, using two- and three-dimensional models. The simulations show that the margination properties of particles improve with increasing carrier size. Spherical particles yield slightly better margination than ellipsoidal carriers; however, ellipsoidal particles exhibit a slower rotational dynamics near a wall favoring their adhesion. In conclusion, micron-sized ellipsoidal particles are favorable for drug delivery in comparison with sub-micron spherical particles

Classification:

Contributing Institute(s):
  1. Theorie der Weichen Materie und Biophysik (IAS-2)
  2. Theorie der Weichen Materie und Biophysik (ICS-2)
Research Program(s):
  1. 451 - Soft Matter Composites (POF2-451) (POF2-451)

Appears in the scientific report 2014
Database coverage:
Medline ; Creative Commons Attribution CC BY 3.0 ; DOAJ ; OpenAccess ; BIOSIS Previews ; JCR ; NCBI Molecular Biology Database ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection ; Zoological Record
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Document types > Articles > Journal Article
Institute Collections > IBI > IBI-5
Institute Collections > IAS > IAS-2
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ICS > ICS-2
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 Record created 2014-06-04, last modified 2024-06-10


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