Cellular Interactions of Liposomes and PISA Nanoparticles during Human Blood Flow in a Microvascular Network

No Preview Available
Citations
Web of Science:
Scopus:
Altmetric:
Altmetric::
Associated Records
File Licence
Editors
Date
2020-08-01
Source Title
Small
Journal Title
Journal ISSN
Volume Title
Publisher
WILEY-V C H VERLAG GMBH
Affiliation
Microbiology and Immunology
Document Type
Journal Article
Subject Code
Citation
Vu, M. N., Kelly, H. G., Wheatley, A. K., Peng, S., Pilkington, E. H., Veldhuis, N. A., Davis, T. P., Kent, S. J. & Truong, N. P. (2020). Cellular Interactions of Liposomes and PISA Nanoparticles during Human Blood Flow in a Microvascular Network. Small, 16 (33), https://doi.org/10.1002/smll.202002861.
Access Status
Access this item via the Open Access location
Access URL
Open Access URL
Linked Resource URL
NHMRC Grant Code
ARC Grant Code
Description
Abstract
A key concept in nanomedicine is encapsulating therapeutic or diagnostic agents inside nanoparticles to prolong blood circulation time and to enhance interactions with targeted cells. During circulation and depending on the selected application (e.g., cancer drug delivery or immune modulators), nanoparticles are required to possess low or high interactions with cells in human blood and blood vessels to minimize side effects or maximize delivery efficiency. However, analysis of cellular interactions in blood vessels is challenging and is not yet realized due to the diverse components of human blood and hemodynamic flow in blood vessels. Here, the first comprehensive method to analyze cellular interactions of both synthetic and commercially available nanoparticles under human blood flow conditions in a microvascular network is developed. Importantly, this method allows to unravel the complex interplay of size, charge, and type of nanoparticles on their cellular associations under the dynamic flow of human blood. This method offers a unique platform to study complex interactions of any type of nanoparticles in human blood flow conditions and serves as a useful guideline for the rational design of liposomes and polymer nanoparticles for diverse applications in nanomedicine.
Notes
Terms of Use
Keywords
Publisher Licence