Authors: Mai N. Vu, Hannah G. Kelly, Adam K. Wheatley, Scott Peng, Emily H. Pilkington, Nicholas A. Veldhuis, Thomas P. Davis, Stephen J. Kent, and Nghia P. Truong
Source: onlinelibrary.wiley.com
Advance Science News, Small Journal
Received: May 6, 2020. Revised: June 4, 2020. Published online: June 25, 2020.
Synopsis: 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 effciency. 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 micro-vascular 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.