A tissue chamber chip for assessing nanoparticle mobility in the extravascular space


Living Systems and Precision Medicine
A tissue chamber chip for assessing nanoparticle mobility in the extravascular space
Saturday 7th December 2019
Lusi, V.; Moore, T. L.; Laurino, F.; Coclite, A.; Perreira, R.; Rizzuti, I.; Palomba, R.; Zunino, P.; Duocastella, M.; Mizrahy, S.; Peer, D.; Decuzzi, P.
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Although a plethora of nanoparticle configurations have been proposed over the past 10 years, the uniform and deep penetration of systemically injected nanomedicines into the diseased tissue stays as a major biological barrier. Here, a ‘tissue chamber’ chip is designed and fabricated to study the extravascular transport of small molecules and nanoparticles. The chamber comprises a collagen slab, deposited within a PDMS mold, and an 800 mm channel for the injection of the working solution. Through fluorescent microscopy, the dynamics of molecules and nanoparticles was estimated within the gel, under different operating conditions. Diffusion coefficients were derived from the analysis of the particle mean square displacements (MSD). For validating the experimental apparatus and the protocol for data analysis, the diffusion D of FITC-Dextran molecules of 4, 40 and 250 kDa was first quantified. As expected, D reduces with the molecular weight of the Dextran molecules. The MSD-derived diffusion coefficients were in good agreement with values derived via fluorescence recovery after photobleaching (FRAP), an alternative technique that solely applies to small molecules. Then, the transport of six nanoparticles with similar hydrodynamic diameters (~ 200 nm) and different surface chemistries was quantified. Surface PEGylation was confirmed to favor the diffusion of nanoparticles within the collagen slab, whereas the surface decoration with hyaluronic acid (HA) chains reduced nanoparticle mobility in a way proportionally to the HA molecular weight. To assess further the generality of the proposed approach, the diffusion of the six nanoparticles was also tested in freshly excited brain tissue slices. In these ex-vivo experiments, the diffusion coefficients were 5-orders of magnitude smaller than for the ‘tissue chamber’ chip. This was mostly ascribed to the lack of a cellular component in the chip. However, the trends documented for PEGylated and HA-coated nanoparticles in vitro were also confirmed ex-vivo. This work demonstrates that the ‘tissue chamber’ chip can be employed to effectively and efficiently test the extravascular transport of nanomedicines while minimizing the use of animals.
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Biomedical Microdevices (2019) 21: 41. https://doi.org/10.1007/s10544-019-0398-5