Re-examining the size/charge paradigm: Differing in vivo characteristics of size- and charge-matched mesoporous silica nanoparticles

Jason L. Townson, Yu Shen Lin, Jacob O. Agola, Eric C. Carnes, Hon S. Leong, John D. Lewis, Christy L. Haynes, C. Jeffrey Brinker

Research output: Contribution to journalArticlepeer-review

73 Scopus citations

Abstract

The combination of nanoparticle (NP) size, charge, and surface chemistry (e.g., extent of modification with polyethylene glycol (PEG)) is accepted as a key determinant of NP/cellular interactions. However, the influence of spatial arrangement and accessibility of the charged molecules on the NP surface vis-à-vis the average surface charge (zeta (ζ) potential) is incompletely understood. Here we demonstrate that two types of mesoporous silica nanoparticles (MSNP) that are matched in terms of primary and hydrodynamic particle size, shape, pore structure, colloidal stability, and ζ potential, but differ in surface chemistry, viz. the spatial arrangement and relative exposure of surface amines, have profoundly different interactions with cells and tissues when evaluated in vitro and in vivo. While both particles are ∼50 nm in diameter, PEGylated, and positively charged (ζ = +40 mV), PEG-PEI (MSNPs modified with exposed polyamines), but not PEG-NMe 3+ (MSNP modified with distributed, obstructed amines) rapidly bind serum proteins, diverse cells types in vitro, and endothelial and white blood cells in vivo (ex ovo chick embryo model). This finding helps elucidate the relative role of surface exposure of charged molecules vs ζ potential in otherwise physicochemically matched MSNP and highlights protein corona neutrality as an important design consideration when synthesizing cationic NPs for biological applications.

Original languageEnglish (US)
Pages (from-to)16030-16033
Number of pages4
JournalJournal of the American Chemical Society
Volume135
Issue number43
DOIs
StatePublished - Oct 30 2013

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