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Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and Their Functionalization for Downstream Processing in Biotechnology
Author(s) -
Lennart Kleinfeldt,
Johannes Gädke,
Rebekka Biedendieck,
Rainer Krull,
Georg Garnweitner
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b01549
Subject(s) - iron oxide nanoparticles , nanoparticle , surface modification , chemical engineering , superparamagnetism , oxide , magnetic nanoparticles , materials science , downstream processing , magnetization , magnetic separation , iron oxide , suspension (topology) , aqueous solution , chemistry , coacervate , nanotechnology , chromatography , organic chemistry , magnetic field , engineering , metallurgy , physics , mathematics , quantum mechanics , homotopy , pure mathematics
In this work, the structuring of iron oxide nanoparticles via spray-drying (SD) of aqueous suspensions is investigated, leading to micrometer-sized aggregates with saturation magnetization comparable to that of the individual nanoparticles. Interestingly, the superparamagnetic behavior is retained despite the multicore structure. Modification of the aggregates via the addition of silica nanoparticles to the suspension allows for control of the resulting magnetization by adjusting the iron oxide content. Moreover, the morphology of the produced aggregates is gradually shifted from irregular inflated-like shapes in case of pure iron oxide aggregates to reach spherical structures when bringing the silica content to only 20%. The aggregates with different magnetization can be effectively separated in a simple column with an attached permanent magnet. Functionalization of pure iron oxide aggregates with a previously coupled ligand holding a nitrilotriacetic acid (NTA)-like moiety and subsequent loading with Ni 2+ ions leads to the ability to bind 6-histidine (His 6 )-tagged target proteins via chelation complexes for magnetic separation. The application of the presented system for the purification of recombinant protein A in multiple cycles is shown. The recyclability of the separation system in combination with the high degree of magnetic separation is promising for future applications in the field of preparative in situ protein purification.

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