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Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and Their Functionalization for Downstream Processing in Biotechnology
[Image: see text] 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 beha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787900/ https://www.ncbi.nlm.nih.gov/pubmed/31616807 http://dx.doi.org/10.1021/acsomega.9b01549 |
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author | Kleinfeldt, Lennart Gädke, Johannes Biedendieck, Rebekka Krull, Rainer Garnweitner, Georg |
author_facet | Kleinfeldt, Lennart Gädke, Johannes Biedendieck, Rebekka Krull, Rainer Garnweitner, Georg |
author_sort | Kleinfeldt, Lennart |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-6787900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67879002019-10-15 Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and Their Functionalization for Downstream Processing in Biotechnology Kleinfeldt, Lennart Gädke, Johannes Biedendieck, Rebekka Krull, Rainer Garnweitner, Georg ACS Omega [Image: see text] 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. American Chemical Society 2019-09-26 /pmc/articles/PMC6787900/ /pubmed/31616807 http://dx.doi.org/10.1021/acsomega.9b01549 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kleinfeldt, Lennart Gädke, Johannes Biedendieck, Rebekka Krull, Rainer Garnweitner, Georg Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and Their Functionalization for Downstream Processing in Biotechnology |
title | Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and
Their Functionalization for Downstream Processing in Biotechnology |
title_full | Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and
Their Functionalization for Downstream Processing in Biotechnology |
title_fullStr | Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and
Their Functionalization for Downstream Processing in Biotechnology |
title_full_unstemmed | Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and
Their Functionalization for Downstream Processing in Biotechnology |
title_short | Spray-Dried Hierarchical Aggregates of Iron Oxide Nanoparticles and
Their Functionalization for Downstream Processing in Biotechnology |
title_sort | spray-dried hierarchical aggregates of iron oxide nanoparticles and
their functionalization for downstream processing in biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787900/ https://www.ncbi.nlm.nih.gov/pubmed/31616807 http://dx.doi.org/10.1021/acsomega.9b01549 |
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