Cited by 38Diatoms and Algae ResearchCellular Mechanics and InteractionsNanoparticle-Based Drug Delivery

Biopebbles: DNA‐Functionalized Core–Shell Silica Nanospheres for Cellular Uptake and Cell Guidance Studies

Leidner, Arnold, Weigel, Simone, Bauer, Jens, Reiber, Jens, Angelin, Alessandro, Grösche, Maximilian, Scharnweber, Tim, Niemeyer, Christof M.·2018·Advanced Functional Materials

Abstract

The development of a versatile class of silica nanoparticles for cell studies is reported. The particles contain a fluorescent dye‐encoded core and a single‐stranded DNA oligonucleotide‐displaying shell. They are accessible in arbitrary size and color through robust protocols for Stöber‐based colloidal synthesis and sturdy chemical surface functionalization. Silica particles in the size range of 100 nm to 1.5 µm diameter containing fluorescein, Cy3 oder Cy5 dye‐encoded cores are synthesized and functionalized with DNA oligonucleotides. These silica biopebbles are conveniently traceable by microscopy and have a high affinity to live cells, which makes them ideal for cell uptake studies, as demonstrated for MCF7 and A431 cancer cells. The biopebbles can be utilized as building blocks for the self‐assembled formation of arbitrary surface patterns on glass substrates. With these architectures, the privileged internalization of the biopebbles can be exploited for improved adhesion and guidance of cells because the particles are no longer ingested by adhered cells due to their physical connection with the solid support. It is believed that the biopebble approach will be useful for a variety of applications, fundamental studies in cell biology and tissue engineering.

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Crossref · 10.1002/adfm.201707572

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  • Using hybridization assays with fluorescently-labelled probes, the authors estimated the number of barcodes available for hybridization on each file to be on the order of 10^8.

    “Using hybridization assays with fluorescently-labelled probes35–37, we estimated the number of barcodes available for hybridization on each file to be on the order of 108 (Supplementary Fig. 7).”

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References 58 · Cited by 38

Authors
Leidner, A., Weigel, S., Bauer, J., Reiber, J., Angelin, A., Grösche, M., Scharnweber, T., & Niemeyer, C. M.
Affiliations
Karlsruhe Institute of Technology (DE)
Corresponding author
Niemeyer, Christof M.
Venue
Advanced Functional Materials
Publisher
Wiley
Published
2018-03-09
Volume
28
Issue
18
ISSN
  • 1616-301X (ISSN-L)
  • 1616-3028
OpenAlex
W2789580484
Cited by
38
References
58
Citations by year
2026: 2 · 2025: 1 · 2024: 1 · 2023: 1 · 2022: 5 · 2021: 9 · 2020: 6 · 2019: 8 · 2018: 5
FWCI
2.26
Type
journal article
Language
en
Open access
closed
Locations
Advanced Functional Materials (publishedVersion)
Funders
  • Deutsche Forschungsgemeinschaft
  • Max-Planck-Gesellschaft
Topics
  • Physical Sciences › Materials Science › Biomaterials › Diatoms and Algae Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
Keywords
silica nanoparticles, DNA-functionalized nanoparticles, core-shell nanospheres, cellular uptake, cell adhesion, cell guidance, Stöber synthesis, MCF-7 cells, A431 cells, tissue engineering

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