journal article·2010

Recognition and transmembrane delivery of bioconjugated Fe 2 O 3 @Au nanoparticles with living cells

Linlin Sun, Jine Wang, Zhenxin Wang

Nanoscale· Volume 2· Issue 2
Publisher page

Abstract

Here, we describe the synthesis of peptide- and/or protein-functionalized Fe(2)O(3) core-Au shell (Fe(2)O(3)@Au) nanoparticles for imaging and targeting of living cells. When functionalized with the transmembrane peptide RRRRRRRR (R(8)), the Fe(2)O(3)@Au nanoparticles (R(8)-Fe(2)O(3)@Au) are able to serve as cellular trafficking agents with excellent biocompatibility. The internalization mechanism and delivery efficiency of the R(8)-Fe(2)O(3)@Au nanoparticles have been characterized with dark-field microscopy and fluorescence confocal scanning laser microcopy. Experimental result suggests that the R(8)-Fe(2)O(3)@Au nanoparticles are internalized initially by binding with the membrane-associated proteoglycans on cell surfaces, especially heparan sulfate proteoglycans (HSPGs), following an energy-dependent endocytosis process to enter into living cells. After conjugation with the epidermal growth factor receptor antibody (anti-EGFR), these nanoparticles can also be used for the recognition of cell membrane antigens to specifically label tumor cells.
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Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Nanoparticle-Based Drug Delivery · RNA Interference and Gene Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

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