Design of Magnetic-Plasmonic Nanoparticle Assemblies via Interface Engineering of Plasmonic Shells for Targeted Cancer Cell Imaging and Separation.
Myeong Soo KimBum Chul ParkYu Jin KimJu Hun LeeThomas Myeongseok KooMin Jun KoYoung Keun KimPublished in: Small (Weinheim an der Bergstrasse, Germany) (2020)
Magnetic-plasmonic nanoparticles have received considerable attention for widespread applications. These nanoparticles (NPs) exhibiting surface-enhanced Raman scattering (SERS) activities are developed due to their potential in bio-sensing applicable in non-destructive and sensitive analysis with target-specific separation. However, it is challenging to synthesize these NPs that simultaneously exhibit low remanence, maximized magnetic content, plasmonic coverage with abundant hotspots, and structural uniformity. Here, a method that involves the conjugation of a magnetic template with gold seeds via chemical binding and seed-mediated growth is proposed, with the objective of obtaining plasmonic nanostructures with abundant hotspots on a magnetic template. To obtain a clean surface for directly functionalizing ligands and enhancing the Raman intensity, an additional growth step of gold (Au) and/or silver (Ag) atoms is proposed after modifying the Raman molecules on the as-prepared magnetic-plasmonic nanoparticles. Importantly, one-sided silver growth occurred in an environment where gold facets are blocked by Raman molecules; otherwise, the gold growth is layer-by-layer. Moreover, simultaneous reduction by gold and silver ions allowed for the formation of a uniform bimetallic layer. The enhancement factor of the nanoparticles with a bimetallic layer is approximately 107 . The SERS probes functionalized cyclic peptides are employed for targeted cancer-cell imaging and separation.
Keyphrases
- molecularly imprinted
- label free
- silver nanoparticles
- gold nanoparticles
- single molecule
- solid phase extraction
- energy transfer
- high resolution
- sensitive detection
- raman spectroscopy
- quantum dots
- visible light
- liquid chromatography
- risk assessment
- mass spectrometry
- working memory
- binding protein
- tandem mass spectrometry
- dna binding
- highly efficient
- transcription factor
- simultaneous determination
- photodynamic therapy
- fluorescent probe