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Characterizing Single Polymeric and Protein Nanoparticles with Surface Plasmon Resonance Imaging Measurements.
Adam M Maley1, George J Lu2, Mikhail G Shapiro2
1Department of Chemistry, University of California-Irvine , Irvine, California 92697, United States.
ACS Nano
|July 11, 2017
Summary
Near-infrared surface plasmon resonance imaging (SPRI) microscopy tracks single polymeric and protein nanoparticles (PPNPs) adsorption in real time. SPRI analysis reveals nanoparticle size, composition, and interactions, advancing nanoparticle characterization.
Area of Science:
- Nanotechnology
- Biophysics
- Materials Science
Background:
- Characterizing individual nanoparticles is crucial for understanding their behavior.
- Real-time, label-free detection methods are needed for dynamic nanoparticle studies.
- Surface Plasmon Resonance Imaging (SPRI) offers potential for nanoscale analysis.
Purpose of the Study:
- To utilize near-infrared SPRI microscopy for real-time detection and characterization of single polymeric and protein nanoparticles (PPNPs).
- To analyze nanoparticle adsorption onto gold thin films.
- To extract information on nanoparticle properties from SPRI response distributions.
Main Methods:
- Employing near-infrared surface plasmon resonance imaging (SPRI) microscopy.
- Monitoring the adsorption of hundreds of single nanoparticles in real time.
- Analyzing the frequency distribution of single-nanoparticle SPRI responses (Δ%RNP).
Main Results:
- Demonstrated real-time detection and characterization of single PPNPs adsorption.
- Analyzed Δ%RNP histograms to determine nanoparticle size, material content, and interparticle interactions.
- Quantified bioaffinity uptake and aggregation of hydrogel nanoparticles and characterized protein nanostructures.
Conclusions:
- Near-infrared SPRI microscopy is a powerful tool for label-free, real-time characterization of single nanoparticles.
- SPRI analysis of adsorption responses provides quantitative insights into nanoparticle properties and interactions.
- This technique is applicable to diverse nanoparticle systems, including hydrogels and protein nanostructures.
Keywords:
NIPAm-based hydrogel nanoparticleconcanavalin Agas vesiclemelittinprotein nanostructuresingle-nanoparticle refractive indexsurface plasmon polaritons
