Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

X-ray Crystallography02:18

X-ray Crystallography

27.1K
The size of the unit cell and the arrangement of atoms in a crystal may be determined from measurements of the diffraction of X-rays by the crystal, termed X-ray crystallography.
Diffraction
Diffraction is the change in the direction of travel experienced by an electromagnetic wave when it encounters a physical barrier whose dimensions are comparable to those of the wavelength of the light. X-rays are electromagnetic radiation with wavelengths about as long as the distance between neighboring...
27.1K
X-ray Diffraction of Biological Samples01:10

X-ray Diffraction of Biological Samples

5.2K
X-ray diffraction or XRD is an analytical tool that utilizes X-rays to study ordered structures such as crystalline organic and inorganic samples, polycrystalline materials, proteins, carbohydrates, and drugs.
According to Bragg's law, when X-rays strike the sample positioned on a stage, the rays are  scattered by the electron clouds around the sample atoms. The  X-ray diffraction or scattering is caused by constructive interference of the X-ray waves that reflect off the internal...
5.2K
X-ray Imaging01:24

X-ray Imaging

11.1K
German physicist Wilhelm Röntgen (1845–1923) was experimenting with electrical current when he discovered that a mysterious and invisible "ray" would pass through his flesh but leave an outline of his bones on a screen coated with a metal compound. In 1895, Röntgen made the first durable record of the internal parts of a living human: an "X-ray" image (as it came to be called) of his wife’s hand. Scientists worldwide quickly began their own experiments with...
11.1K
Atomic Emission Spectroscopy: Lab01:29

Atomic Emission Spectroscopy: Lab

835
AES is a powerful analytical technique, especially effective when used with plasma sources, producing abundant spectra in characteristic emission lines. The Inductively Coupled Plasma (ICP), in particular, yields superior quantitative analytical data due to its high stability, low noise, low background, and minimal interferences under optimal experimental conditions. However, newer air-operated microwave sources are emerging as promising alternatives that could be more cost-effective than...
835
Atomic Fluorescence Spectroscopy01:29

Atomic Fluorescence Spectroscopy

1.2K
Atomic fluorescence spectroscopy (AFS) is an analytical technique that involves the electronic transitions of atoms in a flame, furnace, or plasma being excited by electromagnetic (EM) radiation. When these atoms absorb energy, they become excited and subsequently release energy as they return to their original state. This emitted light, or "fluorescence," is observed at a right angle to the incident beam. Both absorption and emission processes transpire at distinct wavelengths, which...
1.2K
2D NMR: Overview of Heteronuclear Correlation Techniques01:18

2D NMR: Overview of Heteronuclear Correlation Techniques

930
Heteronuclear correlation spectroscopy is an analytical technique that investigates the coupling between different types of nuclei, often a proton and an X-nucleus, such as carbon-13 or nitrogen-15. This method is commonly used in nuclear magnetic resonance (NMR) spectroscopy to gain insights into complex chemical compounds' structural and compositional aspects. A typical heteronuclear correlation spectrum displays X-nucleus chemical shifts on one axis and a proton spectrum on the other...
930

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Fractionation-Free Protein Corona Quantification Through Synchrotron-Based Small-Angle X-ray Scattering.

Small methods·2026
Same author

DDX3X is a Cl<sup>-</sup>-sensitive RNA helicase.

Science signaling·2026
Same author

<i>In Situ</i> Coherent X‑Ray Scattering Investigation of Macropore Formation in Porous Silica.

ACS omega·2026
Same author

Eutectozymes as Soft Hybrid Materials for Advanced Biocatalysis.

Advanced materials (Deerfield Beach, Fla.)·2025
Same author

Decoding Protein Corona Through Synchrotron-Based Small-Angle X‑Ray Scattering.

ACS omega·2025
Same author

Unveiling the physical chemistry of silica binding peptide adsorption.

Journal of colloid and interface science·2025

Related Experiment Video

Updated: Apr 13, 2026

Confocal Microscopy Reveals Cell Surface Receptor Aggregation Through Image Correlation Spectroscopy
06:51

Confocal Microscopy Reveals Cell Surface Receptor Aggregation Through Image Correlation Spectroscopy

Published on: August 2, 2018

7.7K

Distinguishing Protein Corona from Nanoparticle Aggregate Formation in Complex Biological Media Using X-ray Photon

Caroline E P Silva1, Agustin S Picco2, Flavia Elisa Galdino1

  • 1Brazilian Synchrotron Light Laboratory (LNLS), Brazilian Center for Research in Energy & Materials (CNPEM), Campinas, Sao Paulo 13083-970, Brazil.

Nano Letters
|October 3, 2024
PubMed
Summary

X-ray photon correlation spectroscopy (XPCS) reveals silica nanoparticles (SiO2) exhibit consistent Brownian motion in complex biological fluids. This technique offers real-time analysis, overcoming limitations of traditional methods for nanomedicine applications.

Keywords:
AggregationProtein CoronaSilica NanoparticlesX-ray Photon Correlation Spectroscopy (XPCS)

More Related Videos

Detection of Protein Aggregation using Fluorescence Correlation Spectroscopy
14:04

Detection of Protein Aggregation using Fluorescence Correlation Spectroscopy

Published on: April 25, 2021

6.3K
Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells
14:12

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells

Published on: December 11, 2021

6.3K

Related Experiment Videos

Last Updated: Apr 13, 2026

Confocal Microscopy Reveals Cell Surface Receptor Aggregation Through Image Correlation Spectroscopy
06:51

Confocal Microscopy Reveals Cell Surface Receptor Aggregation Through Image Correlation Spectroscopy

Published on: August 2, 2018

7.7K
Detection of Protein Aggregation using Fluorescence Correlation Spectroscopy
14:04

Detection of Protein Aggregation using Fluorescence Correlation Spectroscopy

Published on: April 25, 2021

6.3K
Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells
14:12

Dual-Color Fluorescence Cross-Correlation Spectroscopy to Study Protein-Protein Interaction and Protein Dynamics in Live Cells

Published on: December 11, 2021

6.3K

Area of Science:

  • Nanomedicine
  • Colloid Science
  • Biophysics

Background:

  • Nanoparticles interact with biomolecules in biological systems, leading to protein corona formation and potential aggregation.
  • Understanding nanoparticle behavior in biological fluids is crucial for nanomedicine.
  • Conventional methods struggle to analyze nanoparticles in complex biological media.

Purpose of the Study:

  • To investigate the behavior of silica nanoparticles (SiO2) in diverse biological environments using X-ray photon correlation spectroscopy (XPCS).
  • To assess the impact of biological media complexity and protein corona formation on nanoparticle dynamics.
  • To demonstrate the capabilities of XPCS for real-time nanoparticle analysis.

Main Methods:

  • Application of X-ray photon correlation spectroscopy (XPCS) to study silica nanoparticles (SiO2).
  • Investigation across a range of biological media, from low to high complexity.
  • Tailoring nanoparticle surface and media composition to differentiate between corona-free systems and protein corona/aggregate formation.

Main Results:

  • Silica nanoparticles (SiO2) consistently exhibited Brownian motion, regardless of the biological media's complexity.
  • Differences in nanoparticle behavior were observed based on surface modification and media composition, distinguishing corona-free from protein-coated systems.
  • XPCS provided real-time insights into nanoparticle dynamics in complex biological environments.

Conclusions:

  • XPCS is a powerful technique for real-time nanoparticle analysis in biological media.
  • The study overcomes limitations of traditional methods for characterizing nanoparticle behavior in complex biological systems.
  • Findings offer deeper insights into colloidal behavior and protein corona formation for nanomedicine applications.