Related Experiment Video
Updated: Jun 11, 2025

09:11
Synthesis of Near-Infrared Emitting Gold Nanoclusters for Biological Applications
Published on: March 22, 2020
7.8K
p-Sulfonatocalix[6]arene-Functionalized Gold Nanoparticles: Applications in Drug Delivery and Bioimaging
Suprotim Koley1, Paacha Kandy Risla Sherin1, Minati Nayak1,2
1Radiation & Photochemistry Division, Bhabha Atomic Research Centre, Mumbai 400085, India.
ACS Physical Chemistry Au
|October 4, 2024
Summary
Stable gold nanoparticles functionalized with p-sulfonatocalix[6]arene (SCx6AuNPs) efficiently deliver anticancer drug doxorubicin (Dox). These SCx6AuNPs show reduced toxicity and stimuli-responsive release for targeted cancer therapy and bioimaging.
Area of Science:
- Nanotechnology
- Materials Science
- Biomedical Engineering
Background:
- Noble metal nanoparticles, particularly gold nanoparticles (AuNPs), are widely explored for biomedical applications.
- Macrocyclic hosts offer unique molecular recognition capabilities for functionalizing nanoparticles.
- Surface-functionalized nanoparticles are crucial for targeted drug delivery and diagnostics.
Purpose of the Study:
- To synthesize and characterize stable p-sulfonatocalix[6]arene-functionalized gold nanoparticles (SCx6AuNPs).
- To evaluate the potential of SCx6AuNPs for targeted delivery and stimuli-responsive release of the anticancer drug doxorubicin (Dox).
- To assess the cellular uptake and bioimaging capabilities of SCx6AuNPs.
Main Methods:
- Synthesis and characterization of SCx6AuNPs using UV-vis absorption, transmission electron microscopy (TEM), and surface-enhanced Raman spectroscopy (SERS).
- In vitro evaluation of doxorubicin (Dox) loading, release kinetics, and cytotoxicity assays on cancerous (A549) and normal (W126) cell lines.
- Bioimaging studies using thioflavin T (ThT) dye-loaded SCx6AuNPs to visualize cellular uptake.
Main Results:
- Stable SCx6AuNPs (∼7.5 nm) were successfully synthesized and characterized.
- Efficient loading and stimuli-responsive release of Dox from SCx6AuNPs were demonstrated.
- SCx6AuNPs exhibited decreased cytotoxicity of Dox towards normal cells and selective uptake by cancer cells.
- Bioimaging confirmed efficient cellular uptake of SCx6AuNPs.
Conclusions:
- SCx6AuNPs are promising nanocarriers for targeted drug delivery of anticancer agents like doxorubicin.
- The reduced cytotoxicity and stimuli-responsive release offer advantages for selective cancer therapy.
- SCx6AuNPs possess potential for dual applications in drug delivery and bioimaging.

