Related Experiment Video
Updated: Jul 15, 2025

09:34
Uptake of New Lipid-coated Nanoparticles Containing Falcarindiol by Human Mesenchymal Stem Cells
Published on: February 9, 2019
9.0K
Electrosprayed Core (Cellulose Acetate)-Shell (Polyvinylpyrrolidone) Nanoparticles for Smart Acetaminophen Delivery
1School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai 200093, China.
Pharmaceutics
|September 28, 2023
Summary
Researchers developed novel core-shell nanoparticles using cellulose acetate and polyvinylpyrrolidone for smart drug delivery. These nanoparticles provide biphasic release of acetaminophen, offering rapid and sustained therapeutic effects.
Area of Science:
- Pharmaceutics and Materials Science
- Nanotechnology and Drug Delivery
Background:
- Smart drug delivery systems are crucial for optimizing therapeutic effects by aligning drug release with biological needs.
- Biphasic release, combining pulsatile and extended release, is a key strategy for achieving rapid onset and prolonged therapeutic action.
Purpose of the Study:
- To develop advanced core-shell nanoparticles for biphasic release of acetaminophen (ATP).
- To utilize cellulose acetate (CA) and polyvinylpyrrolidone (PVP) for fabricating a novel drug delivery system.
- To investigate the process-structure-performance relationship of these biomacromolecule-based nanoparticles.
Main Methods:
- Fabrication of core-shell nanoparticles using a modified coaxial electrospraying process.
- Characterization of nanoparticle morphology and structure using scanning electron microscopy (SEM) and transmission electron microscopy (TEM).
- In vitro evaluation of acetaminophen release kinetics to determine pulsatile and sustained release profiles.
Main Results:
- Successfully fabricated core-shell nanoparticles with distinct double-chamber structures and spherical morphologies.
- Achieved biphasic release of acetaminophen: a rapid release of 30% in 0.32 hours and sustained release of 90% over 30.84 hours.
- Confirmed the amorphous state of acetaminophen within the nanoparticles due to excellent compatibility with CA and PVP.
Conclusions:
- The developed core-shell nanoparticles demonstrate a promising platform for smart, biphasic drug delivery.
- The biomacromolecule-based approach offers a viable strategy for designing advanced nano drug delivery systems with controlled release profiles.
- Understanding the process-structure-performance relationships is key to advancing the development of novel nanocarriers.

