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Bioavailability Enhancement: Drug Permeability Enhancement01:27

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Encapsulation and Permeability Characteristics of Plasma Polymerized Hollow Particles
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Core-shell upconversion nanoparticles with suitable surface modification to overcome endothelial barrier.

Chao Lu1, Jianying Ouyang2, Jin Zhang3,4

  • 1Department of Chemical and Biochemical Engineering, University of Western Ontario, London, ON, N6A 5B9, Canada.

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|November 12, 2024
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Summary
This summary is machine-generated.

Modified upconversion nanoparticles (UCNPs) with N, N-trimethyl chitosan (TMC) effectively overcome endothelial barriers for improved bioimaging delivery. This cationic modification enhances nanoparticle transport across biological tissues.

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Area of Science:

  • Materials Science
  • Biomedical Engineering
  • Nanotechnology

Background:

  • Upconversion nanoparticles (UCNPs) offer promising near-infrared (NIR) to visible light conversion for bioimaging.
  • Tissue barriers impede effective nanoparticle delivery for in vivo applications.
  • Surface modification of nanoparticles is crucial for overcoming biological barriers.

Purpose of the Study:

  • To develop core-shell UCNPs modified with N, N-trimethyl chitosan (TMC) to enhance endothelial barrier penetration.
  • To evaluate the transport efficiency and biocompatibility of TMC-modified UCNPs.
  • To assess the potential of these modified UCNPs for improved bioimaging delivery.

Main Methods:

  • Synthesis of core-shell UCNPs (NaGdF4:Yb3+,Tm3+@SiO2) and surface modification with poly(ethylene glycol) (PEG) and TMC.
  • Characterization using XRD, TEM, and zeta potential measurements.
  • In vitro assessment of endothelial barrier integrity (TEER, tight junction proteins) and nanoparticle transport across a model endothelial barrier.

Main Results:

  • TMC modification significantly increased the zeta potential of UCNPs@SiO2-PEG, indicating enhanced cationic properties.
  • TMC-modified UCNPs demonstrated no significant toxicity to HUVECs up to 250 µg/mL.
  • The transport percentage of TMC-modified UCNPs across the in vitro endothelial barrier model was up to 4.56%, significantly higher than unmodified UCNPs.

Conclusions:

  • Core-shell UCNPs surface-modified with TMC can effectively overcome endothelial barriers.
  • The enhanced transport ability suggests improved potential for targeted delivery in bioimaging applications.
  • TMC modification represents a viable strategy to enhance nanoparticle penetration through biological barriers.