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Understanding the effect of etching medium in tuning the surface polarity of silica nanoparticles for tuning the loading and release of anticancer drugs


EMSL Project ID
49752

Abstract

Silica nanoparticles have traditionally been used in drug delivery owing to their easy synthesis, nearly inert behaviour and ability to tune its surfaces for attaching targeting moieties. Recently etching silica nanoparticles with selected etching agents have also been explored as means of increasing the drug adsorption capacity as etching increases the active surface area available for adsorption of drugs. It is generally assumed that increase in surface area results in increase in drug adsorption as well as its release in the suitable medium. Our recent experimentation with etching silica nanoparticles surfaces for increasing the adsorption of docetaxel, a hydrophobic anticancer drug, suggest that the etching medium can significantly influence the drug uptake and release. While etching increases the surface area of the silica nanoparticles it also chemically modifies its surfaces resulting higher uptake of the hydrophobic drug as compared to unetched silica nanoparticles. However the cumulative drug release from the etched silica nanoparticles was lower than the drug release from unetched silica nanoparticles suggesting that the drug was adsorbed more strongly on the etched surface than the unetched surfaces. Based on this observation it is hypothesized that etching silica nanoparticles modifies the polarity of the surfaces resulting in strong interaction of the hydrophobic drug with silica nanoparticles. Based on this hypothesis the aim of the present study is to evaluate the surface chemistry of silica nanoparticles etched in different mediums and correlate with the experimental observations of drug uptake and release studies. This study would result in modifying the design of silica based drug delivery vehicles for fighting against diseases such as cancers.

Project Details

Start Date
2017-03-20
End Date
2019-09-30
Status
Closed

Team

Principal Investigator

Mark Engelhard
Institution
Environmental Molecular Sciences Laboratory

Team Members

Katherine Koh
Institution
Pacific Northwest National Laboratory

Nicholas Nelson
Institution
Pacific Northwest National Laboratory

Matthew Linford
Institution
Brigham Young University

Vijayakumar Murugesan
Institution
Pacific Northwest National Laboratory

Ajay Karakoti
Institution
Pacific Northwest National Laboratory

Abhijeet Karkamkar
Institution
Pacific Northwest National Laboratory

Sebastien Kerisit
Institution
Pacific Northwest National Laboratory

Janos Szanyi
Institution
Pacific Northwest National Laboratory

Eugene Ilton
Institution
Pacific Northwest National Laboratory

Greg Coffey
Institution
Pacific Northwest National Laboratory

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