In protein-rich environments such as the blood, the formation of a protein corona on receptor-targeting nanoparticles prevents target recognition. As a result, the ability of targeted nanoparticles to selectively bind to diseased cells is drastically inhibited. Backfilling the surface of a targeted nanoparticle with polyethylene glycol (PEG) molecules is demonstrated to reduce the formation of the protein corona and re-establishes specific binding. The length of the backfilled PEG molecules must be less than the length of the ligand linker; otherwise, PEG interferes with the binding of the targeting ligand to its corresponding cellular receptor
International audiencePolymer nanoparticles (NPs) are extensively studied as drug delivery systems f...
Investigation of the nanoparticle protein corona, the shell of plasma proteins formed around nanopar...
Investigation of the nanoparticle protein corona, the shell of plasma proteins formed around nanopar...
In protein-rich environments such as the blood, the formation of a protein corona on receptor-target...
Uptake and intracellular trafficking of nanoparticles upon exposure to the cells are tightly regulat...
Protein corona can alter the physiochemical properties of targeting nanoparticles (NPs), as well as ...
Surface functionalization of nanoparticles with polyethylene glycol (PEG) has been widely demonstrat...
Currently, ligand binding to nanoparticle surface is the most widespread strategy for targeting spec...
The conjugation of receptor ligands to shielded nanoparticles is a widely used strategy to precisely...
The current gold standard to reduce non-specific cellular uptake of drug delivery vehicles is by cov...
Here we have investigated the effect of enshrouding polymer-coated nanoparticles (NPs) with polyethy...
Multiple studies highlight the strong prevalence of anti-poly(ethylene glycol) (anti-PEG) antibodies...
Although there are a large number of studies available for the evaluation of the therapeutic efficac...
International audienceCovering the surface of a nanoparticle with polyethylene glycol (PEG) is a com...
With respect to the intriguing biocompatibility and the stealthy functions of poly(ethylene glycol),...
International audiencePolymer nanoparticles (NPs) are extensively studied as drug delivery systems f...
Investigation of the nanoparticle protein corona, the shell of plasma proteins formed around nanopar...
Investigation of the nanoparticle protein corona, the shell of plasma proteins formed around nanopar...
In protein-rich environments such as the blood, the formation of a protein corona on receptor-target...
Uptake and intracellular trafficking of nanoparticles upon exposure to the cells are tightly regulat...
Protein corona can alter the physiochemical properties of targeting nanoparticles (NPs), as well as ...
Surface functionalization of nanoparticles with polyethylene glycol (PEG) has been widely demonstrat...
Currently, ligand binding to nanoparticle surface is the most widespread strategy for targeting spec...
The conjugation of receptor ligands to shielded nanoparticles is a widely used strategy to precisely...
The current gold standard to reduce non-specific cellular uptake of drug delivery vehicles is by cov...
Here we have investigated the effect of enshrouding polymer-coated nanoparticles (NPs) with polyethy...
Multiple studies highlight the strong prevalence of anti-poly(ethylene glycol) (anti-PEG) antibodies...
Although there are a large number of studies available for the evaluation of the therapeutic efficac...
International audienceCovering the surface of a nanoparticle with polyethylene glycol (PEG) is a com...
With respect to the intriguing biocompatibility and the stealthy functions of poly(ethylene glycol),...
International audiencePolymer nanoparticles (NPs) are extensively studied as drug delivery systems f...
Investigation of the nanoparticle protein corona, the shell of plasma proteins formed around nanopar...
Investigation of the nanoparticle protein corona, the shell of plasma proteins formed around nanopar...