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MP-SPR for drug delivery

Drug delivery is an essential part of the drug formulation process. With novel biopharmaceuticals, the internalization of a drug has to be facilited by nanodrug carriers. Also novel gel and patch formulations require deep understanding of drug-nanoparticle, nanoparticle-target, nanoparticle-living cell interaction as well as release of drug from material.

Nanoparticles for drug delivery and for contrast agents are typically made of polymers, silica, metals, liposomes, viruses, DNA polyplexes and newly also exosomes and other microvesicles.


See five reasons to choose MP-SPR for drug delivery studies:

  • Size does not matter
  • From targeting to internalization studies
  • Aggregating nanoparticles? Just try MP-SPR!
  • From static to dynamic measurements of nanoparticles
  • From SEM to MP-SPR and back to SEM

See five key questions about drug delivery that MP-SPR can answer:

  • What is the best nanoparticle for drug delivery?
  • What is the absorption route of a drug nanocarrier?
  • How does nanoparticle X interact with lipid bilayer?
  • What is the release rate of drug X from material Y?
  • How does a nanoparticle or virus enter the cell?

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