Kiss-and-run drug delivery

Jeanne Therese Andres writes about a HOT ChemComm article for Chemistry World

Carriers that release hydrophobic substances at cell membranes but do not enter the cells themselves could be the foundation for a new way to deliver drugs into cells, according to a team of scientists in Germany.

  
 The carrier touches the cell membrane for around 100ms to release its cargo which ends up inside lipid droplets (LD) in the cell

Many drugs are not water- or blood-soluble, so nanocarriers are typically used to encapsulate and transport drugs through the bloodstream to target sites where they are then taken inside the cell before releasing their drug cargo. Previous efforts focussed on ensuring successful nanocarrier uptake, as this was assumed to be the best way to deliver drugs into cells. ‘But now, with our new “kiss-and-run” mechanism, we no longer need to worry about whether the carrier can enter the cell,’ says team leader Volker Mailänder from the Max Planck Institute for Polymer Research, ‘only the drug itself needs to do that.’

Mailänder and his team tested their approach using biodegradable poly-L-lactide nanoparticles that fleetingly touch the cell’s phospholipid layer for around 100ms to release their cargo, in this case a hydrophobic dye that was left to stain the cell membrane, before quickly detaching from the cell – hence the term ‘kiss-and-run.’ They later found that the dye, representing water-insoluble drug cargo, was ultimately stored as lipid droplets within the cell.


Read the full article in Chemistry World»

Read the original journal article in ChemComm:
Drug delivery without nanoparticle uptake: delivery by a kiss-and-run mechanism on the cell membrane
Daniel Hofmann, Claudia Messerschmidt, Markus B. Bannwarth, Katharina Landfester and Volker Mailänder  
Chem. Commun., 2014, Advance Article, DOI: 10.1039/C3CC48130A

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