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Chasing Tiny Vehicles: Microscope Shows How Nanoferries Invade Cells

Date:
July 22, 2009
Source:
Ludwig-Maximilians-Universitaet Muenchen (LMU)
Summary:
In future therapies, synthetic nanoparticles may well be able to ferry medicines and even genes to targets inside the body. These nanovehicles can now be directly tested and optimized using a highly sensitive microscopic method that can trace single particles all the way into a cell.

In future therapies, synthetic nanoparticles may well be able to ferry medicines and even genes to targets inside the body. These nanovehicles can now be directly tested and optimized using a highly sensitive microscopic method that can trace single particles all the way into a cell.

Nanoparticles are just billionths of a millimeter in size. Exhibiting novel and often surprising properties, they are finding their way into an endless stream of equally innovative products. In medical therapies, for example, tiny nanovehicles could one day ferry drugs or even genes into cells. So far, the only way of testing these approaches has been to wait for the desired effect to show – the activation of a transported gene inside a cell for example. 

Under the direction of LMU Munich physicochemist Professor Christoph Bräuchle, a research group cooperating with Dr. Christian Plank of the Technische Universität München (TUM) has now used a highly sensitive microscopic technique to pursue individual nanoparticles as they make their way into target cells – in real-time and at high spatial and temporal resolution. They tested magnetic nanoparticles that could be used, among other things, in cancer therapy. This approach should also allow a better understanding of existing nanovectors as well as the development of new systems.

Nanoparticles are so small that many barriers in the body simply can't stop them. They can also use the bloodstream to reach any part of the body. Researchers and doctors alike hope that these tiny vehicles will one day be put to work in therapies carrying drugs directly to the seat of a disease. “Even genes can be transported this way,” says Plank. “That means we could be seeing new breakthroughs in gene therapy soon, which has seen more than its fair share of setbacks. After all, lacking most are functional transporters.” Such vehicles or vectors have been developed mainly from viruses until now. But even deactivated viruses can sometimes trigger unwanted side-effects. Nanoferries, on the other hand, have been tailored to deliver genes or drugs directly to the target without side-effects.

For such a targeted delivery, however, nanoferries need a kind of search mechanism to guide them to where their cargo is needed. Magnetic particles have already been tried in cancer therapies: They have been administered by infusion and then directed – via magnetic fields –  to a tumor whose cells they should invade directly. But until now, is has been impossible to observe nanoparticles along their route, especially into living tumor cells. It is a prerequisite, though, for therapeutic approval and the definition of functional doses to know the exact path of these carriers and the efficiency of their transport and uptake by cancer cells.

So far, only the appearance or absence of the desired therapeutic effect would tell whether an approach was even promising or not.  “It’s like a black box,” Bräuchle says. “You put something in at one end, then wait and see if anything comes out at the other end. What happens in between is anyone’s guess.” Now, his workgroup has employed highly sensitive single-molecule fluorescence microscopy to follow the nanoferries on their voyage. This highly sensitive method works by tagging individual particles with a dye that acts like a “molecular lamp” to light up the particle’s path into the cell.

“Thus, we have traced magnetic lipoplex nanoparticles and made movies of their transport,” reports Anna Sauer, first author of the study. “We were able to watch the particles in real-time and at high temporal and spatial resolution as they made their way into the cells.” In doing so, the research team could even define separate phases: how the particles reached the cell membrane, came to rest there and then ultimately – enclosed in a membrane vesicle – invaded the cells. The vesicles move randomly, often downright erratically inside the cell, until a so-called motor protein binds them and quickly transports them towards the cell nucleus – the ultimate target for the gene.

The research team is now in a position to characterize and describe in great detail the individual steps along this path. “Our new approach has also revealed bottlenecks in nanoferry transport,” Bräuchle reports. “We saw, for example, that the magnetic field can only direct particles outside cells. But, contrary to expectations, it did not facilitate entry into cells. Thanks to these new insights, existing nanoferries can be suitably optimized in future, and even new systems developed.” 

The work was performed in the scope of the clusters of excellence NIM and CiPSM.


Story Source:

The above story is based on materials provided by Ludwig-Maximilians-Universitaet Muenchen (LMU). Note: Materials may be edited for content and length.


Journal Reference:

  1. Sauer et al. Dynamics of magnetic lipoplexes studied by single particle tracking in living cells. Journal of Controlled Release, 2009; 137 (2): 136 DOI: 10.1016/j.jconrel.2009.04.003

Cite This Page:

Ludwig-Maximilians-Universitaet Muenchen (LMU). "Chasing Tiny Vehicles: Microscope Shows How Nanoferries Invade Cells." ScienceDaily. ScienceDaily, 22 July 2009. <www.sciencedaily.com/releases/2009/07/090720083217.htm>.
Ludwig-Maximilians-Universitaet Muenchen (LMU). (2009, July 22). Chasing Tiny Vehicles: Microscope Shows How Nanoferries Invade Cells. ScienceDaily. Retrieved September 30, 2014 from www.sciencedaily.com/releases/2009/07/090720083217.htm
Ludwig-Maximilians-Universitaet Muenchen (LMU). "Chasing Tiny Vehicles: Microscope Shows How Nanoferries Invade Cells." ScienceDaily. www.sciencedaily.com/releases/2009/07/090720083217.htm (accessed September 30, 2014).

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