Nanoparticles for diabetic nephropathy

Poor target cell specificity is currently a major shortcoming of nanoparticles. It causes significant material loss and poor availability. Designed nanoparticles that identify cells in a virus-like manner could provide a solution. The invention involves virus-mimetic nanoparticles able to transport drugs into their target kidney cells. The nanoparticles use a novel recognition process similar to virus organisms.
Life Sciences
Therapeutics
Reference
b79122
IP right year
2022
IP status
Pending in US, CN, EP, JP
Patentee
University of Regensburg
Contact
Erol Ceylan

Challenge and innovation

A major limitation in treating mesangial cell-associated diseases such as IgA nephropathy, diabetic nephropathy, or lupus nephritis is the poor drug availability in the glomerular mesangium; effectively delivering therapeutics via targeted nanoparticles combined with an appropriate nanoparticle target retention time to trigger relevant biological effects in the mesangium remains difficult.

The invention described here involves virus-mimetic nanoparticles that are able to transport drugs into the mesangium of the kidney. The nanoparticles use a novel sequential recognition process that is used in a similar way by viruses to recognize their target cells. In contrast to other nanomaterials, the virus-mimetic particles are able to effectively accumulate in the cells of the mesangium. Active targeting of nanoparticles with surface-bound ligands to the glomerular mesangium represents a promising strategy to improve drug availability

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