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Nanofluidic Device Enables Development of Exosome-Based Drug Delivery Vehicles
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Nanofluidic Device Enables Development of Exosome-Based Drug Delivery Vehicles

Nanofluidic Device Enables Development of Exosome-Based Drug Delivery Vehicles
News

Nanofluidic Device Enables Development of Exosome-Based Drug Delivery Vehicles

Novel nanofluidic device for efficient exosome-based drug delivery. Credit: Prof. YANG Hui's group
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A research group led by Prof. YANG Hui from the Shenzhen Institute of Advanced Technology (SIAT) of the Chinese Academy of Sciences has reported a novel nanofluidic device for high-throughput preparation of exosome-based drug delivery vehicles.

Their study was published in Small.

Exosomes are biological nanoparticles that are secreted into extracellular space or body fluid by almost all cell types, with a diameter of about 30 ~ 200 nm. Since exosomes exhibit a naturally derived composition and function as intercellular communication tools, they have great potential as smart vehicles for cargo delivery.

However, the commonly used methods for preparing exosomes that can carry desired cargo suffer from low loading efficiency and excessive damage to both exosomes and their cargo.

In this study, Prof. YANG's group proposed a high-throughput nanofluidic device called an "exosome nanoporator (ENP)," which can load a variety of exogenous cargo into exosomes.

The ENP can accurately control the characteristics of fluid in nanoscale by nanofluidic technology, so as to realize highly controllable preparation conditions for exosome-based drug delivery vehicles.

Moreover, the researchers manufactured nanofluidic channels with precise geometries, enabling 30,000 modules working in parallel in a single device.

By transporting exosomes through the nanochannels, exosome membranes are permeabilized by mechanical compression and fluid shear, generating transient nanopores on the exosome membranes and allowing an influx of cargo molecules into exosomes from the surrounding solution while maintaining exosome integrity.

The researchers selected a clinically approved chemotherapeutic antitumor drug, i.e., doxorubicin hydrochloride, as the cargo model, and confirmed that the ENP could efficiently load it into exosomes. "We found that the exosomes treated by the ENP can deliver their drug cargos to human non-small cell lung cancer cells and induce cell death. This indicates potential opportunities for the device to develop new exosome-based delivery vehicles for medical and biological applications," said Prof. YANG.

In the future, this new strategy is expected to develop into a platform to load different exogenous substances with biological significance and clinical therapeutic effects into exosomes.

Reference: 
Hao R, Yu Z, Du J, et al. A High-throughput nanofluidic device for exosome nanoporation to develop cargo delivery vehicles. Small. 2021;17(35):2102150. doi: 10.1002/smll.202102150

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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