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Completed NON-SBIR/STTR RPGS NIH (US)

Optical nanosensor for 3D force sensing in intact tissues of live animals

$2.38M USD

Funder NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
Recipient Organization University of Colorado
Country United States
Start Date Feb 01, 2021
End Date Jan 31, 2023
Duration 729 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10109869
Grant Description

PROJECT SUMMARY Physical forces are known to impact cell functions in a fundamental way. While the study dates back some 100-years, the scientific interests have significantly increased in the past decades. However, despite the extensive studies, obtaining precise force information in live animals remains an elusive task.

Currently, a vast majority of, if not all, force sensing studies have only been carried out in cultured cells.

Yet, it is well-documented that one of the most prominent differences between cell culture and intact tissues is the change of mechanical forces and cell- cell adhesion.

Therefore, precise measurements of forces inside biological tissues of live animals are desperately needed to advance the field.

The goal of this project is to develop a novel force sensing technique that allows non-invasive sensing of force distribution across 3D volume of biological tissue in a live animal.

It promises highly sensitive force measurements with simple fluorescence measurements that can be conducted in a standard confocal microscope. The nanosensor is composed of metal nanodisk, upconversion nanoparticle and flexible polymer. Upconversion nanoparticle is excited by an infrared light and emits visible fluorescence.

The infrared excitation provides many benefits including no background fluorescence and high sensitivity.

The nanosensor produces fluorescence signal that is highly sensitive to local deformations, enabling detection of force as small as 1 nN and local deformation down to ~1 nm. Finally, we have established a state-of-art two-photon microscope system to perform fluorescence imaging in live mice.

We have developed a number of fluorescence tagged mouse models that resolve epidermal and hair follicle lineages and monitor the adhesion, migration and proliferation of epithelial cells. This system will allow us to test and fine-tune our designs in a physiologically relevant condition.

All Grantees

University of Colorado

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