Award Abstract # 2002511
Multi-Modal Data-Driven Platform for Multiplexed Cellular Antigen Classification using Nano-electronic Barcoded Particles for Whole Blood Applications

NSF Org: ECCS
Div Of Electrical, Commun & Cyber Sys
Recipient: RUTGERS, THE STATE UNIVERSITY
Initial Amendment Date: December 17, 2019
Latest Amendment Date: December 17, 2019
Award Number: 2002511
Award Instrument: Standard Grant
Program Manager: Svetlana Tatic-Lucic
staticlu@nsf.gov
 (703)292-0000
ECCS
 Div Of Electrical, Commun & Cyber Sys
ENG
 Directorate For Engineering
Start Date: February 1, 2020
End Date: January 31, 2024 (Estimated)
Total Intended Award Amount: $500,000.00
Total Awarded Amount to Date: $500,000.00
Funds Obligated to Date: FY 2020 = $500,000.00
History of Investigator:
  • Umer Hassan (Principal Investigator)
    umer.hassan@rutgers.edu
  • Mehdi Javanmard (Co-Principal Investigator)
Recipient Sponsored Research Office: Rutgers University New Brunswick
3 RUTGERS PLZ
NEW BRUNSWICK
NJ  US  08901-8559
(848)932-0150
Sponsor Congressional District: 12
Primary Place of Performance: Rutgers University New Brunswick
NJ  US  08854-8058
Primary Place of Performance
Congressional District:
06
Unique Entity Identifier (UEI): M1LVPE5GLSD9
Parent UEI:
NSF Program(s): CCSS-Comms Circuits & Sens Sys
Primary Program Source: 01002021DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 090E, 104E
Program Element Code(s): 756400
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

This project is to develop a platform that can classify human leukocytes, which play a critical role in the body?s defense against a plethora of diseases like sepsis, cancer, and other chronic and acute diseases. State-of-the-art healthcare facilities rely on bulky and costly instruments which require manual sample processing and highly trained technical staff to perform blood analysis. In this work, an artificial intelligence enabled data-driven biosensor platform will be developed for hematology analysis. It will be based on multi-modal sensing, integrated microfluidics, and the ability to perform automated sample processing from whole blood samples. Furthermore, the proposed sensing platform will be equipped with real-time measurement capability and machine learning models to train the sensors data and provide reconfigurability and resource optimization as required. The proposed dynamic reconfigurable data driven biosensor will advance biomedical research and will have great potential to benefit human health and welfare. This cross disciplinary project will train undergraduate and graduate students in areas of sensors, systems, and bionanotechnology. The project will enable the integration of research into educational efforts directed towards engineering students. The PIs outreach activities will include engaging K-12 students, the local health-care industry, and the general public through educational lectures and making them available online for broad dissemination of knowledge.

The proposal will enable the development of a next generation in-vitro diagnostic platform equipped with multi-model sensing and nano-barcoded particles to perform reconfigurable biomarker selection in whole blood samples. Human blood cells play a critical role in immune system activation in response to infections. The concentration of these immune cells in whole blood and their membrane receptor densities may change in different diseases and their respective pathogenesis. The heterogeneity of the cellular classification needs to be quantified to provide a personalized diagnostics and monitoring system for patients in a hospital setting. The biosensing platform will be integrated with multi-modal sensing including electrical and optical detectors which will allow to correct for inherent device-to-device variation to improve sensor performance. Immune cells conjugated with functionalized nano-barcoded particles will be quantified simultaneously with an impedance detector and smartphone image sensor. Further, the proposed biosensor will be equipped with real-time data analysis using machine learning to enable a reconfigurable system for resource optimization and biomarker selection. An integrated biochip will be used to perform reconfigurable multiplexing and quantify multiple inflammatory biomarkers from patient blood samples. The proposed sensor will enable multiplexed cellular antigen classification from a drop of whole blood with time to result (TOR) for less than 30 minutes. Sensors will be benchmarked with patient clinical samples. Furthermore, it is envisioned that the biosensor platform to be generic and reconfigurable with pre-functionalized cartridges that can be swapped out for different infectious diseases.

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

Note:  When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher. Some full text articles may not yet be available without a charge during the embargo (administrative interval).

Some links on this page may take you to non-federal websites. Their policies may differ from this site.

Ashley, Brandon K. and Hassan, Umer "Point?of?critical?care diagnostics for sepsis enabled by multiplexed micro and nano sensing technologies" WIREs Nanomedicine and Nanobiotechnology , v.13 , 2021 https://doi.org/10.1002/wnan.1701 Citation Details
Ashley, Brandon K. and Sui, Jianye and Javanmard, Mehdi and Hassan, Umer "Functionalization of hybrid surface microparticles for in vitro cellular antigen classification" Analytical and Bioanalytical Chemistry , v.413 , 2021 https://doi.org/10.1007/s00216-020-03026-4 Citation Details
Sami, Muhammad A. and Tayyab, Muhammad and Parikh, Priya and Govindaraju, Harshitha and Hassan, Umer "A modular microscopic smartphone attachment for imaging and quantification of multiple fluorescent probes using machine learning" The Analyst , v.146 , 2021 https://doi.org/10.1039/D0AN02451A Citation Details
Ashley, Brandon K. and Mukerji, Ishika and Hassan, Umer "Investigating Cell-Particle Conjugate Orientations in a Microfluidic Channel to Ameliorate Impedance-based Signal Acquisition and Detection *" 2021 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC) , 2021 https://doi.org/10.1109/EMBC46164.2021.9630171 Citation Details
Ashley, Brandon K. and Hassan, Umer "Time?domain signal averaging to improve microparticles detection and enumeration accuracy in a microfluidic impedance cytometer" Biotechnology and Bioengineering , v.118 , 2021 https://doi.org/10.1002/bit.27910 Citation Details

Please report errors in award information by writing to: awardsearch@nsf.gov.

Print this page

Back to Top of page