AuburnDx · Rapid Biosensors

A rapid biosensor platform for food animal, companion animal and human health

AuburnDx field reader and single-use biosensor chip
~20s
Time to answer at the point of collection
<1,000 cp/mL
Limit of detection — PCR-class sensitivity
~60¢
Chip cost at scale on a standard wafer line
1 reader · n chips
One reader, one chip per pathogen — reconfigurable
Team & Institutional Backing

Built at Auburn — engineered for translation

Jennifer Nay

Jennifer Nay

Chief Executive Officer

Operator and commercial lead for AuburnDx. Veterinary practice owner and hospital administrator. Auburn University Adjunct Professor and Entrepreneur in Residence.

Dr. Cris Young

Dr. Cris Young

President

Veterinary and animal-health domain lead. Former USDA National Director, cattle industry expert. Professor of Practice at Auburn. Leads Part 3 — Food Animal health impact.

Dr. Masoud Mahjouri-Samani

Dr. Masoud Mahjouri-Samani

Principal Investigator

Associate Professor, ECE Auburn. Inventor of the FET nanomaterial biosensor and PI of the Laser-Assisted Science and Engineering Lab. Leads Part 2 — the technology.

Institutional backing & IP

Auburn University · Auburn IP Exchange · Laser-Assisted Science & Engineering Lab · U.S. Patent No. 12,123,845 B2, issued October 22, 2024 · Auburn New Venture Accelerator portfolio company.

Auburn University AuburnDx
Part 1

Jennifer Nay — Business Execution

Jennifer Nay, Chief Executive Officer, AuburnDx
Chief Executive Officer, AuburnDx Veterinary practice owner and hospital administrator.
2×
Veterinary Practice Owner & Hospital Administrator
6 yrs
Assisting the commercialization of research at Auburn
30+ yrs
in finance, operations and entrepreneurship

At Auburn University

  • Entrepreneur-in-Residence at the New Venture Accelerator — mentoring faculty and student-led start-up teams.
  • Adjunct professor of Entrepreneurship, Harbert College of Business.
  • Works closely with Auburn's IP Exchange to commercialize research.

In Veterinary Practice

  • Ran the business side of 2 all-Idexx veterinary hospitals.
  • Built Animal Medical Center from a one-doctor day practice into a 24-hour emergency and critical care hospital: 50 staff, 10 doctors, referrals from 80+ practices.
  • Owner with husband of a veterinary campus in Richmond, VA.
  • New concept practice in Auburn opening August 25, 2026.
MBA, Auburn University · B.S. Finance, Radford University
In the Press

Attention-grabbing research

WAFF 48 News coverage
WAFF 48 News, Alabama — "Engineers develop instant COVID test kit."
News coverage of the AuburnDx biosensor
The instant test kit made headlines for turning a 20-second read into an actionable result.
The Device

Reader + single-use chip

1

One reader, one chip per pathogen

Field reader plus a disposable chip.

2

Chip cost ~60¢ at scale

Standard wafer line — prototyped at Auburn and X-FAB.

3

Drop sample, get answer

Insert chip, add sample, push button. Results in seconds.

AuburnDx single-use biosensor chip
Sample Collection

Any bodily fluid, from any species

Food animal — cattle, swine and poultry

Food Animal

Cattle, swine and poultry
  • Raw milk — bulk tank or individual cow
  • Whole blood · serum
  • Nasal and oral swabs
  • Oral fluid — pen-level, swine
  • Cloacal swab — poultry
Companion animal — dogs and cats

Companion Animal

Dogs and cats
  • Whole blood · serum · plasma
  • Saliva
  • Urine
  • Ear and skin swabs
  • Fecal slurry
Human health — point of care and at home

Human Health

Point of care and at home
  • Saliva
  • Fingerstick whole blood
  • Serum
  • Nasal swab
  • Urine
No swab-and-ship, no extraction, no cold chain. The sample goes straight onto the chip — same chip body, same reader, whichever species it came from.
Why It Wins

Six advantages over every incumbent format

Faster
20 seconds

Time to answer at the point of collection — not a one-to-three-day round trip to a reference lab.

More Accurate
<1,000 cp/mL

A limit of detection an order of magnitude below the approved rapid assays on the market today.

Reconfigurable
1 reader, n chips

Same chip body, same reader. Only the capture antibody changes from one target to the next.

Multi-Sensor
n targets, 1 chip

Several capture chemistries on a single chip, so one sample returns a panel rather than one answer.

Cost-Effective
~60¢ per chip

Produced at wafer scale on semiconductor fabrication lines, not through biological reagent manufacture.

Eco-Friendly
No cold chain

No refrigerated logistics, no extraction consumables and no reagent chain to maintain in the field.

Validated Performance

Faster than rapid tests, more sensitive than rapid tests, simpler than PCR

Validated in-house to date:

USDA PCR BinaxNOW CareStart LumiraDx AuburnDx
Retail price / test $25–80 $12 $14 $13.60 $5–10
Sample prep RNA extraction 2 min 2 min 2 min Drop & read
Time to result 4–24 hr 15 min 10 min 12 min 20 sec
Limit of detection ≈ 100 cp/mL 22,500 cp/mL 315,000 cp/mL 22,500 cp/mL 1,000 cp/mL
Setting Centralized lab (NAHLN) Point of care Point of care Point of care Clinic / Field / Barn
VALIDATED IN-HOUSE TO DATE SARS-CoV-2 spike·Influenza A/B·MRSA
Part 2

Dr. Masoud Mahjouri-Samani — The Inventor

Dr. Masoud Mahjouri-Samani, Principal Investigator
Principal Investigator, AuburnDx Godbold Associate Professor of Electrical & Computer Engineering, Auburn University
120+
peer-reviewed articles published
$11M+
research funding as PI or co-PI
~20 yrs
in nanomaterials and nanofabrication

What he brings to the biosensor

  • Nanomaterial-enabled sensing platforms built on two-dimensional semiconducting materials, functionalized interfaces, and liquid-gated device configurations.
  • The full stack in-house — nanomaterial synthesis, electrode and sensing-layer fabrication, surface functionalization, and electrical characterization.
  • Calibration, signal processing, and the electronic readers that turn a sensor response into a quantitative result.
  • Multiple patents in nanomanufacturing and two-dimensional electronic devices.
B.S. and Ph.D., Electrical Engineering, University of Nebraska–Lincoln · Postdoctoral Research Associate, Oak Ridge National Laboratory · Funded by NASA, NSF, U.S. Army and FAA
The Science

How a binding event becomes a number

1

Functionalize

The WSe2 channel is activated with MUA linker chemistry, then coated with a target-specific antibody.

2

Apply sample

A drop of raw sample meets the liquid gate. No extraction, no amplification, no reagent chain.

3

Transduce

Antigen binding perturbs surface charge, shifting current through the transistor channel directly.

4

Read

The reader tracks current against time and returns a quantitative result in about 20 seconds.

The stack: WSe2 two-dimensional channel · activated MUA linker · antibody-functionalised surface · liquid-gated FET readout · limit of detection below 1,000 copies / mL
The AuburnDx sensing stack — WSe2 channel, MUA linker, antibody surface and FET readout
The Technology

Field-effect transistor biosensor on engineered nanomaterials

WSe₂ FET sensing surface

Sub-monolayer nanomaterial transduces a binding event into a direct electrical signal — no fluorescence, no amplification, no enzyme.

Activated MUA linker chemistry

Antibody is covalently anchored at controlled density; the same chip body accepts any antibody pair we choose to functionalize.

20-second drop-to-readout

Apply sample, watch real-time current shift. No incubation, no buffer exchange, no read-window guessing.

Single reader, recurring chips

Microcontroller-driven handheld unit. Razor / razor-blade economics: capital in once, consumables forever.

WSe2 field-effect transistor biosensor schematic
Activated MUA linker chemistry on the chip surface
U.S. Patent No. 12,123,845
Patent Position

Issued — U.S. Patent No. 12,123,845

1

Issued

U.S. Patent No. 12,123,845 B2, issued October 22, 2024 — protecting the FET nanomaterial biosensor platform.

2

University-backed

Filed through Auburn IP Exchange, with additional patents in nanomanufacturing and two-dimensional electronic devices held by the lab.

Part 3

Dr. Cristopher A. Young — Veterinary/Animal Science Expert

Dr. Cris Young, President, AuburnDx
President, AuburnDx Professor of Practice at Auburn University — College of Veterinary Medicine, and Animal Sciences in the College of Agriculture
8 states
of APHIS Veterinary Services field operations directed
27 yrs
U.S. Army Reserve Veterinary Corps — retired Colonel
30+ yrs
across practice, federal regulation and biosecurity

What he brings to AuburnDx

  • Federal regulatory fluency — former Area Veterinarian in Charge for Florida and Georgia, Field Operations Director of APHIS Veterinary Services across eight states and National Director of the US Ruminant Animal Health Center.
  • Outbreak response and biosurveillance at national scale — serving as Incident Commander for five years, now part of the Auburn team building AU-BISR for early detection of biological threats to agriculture.
  • Policy access — testified before the U.S. House Committee on Homeland Security on threats to food, agriculture and veterinary defense (holds a TS clearance).
  • Board-certified in veterinary preventive medicine — an epidemiologist who designed and managed national surveillance programs.
D.V.M., Auburn University · M.P.H., Western Kentucky University · Diplomate, American College of Veterinary Preventive Medicine · Adjunct Professor, University of Georgia
Validation & Extensibility

What we've proven — and what it implies

1 · Validated to date

  • Viral antigens
  • SARS-CoV-2 spike protein
  • Influenza A and B
  • Bacterial pathogens
  • MRSA
  • Soluble proteins
  • Bovine serum albumin (BSA)

2 · Now assumed testable

  • Any enveloped virus with a capture antibody
  • Food animal — HPAI H5N1
  • Food animal — BVDV · BRSV · IBR (BoHV-1)
  • Food animal — Bovine parainfluenza-3 · bluetongue
  • Companion — Canine parvovirus · canine influenza
  • Human — Seasonal influenza · RSV
  • Bacteria identifiable by a surface antigen
  • Food animal — E. coli O157:H7 · Salmonella spp.
  • Food animal — Mannheimia haemolytica · Pasteurella
  • Food animal — Histophilus somni · Mycoplasma bovis
  • Companion — Leptospira · Bordetella bronchiseptica
  • Human — Staphylococcus aureus (MSSA)
  • Protein biomarkers with an antibody pair
  • Food animal — Pregnancy-associated glycoproteins
  • Food animal — Haptoglobin · serum amyloid A
  • Food animal — Colostrum IgG · milk somatic markers
  • Companion — Heartworm antigen · canine CRP
  • Human — hCG (pregnancy)

3 · Hypothetical

  • Viral
  • Food animal — African swine fever · PRRSV
  • Food animal — Foot-and-mouth disease · Newcastle
  • Food animal — Swine influenza · bovine leukaemia virus
  • Companion — Rabies (lyssavirus antigen)
  • Companion — Canine distemper · FeLV · FIV
  • Human — HIV · HPV
  • Bacterial
  • Food animal — Brucella abortus · Listeria
  • Food animal — Mycobacterium bovis (bovine TB)
  • Food animal — M. avium paratuberculosis (Johne's)
  • Food animal — Campylobacter · Clostridium perfringens
  • Companion — Borrelia burgdorferi · Ehrlichia
  • Human — Mycobacterium tuberculosis
  • Soluble proteins
  • Food animal — Aflatoxin M1 in milk (mycotoxin)
  • Food animal — Beta-lactam and antibiotic residues
  • Food animal — Progesterone · cortisol (haptens)
  • Companion — Feline SDMA · pancreatic lipase
  • Companion — Cardiac troponin I
  • Human — PSA · CA-125 (cancer antigens)
Platform Extensibility

One chip body, every food-animal pathogen we already know how to capture

Proven across three pathogen classes already — viral (SARS-CoV-2), influenza, and bacterial (MRSA). Each new target requires only a new antibody pair on the same chip architecture.

DAIRY & BEEF
  • BVDV — Bovine viral diarrhea
  • BRSV — Bovine respiratory syncytial
  • Mycoplasma bovis
  • Mycobacterium paratuberculosis (Johne's)
  • Staphylococcus aureus — mastitis
  • E. coli O157:H7
POULTRY
  • HPAI H5N1 — primary panel
  • Newcastle disease virus
  • Infectious bronchitis virus
  • Mycoplasma gallisepticum
  • Salmonella enteritidis
  • Campylobacter jejuni
SWINE & EXOTIC
  • African swine fever virus
  • Foot-and-mouth disease virus
  • PRRSV
  • PCV2
  • Classical swine fever
  • Listeria monocytogenes (cross-species)

Each panel adds incremental ARPU on the same instrument base — the IDEXX SNAP playbook, accelerated.

Primary Use Case

HPAI H5N1 detection across the National Milk Testing Strategy

STAGE 1

Plant silo

Drop-and-read on bulk milk silo samples. Replace overnight PCR turnaround with 20-second screening at intake.

STAGE 2/3

State bulk-tank

On-route mobile screening for state milk programs. Same chip, same reader, no lab handoff.

STAGE 3

Affected herd

Pen-side raw-milk and/or nasal-swab testing for herd-level case finding during a Stage 3 response.

FEDERAL ORDER

Pre-movement

Lactating-cow pre-movement testing in minutes — opens the interstate gate without sending samples to NAHLN.

Why AuburnDx wins this use case

PCR is sensitive but slow, lab-bound, and expensive per sample. Lateral-flow is fast but blind below ~22,500 cp/mL. AuburnDx is the first format that delivers PCR-class sensitivity with rapid-test economics and field-test speed — exactly what NMTS Stages 1–4 require as the program scales.

Commercial Model

Reader-and-cartridge economics

Chip
$5–10
per chip (retail)

≈ 60¢ COGS at scale via standard CMOS wafer line; 80–90% gross margin headroom.

Instrument
≈ $60
handheld field reader

≈ $15 simple device COGS at scale could be conservatively sold at $60 for a 75% profit margin.

Recurring
n panels
per customer, per year

Every new disease panel rides the installed base — no instrument refresh required.

Customer segments

Dairy

≈ 27,000 U.S. dairy operations

Poultry

≈ 232,000 commercial flocks

Reference labs

NAHLN + LAB Co. networks

Veterinary clinics

> 50,000 small/mixed practices

Market

A platform that compounds across human and animal diagnostics

$5.0B

Global companion + production animal diagnostics market (2025E)

$8.3B in-vitro diagnostics for infectious disease (2022) — every dollar of which is addressable by a faster, multi-target platform.
Why the TAM compounds

HPAI surveillance (now)

USDA NMTS; ~27k dairies × ongoing testing × 5-year mandate horizon.

Poultry biosecurity (12 months)

Pre-harvest influenza.

Production animal expansion (24 months)

BVDV, BRSV, mastitis pathogens — premium-margin replacement of slow costlier tests.

Roadmap

From validated chip to partnered clinic/field deployment

Today

Validated

COVID, Influenza A/B, and MRSA functionalization completed. FET reader prototypes in hand.

  • 3 antibody chemistries proven
  • Reader prototype
  • Auburn microfab + X-FAB
Q3–Q4 2026

MVP

Complete market-ready MVP: production chip SKU, finalized reader firmware, packaging, and pre-validation kit.

  • Market-ready MVP
  • Reader firmware 1.0
  • Test validation
Q1–Q2 2027

H5N1 testing

H5N1 functionalization & analytical validation at a partner BSL-3 facility and test onsite in the field.

  • BSL-3 partner lab
  • H5 LoD confirmed on live virus
  • USDA-CVB pre-submission
H2 2027 →

Clinic / Field

USDA conditional license, and expansion to multi-pathogen panels.

  • USDA-CVB conditional license
  • Multi-panel expansion
Next Steps

Where we'd like this to go.

The fit

Built for a commercial platform like yours — scale-up is the remaining work.

The goal

Get the technology into food and companion animal health, fast.

The ask

Find this IP a long-term home inside IDEXX.

Contact:

Jennifer Nay — CEO, AuburnDx  ·  jgn0012@auburn.edu

The Platform

Today you can test fast, or test well. Not both.

Infectious disease testing runs on two modalities. Neither closes the gap.

MOLECULAR

Molecular (PCR)

Amplifies nucleic acid, so it detects at low viral load — early enough to contain. It costs a shipped sample and days of turnaround.

IMMUNOASSAY

Lateral-flow immunoassay

Reads a binding reaction on site in minutes, but needs high antigen titer — early infections read negative.

THE GAP

The blind window

The two have never converged because the readouts are physically incompatible — amplification and reagent chemistry versus an optical endpoint. So the industry runs both: reference labs for sensitivity, point-of-care for speed. The blind window between them is where containment stops being cheap.

Comparison of molecular and immunoassay testing modalities

AuburnDx is the first format that delivers PCR-class sensitivity with rapid-test economics and field-test speed.