THE SCIENCE

The science behind Em-Lux

Em-Lux measures the fluorescence lifetime of NADH, a coenzyme in cellular energy metabolism, without touching the cells. It is designed to assess embryos, and egg assessment is in development on the same instrument. This page covers the biology, what Em-Lux measures, the published research and both applications.

Animated blastocyst with flickering mitochondria and a glowing inner cell mass
THE EMBRYO

The embryo and the inner cell mass

By day five, an embryo is a blastocyst. Its outer layer, the trophectoderm, forms the placenta. The inner cell mass becomes the fetus. A PGT-A biopsy samples the outer layer; Em-Lux images the inner cell mass without contact.

Within the inner cell mass, the epiblast cells become the fetus; the primitive endoderm forms the yolk sac. Inside each cell, mitochondria produce energy for development. NADH, a coenzyme in this process, fluoresces naturally.

Video, 1 min 19 s, with narration: the inner cell mass from fertilization to day five, and how Em-Lux and EMMI assess it.
Fluorescence lifetime map of a human embryo imaged on Em-Lux
Lifetime map of a human blastocyst imaged on Em-Lux
WHAT WE MEASURE

What Em-Lux measures

NADH fluoresces naturally. Its fluorescence lifetime is different when it is bound to enzymes than when it is free, which reflects how the cell is producing energy. Nothing is added to the sample.

NADH lifetimeReflects energy metabolism
Bound and free fractionsShare of NADH engaged with enzymes
Inner cell massMeasured in the region that becomes the fetus

Additional molecules, such as FAD, are on our development roadmap.

PUBLISHED RESEARCH

Published research on FLIM in embryos

10,000+
articles on NADH fluorescence as a metabolic marker, since 1950
1,000+
articles on FLIM of NADH as a metabolic marker, since 1990
~100
articles on FLIM of NADH in embryology, since 2010
MOUSE AND HUMAN

Culture stress

Embryos under nutrient or osmotic stress separate from controls.

MOUSE

Glycolysis

Blocking key metabolic enzymes in mouse oocytes and embryos shifts the lifetime signature; the authors reported that imaging did not significantly impair mouse embryo development (Sanchez et al., 2019).

MOUSE AND HUMAN

Development

Published work reports signatures that change in a consistent way from zygote to blastocyst.

HUMAN

Ploidy

FLIM found significant metabolic differences between euploid and aneuploid human blastocysts (Shah et al., 2022).

Summaries of published studies. See References below.

EMBRYOS AND EGGS

One instrument, two points in the IVF cycle

Em-Lux measures the same metabolic signal at two decision points: before an egg is frozen or fertilized, and before an embryo is transferred or frozen. Embryo assessment is the focus of our current research. Egg assessment is in our development pipeline.

  1. 01Egg retrievalMature eggs are collected.
  2. 02Egg assessmentMetabolic read of each egg before freezing or fertilization. In development.
  3. 03FertilizationIVF or ICSI.
  4. 04CultureDays 1 to 5 in the incubator.
  5. 05Embryo assessmentInner cell mass scan and EMMI score on day 5 or 6. Investigational.
  6. 06Transfer or freezeThe clinical team decides.
APPLICATION 1Embryo assessmentInner cell mass metabolism, combined with morphology and patient data into a viability score and ranking.Read more →APPLICATION 2Egg assessmentA metabolic read of each mature egg, before it is frozen or fertilized, on the same instrument.Read more →
APPLICATION 1: EMBRYOS

Embryo assessment

INVESTIGATIONAL ยท IN CLINICAL RESEARCH

Em-Lux images each embryo at the blastocyst stage and measures metabolism in the inner cell mass, the region that becomes the fetus. EMMI combines that measurement with morphology and patient data to report a viability score for each embryo, and ranks the embryos in the dish.

When
Day 5 or 6 blastocyst, before transfer or freezing
Where
Inner cell mass, imaged without contact
Signal
NADH fluorescence lifetime and bound and free fractions
Combined with
Morphology and patient data, in EMMI
Output
A viability score per embryo and a ranking within the cohort
Scan time
About 1 minute per embryo
Animated blastocyst showing the trophectoderm, blastocoel and inner cell mass
Schematic of a day 5 blastocyst. Em-Lux measures the inner cell mass.

Decisions it is designed to inform

Which embryo to transfer first

A ranking of the embryos in a cohort to support the embryologist's choice. The final decision stays with the clinical team.

Which embryos to freeze

Additional information when deciding which embryos to vitrify for later use.

A view alongside PGT-A

A metabolic measure that needs no biopsy, designed to be used with existing methods rather than replace them.

Research basis: published FLIM studies in mouse and human embryos, including metabolic differences between euploid and aneuploid human blastocysts (Shah et al., 2022), and Noor data presented at PCRS 2026 (Nel-Themaat et al.).

Animation of a mature human egg with its parts labeled
Schematic of a mature egg. Mitochondria in the cytoplasm supply its energy.
APPLICATION 2: EGGS

Egg assessment

IN DEVELOPMENT PIPELINE

There is no standard objective method today to assess an egg before it is frozen or fertilized. Em-Lux is being developed to measure the same metabolic signal in mature eggs, on the same instrument used for embryos.

When
Mature (metaphase II) eggs after retrieval, before freezing or fertilization
Where
The egg cytoplasm, where mitochondria produce energy
Signal
NADH fluorescence lifetime, the same signal used for embryos
Published basis
NADH lifetime has been measured in oocytes and in the cumulus cells around them (Sanchez et al., 2019; Venturas et al., 2023)
Output
An egg-level metabolic measure; scoring is in development

Potential applications

Egg freezing

Information on egg quality when patients decide how many eggs to bank.

Choosing eggs to fertilize

A way to prioritize eggs when not all of them can be used.

Donor eggs and egg banks

Designed to give a shared measure across donors, clinics and banks.

One instrument

Eggs and embryos assessed on the same system in the lab.

SIDE BY SIDE

Embryos and eggs at a glance

Embryo and egg assessment compared
 Embryo assessmentEgg assessment
StageDay 5 or 6 blastocystMature egg, after retrieval
Region measuredInner cell massCytoplasm
SignalNADH fluorescence lifetimeNADH fluorescence lifetime
Contact with the cellNone; light onlyNone; light only
Decision it is designed to informTransfer order and which embryos to freezeWhich eggs to freeze or fertilize
AI outputEMMI viability score and rankingIn development
StatusInvestigational; in clinical researchIn development pipeline

Both applications are investigational and not FDA cleared.

NEXT

From measurement to a score

See how Em-Lux captures this signal in the lab, and how EMMI combines it with morphology and patient factors.

See Em-Lux and EMMIFor clinics
References (9)
  1. Nel-Themaat L, Azartash K, Menjivar N, Hellriegel C. A novel non-invasive selection platform for assessing embryo metabolic state and ploidy. PCRS 2026.
  2. Shah JS, Venturas M, Sanchez TH, Penzias AS, Needleman DJ, Sakkas D. Fluorescence lifetime imaging microscopy (FLIM) detects differences in metabolic signatures between euploid and aneuploid human blastocysts. Hum Reprod 2022;37(3):400-410.
  3. Sanchez T, Venturas M, Aghvami SA, et al. Combined noninvasive metabolic and spindle imaging as potential tools for embryo and oocyte assessment. Hum Reprod 2019.
  4. Venturas M, et al. Noninvasive metabolic profiling of cumulus cells, oocytes, and embryos via fluorescence lifetime imaging microscopy. Hum Reprod 2023.
  5. Ma N, et al. Label-free assessment of pre-implantation embryo quality by the FLIM-phasor approach. Sci Rep 2019.
  6. Skala MC, et al. In vivo multiphoton microscopy of NADH and FAD redox states, fluorescence lifetimes, and cellular morphology. PNAS 2007.
  7. Blacker TS, et al. Separating NADH and NADPH fluorescence in live cells and tissues using FLIM. Nat Commun 2014.
  8. Leese HJ. Metabolism of the preimplantation embryo: 40 years on. Reproduction 2012.
  9. Cao R, et al. Multiphoton FLIM imaging of NAD(P)H and FAD with one excitation wavelength. J Biomed Opt 2020.