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FluoPulse™ system is the first commercial, plug-and-play Fluorescence Lifetime Fiber Photometry (FLiP) system available on the market, designed for neuroscience. This system measures changes in a biosensor's fluorescence lifetime, and is an essential tool to monitor intracellular biochemical reactions in the brains of freely moving animals.

The term "fluorescence lifetime" denotes the time lapse between the laser excitation and the release of fluorescence by the biosensor. Specially designed biosensors have unique lifetime distributions depending on whether they are in bound or unbound states. This disparity can be leveraged to study changes in neurophysiological states of key neural populations, including protein-protein interactions, changes in protein conformation, and the presence of neurotransmitters or other molecules of interest.

The FluoPulse™ system is designed to measure fluorescence lifetimes ranging between 1-10 ns and can resolve differences in lifetime of 10-50 ps. Thus, it is compatible with most biosensors designed for Fluorescence Lifetime Microscopy (FLIM) and Förster’s Resonance Energy Transfer (FRET), including FLIM-AKAR, tq-Ca-FLITS, etc. We strongly recommend using biosensor with modest changes in intensity (<2x) for optimal lifetime measures.

The FluoPulse™ system includes:

  1. FluoPulse™ Cube contains optics, swappable bandpass and neutral density filters. It also contains excitation lasers and photodetectors for high temporal precision lifetime measurements. Users can customize the FluoPulse™ Cube according to experimental needs*.
  2. FluoPulse™ Console contains ultra-fast electronics for analog data sampling and 8 Digital Input/Output ports to synchronize behavioral measures. The FluoPulse™ Console is compatible with all configurations of the FluoPulse™ Cube.

The FluoPulse™ system uses a novel low-power Waveform Sampling method to measure the fluorescence lifetime in freely behaving animals. While traditional fluorescence lifetime measurement, Time-Correlated Single Photon Counting (TCSPC), collects single photons at a time, the waveforms sampling method is designed to collect multiple photons simultaneously, providing a higher sampling rate (up to 25 Hz) and precision.

Furthermore, fluorescence lifetime photometry measurements offer several advantages compared to classic, intensity-based photometry. Since lifetime is a molecular property, it is less susceptible to issues like photobleaching, expression levels, excitation power, and movement artifacts, which commonly pose challenges in intensity-based photometry. Consequently, fluorescence lifetime measures are more consistent between different animals and are exceptionally reliable for prolonged experimental paradigms spanning weeks and months, a critical timeframe for clinical studies.

Thus, the FluoPulse™ system provides a state-of-the-art tool to measure fluorescence lifetime in a freely-moving animal, and opens avenues for discoveries in neuroscience and other fields where fluorescence lifetime offers valuable insights into the sample under investigation.

* In the configuration with red fluorophore, please note that Doric does not provide the 561 nm laser source. Contact us for more details on the laser requirements.

FluoPulse™ Cube

Built-in detectors
Wavelength detection range F1 500 to 550 nm
Wavelength detection range F2 580 to 680 nm
Built-in laser diodes
Excitation wavelength options 405, 450, 488 nm
Maximum Average Power - 40 µW @ 405 nm
- 30 µW @ 450 nm
- 20 µW @ 488 nm
Pulse Duration 450 ps
Pulse Repetition Rate 400 kHz
Fiber connection
Optical fiber core diameter 200 or 400 µm
NA 0.37
Optical fiber port connector Sample Port:FC/APC
Optogenetic port (optionnal): FC/PC
Physical properties
Dimensions Cube (width x depth x height) without knobs, connectors 165 x 76 x 51 mm
Mass Cube 950 g



FluoPulse™ Console

Fluorescence Lifetime
Lifetime range 1-10 ns
Sample rate with 1 excitation 5 to 40 Hz
Measurement precision 10-50 ps
Dynamic range 5 dB
Digital Inputs / Outputs
DIO count 8
Voltage level 5 / 3.3 / TTL V
DIO Sampling rate 10 - 50 kHz
Computer interface USB 3.0
Physical properties
Dimensions Console (width x depth x height) without connectors 165 x 76 x 75 mm
Mass Console 750 g
Drawing

Fluorescence Lifetime Photometry Cube 4

Fluorescence Lifetime Photometry Cube 6

Fluorescence Lifetime Photometry Console

Fluorescence Lifetime Filter

User Manuals Fr En

FluoPulse™

The standard FluoPulse system includes :

  • FLiP Console, the core of the system
  • FLiP Cube with built-in laser diodes with their drivers, and integrated high-speed detectors with their amplifiers
  • Doric Neuroscience Studio software
  • All necessary cables and an output fiber optic patch cord

Optional items:

Accessories:

Other light sources and fluorophore combinations are possible.

Here is a lis of some of the msot common fluorescence lifetime biosensors. In particular, we've highlighted the biosensors that have already been successfully used by clients with the FluoPulse™ system. Note that we've also included some bioRxiv papers showcasing latest innovations.

This paper, also has a more exhaustive summary: https://www.mdpi.com/2079-6374/13/10/939 but it's only from 2023.

Lifetime Biosensor Substrate Excitation Δ tau (ns) ΔF/F0 < 2x* Test with Doric Reference
Tq-Ca-FLITS Calcium 450 nm ~1.6 ns https://www.nature.com/articles/s41467-021-27249-w
G-Ca-FLITS Calcium 488 nm ~1 ns https://www.biorxiv.org/content/10.1101/2024.11.05.622032.full.pdf
RCaMP1h Calcium 560 nm ~0.1 ns x https://www.cell.com/cell-metabolism/fulltext/S1550-4131(17)30421-7
LifeCamp Calcium 488 nm ~1 ns ? https://www.biorxiv.org/content/biorxiv/early/2025/12/25/2025.12.23.696288.full.pdf
dLight3.8 Dopamine 488 nm ~0.1 ns x ✓ (can saturate) https://www.biorxiv.org/content/biorxiv/early/2024/11/11/2024.11.11.622990.full.pdf
GRAB-Ach3.0 Ach 488 nm ~0.1 ns x https://www.science.org/doi/full/10.1126/sciadv.adi0643
Rncp-iGluSnFR1 Glutamate 560 nm ∼0.6 ns x https://www.sciencedirect.com/science/article/abs/pii/S0026265X25009257
FLIM-AKAR PKA 488 nm ~0.2 ns https://www.nature.com/articles/s41598-024-53313-8
CKAR3 PKC 450 nm ~0.4 ns https://www.nature.com/articles/s41467-025-61729-7.pdf#page=1.25
sDarken Serotonin 488 nm ~0.5 ns x https://www.biorxiv.org/content/10.1101/2024.01.04.574197.full.pdf
iGlucoSnFR-TS Glucose 405 nm ~0.1 ns https://pmc.ncbi.nlm.nih.gov/articles/PMC6565483/pdf/nihms-1526614.pdf
LiLac Lactate 450 nm ~1.2 ns https://static-content.springer.com/esm/art%3A10.1038%2Fs41467-022-30685-x/MediaObjects/41467_2022_30685_MOESM1_ESM.pdf
sR-TOLLEC pH 450 nm 0.8 https://www.biorxiv.org/content/10.64898/2025.12.25.693346v1.full.pdf
qMaLioffG ATP 488 nm 488 nm

*An ideal biosensor should have an intensity change under two-fold, for optimal FluoPulse™ detector range (prevent saturation) and for accurate lifetime measures. Generally, FRET-FLIM biosensors meet this criterion, while biosensors that were generated from intensity biosensors do not. When using biosensors with large intensity changes, care must be taken to avoid saturation (adjust titre, detector gain and excitation power).

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