Precise, every time

Precise,
every time

Bringing diagnosis at the bed-site of critically ill patients to improve their quality of life

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The Risks of Delaying Patient Dosage Adjustment.

Patient’s dosage adjustment is crucial in emergency cases where the drug concentration should be quantified in minutes,  but the conventional analytical techniques for therapeutic drug monitoring (TDM) in hospitals provide results in hours or days, risking the patient's life.

A Breakthrough in Drug Quantification.

In Fluilux we develop a first in-class, highly flexible, fast and cost-effective device, based on advanced spectroscopy and integrated microfluidics, to perform drug quantification  in samples of critically ill patients.

Fluilux Prototype
Fluilux Prototype
Fluilux Prototype
  • Fluilux Icon
  • Precise Every Time
  • Fluilux Icon
  • Light Speed Solutions
  • Fluilux Icon
  • Precise Every Time
  • Fluilux Icon
  • Light Speed Solutions

Step 1

Loading of the patient’s sample in the microfluidic cartridge

Step 2

In situ disc rotation, drug separation and trapping in the nanostructured substrate

Step 3

Substrate scanning, data collection and analysis 

Step 4

Quantification results about the drug concentration with digital interface to help doctor’s decision

EU PROJECT.

EU PROJECT.

Automated Clinical Platform for Personalized Antibiotherapy in Critical Units Based on Surface-Enhanced Raman Spectroscopy. (ACU-SERS).

PROJECT DESCRIPTION

BACKGROUND AND APPROACH

PROJECT DESCRIPTION

BACKGROUND AND APPROACH

PROJECT DESCRIPTION

BACKGROUND AND APPROACH

technology.

technology.

Novel and integrated technology

Our device is made of an integrated benchtop analyzer with a digital interface for quick drug analysis results.

Compact design

The benchtop system is compact (25 x 35 x 30 cm3) and light (~7 Kg), containing a miniaturized Raman spectrometer, a microfluidic platform with integrated nanostructured substrates, and a motor to spin the cartridge.

Label-free

Non need of markers or labeling on the singing element.

Rapid results

Our system can provide quantitative drug content in a biological sample within ~15 min.

Easy to operate

Sample preparation and analysis are fully automated, it does not require skilled technicians, reducing human error.

Flexible

Each cartridge can be used to run multiple samples in parallel (up to 8).

Versatile

The same cartridge and analyzer design can be used across multiple drugs.

Connectivity

Our design can be coupled with connectivity to Laboratory Information Systems (LIS), facilitating clinical flows.

testimonials.

Testing for antibiotics in critically ill patients in the ICU is an area where a fast and low-complexity platform like yours could add significant value.

Jason Roberts, PhD, Professor

Centre for Clinical Research. University of Queensland, Australia

With the specifications for your platform, major companies in the TDM field could have an interest in becoming a partner.

Teun van Gelder, MD, Professor

Clinical Pharmacology. Leiden University Medical Center Leiden, The Netherlands and Former president of the International Association of TDM and Clinical Toxicology (IATDMCT)

To ensure that TDM is feasible and can deliver personalized antibiotic dosing schemes, a point-of-care device is needed to provide answers around-the clock.

Anders Perner, PhD, Professor

Department of Intensive Care, Rigshospitalet, Copenhagen, Denmark

meet the team.

Gohar Soufi
Gohar Soufi
Gohar Soufi

Gohar Soufi
PhD

MSc. Analytical Chemistry. Chemical spectroscopy & Data analysis

Yaman Goksel
Yaman Goksel
Yaman Goksel

Yaman Göksel
PhD

MSc. Materials science and engineering, SERS sensors & assay development.

Isidro Badillo Ramirez
Isidro Badillo Ramirez
Isidro Badillo Ramirez

Isidro Badillo-Ramírez
PhD

MSc. Chemical spectroscopy, SERS technology & vibrational spectroscopy.

Roman Slipets
Roman Slipets
Roman Slipets

Roman Slipets

MSc. Radio-physics and electronic Hardware & Software Development.

News.

Stay up-to-date on the latest news and current events.

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This project has received funding from the European Union’s Horizon Europe programme under grant agreement No 101158666. 

Funded bythe European Union