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Scientific
   approach

1 er
  LABORATOIRE
  INDEPENDANT
  en Europe
 100%
dédié à l'identification des
Perturbateurs Endocriniens

Key points of our tests


Tests validated or in validation process by OECD
Performed on whole endocrine systems exposed in vitro

Ethical alternative method to animal testing
Tailor-made protocols adapted to your needs

Explanation of our testing methodologie


We perform testing on different types of samples in order to respond to different questions :
• Detect potential endocrine activity
• Measure effects of these activities on living organisms
• Identify modes of action

At early stage hormonal mechanisms are similar to those of adults and they are well maintained through the evolution of species.
In order to conduct tests we use we use Medaka (fish from asian ricefields) eggs and Xenopus (amphibian) eggs, just after hatching. Samples are tested during 24 to 96 hours after induction with hatched eggs.



Fish fry induced by exposure to the estrogenic hormone (ethinyl estradiol).
The fluorescence is induced in the liver.
Eggs harbor a genetic construct composed of the promoter of the naturally occurring target gene driving expression of a fluorescent gene (GFP).
The level of fluorescence is proportional to the effect.

Endocrine disruption is revealed by an increase or decrease in fluorescence.
Fluorescence reveals the natural reaction of the organisms

Interview with our team of experts on the endocrine system:

 Why choose a whole organism performed in vitro?

 What are the main advantages of this technology?

 Which endocrine axes should be tested (estrogenic, androgenic, thyroid)?

 Can one test identify an endocrine disruptor?

 What are the communication rules regarding Endocrine Disruption?


Results at a glance

In order to facilitate understanding of the results and to adapt each report as much as possible to its end use, we can deliver results on several levels: 
       
  • Hormonal equivalence   
  • Raw data    
  • Histograms   
  • Images   
  • Simplified data
This depends on the planned use: regulatory focus, R&D, evaluation of your raw materials and finished products, portfolio screening, ...


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