Development of pharmaceutical active ingredients

Efficient and sustainable processes

Obtaining innovative ingredients in response to production safety requirements

Research and innovation for more effective and sustainable health

At AINIA, we constantly seek innovative solutions for obtaining ingredients and active ingredients that enable our collaborating companies to be more competitive in the market. We prioritise alternative compounds obtained through sustainable, safe processes, with proven evidence of their biological effect.

In line with our commitment to responsible innovation, we use alternative techniques to animal experimentation, which enables us to verify the efficacy of compounds while ensuring the development of the expected effect, faster and at lower cost.

At AINIA, we add value

  • More relevant data than standardised methods.
  • Candidate screening with greater safety and lower cost.
  • Mechanism of action studies in specific cellular models.

Development of pharmaceutical active ingredients

Development of pharmaceutical active ingredients using supercritical fluids: we extract, in a single extraction and purification stage, high concentrations of the active ingredient with high purity. These processes are clean, leave no type of residue or contaminant, and therefore do not require the management of discharges or by-products.

On the other hand, we design biosynthesis processes that begin with the selection of microorganisms for the industrial production of active ingredients with functional activity. Biofactories are also used to obtain molecules such as pharmaceutical active ingredients. We have our own collection of more than 400 natural strains with various functionalities.

We design microencapsulation processes to ensure the protection and controlled release of the principles that develop the biological activity for which they have been considered.

We have an integral in vitro model capable of studying the release and absorption of active ingredients for their formulation in pharmaceutical products, which enables more biorelevant preclinical data to be obtained than standardised analysis methods.

Integral platform for formulation and efficacy

We have an integral in vitro model to evaluate the release (bioaccessibility) and absorption (bioavailability) of active ingredients in pharmaceutical products:

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Lidia Tomás
Head of Preclinical in vitro Studies

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