Enhanced Solubility & Bioavailability
Unleash the true potential of your API/Drug Product through Eurofins CDMO's spray drying services. Our expansive network of companies presents a comprehensive range of solutions, including cGMP spray drying. With a focus on both clinical and small-scale commercial needs, we offer Spray Drying Development & GMP Spray Drying Manufacturing services, augmented by critical supportive measures such as supersaturation studies, solid-state characterization, and stability/stress assessments.
Our Expertise
- Solid State Characterization
- Screening and Development of Spray dried formulations to be tested in animal PK studies
- Miniaturized Approach: We offer a unique method that optimizes API consumption, allowing efficient formulation testing.
- Clinical and Small-Scale Commercial cGMP Spray Drying
- API and Drug Product Development & Manufacturing
- Analytical Services (solubility testing, supersaturation studies, evaluation of miscibility, solid state characterization, stability/stress studies)
- Aqueous and Organic Solvent Processing
- Seamless Transfer Activities: Our expertise supports smooth transitions to Contract Manufacturing Organizations (CMOs)
The advantages
- Enhanced Solubility & Bioavailability: Transform poorly soluble compounds into effective therapeutic solutions.
- API Complexation with Polymers: Achieve improved performance and stability
- Controlled Particle Characteristics: Precision in particle characteristics and control through advanced spray drying techniques.
- Continuous Processing & Scale-Up
Applications of Spray Drying for pharmaceuticals:
- Development of amorphous solid dispersions to improve the solubility & bioavailability of poorly soluble compounds
- Solidification of biologics for further processing into a tablet, capsule or other final Drug Product
- Solidification of nanosuspensions into a tablet, capsule or other final Drug Product
- Powder encapsulation in view of taste masking or controlled release
Talk to our experts