Pioneering the convergence of 3D bioreactor engineering, targeted exosome modification, and validated disease models to unlock the next generation of regenerative therapeutics.
Our proprietary technology stack addresses the critical bottlenecks in exosome-based medicine: scalable production, precise targeting, and rigorous validation.
Proprietary perfusion-based 3D bioreactor platform achieves 50-100x higher exosome yield compared to traditional 2D culture, with consistent particle quality and scalability from lab to GMP production.
Surface display technology enables precise tissue and cell-type targeting through engineered ligands, achieving >90% targeting accuracy in validated disease models with minimal off-tissue distribution.
Comprehensive library of 260+ validated disease models across oncology, neurology, immunology, and metabolic disorders enables rapid preclinical assessment and IND-enabling studies.

Our closed-system 3D bioreactor integrates real-time monitoring of pH, dissolved oxygen, glucose consumption, and lactate production with automated perfusion control, ensuring batch-to-batch consistency critical for regulatory compliance.

Every batch undergoes comprehensive characterization using NTA, TEM, Western blot, and multi-color flow cytometry. Our QC protocol exceeds MISEV2023 guidelines with 47 quality checkpoints per production lot.
Our growing IP portfolio covers bioreactor design, surface engineering methods, cargo loading technologies, and therapeutic applications across multiple indications.
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