STEP 1
Biological Input
Assess the target material, activity, and stability challenge.
The Science That Makes Biologics Shelf-Stable
Our proprietary stabilization platform combines proprietary formulations with specialized drying protocols to immobilize sensitive biological materials within a protective vitrified matrix — helping preserve activity, improve shelf life, and enable ambient-stable product formats.
STEP 2
Stabilization System
Apply proprietary chemistry tailored to the material.
STEP 3
Specialized Drying
Dry under conditions designed to minimize biological stress.
STEP 4
Protective Vitrified Matrix
Immobilization within a protective glass-like state
STEP 5
Commercial Product Formats
Commercial ambient-stable biological products
The Four Pillars of VitriStableâ„¢ Technology
Proprietary Formulation Science
Proprietary stabilization formulations designed to protect sensitive biological materials during dehydration, storage, and distribution.
Optimized Drying Protocols
Controlled drying protocols tailored to the material’s stability profile, balancing water removal with preservation of viability, activity, and performance.
Conventional Equipment Compatibility
Designed to work within existing production environments and conventional lyophilization infrastructure without requiring specialized new equipment.
Protected IP Portfolio
A proprietary formulation-and-process platform supported by patent protection, know-how, and application-specific optimization.
The VitriStableâ„¢ Development Process
01
02
Material Assessment
Evaluation of the material’s baseline viability, activity, and stability profile to determine key sensitivities and establish a starting point for formulation development.
Formulation Design
Development of proprietary stabilization formulations tailored to the material’s sensitivity profile, performance requirements, and intended product format.
03
Protocol Optimization
Refinement of drying protocols to support protective vitrification while preserving viability, activity, and performance in the final dry state.
04
05
Scale-Up Validation
Evaluate optimized VitriStableâ„¢ formulations and protocols in larger-scale or partner-relevant environments to confirm reproducibility, process compatibility, and commercial readiness.
Implementation Pathway
Translate validated VitriStableâ„¢ formulations and protocols into a partner-ready pathway for integration, licensing, and commercialization.
The VitriStableâ„¢ Advantage
Stabilization Comparison
A differentiated technology versus conventional drying methods for sensitive biological materials.
Conventional Freeze-Drying
Stability
Often requires cold chain
SURVIVAL / ACTIVITY
Variable retention
process stress
Freezing + dehydration
Throughput
Slow: 1-5 day cycles
product enablement
Stability-limited
PROPRIETARY TECHNOLOGY
VitriStableâ„¢ Platform
Stability
Target: 2+ years at 25°CAmbient-stable formats
SURVIVAL / ACTIVITY
High-retention design
process stress
Low-temp vaporization
Throughput
Rapid: 1-5 hours
product enablement
Format-ready stable powder
Conventional Spray Drying
Stability
Material-dependent
SURVIVAL / ACTIVITY
Often compromised
Process stress
Heat + atomization
throughput
Fast: minutes
product enablement
Heat-limited
*Results and targets vary by material, formulation, and application. Development may include elevated-temp testing at 37–40°C under accelerated conditions.