Low-volume dissolution-absorption testing system

Optimize your development of oral formulations with a device that enables low-volume, real-time dissolution and absorption testing, streamlining your evaluation of drug solubility and permeability for precise in-vitro analysis.

Performs In-Vitro Dissolution and Absorption Testing

The MicroFLUX system from Pion Inc. is designed for low-volume in-vitro assessment of drug dissolution and absorption processes, streamlining early-stage pharmaceutical formulation. This innovative device features a dual-chamber setup with a biomimetic membrane, enabling simultaneous analysis of dissolution and permeation. Compatible with various aqueous and biorelevant media, it facilitates rapid evaluation by using fiber-optic UV probes for real-time concentration monitoring. The system integrates seamlessly into benchtop operations, offering valuable insights into drug-excipient interactions and supporting biopharmaceutical development with compliance-ready tools. By combining dissolution and absorption into one assay, the MicroFLUX system enhances efficiency and precision for R&D and laboratory environments, particularly for studies on bioequivalence and low-solubility drugs.

Benefits

  • Enhances formulation development by providing real-time, simultaneous dissolution and absorption insights.
  • Reduces material waste with low-volume sample and media requirements.
  • Accelerates research with rapid, in-vitro testing capabilities.
  • Improves understanding of drug-excipient interactions, aiding in bioequivalence and solubility studies.
  • Integrates efficiently into existing lab setups for seamless operation.

General


Applications
Biopharmaceuticals,Oral formulations,Pharmaceuticals
End products
Drug excipient interaction studies,Low-solubility pharmaceuticals,Aripiprazole formulations,Bioequivalence study formulations,Biorelevant drug solutions,Dissolution-permeation assays
Steps before
Compound Screening,Oral Formulation Delivery,Physicochemical Characterization
Steps after
Bioequivalence Prediction,Flux Measurements Analysis,Excipient Impact Analysis
Input ingredients
drug substance,aqueous and biorelevant medias,samples,excipients
Output ingredients
dissolution rate,flux parameters,absorption concentration,in vitro dissolution-absorption analysis
Market info

Technical Specifications


Low-volume absorption chamber
Yes
Biomimetic gastrointestinal tract permeation membrane
Yes
Compatible media
Aqueous and biorelevant medias
Real-time concentration monitoring
Yes
Integration with Dynamic Dissolution Monitor
Yes
UV probe technology
Fiber-optic
Dissolution curve modeling tools
AuPRO software

Operating Characteristics


Working Mechanism
In-vitro dissolution-absorption
Integrated Steps
Simultaneous dissolution and absorption
Batch vs. Inline Flow
Batch
Automation Level
Real-time monitoring
Changeover Time
N/A
Cleaning Method
Manual

Material Compatibility


Density/particle size
0.5–2.5 g/cm³ / 50–1000 µm

Product type Characteristics


Chamber Type
Low-volume absorption and donor chambers
Media Compatibility
Aqueous and biorelevant medias
Monitoring Capability
Real-time concentration
Integration with Instruments
Rainbow Dynamic Dissolution Monitor®
Measurement Type
UV probes for concentration monitoring

Physical Characteristics


Low-volume absorption chamber
Yes
Donor chamber size
Low-volume
Permeation membrane
Biomimetic gastrointestinal tract
Compact footprint
Yes
Fiber-optic UV probe configuration
Positioned in donor and receiver compartments

Custom Options


Control panel type
HMI touch screen
Integration possibilities
Compatible with Rainbow Dynamic Dissolution Monitor®