NanoDis System – compliant solution for Nanoparticle Dissolution

The Agilent NanoDis System provides formulation scientists with accurate release profiles of APIs using conventional dissolution test apparatus in an automated, compliant manner. This functionality enables dissolution analysts to uncover the best nanoparticle formulation faster, and achieve accurate and reliable results in any dissolution tests for tablets or liposome drug products.

Agilent Dissolution System
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Conquer Your Filtration Challenges

Users benefit from a complete, automated solution, including dissolution, filtration, and sampling, compliant with cGMP regulations.

For nano, and more. Equipped with hollow fiber filtration, the NanoDis System is particularly suitable for nanoparticle formulations. It can also be used for liposomes, parenterals, and any other products with filtration challenges requiring release-rate testing.

For speed-to-market. The automated, software-driven workflow helps achieve predictive dissolution profiles in less time, facilitating faster formulation development, validation, and time to market.

NanoDis System – compliant solution for Nanoparticle Dissolution

  • Rugged and robust methodology using conventional USP apparatus. Methods are easily transferred to QA/QC.
  • An uninterrupted dissolution process as media and any dispersed nanoparticles are recycled back to the 708-DS vessels
  • Full compliance - all methods are operated, electronically documented and auditable (DWS)
  • System is comprised of existing and compliant hardware and software solutions: 708-DS, peristaltic pump, 850-DS, and Dissolution Workstation

Dissolution Workstation Software (DWS)

  • Flexible – up to 4 systems online at any time
  • Compliant – designed for 21 CFR Part 11 environments
  • Efficient – paperless solution reduces manual transcription and remote access
  • Secure – integrated data security with easy export features
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