Precision that Powers Biopharma Breakthroughs.
From preclinical development to commercial manufacturing.
Prometheus Panta C generates high-quality protein stability and aggregation data with the precision and efficiency needed throughout the drug development process — from preclinical research to commercial manufacturing.
By combining four advanced optical technologies, Panta C enables streamlined developability assessment, process monitoring, and characterization of protein identity — all while minimizing sample volume and offering features that support data integrity and 21 CFR Part 11 compliance.
With advanced optical technology, get high-quality, precise stability data that thoroughly characterize and identify your biologics. Develop fundamental insights to build on in later stages.
De-risk your asset and your process with a robust instrument that delivers a repeatable output, and information that you can trust. Don’t lose time redoing experiments or questioning the validity of your data.
Save time and sample volume by measuring multiple stability parameters in parallel, in less than two hours. Be up and running within a day, ready to develop meaningful data with an easy workflow comprising few steps.
With just a few clicks, PR. Panta C Control Software lets you design and execute single and multi-parameter stability experiments in compliance with 21 CFR Part 11 regulations.
In accordance with regulatory requirements, the Software facilitates the separation of tasks by providing five distinct user access groups, each with predefined permissions: Operator, Reviewer, Supervisor, Administrator, and Service Engineer.
1) Thermal unfolding measurements, including the acquisition of data from nanoDSF, DLS and Backreflection technologies in parallel, across a thermal ramp.
2) Particle sizing analysis using isothermal DLS data acquisition.
Johnson and Johnson Innovative Medicine.
Dr. Marius Müller, Team Lead Fill & Finish.
Characterize thermal and colloidal stability to select protein constructs for further development. Screen out poor candidates with undesirable properties early, to minimize development and commercialization risk of your program.
Strengthen the CMC package for your biopharmaceutical in all phases of drug development, from preclinical to commercialization. Track process performance and molecule behavior with high-quality data for your records.
Compare molecules to their physiological counterparts or other relevant reference products. Develop algorithms for identification at various stages and establish protein fingerprints using thermal unfolding curves.
See how Johnson and Johnson Innovative Medicine implemented nanoDSF to efficiently perform identifiy testing of biologics drug substance.
In this video, Dr. Marius Müller from J&J Innovative Medicine describes how he successfully performs ID testing of Drug Substance with Prometheus Panta C. You’ll learn about:
NanoTemper Technologies.
Dr. Stefan Duhr, CEO and Founder.