

The typical use of WinNonlin is via a graphical user interface. Here, we provide a step-wise illustration of how to perform a calculation of microsomal clearance from UNIFI data acquired on Xevo G2-S QTof using WinNonlin.Commercial software Phoenix WinNonlin is the most widely used NCA tool, and as such stands as the main reference tool. All of these features help to minimize errors and enable the more confident analysis of large data sets. The exported data can be brought into third-party packages without manual copying or transcription and the table layouts preferences can be saved within UNIFI. Flexibility in defining and customizing columns to be exported (i.e.: filter data performed in human species at a specific dose or time points). Entire processed datasets or filtered subsets data (such as separate tables for QCs, Unknowns, etc.).Summary and custom calculations (support for built in UNIFI calculations such as max, min, average values, etc.).Custom columns (user customizable values).


Electronic and customizable data transfer/integration between instrumentation software and third-party software platforms (WinNonlin, Spotfire, etc.) is the preferred approach and is essential for handling and processing large amounts of data with both accuracy and speed.Įnhanced export using UNIFI Software provides the following features: Calculation of PK parameters are commonly performed to establish the viability of a drug candidate or series and help prioritization efforts. It is critical for LC-MS software to support easy transfer of results to a variety of third-party software packages in order to extract and provide key information to support drug discovery and development.Īn example of this is to use LC-MS data to calculate pharmacokinetics parameters using industry-standard software packages such as Phoenix WinNonlin (Certara, St. How we convert this data to drive decisions is often the bottleneck as many different software tools are used in a typical DPMK lab. Generating LC-MS data is an integral part of drug metabolism pharmacokinetic (DMPK) departments.
