Zhe Yin, Kenneth J. Fountain, Doug McCabe and Diane M. Diehl, Waters Corporation, Milford, Massachusetts, USA
Introduction
As UPLC users convert or replace their existing HPLC systems with UPLC systems there is a transition period where a method
must be run on both platforms. Thus, having the same particle substrate and bonded phases available in HPLC and UPLC particle
sizes can significantly ease the burden of method development and transfer from one platform to another. In addition to the
ethylene bridged hybrid (BEH) particle, three new high strength silica (HSS) stationary phases for HPLC applications are introduced.
Scalability between both column diameter and particle size is demonstrated on both UPLC and HPLC instrumentation.
Results and Discussion
 Figure 1
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Figure 1 shows the scalability between UPLC and HPLC columns for the separation of paroxetine-related compounds on HSS C18 SB. Gradient, flow-rate and injection volume were properly scaled between different particle sizes and column dimensions.
The system volume was properly compensated for when transferring method between UPLC and HPLC instrumentations. Chromatographic
resolution and selectivity were maintained across all separation platforms.
 Figure 2
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Figure 2 demonstrates the scalability between columns with different internal diameters for the separation of a forced degradation
sample of glimepiride.
Conclusions
A successful method transfer requires careful consideration of key parameters including system volume, column dimension and
particle size, injection volume and gradient profile. Methods can be easily transferred between different systems (UPLC →
HPLC → prep), particle sizes and column diameters on the new HSS columns.
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