TY - JOUR
T1 - Post column derivatisation analyses review : is post-column derivatisation incompatible with modern HPLC columns?
AU - Jones, Andrew
AU - Pravadali-Cekic, Sercan
AU - Dennis, Gary R.
AU - Shalliker, R. Andrew
PY - 2015
Y1 - 2015
N2 - Post Column derivatisation (PCD) coupled with high performance liquid chromatography or ultra-high performance liquid chromatography is a powerful tool in the modern analytical laboratory, or at least it should be. One drawback with PCD techniques is the extra post-column dead volume due to reaction coils used to enable adequate reaction time and the mixing of reagents which causes peak broadening, hence a loss of separation power. This loss of efficiency is counter-productive to modern HPLC technologies, -such as UHPLC. We reviewed 87 PCD methods published from 2009 to 2014. We restricted our review to methods published between 2009 and 2014, because we were interested in the uptake of PCD methods in UHPLC environments. Our review focused on a range of system parameters including: column dimensions, stationary phase and particle size, as well as the geometry of the reaction loop. The most commonly used column in the methods investigated was not in fact a modern UHPLC version with sub-2-micron, (or even sub-3-micron) particles, but rather, work-house columns, such as, 250ÃÂ4.6mm i.d. columns packed with 5μm C18 particles. Reaction loops were varied, even within the same type of analysis, but the majority of methods employed loop systems with volumes greater than 500μL.A second part of this review illustrated briefly the effect of dead volume on column performance. The experiment evaluated the change in resolution and separation efficiency of some weak to moderately retained solutes on a 250ÃÂ4.6mm i.d. column packed with 5μm particles. The data showed that reaction loops beyond 100μL resulted in a very serious loss of performance.Our study concluded that practitioners of PCD methods largely avoid the use of UHPLC-type column formats, so yes, very much, PCD is incompatible with the modern HPLC column.
AB - Post Column derivatisation (PCD) coupled with high performance liquid chromatography or ultra-high performance liquid chromatography is a powerful tool in the modern analytical laboratory, or at least it should be. One drawback with PCD techniques is the extra post-column dead volume due to reaction coils used to enable adequate reaction time and the mixing of reagents which causes peak broadening, hence a loss of separation power. This loss of efficiency is counter-productive to modern HPLC technologies, -such as UHPLC. We reviewed 87 PCD methods published from 2009 to 2014. We restricted our review to methods published between 2009 and 2014, because we were interested in the uptake of PCD methods in UHPLC environments. Our review focused on a range of system parameters including: column dimensions, stationary phase and particle size, as well as the geometry of the reaction loop. The most commonly used column in the methods investigated was not in fact a modern UHPLC version with sub-2-micron, (or even sub-3-micron) particles, but rather, work-house columns, such as, 250ÃÂ4.6mm i.d. columns packed with 5μm C18 particles. Reaction loops were varied, even within the same type of analysis, but the majority of methods employed loop systems with volumes greater than 500μL.A second part of this review illustrated briefly the effect of dead volume on column performance. The experiment evaluated the change in resolution and separation efficiency of some weak to moderately retained solutes on a 250ÃÂ4.6mm i.d. column packed with 5μm particles. The data showed that reaction loops beyond 100μL resulted in a very serious loss of performance.Our study concluded that practitioners of PCD methods largely avoid the use of UHPLC-type column formats, so yes, very much, PCD is incompatible with the modern HPLC column.
KW - amino acids
KW - antioxidants
KW - chromatographic analysis
KW - derivatization
KW - high performance liquid chromatography
UR - http://handle.uws.edu.au:8081/1959.7/uws:31703
U2 - 10.1016/j.aca.2015.07.003
DO - 10.1016/j.aca.2015.07.003
M3 - Article
VL - 889
SP - 58
EP - 70
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
ER -