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. Author manuscript; available in PMC: 2011 Nov 16.
Published in final edited form as: J Chromatogr A. 2007 Dec 7;1182(1):41–55. doi: 10.1016/j.chroma.2007.11.104

Table 4.

The Total Retention and the Percent Cation Exchange Contribution on SO3-HC-C8 Phases

Stationary
Phases
Gradient
Washing
[TEAH+]
(mM)
Retention Solutesc
A B C D E F
SO3-HC-C8-H No 120 k’totala 1.26 1.67 2.07 2.38 3.43 3.98
%k’IEXb 100d 100d 85 86 81 84
12 k’totala 12.82 17.35 17.87 20.75 28.36 33.94
%k’IEXb 100 100 98 98 98 98
SO3-HC-C8-L No 20 k’totala 1.29 1.91 2.04 2.38 3.17 3.92
%k’IEXb 91 87 83 83 80 81
2 k’totala 11.86 16.85 17.29 20.23 26.05 32.51
%k’IEXb 99 99 98 98 98 98
SO3-HC-C8-L Yes 20 k’totala 1.03 1.50 1.57 1.83 2.38 2.87
%k’IEXb 100d 95 94 92 89 90
2 k’totala 10.51 14.33 14.81 17.03 21.51 26.10
%k’IEXb 100 100 99 99 99 99
a

The total retention at different [TEAH+ ] calculated from Eq. (5) using the BIEX and k’IEX obtained from the linear regression of k’ vs. 1/[TEAH+]

b

The percentage of cation exchange contribution to the total retention at different [TEAH+] calculated from Eq. (5) using the BIEX and k’IEX obtained from the linear regression of k’ vs. 1/[TEAH+]

c

Solutes: A: morphine; B: hydromorphone; C: cathinone; D: ephedrine; E: 3,4-methylenedioxyamphetamine; F: methamphetamine (see Fig. 3 for the compound structures)

d

A percentage slightly higher than 100% is obtained because k’RP is a small negative value, which could be caused by either the error of the linear regression or the very small retention of the dead time marker uracil.