“…For this reason we chose a column with smaller ID than the previously used 4.6 mm ID column, which can be run under moderate conditions with respect to flow rate and reasonable retention times even with more strongly retained analytes. The difference in retention could be reduced by partial dynamic deactivation of the support by inclusion of Tween 60 | 174 in the methanol modifier as described earlier in reversed phase LC [18]. The intention of that work was to develop a chromatographic system that made it possible to inject clevidipine dissolved in a complex matrix, Intralipid | [18].…”
Section: Chromatography Of Dihydropyridines On Hypercarbmentioning
confidence: 98%
“…The difference in retention could be reduced by partial dynamic deactivation of the support by inclusion of Tween 60 | 174 in the methanol modifier as described earlier in reversed phase LC [18]. The intention of that work was to develop a chromatographic system that made it possible to inject clevidipine dissolved in a complex matrix, Intralipid | [18].…”
Section: Chromatography Of Dihydropyridines On Hypercarbmentioning
confidence: 98%
“…The time course is illustrated in Figure 3, starting with a Tween 60 | deactivated basal system. Equilibration is reached within about 12,000 column volumes after introduction of selector in the methanol Tween 60| This time can be reduced by using a bolus dose of Tween 60 | [18].…”
Section: Effect Of Counter-ion Concentration On Enantioselectivitymentioning
confidence: 99%
“…A typical equilibration profile is given in Figure 3. The dip in the curve at 12,000 column volumes was caused by an intermittent increase in the Tween 60 | concentration in order to speed up the equilibration time as described in reversed LC mode [18]. Initially a column temperature of 40 ~ was used but increasing it to 70 ~ reduced retention factors by ca.…”
Section: Equilibration Of Chromatographic Systemmentioning
SummaryA chromatographic method is described for separation of substituted dihydropyridines on Hypercarb, porous-graphitic carbon as support and methanol-modified carbon dioxide containing Tween 60 | deactivation additive, as mobile phase.Enantiomers of a dihydropyridine substituted acid were resolved after addition of Z-(L)-arginine as ion-pairing counter ion. A 0.2 mM concentration was sufficient to achieve a resolution factor > 2 or baseline resolution. The system was used to estimate the minor enantiomer below 0.1% level.
“…For this reason we chose a column with smaller ID than the previously used 4.6 mm ID column, which can be run under moderate conditions with respect to flow rate and reasonable retention times even with more strongly retained analytes. The difference in retention could be reduced by partial dynamic deactivation of the support by inclusion of Tween 60 | 174 in the methanol modifier as described earlier in reversed phase LC [18]. The intention of that work was to develop a chromatographic system that made it possible to inject clevidipine dissolved in a complex matrix, Intralipid | [18].…”
Section: Chromatography Of Dihydropyridines On Hypercarbmentioning
confidence: 98%
“…The difference in retention could be reduced by partial dynamic deactivation of the support by inclusion of Tween 60 | 174 in the methanol modifier as described earlier in reversed phase LC [18]. The intention of that work was to develop a chromatographic system that made it possible to inject clevidipine dissolved in a complex matrix, Intralipid | [18].…”
Section: Chromatography Of Dihydropyridines On Hypercarbmentioning
confidence: 98%
“…The time course is illustrated in Figure 3, starting with a Tween 60 | deactivated basal system. Equilibration is reached within about 12,000 column volumes after introduction of selector in the methanol Tween 60| This time can be reduced by using a bolus dose of Tween 60 | [18].…”
Section: Effect Of Counter-ion Concentration On Enantioselectivitymentioning
confidence: 99%
“…A typical equilibration profile is given in Figure 3. The dip in the curve at 12,000 column volumes was caused by an intermittent increase in the Tween 60 | concentration in order to speed up the equilibration time as described in reversed LC mode [18]. Initially a column temperature of 40 ~ was used but increasing it to 70 ~ reduced retention factors by ca.…”
Section: Equilibration Of Chromatographic Systemmentioning
SummaryA chromatographic method is described for separation of substituted dihydropyridines on Hypercarb, porous-graphitic carbon as support and methanol-modified carbon dioxide containing Tween 60 | deactivation additive, as mobile phase.Enantiomers of a dihydropyridine substituted acid were resolved after addition of Z-(L)-arginine as ion-pairing counter ion. A 0.2 mM concentration was sufficient to achieve a resolution factor > 2 or baseline resolution. The system was used to estimate the minor enantiomer below 0.1% level.
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