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High performance capillary electrophoresis - T.E.A.M.

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Modes<br />

Mode<br />

Capillary zone<br />

<strong>electrophoresis</strong><br />

Micellar<br />

electrokinetic<br />

chromatography<br />

Capillary gel<br />

<strong>electrophoresis</strong><br />

Isoelectric<br />

focusing<br />

Isotachophoresis<br />

Table 8<br />

Modes of CE<br />

Basis of<br />

separation<br />

Free solution<br />

mobility<br />

Hydrophobic/<br />

ionic interactions<br />

with micelle<br />

Size and charge<br />

Isoelectric point<br />

Moving<br />

boundaries<br />

The versatility of CE is partially derived from its numerous<br />

modes of operation. The separation mechanisms of each<br />

mode are different and thus can offer orthogonal and<br />

complementary information. The basic methods encompassed<br />

by CE include <strong>capillary</strong> zone <strong>electrophoresis</strong> (CZE),<br />

micellar electrokinetic chromatography (MEKC), <strong>capillary</strong><br />

gel <strong>electrophoresis</strong> (CGE), <strong>capillary</strong> isoelectric focusing<br />

(CIEF), and <strong>capillary</strong> isotachophoresis (CITP).<br />

The separation mechanisms of each mode are illustrated in<br />

figure 21 and described in table 8. For the most part, the<br />

different modes are accessed simply by altering the buffer<br />

composition. Each mode is described below, with emphases<br />

on basic operation and relevant applications.<br />

Figure 21<br />

Illustration of zonal, IEF and ITP <strong>electrophoresis</strong><br />

Zone <strong>electrophoresis</strong><br />

a)<br />

t = 0<br />

t > 0<br />

IEF<br />

Capillary filled with mixture of sample and ampholytes<br />

b)<br />

t = 0<br />

Low pH<br />

pH gradient<br />

<strong>High</strong> pH<br />

t > 0<br />

ITP<br />

c)<br />

T<br />

L<br />

t = 0<br />

T<br />

L<br />

t > 0<br />

46

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