Zusammenfassung der Ressource
CAPILLARY
ELECTROPHORESIS
- ELECTROPHORESIS: HOW DOES IT WORK?
- differential migration of
charged sp. in applied DC
- rate depends on
CHARGED:SIZE
RATIO
- migration rate
ν= μeE
Anmerkungen:
- μe = electrophoretic mobility
α = ionic charge
1/α = frictional factors (size & shape, viscosity)
E = applied field strength
- electric field strength
related to magnitude
and length over which
- migration rate :
ν= μe x V/L
Anmerkungen:
- V: voltage
L: length of slab/capillary
- Plate #:
N= μeV/2D
Anmerkungen:
- D: diffusion coefficient of solute
- RESISTANCE (joule heating)
- V = I x R
Anmerkungen:
- I = current
R = resistance
- if use gel - produce heat.
limit V applied for slab elect.
~500v
- Capillary typically
10-100μm ID and
30-100cm long (large
surface:volume ratio =
better cooling)
- P = I^2/R
Anmerkungen:
- P = power dissipation = amt heat produced
long capillary and small cross sectional area = high R
- voltages we can use in cap.ele.
typical applied voltage 10-25kV =
E of 100-400 Vcm-1 typical N =
100,000 –200,000(HPLC 5,000
–20,000)
- ELECTROOSMOTIC FLOW
- high V applied -
buffer-filled-Si cap. -
bulk liq twds CATHODE
- pressure-induced
- electroosmotic flow
- EO Flow generally >
electrophoretic migratn
- buffer = mob. phase
- EO flow = mob. phase pump
- all analytes are swept through
column regarding the charged
(CATION - NEUTRAL - ANION)
- electroosmotic flow
velocity ν= μeoE
Anmerkungen:
- μeo= electroosmotic mobility
- ion velocityν= (μe+ μeo)E
- migration rate
tm= l/ (μe+ μeo)E
= IL(μe+ μeo)V
Anmerkungen:
- L= Length of capillary
l = length to detector
- N = 16(tm/W)^2
- CE HARDWARE
- Small vol- cap (4-5μL),
injector/detector < 10nL (the
result not concentrated)
- Cap: fused silica,
external coating of
polyimide (flexibility &
durability)
- can reverse the
polarity: anions elute
first
- Sample Injection
- 5 -50 nL
- tips that can sample
directly from cell/cell
substructure
- Can be automated
- electrokinetic
Anmerkungen:
- Voltage--> sample flow with EO flow + ion movement
Injects larger amts of more mobile ions
- pressure
- Detectors (= HPLC)
- Optical
- Problem with low volumes =
short pathlength = low
absorbance or fluorescence
- modify cell to increase the pathlength
- Z-cell
Anmerkungen:
- - path length 10 x the cap. diameter
- increase path length -> decreases in peak efficiency = add spherical ball lenses btwn source-zcell-detector.
- Increase sensitivity
- Bubble cell
Anmerkungen:
- bubble formed near the end of the capillary
- Multireflection cell
Anmerkungen:
- a reflective coating of silver is deposited on the end of the capillary
- Adsorption & fluoro.
(limits in conc terms, but
equal or better in mass
detection limits)
- Indirect detection
- for compounds that don't
have suitable
chromophore/molar
absorptivity - add ionic
chromophore in the buffer,
see any reduction in that
signal
- Electrochemical
- conductivity & amperometry
- MS
- small volume of flow rate
(1uL/min) allow to couple w
MS
- common use of
electrospray Ionisation
(ESI)
- use volatile buffer
- CE/MS - use to
detect proteins,
DNA fragments n
peptides. (large
biomolecules)
- APPLICATIONS OF CE
- Capillary Zone
Electrophoresis
- small ions
- cation separations- wall
untreated, analytes flow with EO flow
twrds cathode
- Anions separation-
wall treated, reversed EO flow
twrds anode
- molecular sp.
- ions or non-ion
(derivatization) -
herbicides, persticides,
proteins, aa. etc
- - buffer composition is constant -
ionic components migrate into zones
(complete resolved zone have buffer
between zones)
- Capillary Gel Electrophoresis
- performed in porous gel
polymer matrix w a
buffer mixture that fills
the pores of the gel
- types of gel :
polyacrylamide
polymer, agarose,
methyl cellulose etc.
- Capillary Isoelectric Focusing
- separate amphiprotic sp. (aa,
proteins - have weak COOH and
AMINE gp.)
Anmerkungen:
- amphiprotic - sp in a soln is capable to donate or accept a proton.
- buffer mixture that
continuously varies in pH
along its length