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. 2011 Mar 15;27(6):3150-6.
doi: 10.1021/la104242p. Epub 2011 Feb 21.

Electrophoretic transport of biomolecules through carbon nanotube membranes

Affiliations

Electrophoretic transport of biomolecules through carbon nanotube membranes

Xinghua Sun et al. Langmuir. .

Abstract

Electrophoretic transport of proteins across electrochemically oxidized multi-walled carbon nanotube (MWCNT) membranes has been investigated. A small charged protein, lysozyme, was successfully pumped across MWCNT membranes by an electric field while rejecting larger bovine serum albumin (BSA). Transport of lysozome was reduced by a factor of about 30 in comparison to bulk mobility and consistent with the prediction for hindered transport. Mobilities between 0.33 and 1.4 × 10(-9) m(2) V(-1) s(-1) were observed and are approximately 10-fold faster than comparable ordered nanoporous membranes and consistent with continuum models. For mixtures of BSA and lysozyme, complete rejection of BSA is seen with electrophoretic separations.

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Figures

Figure 1
Figure 1
Schematic U-tube diffusion set-up and schematic of membrane with oxidized CNTs for biomolecular electrophoresis transport study.
Figure 2
Figure 2
Typical SEM top-view images of (a) microtome cut and (b) electrochemically oxidized MWCNT membranes.
Figure 3
Figure 3
(a) SEC-HPLC chromatograms of the permeate solution collected at -1V and pH 7.0 electrophoresis for 24 hr and (b) 12.5 μg/ml (0.87 nmol/ml) lysozyme standard prepared in pH7.0 PB.
Figure 4
Figure 4
Voltage dependence of the membrane area based electrophoresis flux of positively charged lysozyme dissolved in pH 7.0 PB.
Figure 5
Figure 5
Electrophoresis enhancement Eep, for lysozyme (diamond), Ru2+ (square) and MV2+ (triangle) at different applied voltage. Lysozyme and MV2+ were dissolved in pH 7.0 PB and Ru2+ was dissolved in DI water.
Figure 6
Figure 6
Chromatograms of (left) permeate collected in the electrophoretic separation of charged lysozyme from neutral BSA in pH 4.7 PB at applied voltage of -2 V, and (right) standard mixture containing 2.5 μg/ml BSA and 2.5 μg/ml lysozyme to demonstrate detection limit of SEC-HPLC analysis.

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