Issue 9, 2012

Polydopamine-graft-PEG antifouling coating for quantitative analysis of foodproteins by CE

Abstract

In this paper, firstly the surface plasma resonance (SPR) was used to evaluate the antifouling property of polydopamine-graft-poly(ethylene glycol) (PEG) copolymer coating, and then the quantitative analysis of food proteins (such as hen eggs and milk powder) was investigated by capillary electrophoresis (CE) method using polydopamine-graft-PEG copolymer coated capillary. The great separations of lysozyme, conalbumin and ovalbumin from hen egg white could be achieved in phosphate–citrate buffer (pH 3.20) with an applied voltage of +20 kV in polydopamine-graft-PEG copolymer coated capillary. The range of protein recovery percentage of the three kinds of egg white proteins was 96.67% to 101.02%. According to the quantitative analysis results, the protein content of lysozyme, conalbumin and ovalbumin in hen egg white was 13.268 mg mL−1, 28.360 mg mL−1 and 157.418 mg mL−1, respectively. Whey proteins (β-lactoglobulin A, β-lactoglobulin B and α-lactalbumin) in nonfat milk powder could be separated completely with an applied voltage of −20 kV in sodium tetraborate buffer (pH 8.5). The protein recovery of β-lactoglobulin A, β-lactoglobulin B and α-lactalbumin was in the range of 86.40–94.38%. Finally, the quantitative protein content of β-lactoglobulin A, β-lactoglobulin B and α-lactalbumin in nonfat milk powder was 1.418 mg mL−1, 0.129 mg mL−1, and 0.073 mg mL−1, respectively. Also the egg white proteins could be separated consecutively 25 times without a noticeable loss in separation efficiency using polydopamine-graft-PEG copolymer coated capillary in one day.

Graphical abstract: Polydopamine-graft-PEG antifouling coating for quantitative analysis of food proteins by CE

Supplementary files

Article information

Article type
Paper
Submitted
07 Feb 2012
Accepted
08 Jun 2012
First published
13 Jun 2012

Anal. Methods, 2012,4, 2852-2859

Polydopamine-graft-PEG antifouling coating for quantitative analysis of food proteins by CE

L. Chen, R. Zeng, L. Xiang, Z. Luo and Y. Wang, Anal. Methods, 2012, 4, 2852 DOI: 10.1039/C2AY25129A

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