4.5 Article

Simplified Microchip Electrophoresis for Rapid Separation of Urine Proteins

Journal

JOURNAL OF CLINICAL LABORATORY ANALYSIS
Volume 28, Issue 2, Pages 104-109

Publisher

JOHN WILEY & SONS INC
DOI: 10.1002/jcla.21651

Keywords

UV detection; selectivity of proteinuria; ethylamine; urine proteins; calcium lactate; microfluidic chip electrophoresis

Funding

  1. State 863 High Technology R & D Project of China [2002AA404310, 2004AA404252]
  2. Technology Project of Jiangsu [H200216]

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Background Urine protein test has been widely used in clinics, but to determine the type of proteinuria is usually difficult due to technical limitations. Methods In the current study, a rapid and simple method to separate and determine urine proteins by a microchip electrophoresis (ME) system has been developed in which only 4 min are required. Results Optimal separation conditions have been established by using 15 s injection time at 500 and 1,500 V separation voltage in 75 mmol/l borate buffer containing 0.8 mmol/l calcium lactate and 1% phi ethylamine (pH 10.55). Relative standard deviation (RSD) of migration time with purified human albumin and human transferring was 2.68% and 2.24%, and RSD of the peak area was 5.85% and 4.96%, respectively. The linear detection range was 1.0-15.0 g/l for purified human albumin and 1.0-10.0 g/l for human transferrin, with the same detection limit (S/N = 3) of 0.4 g/l. Finally, comparing to conventional agarose gel electrophoresis, the same results were obtained by using ME by testing clinical samples including 60 selective proteinuria, 105 nonselective proteinuria, and 6 overflow proteinuria. Conclusion This newly established ME could have broad applications to determine the type of proteinuria in clinics.

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