Quantitation of underivatized branched-chain amino acids in sport nutritional supplements by capillary electrophoresis with direct or indirect UV absorbance detection

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Abstract

The branched-chain amino acids (BCAAs) including leucine (Leu), isoleucine (Ile) and valine (Val) play a pivotal role in the human body. Herein, we developed capillary electrophoresis (CE) coupled with conventional UV detector to quantify underivatized BCAAs in two kinds of sport nutritional supplements. For direct UV detection at 195 nm, the BCAAs (Leu, two enantiomers of Ile and Val) were separated in a background electrolyte (BGE) consisting of 40.0 mmol/L sodium tetraborate, and 40.0 mmol/L β-cyclodextrin (β-CD) at pH 10.2. In addition, the indirect UV detection at 264 nm was achieved in a BGE of 2.0 mmol/L Na2HPO4, 10.0 mmol/L p-aminosalicylic acid (PAS) as UV absorbing probe, and 40.0 mmol/L β-CD at pH 12.2. The β-CD significantly benefited the isomeric separation of Leu, L- and D-Ile. The optimal conditions allowed the LODs (limit of detections) of direct and indirect UV absorption detection to be tens μmol/L level, which was comparable to the reported CE inline derivatization method. The RSDs (relative standard deviations) of migration time and peak area were less than 0.91% and 3.66% (n = 6). Finally, CE with indirect UV detection method was applied for the quantitation of BCAAs in two commercial sport nutritional supplements, and good recovery and precision were obtained. Such simple CE method without tedious derivatization process is feasible of quality control and efficacy evaluation of the supplemental proteins.

Figures

  • Fig 1. Separation of BCAAs affected by the concentration of β-CD (A) and the wavelength (B) at the direct UV detection mode. The optimization process in A was obtained by adding β-CD in 40.0 mM sodium tetraborate (pH 10.2), and detected at 195 nm. The separation profiles in B were at optimal BGE. Capillary: 60 cm long (effective length 50 cm) and 75 μm I.D. Sample: 2.0 mmol/L Leu, Ile and Val. Sample introduction: 0.5 psi for 5 s. Separation voltage: +15 kV.
  • Table 1. Analytical parameters for direct and indirect UV detection of BCAAs.
  • Fig 2. Indirect UV detection of BCAAs affected by the concentration of PAS (A) and the wavelength (B). The optimization process in A was obtained by different PAS concentration in 40.0 mM β-CD, 2.0 mmol/L Na2HPO4 (pH12.2), and detected at 264 nm. The separation profiles in B were at optimal BGE. Sample: 1.0 mmol/L Leu, Ile and Val. Others as in Fig 1.
  • Fig 3. Identification of BCAAs in hydrolysates of the sports nutrition supplements by direct (A) and indirect (B) UV detection mode. The hydrolysates were 20- and 50-fold dilution, respectively for direct and indirect UV detection. Optimal BGE and others as in Figs 1 and 2.
  • Table 2. Amounts of BCAAs in supplemental proteins with indirect UV detection.

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APA

Qiu, J., Wang, J., Xu, Z., Liu, H., & Ren, J. (2017). Quantitation of underivatized branched-chain amino acids in sport nutritional supplements by capillary electrophoresis with direct or indirect UV absorbance detection. PLoS ONE, 12(6). https://doi.org/10.1371/journal.pone.0179892

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