Issue 27, 2016

Determination of ascorbic acid in the retina during chicken embryo development using high performance liquid chromatography and UV detection

Abstract

The retina is a specialized tissue of the central nervous system (CNS) and it is the only part of the CNS that can be visualized non-invasively. During vertebrate development, the retina originates together with the optic nerve as outgrowths of the developing brain, and in this respect, the avian retina is a very convenient model for neurochemical studies of the CNS. In this study, a HPLC-UV method was developed and validated for the determination of ascorbic acid (AA) in the chicken embryo retina. AA has an important role in the retina because of its antioxidant properties. The developed method showed very good figures of merit (recovery = 91 ± 2%; repeatability and intermediate precision better than 1.67% and 2.53% and a limit of quantification of 0.03 mg L−1). Retinas of two embryo ages (12 days and 18 days) showed AA concentrations of 0.0107 ± 0.0010 and 0.0055 ± 0.0005 μg of AA per μg of protein, respectively, and the statistical comparison of results confirmed the decrease of the AA level. These results seem to correlate well with oxidative stress protection, but this fact is still under investigation. As far as we are aware, this is the first study that demonstrates the HPLC-UV determination of ascorbic acid in the chicken embryo retina and its variation along embryo development.

Graphical abstract: Determination of ascorbic acid in the retina during chicken embryo development using high performance liquid chromatography and UV detection

Article information

Article type
Paper
Submitted
28 Apr 2016
Accepted
22 May 2016
First published
07 Jun 2016

Anal. Methods, 2016,8, 5441-5447

Determination of ascorbic acid in the retina during chicken embryo development using high performance liquid chromatography and UV detection

D. R. S. Lima, M. Cossenza, C. G. Garcia, C. C. Portugal, F. F. D. C. Marques, R. Paes-de-Carvalho and A. D. Pereira Netto, Anal. Methods, 2016, 8, 5441 DOI: 10.1039/C6AY01249C

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