CICTERRA   20351
CENTRO DE INVESTIGACIONES EN CIENCIAS DE LA TIERRA
Unidad Ejecutora - UE
artículos
Título:
Direct Determination of Saccharin and Acesulfame-K
Autor/es:
NATALIA E. LLAMAS, MARÍA S. DI NEZIO, MIRIAM E. PALOMEQUE, BEATRIZ S. FERNÁNDEZ BAND
Revista:
Food Analytical Methods
Editorial:
Springer
Referencias:
Lugar: New York; Año: 2008 vol. 1 p. 43 - 48
ISSN:
1936-9751
Resumen:
Abstract A simple and rapid analytical procedure for
determination of saccharin (SAC) and acesulfame-K (ACK)
based on UV-vis measurements and partial least squares
(PLS) was proposed. Thus, an experimental design at levels
2 and 15 mg l-1 for SAC and 2 and 20 mg l-1 for AC-K
was applied. Because real samples usually contain SAC and
AC-K combined with aspartame (ASP), this interference
was also included in the model. The procedure was
successfully applied for SAC and AC-K simultaneous
determination in sweeteners and fruit juice powders,
without any separation step to remove ASP. The results
were validated by using spiked samples, and the obtained
recoveries were satisfactory.
A simple and rapid analytical procedure for
determination of saccharin (SAC) and acesulfame-K (ACK)
based on UV-vis measurements and partial least squares
(PLS) was proposed. Thus, an experimental design at levels
2 and 15 mg l-1 for SAC and 2 and 20 mg l-1 for AC-K
was applied. Because real samples usually contain SAC and
AC-K combined with aspartame (ASP), this interference
was also included in the model. The procedure was
successfully applied for SAC and AC-K simultaneous
determination in sweeteners and fruit juice powders,
without any separation step to remove ASP. The results
were validated by using spiked samples, and the obtained
recoveries were satisfactory.
-1 for SAC and 2 and 20 mg l-1 for AC-K
was applied. Because real samples usually contain SAC and
AC-K combined with aspartame (ASP), this interference
was also included in the model. The procedure was
successfully applied for SAC and AC-K simultaneous
determination in sweeteners and fruit juice powders,
without any separation step to remove ASP. The results
were validated by using spiked samples, and the obtained
recoveries were satisfactory.