Artigo Revisado por pares

A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations

2010; Elsevier BV; Volume: 54; Issue: 5 Linguagem: Inglês

10.1016/j.jpba.2010.11.036

ISSN

1873-264X

Autores

Eric Deconinck, S. Crevits, P. Baten, P. Courselle, J. De Beer,

Tópico(s)

Lanthanide and Transition Metal Complexes

Resumo

A fully validated UHPLC method for the identification and quantification of folic acid in pharmaceutical preparations was developed. The starting conditions for the development were calculated starting from the HPLC conditions of a validated method. These start conditions were tested on four different UHPLC columns: Grace Vision HT™ C18-P, C18, C18-HL and C18-B (2 mm × 100 mm, 1.5 μm). After selection of the stationary phase, the method was further optimised by testing two aqueous and two organic phases and by adapting to a gradient method. The obtained method was fully validated based on its measurement uncertainty (accuracy profile) and robustness tests. A UHPLC method was obtained for the identification and quantification of folic acid in pharmaceutical preparations, which will cut analysis times and solvent consumption.

Referência(s)