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Keywords
(9)
Gradient Method
Measurement Uncertainty
Method Validation
Pharmaceutical Preparation
Stationary Phase
folic acid
Liquid Chromatographic
Ultra High Pressure
Water Soluble
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A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations
A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations,10.101
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A validated ultra high pressure liquid chromatographic method for qualification and quantification of folic acid in pharmaceutical preparations
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E. Deconinck
,
S. Crevits
,
P. Baten
,
P. Courselle
,
J. De Beer
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 (2mm×100mm, 1.5μm). 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.
Journal:
Journal of Pharmaceutical and Biomedical Analysis - J PHARMACEUT BIOMED ANAL
, vol. 54, no. 5, pp. 995-1000, 2011
DOI:
10.1016/j.jpba.2010.11.036
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