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Stationary cuvette: a new approach to obtaining analytical curves by UV–VIS spectrophotometry
Author(s) -
Silva K. G. H.,
Júnior F. H. Xavier,
Farias I. E. G.,
Silva A. K. A.,
Neto J. A. Caldas,
Souza L. C. A.,
Santiago R. R.,
Júnior F. Alexandrino,
Júnior T. Nagashima,
Soares L. A. L.,
SantosMagalhães N. S.,
Egito E. S. T.
Publication year - 2009
Publication title -
phytochemical analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 72
eISSN - 1099-1565
pISSN - 0958-0344
DOI - 10.1002/pca.1122
Subject(s) - cuvette , chemistry , absorbance , spectrophotometry , dilution , chromatography , reproducibility , linearity , process analytical technology , analytical chemistry (journal) , accuracy and precision , chemometrics , process engineering , ultraviolet visible spectroscopy , analytical procedures , pharmaceutical formulation , statistics , thermodynamics , mathematics , optics , work in process , physics , quantum mechanics , marketing , business , engineering , organic chemistry
Background Investigations in the field of pharmaceutical analysis and quality control of medicines require analytical procedures that achieve suitable performance. An analytical curve is one of the most important steps in the chemical analysis presenting a direct relationship to features such as linearity. Objective This study has the aim of developing a new methodology, the stationary cuvette, to derive analytical curves by spectroscopy for drug analysis. Methodology The method consists basically of the use of a cuvette with a path length of 10 cm, containing a constant volume of solvent in which increasing amounts of a stock solution of the sample are added, droplet by droplet. After each addition, the cuvette is stirred and the absorbance is measured. This procedure was compared with the currently used methodology, which requires a labour‐intensive dilution process, and possible sources of variation between them were evaluated. Results The results demonstrated that the proposed technique presented high sensitivity and similar reproducibility compared with the conventional methodology. In addition, a number of advantages were observed, such as user‐friendliness, cost‐effectiveness, accuracy, precision and robustness. Conclusion The stationary cuvette approach may be considered to be an appropriate alternative to derive analytical curves for analysing drug content in raw materials and medicines through UV–VIS spectrophotometry. Copyright © 2009 John Wiley & Sons, Ltd.