IJUP08 - Universidade do Porto
IJUP08 - Universidade do Porto
IJUP08 - Universidade do Porto
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Development of an automatic multi-pumping flow system for the<br />
spectrophotometric determination of trimipramine<br />
D. Ribeiro 1 , J. Prior 1 , J. Santos 1 and J. Lima 1<br />
1 Requimte, Department of Physical-Chemistry, Faculty of Pharmacy, University of <strong>Porto</strong>,<br />
Portugal.<br />
Trimipramine maleate, is a tricyclic antidepressant agent, that belongs to the<br />
dibenzoazepine class, with an anxiety-reducing sedative activity. The intensive<br />
therapeutical utilisation of dibenzoazepine derivates increases the need to improve or<br />
develop new methods for their determination in body fluids and in pharmaceutical<br />
preparations [1].<br />
In the present work, an automatic metho<strong>do</strong>logy of flow analysis exploiting the multipumping<br />
[2] concept was developed for the spectrophotometric determination of<br />
trimipramine in commercially available pharmaceutical formulations. The trimipramine<br />
determination was based on the reaction of the drug with ammonium monovanadate<br />
reagent in acidic medium yielding a coloured compound with a maximum of absorbance at<br />
620 nm [3]. The improved flow mixing conditions during sample and reagents insertion<br />
and transport, due to the chaotic movement of the solutions originated by the pulsed flow<br />
characteristic of multi-pumping systems, assured a fast reaction zone homogenization in a<br />
reduced residence time, which was particularly advantageous for carrying out analytical<br />
determinations that involved highly viscous solutions, as is the case of the sulphuric acid<br />
solution used in the determination of trimipramine, without impairing the sampling rate.<br />
A linear working range for trimipramine concentrations of up to 50 mg L-1 (r = 0.9998; n<br />
= 6) was obtained and the detection limit was about 1.15 mg L-1. The sampling rate was<br />
approximately 50 determinations per hour. The obtained results were in agreement with<br />
those furnished by the reference procedure [4], with relative deviations lower then 4.7%.<br />
The proposed metho<strong>do</strong>logy allowed the rapid quantification of trimipramine, which could<br />
represent an advantageous alternative for the pharmaceutical control at industrial level, and<br />
additionally, required low quantities of reagents and produced reduced volumes of<br />
residues.<br />
References:<br />
[1] Baldessarini, R.J. (2001), Drugs and the treatment of psychiatric disorders. Depression and<br />
anxiety disorders, in Gilman, A.G., Hardman, J.G., and Limbird, L.E. (Eds.) The pharmacological<br />
basis of therapeutics, 10th ed., New York: McGraw Hill Co., pp. 447-483.<br />
[2] Lapa, R.A.S., Lima, J.L.F.C., Reis, B.F., Santos, J.L.M., Zagatto, E.A.G. (2002), Multipumping<br />
in flow analysis: concepts, instrumentation, potentialities, Anal. Chim. Acta, 466, 125-<br />
132.<br />
[3] Misiuk, W. (2000), Spectrophotometry assay of imipramine and desipramine using ammonium<br />
metavanadate and its application to pharmaceutical preparations, J. Pharm. Biomed. Anal., 22, 189-<br />
196.<br />
[4] Trimipramine Maleate monograph, tablets (2005), in British Pharmacopoeia, vol. III, Lon<strong>do</strong>n:<br />
The Stationary Office, pp. 2853.<br />
37