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   <subfield code="a">Electroanalytical study of benzodiazepinooxazoles: Haloxazolam</subfield>
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   <subfield code="c">[F. Rodríguez, R. Jiménez, R. Alonso]</subfield>
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   <subfield code="a">Summary: The polarographic behaviour of 10-bromo-11 b-(2-fluorophenyl)-2,3,7,11 b-tetrahydrooxazolo [3,2-d][1,4] benzodiazepin-6(5H)-one (Haloxazolam) was studied in the pH range 1-13. Haloxazolam suffers a hydrolysis process, which can be followed by polarography. The reduction processes of Haloxazolam and its hydrolysis products are irreversible and their currents are diffusion-controlled. This behaviour was compared with that observed for other members of benzodiazepinooxazoles. Two polarographic methods have been developed upon the basis of the reduction of both the protonated iminium form (0.05 mol/l HCl, measurement time: 5 min) and the benzophenone produced in the hydrolysis process (pH 13.25, measurement time: 17 min). The relationship between reduction peak current and concentration is linear up to at least 6.62×10−5 mol/l for both methods. A higher sensitivity was obtained for the method based on the benzophenone reduction (detection limit 1.06×10−7 mol/l; 40 μg/l). The reproducibility of the both methods in terms of relative standard deviation was inferior to 2%.</subfield>
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   <subfield code="u">Departamento de Química Analitica, Facultad de Ciencias, Universidad del Pais Vasco, Apdo. 644, E-48 080, Bilbao, Spain</subfield>
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