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   <subfield code="u">Laboratory of Analytical Chemistry, Department of Inorganic and Analytical Chemistry, University of Ioannina, Ioannina, Greece</subfield>
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   <subfield code="a">High-sensitivity spectrophotometric determination of trace amounts of Levodopa, Carbidopa and α-Methyldopa</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Prodromos Issopoulos]</subfield>
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   <subfield code="a">Summary: A simple, sensitive and accurate spectrophotometric method for the determination of Levodopa (LVDA)(I), Carbidopa (CBDA)(II) and α-Methyldopa (α-MDA)(III) at the ppb level has been developed. This method is based on the oxidation of (I), (II) and (III) by Fe(III), using a Fe(III)-o-Phenanthroline mixture and is followed by the formation of a highly stable orange-red coloured tris-complex [Fe(II)-(o-Phenanthroline)3]2+ in a moderate acidic medium (pH=5.0±0.2) which exhibits an absorption maximum at λ=510 nm. The apparent molar absorptivities were 1.26×105, 1.02×105 and 1.29×105 l mol−1 cm−1 and the Sandell's sensitivities were 1.57, 2.20 and 1.60 ng cm−2 for (I), (II) and (III), respectively. Beer's law is obeyed in a concentration range from 50 to 2500 ppb for (I) and (III) and from 100 to 4000 ppb for (II). The slope and the intercept of the regression lines for each of these drugs were calculated with correlation coefficients of 0.9999 for (I) and (III) and 0.9998 for (II). The results obtained from the determination of the drugs studied, using both the described procedure and the corresponding official method, were statistically compared by means of the Student's t-test and by the variance ratio F-test, and no significant difference was observed.</subfield>
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   <subfield code="a">Springer-Verlag, 1990</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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