0000000000684639

AUTHOR

Anatol Kojło

Immobilization of Hexacyanoferrate (III) for a Flow Injection-Spectrophotometric Determination of Promazine

Abstract An automated flow injection method for the determination of promazine is described. The method is based on the oxidation of promazine by hexacyanoferrate (III) and spectrophotometric monitorization of oxidized drug. The chemical and FIA variables were optimized. The calibration graph was linear over the concentration range 2,5–25 ppm of promazine hydrochloride. Some interfering substances were also investigated. The method was applied for the determination of promazine in pharmaceutical formulations.

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FIA-spectrophotometric determination of N-substituted phenothiazine derivatives by oxidation with a solid-phase reactor of manganese dioxide incorporated in polyester resin beads

Abstract The determination of several N -substituted phenothiazine derivatives was carried out by the reaction of the drug with managanese dioxide entrapped in a polymeric material in a packed-bed reactor; the oxidized drug was monitored at λ max . The calibration graph is linear over the range 5–50 μg/ml of phenothiazine derivatives with a relative standard deviation of 0.5–1% (at 10 μg/ml) and sample throughput of 40–48 h −1 . The influence of foreign compounds was studied and the method was applied to the determination of six different phenothiazine derivatives in pharmaceutical formulations.

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Spectrophotometric determination of promazine with an oxidative column in FIA manifolds

Abstract A simple flow-injection spectrophotometric method for the determination of promazine is described. The two proposed procedures are based on the oxidation of analyte with a manganese dioxide column. Concentrations of promazine in the ranges 2–20 and 1–6 are determined with a relative standard deviation of 1.0%. The injection rates are 62 and 80 samples h −1 , respectively. The influence of foreign species and the determination of promazine in a pharmaceutical formulation are also reported.

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FIA-fluorimetric determination of adrenaline by oxidation with a solid-phase reactor of manganese dioxide incorporated in polyester resin beads

Abstract The FIA-spectrofluorimetric determination of adrenaline was carried out by reaction of the drug with manganese dioxide entrapped in a polymeric material in a solid-phase reactor; the oxidized drug was monitored fluorimetrically at 540 nm (Ioxg. 330.0 nm). The calibration graph for adrenaline was linear over the range 0.5 - 20 μg ml−1 with a relative standard deviation of 2.0% (at 5 ug ml−1) and the sample throughput of 65 h−1. The influence of foreign compounds was studied and the method was applied to the determination of adrenaline content in a pharmaceutical formulation . ∗Present address: Institut of Chemistry, Warsawa University, Bialystok Branch, Bialystok, Poland.

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Spectrophotometric determination of adrenaline with an oxidative column in a FIA assembly

Abstract A single channel FIA assembly is proposed for the spectrophotometric determination of adrenaline, the aqueous sample solution is directly injected into the carrier stream leading the sample through a manganese dioxide column at 80°C, and on to the spectrophotometer flow-cell. The calibration graph is linear up to 17 ppm of adrenaline. The influence of other substances has been studied and the method has been applied to the determination of adrenaline in a pharmaceutical formulation.

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