Diamond paste-based electrodes for determination of Cr(III) in pharmaceutical compounds

A new class of monocrystalline diamond paste-based electrodes is proposed for the determination of chromium(III) at trace levels in vitamins. Three types of monocrystalline diamond—natural diamond 1 (natural diamond), synthetic diamond 50 (synthetic-1), and synthetic diamond 1 (synthetic-2)—were used for electrode construction. The linear concentration ranges are between 10^–10 and 10^–8; 10^–9 and 10^–7, and 10^–10 to 10^–8 mol L^–1, with limits of detection of 10^–12, 10^–12, and 10^–11 mol L^–1, when natural diamond, synthetic-1, and synthetic-2, respectively, are used as electrode materials. For electrodes based on natural diamond and synthetic-1 it was found that Cr(III) yields a peak at about +0.275±0.015 V (vs. Ag/AgCl) within a predetermined positive potential range situated between +0.4 and +0.2 V, while for the electrode based on synthetic-2 the peaks are found at +0.300±0.015 V (vs. Ag/AgCl). The proposed method is reliable for the determination of chromium(III) at trace levels in two vitamin tablets (RSD<0.2%).     

Utilization of maltodextrin based enantioselective, potentiometric membrane electrodes for the enantioselective assay of S-perindopril

Enantioselective, potentiometric membrane electrodes (EPMEs) based on carbon paste impregnated with different maltodextrins {dextrose equivalent (DE) 4.0-7.0 (I), 13.0-17.0 (II) and 16.5-19.5 (III)} as chiral selectors for the assay of S-perindopril is described. The proposed electrodes could be reliably employed in the assay of S-perindopril raw material and from its pharmaceutical formulation, Coversyl^® tablets. The electrode based on maltodextrin (I) showed the best enantioselectivity and time-stability. The surfaces of the electrodes are easily renewable by simply polishing on an alumina paper.     

Macrocyclic antibiotics as chiral selectors in the design of enantioselective, potentiometric membrane electrodes for the determination of S-flurbiprofen

Construction of three novel enantioselective, potentiometric membrane electrodes based on carbon paste impregnated with different macrocyclic antibiotics vancomycin and teicoplanin as chiral selectors are described. The solutions for the construction of electrodes were prepared in phosphate buffer pH 4 for the vancomycin-based electrode (VCM), pH 6 and pH 6/40% acetonitrile solutions for teicoplanin-based electrodes, TCP I and II, respectively. The proposed electrodes were applied in the assay of S-flurbiprofen raw material and its pharmaceutical formulation by use of direct potentiometry, VCM electrode exhibiting the best enantioselectivity. The surfaces of the electrodes are easily renewable by simply polishing on an alumina paper.     

Carbon and diamond paste microelectrodes based on Mn(III) porphyrins for the determination of dopamine

Three Mn(III) porphyrins were used for the design of carbon paste and diamond paste based microelectrodes, which were employed for the determination of dopamine in pharmaceutical and biological samples using differential pulse voltammetry (DPV). The limits of detection lie between 1.6 × 10⁻¹³ and 2.0 × 10⁻⁶ mol L⁻¹ while the sensitivities were between 230 pA μmol L⁻¹ and 3.24 μA mol L⁻¹. Dopamine was recovered reliable from pharmaceutical and biological samples in percentages higher than 91.00% and 92.00%, respectively. The surface of the microelectrodes can easily be renewed by simple polishing, obtaining a fresh surface ready for use in a new assay.     

Enantioselective, potentiometric membrane electrodes based on cyclodextrins: application for the determination of R-baclofen in its pharmaceutical formulation

Two enantioselective, potentiometric membrane electrodes based on α- and γ-cyclodextrins were proposed for the assay of R-baclofen. The slopes of the electrodes were 59.50 and 51.00 mV/pR-baclofen for α- and γ-cyclodextrin-based electrodes, respectively. The detection limits of the proposed electrodes were 7 × 10⁻⁹ mol l⁻¹ for α-cyclodextrin-based electrode and 1.44 × 10⁻¹⁰ mol l⁻¹ for γ-cyclodextrin-based electrode. The enantioselectivity was determined over S-baclofen. The proposed electrodes can be employed for the assay of R-baclofen raw materials and its pharmaceutical formulation, Norton-Baclofen^® tablets. The surfaces of the electrodes are stable and easily renewable by polishing on alumina paper.     

Sequential injection spectrophotometric determination of ritodrine hydrochloride using 4-aminoantipyrine

A sequential injection spectrophotometric determination of ritodrine hydrochloride is described. The method is based on the condensation of aminoantipyrine with phenols in the presence of an alkaline oxidizing agent to yield a pink coloured product the absorbance of which is monitored at 503 nm. Different sequential injection analysis (SIA) parameters including reagent concentrations have been optimised and used to obtain the analytical figures of merit. A linear concentration range of 3.1-123.5 μmol L⁻¹ and a detection limit (as 3σ-value) of 1.0 μmol L⁻¹ were obtained. The precision was 2.4 and 2.3% relative standard deviation (R.S.D.) at 6.2 and 15.4 μmol L⁻¹, respectively. This method is superior over previously reported ones in terms of linear range, short analysis time, high sample throughput, excellent reagent economy and minimum waste generation.     

Macrocyclic antibiotics as chiral selectors in the design of enantioselective, potentiometric membrane electrodes for the determination of l- and d-enantiomers of methotrexate

Three enantioselective, potentiometric membrane electrodes (EPMEs) based on macrocyclic glycopeptide antibiotics—vancomycin and teicoplanin (modified or not with acetonitrile)—were proposed for the determination of l- and d-enantiomers of methotrexate (Mtx). The linear concentration ranges for the proposed enantioselective membrane electrodes were between 10⁻⁶ and 10⁻³ mol l⁻¹ for l- and d- methotrexate. The slopes of the electrodes were 58.00 mV/pl-Mtx for vancomycin-based electrode; 57.60 mV/pd-Mtx for teicoplanin-based electrode and 55.40 mV/pd-Mtx for teicoplanin modified with acetonitrile-based electrode. The detection limits of the proposed electrodes were of 10⁻⁸ mol l⁻¹ magnitude order. The surfaces of the electrodes are stable and easily renewable by polishing on alumina paper. All proposed electrodes proved to be successful for the determination of the enantiopurity of Mtx as raw material and of its pharmaceutical formulations (tablets and injections).     

Enantioanalysis of l-2-hydroxyglutaric acid in urine samples using enantioselective, potentiometric membrane electrodes based on maltodextrins

Quantitative assay of l-2-hydroxyglutaric acid (l-2-HGA) is important for the diagnosis of l-2-hydroxyglutaric aciduria. Three enantioselective, potentiometric membrane electrodes (EPMEs) based on maltodextrins with different dextrose equivalent (DE) (DE: 4.0-7.0 (I), 13.0-17.0 (II), 16.5-19.5 (III)), were designed for the enantioanalysis of l-2-HGA. The enantioselective, potentiometric membrane electrodes can be used reliably for enantiopurity assay of l-2-HGA using the direct potentiometric method in the ranges of 10⁻⁹-10⁻⁵, 10⁻⁶-10⁻³ and 10⁻⁸-10⁻⁵ mol L⁻¹ for the enantioselective, potentiometric membrane electrodes based on maltodextrins I, II and III, respectively, with very low detection limits. A high reliability was obtained when the electrodes were used for the assay of l-2-HGA in urine samples.     

Diamond paste based electrodes for the determination of Pb(II) at trace concentration levels

Three types of monocrystalline diamond: natural diamond 1 μm, synthetic diamond 50 μm (synthetic-1), and synthetic diamond 1 μm (synthetic-2) were used for electrodes’ construction. The linear concentration ranges recorded for Pb(II), when natural diamond, synthetic-1 and synthetic-2 based electrodes were used were between 10⁻⁹ and 10⁻⁶; 10⁻¹⁰ and 10⁻⁷; and between 10⁻¹⁰ and 10⁻⁸ mol l⁻¹, respectively. Low detection limits which lie between 10 and 100 pmol l⁻¹ proves the sensitivity of the electrodes. It was found that Pb(II) yielded a peak at about +0.3±0.02 V (versus Ag/AgCl) for all the electrodes. Lead was determine with high reliability from water and tea samples at trace concentration levels using the proposed diamond paste based electrodes.     

Validation criteria for developing ion-selective membrane electrodes for analysis of pharmaceuticals

 The problem of validation criteria for developing ion-selective membrane electrodes for the analysis of pharmaceuticals arises from the connection between the reliability of ion-selective membrane electrodes construction and the reliability of the analytical information. Liquid membrane selective electrodes are more suitable for validation than the solid variety. The influence of the stability of ion pair complexes from the membrane on various parameters (e.g. response, limit of detection, and selectivity) is discussed. Validation criteria are proposed. Received: 18 September 1997 · Accepted: 17 November 1997