Determination of potassium ions in pharmaceutical samples by FIA using a potentiometric electrode based on ionophore nonactin occluded in EVA membrane

被引:27
作者
Garcia, CAB [1 ]
Rover, L
Neto, GD
机构
[1] UFS, Dept Chem, BR-49100000 Sao Cristovao, SE, Brazil
[2] Divino Salvador Coll, BR-13300000 Itu, SP, Brazil
[3] Univ Sao Francisco, Ctr Hlth & Biol Sci, BR-12900000 Braganca Paulista, SP, Brazil
关键词
potassium determination; potentiometric electrode; pharmaceutical samples;
D O I
10.1016/S0731-7085(02)00598-8
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple and rapid method was developed for the K+ ions determination employing a flow injection system using a flow-through electrode based on the naturally-occurring antibiotic ionophore nonactin occluded in a polymeric membrane. The nonactin ionophore was trapped in poly(ethylene-co-vinyl acetate) (EVA) matrix (40% w/w in vinyl acetate) and dispersed on the surface of a graphite-epoxy tubular electrode. The plasticizer-free all-solid-state potassium-selective electrode showed a linear response for K+ concentrations between 5.0 x 10(-5) and 5.0 x 10(-2) M (r = 0.9995) with a near-Nernstian slope of 51.5 mV per decade, when Tris-HCI buffer (pH 7.0;0,1 M) was employed as a carrier. The potentiometric-FIA system allows an analytical frequency of 120 samples per hour with a precision of 3.6%. The relative standard deviations (R.S.D.) for K+ determination in pharmaceuticals samples, without any previous treatment, were lower than 4.0%, comparable to those obtained by flame photometry. Ammonium is the main analytical interference and the electrode response time was 5 s at 25 degreesC. The useful lifetime of the tubular sensor is longer than 3 months in continuous use. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 18
页数:8
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