کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1181931 1491638 2014 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A New Screen-printed Ion Selective Electrode for Determination of Citalopram Hydrobromide in Pharmaceutical Formulation
ترجمه فارسی عنوان
الکترودهای انتخابی یونی جدید برای تعیین هیدرومبروت سیتالوپرام در فرمولاسیون دارویی
کلمات کلیدی
الکترود انتخابی یون سیالوپورام، الکترود چاپی آماده سازی دارویی، تعیین پتانسیومتریک
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی

Novel citalopram screen-printed ion selective electrodes were fabricated, characterized and used for the determination of citalopram in pharmaceutical formulations. The proposed sensors incorporated potassium tetrakis(p-chlorophenyl) borate (KTpClPB) ionophore (electrode V) and citalopram-phosphotungstate (CP-PT) ion pair complex (electrode X) as electroactive materials in screen-printed electrodes and tricresylphosphate (TCP) as solvent mediator. The fabricated electrodes demonstrated near Nernstain response over wide linear range of 4.9 × 10−7−1.0 × 10−2 M and 1.0 × 10−6−1.0 × 10−2 M citalopram with lower limit of detection of 4.9 × 10−7 M and 1.0 × 10−6 M and slope of (60.47 ± 0.80) mV decade−1 and (59.93 ± 1.45) mV decade−1 for electrode (V) and (X), respectively. The results showed that the proposed sensors had the characteristics such as fast and stable response, good reproducibility, long term stability (5 and 4 months) and applicability over a wide pH range of 2–9 and 2–8 for electrodes (V) and (X). The sensors displayed good selectivity for citalopram with respect to number of common foreign inorganic, organic species, excipients and the fillers added to the pharmaceutical preparation. The sensors were successfully applied for the determination of citalopram in tablet, urine and serum.

The static response time of the electrodes was measured after successive immersion of the electrodes in a series of CPB solutions, in each of which the CPB concentration increased 10−fold, from 4.9 × 10−7 M to 1.0 × 10−2 M. The static response time thus obtained was less than 7 and 9 s for 1.0 × 10−2 M and 1.0 × 10−3 M CPB concentration. At lower concentrations, however, the response time was little longer and reached 12 and 13 s for electrode (V) and electrode (X), respectively.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chinese Journal of Analytical Chemistry - Volume 42, Issue 4, April 2014, Pages 565–572
نویسندگان
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