首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Sequential injection spectrophotometric determination of tetracycline antibiotics in pharmaceutical preparations and their residues in honey and milk samples using yttrium (III) and cationic surfactant
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Sequential injection spectrophotometric determination of tetracycline antibiotics in pharmaceutical preparations and their residues in honey and milk samples using yttrium (III) and cationic surfactant

机译:钇(III)和阳离子表面活性剂顺序注射分光光度法测定药物制剂中的四环素抗生素及其在蜂蜜和牛奶中的残留量

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A sequential injection analysis (SIA) spectrophotometric method for determining tetracycline (TC), chlortetracycline (CTC) and oxytetracycline (OTC) in different sample matrices were described. The method was based on the reaction between tetracyclines and yttrium (III) in weak basic micellar medium, yielding the light yellow complexes, which were monitored at 390, 392 and 395 nm, respectively. A cationic surfactant, cetyltrimethylammonium bromide (CTAB) was used to obtain the micellar system. The linear ranges of calibration graphs were between 1.0 × 10~(-5) and 4 × 10~(-4) mol L~(-1), respectively. The molar absorptivities were 5.24 × 10 ~5, 4.98 × 10~4 and 4.78 × 10~4 L mol~(-1) cm~(-1). The detection limits (3σ) were between 4.9 × 10~(-6) and 7.8 × 10~(-6) mol L~(-1) whereas the limit of quantitations (10σ) were between 1.63 × 10 ~(-5) and 2.60 × 10~(-5) mol L~(-1) the interday and intraday precisions within a weak revealed as the relative standard deviations (R.S.D., n = 11) were less than 4%. The method was rapid with a sampling rate of over 60 samples h~(-1) for the three drugs. The proposed method has been satisfactorily applied for the determination of tetracycline and its derivatives in pharmaceutical preparations together with their residues in milk and honey samples collected in Chiang Mai Province. The accuracy was found to be high as the Student's t-values were found to be less than the theoretical ones. The results were compared favorably with those obtained by the conventional spectrophotometric method.
机译:描述了一种顺序注射分析(SIA)分光光度法,用于测定不同样品基质中的四环素(TC),金霉素(CTC)和土霉素(OTC)。该方法基于弱碱性胶束介质中四环素与钇(III)之间的反应,生成浅黄色络合物,分别在390、392和395 nm处进行监测。阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)用于获得胶束系统。校正曲线的线性范围分别在1.0×10〜(-5)和4×10〜(-4)mol L〜(-1)之间。摩尔吸光度为5.24×10〜5、4.98×10〜4和4.78×10〜4 L mol〜(-1)cm〜(-1)。检出限(3σ)在4.9×10〜(-6)和7.8×10〜(-6)mol L〜(-1)之间,而定量限(10σ)在1.63×10〜(-5)之间当相对标准偏差(RSD,n = 11)小于4%时,在弱点内的日间和日内精度为2.60×10〜(-5)mol L〜(-1)。该方法快速,三种药物的采样率超过60个样本h〜(-1)。该方法已令人满意地用于测定药物制剂中的四环素及其衍生物,以及清迈省采集的牛奶和蜂蜜样品中的残留量。由于发现学生的t值小于理论值,因此发现准确性较高。将结果与通过常规分光光度法获得的结果进行了比较。

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