首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >USE OF SOLID-PHASE EXTRACTION CARTRIDGES WITH DIFFERENTIAL-PULSE CATHODIC STRIPPING VOLTAMMETRY AT A HANGING MERCURY DROP ELECTRODE - DETERMINATION OF NEDOCROMIL SODIUM AND PENTAMIDINE ISETHIONATE IN URINE
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USE OF SOLID-PHASE EXTRACTION CARTRIDGES WITH DIFFERENTIAL-PULSE CATHODIC STRIPPING VOLTAMMETRY AT A HANGING MERCURY DROP ELECTRODE - DETERMINATION OF NEDOCROMIL SODIUM AND PENTAMIDINE ISETHIONATE IN URINE

机译:悬挂汞滴电极上使用差分脉冲阴极溶出伏安法分离固相萃取物的测定克己酸钠和戊酸乙二胺磺酸钠的测定

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Nedocromil sodium (an antiasthma drug) and pentamidine isethionate (an antiprotozoal agent) were determined in urine by cathodic stripping voltammetry after adsorptive accumulation at a hanging mercury drop electrode as examples of the use of solid-phase extraction cartridges with this technique. Prior separation from matrix interferents was necessary and this was carried out using either a C-18 solid-phase extraction cartridge or liquid-liquid extraction. For nedocromil, a recovery of 100.5 +/- 6.5% (+/- 2 standard deviations) was obtained from urine spiked with 0.42 mu g ml(-1) of the drug using a C-18 cartridge (five determinations). A 97% recovery of pentamidine isethionate was obtained by solid-phase extraction when the drug was added to urine at a level of 1.48 mu g ml(-1). At lower levels of pentamidine isethionate, better recovery was obtained using liquid-liquid extraction: recoveries of between 60 and 100% were obtained at levels of 0.04-29.6 mu g ml(-1). Linear calibration graphs were obtained for the determination of both drugs at concentration levels in the measured solution lower than 1 x 10(-7) mol l(-1) (i.e., less than approximately 0.05 mu g ml(-1)): standard additions method was preferred for quantification. Relative standard deviations of 4.5% for the determination of pentamidine isethionate and of 5.2% for the determination of nedocromil (n = 5) were obtained for urine samples containing 2.96 mu g ml(-1) of pentamidine isethionate and 0.42 mu g ml(-1) of nedocromil. [References: 17]
机译:作为在此技术中使用固相萃取柱的示例,在悬挂式汞滴电极上吸附积累后,通过阴极溶出伏安法测定了尿液中的奈多克罗米酸钠(一种抗哮喘药)和戊二甲磺酸羟乙磺酸盐(一种抗原虫剂)。必须事先从基质干扰物中分离出来,这可以使用C-18固相萃取柱或液-液萃取进行。对于奈多克罗米,使用C-18药筒从加有0.42μgml(-1)药物的尿液中回收100.5 +/- 6.5%(+/- 2个标准差)(五个测定)。当将药物以1.48μg ml(-1)的水平添加到尿液中时,通过固相萃取可回收97%的乙tam异羟乙磺酸盐。在较低浓度的喷他eth羟乙磺酸盐下,使用液-液萃取可获得更好的回收率:0.04-29.6μg ml(-1)的回收率在60%至100%之间。获得线性校准图,用于测定被测溶液中浓度低于1 x 10(-7)mol l(-1)(即小于约0.05μg ml(-1))的两种药物:标准首选添加法进行定量。对于尿液中含有2.96μgml(-1)的喷他戊定羟乙磺酸盐和0.42μgml- 1)奈多克罗米尔。 [参考:17]

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