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A sequential injection fluorometric procedure for the determination of procaine in human blood and pharmaceuticals

机译:顺序注射荧光法测定人血和药品中的普鲁卡因

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An automated procedure for the assay of procaine hydrochloride in human blood and pharmaceuticals was developed using a sequential injection (SI) technique with fluorometric detection and fluorescamine as the fluorescence probe. A few microliters of fluorescamine and procaine hydrochloride solutions were used in the SI system leading to the formation of a derivative, which was then excited by a 400-nm LED and whose emitted fluorescence was monitored at a wavelength of 494 nm. A linear calibration graph was obtained with 10-200 ng mL(-1) (procaine) by loading 10.0 mu L of sample solution and 5.0 mu L of fluorescamine solution (both 0.125 % m/v). A detection limit of 2.6 ng mL(-1), defined as 3 times the blank standard deviation (3 sigma), was achieved along with a sampling frequency of 25 h(-1) and a precision of 2.1 % RSD at the 50.0 ng mL(-1) level. Procaine contents in injection solutions from various pharmaceutical manufactures were analyzed and reasonable agreement was achieved between the values obtained by using the present procedure and the documented spectrophotometry, and both were coincident with the nominal concentrations. In addition, the degradation of procaine in human blood was investigated. A fast degradation of procaine in human blood was observed for the first 30 min, while afterwards the degradation was retarded.
机译:使用顺序注射(SI)技术开发了一种用于测定人血和药物中盐酸普鲁卡因的自动化程序,该技术采用荧光检测和以荧光胺为荧光探针。在SI系统中使用了几微升的氟胺和盐酸普鲁卡因溶液,导致形成了衍生物,然后将其用400 nm LED激发,并在494 nm的波长处监控其发射的荧光。通过加载10.0μL样品溶液和5.0μL荧光胺溶液(均为0.125%m / v),用10-200 ng mL(-1)(普鲁卡因)获得线性校准图。检测限为2.6 ng mL(-1),定义为空白标准偏差(3 sigma)的3倍,采样频率为25 h(-1),在50.0 ng处的精密度为2.1%RSD mL(-1)浓度。分析了来自各种制药商的注射液中普鲁卡因的含量,并通过使用本程序获得的值与记录的分光光度法之间取得了合理的一致,并且两者均与标称浓度一致。另外,研究了人血中普鲁卡因的降解。在最初的30分钟内观察到普鲁卡因在人血中的快速降解,但此后降解被抑制。

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