首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Simple spectrofluorometric determination of p-aminobenzoic and p-aminosalicylic acids in biological fluids by use of terbium-sensitized luminescence.
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Simple spectrofluorometric determination of p-aminobenzoic and p-aminosalicylic acids in biological fluids by use of terbium-sensitized luminescence.

机译:通过使用sensit敏化的发光方法简单的荧光光谱法测定生物流体中的对氨基苯甲酸和对氨基水杨酸。

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摘要

A novel, sensitive, and selective method has been developed for determination of p-aminobenzoic (PABA) and p-aminosalicylic (PAS) acids in the N-benzoyl-L-tyrosyl-PABA/ PAS test. PAS is measured as a ternary complex with terbium and EDTA (lambda(ex) = 324 nm, lambda(em) = 546 nm) in alkaline aqueous solution (pH approximately 12.6), whereas both compounds (PABA and PAS) are measured as ternary complexes with terbium and tri-n-octylphosphine oxide (lambda(ex) = 292 nm, lambda(em) = 546 nm) in weakly acidic aqueous solution (pH approximately 5.5). We inve stigated and implemented optimum conditions for formation of these complexes, yielding respective detection limits for PABA and PAS of 0.07 and 0.02 micromol/L and ranges of application of 0-10 and 0-40 micromol/L (final concentration). The method has been successfully applied to determinations of PABA and PAS in urine and, after alkaline hydrolysis, to determinations of PABA in serum that has been deproteinized with acetonitrile. Within-run imprecision of the PABA determination ranges from 0.8% to 4.2 % for urine samples and from 3.9% to 8.2% for serum samples; day-to-day imprecision varies from 3.2% to 10% for serum samples.
机译:已开发出一种新颖,灵敏且选择性的方法来测定N-苯甲酰基-L-酪氨酰-PABA / PAS测试中的对氨基苯甲酸(PABA)和对氨基水杨酸(PAS)酸。在碱性水溶液(pH值约为12.6)中,PAS是与with和EDTA的三元络合物(λ(ex)= 324 nm,λ(em)= 546 nm)的三元络合物,而两种化合物(PABA和PAS)都以三元络合物的形式进行测量在弱酸性水溶液(pH值约5.5)中与ter和三正辛基膦氧化物(λ(ex)= 292 nm,λ(em)= 546 nm)形成配合物。我们研究并实施了形成这些复合物的最佳条件,从而分别得出PABA和PAS的检出限为0.07和0.02 micromol / L,应用范围为0-10和0-40 micromol / L(最终浓度)。该方法已成功地应用于尿液中PABA和PAS的测定,碱性水解后,已被乙腈脱蛋白的血清中PABA的测定成功。尿液样本中PABA测定的运行中不准确度在0.8%至4.2%之间,血清样本在3.9%至8.2%之间。血清样品的日常不准确度从3.2%到10%不等。

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