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Determination of selected β-receptor antagonists in biological samples by solid-phase extraction with cholesterolic phase and LC/MS

机译:胆固醇相和LC / MS固相萃取法测定生物样品中所选的β受体拮抗剂

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摘要

A new method is presented for the determination of five selected β-receptor antagonists by HPLC, which emphasizes sample preparation via retention on a new type of silica gel sorbent used for solid-phase extraction (SPE). Sorbents of this type were obtained by the chemical modification of silica gels of various porosities by cholesterol ligands. The cholesterol-based packing material was investigated by spectroscopic methods and elemental analysis. The recoveries obtained with the extraction procedure were optimum over a relatively broad sample pH range (3.08–7.50). Analytical factors such as the sample loading, the washing step and elution conditions, the concentration of β-receptor antagonists to be extracted, and the type of sorbent were found to play significant roles in the sample preparation procedure and would therefore need to be controlled to achieve optimum recoveries of the analytes. Under optimum conditions, the recoveries of nadolol, acebutolol, esmolol, oxprenolol and propranolol from spiked buffers, blood and urine were reproducible and dependent on the polarity or hydrophilicity of the compounds. The above analytes were determined by reverse-phase high-performance liquid chromatography (HPLC) with UV and ESI-ion trap mass spectrometry (MS) detection. The described method was found to be suitable for the routine measurement of compounds that are both polar and basic, and can be applied for the analysis of biological samples such as urine and blood in clinical, toxicological or forensic laboratories. The recovery measurements were performed on spiked human urine and serum, and on real samples of mouse blood serum.
机译:提出了一种通过HPLC测定五种选定的β受体拮抗剂的新方法,该方法强调了保留在用于固相萃取(SPE)的新型硅胶吸附剂上的样品制备方法。这种类型的吸附剂是通过胆固醇配体对各种孔隙率的硅胶进行化学修饰而获得的。通过光谱方法和元素分析研究了基于胆固醇的包装材料。在较宽的样品pH范围(3.08–7.50)范围内,通过萃取程序获得的回收率是最佳的。已发现分析因素,例如样品上样量,洗涤步骤和洗脱条件,要提取的β受体拮抗剂的浓度以及吸附剂的类型在样品制备过程中起着重要作用,因此需要控制到实现分析物的最佳回收率。在最佳条件下,可从加标的缓冲液,血液和尿液中回收萘多洛尔,醋丁洛尔,艾司洛尔,奥普萘洛尔和普萘洛尔,并且这些化合物的极性或亲水性均可以再现。上述分析物是通过反相高效液相色谱(HPLC)以及UV和ESI离子阱质谱(MS)检测来测定的。发现所描述的方法适用于极性和碱性化合物的常规测量,并可用于临床,毒理学或法医实验室中生物样品(如尿液和血液)的分析。对加标的人尿液和血清以及小鼠血清的真实样品进行回收率测量。

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