重复冻干:尿液标准物质制备的新方法

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
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引用次数: 0

摘要

在尿液药物检测中,通常会设定一个临界值来确定样本是阴性还是阳性。含有参比物质的基质有助于抵消尿液基质对不同实验室的不利影响,从而提高最终结果的一致性。然而,作为一种生物基质,尿液容易出现腐败等问题,因此很难用作参比样本。本研究选择了临床上常用的吗啡、硝西泮、劳拉西泮、丁丙诺啡、唑吡坦、咪达唑仑、地西泮和氯氮平作为目标分析物,并进一步优化了制备过程,重复冻干,以期获得更有效、更稳定、更准确的尿液基质参比物(mRMs)。通过密度测定,研究了制备冻干样品的合适尿液密度(1.010-1.017 kg/m3)。反复冻干可获得更致密的粉末,降低塌陷的可能性,提高冻干尿液样本的质量。冻干尿液 mRM 可在室温下保存一个月,或在冷藏条件下(4 ℃)保存六个月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repeated lyophilization: A neo-method for urine-based reference materials preparation

In urine drug testing, a cut-off value is often imposed to determine whether the sample is negative or positive. A matrix containing a reference substance helps counteract the adverse effects of the urine matrix across different laboratories to improve the consistency of final results. However, as a biological matrix, urine is prone to corruption and other problems that make it difficult to use as a reference sample. In this study, morphine, nitrazepam, lorazepam, buprenorphine, zolpidem, midazolam, diazepam, and clozapine commonly used in clinical practice were selected as target analytes, and the preparation process was further optimized to repeated lyophilization, in order to obtain more effective, stable, and accurate urine matrix reference materials (mRMs). The appropriate urine density (1.010–1.017 kg/m3) for preparing lyophilized samples was investigated through density determination. Conducting repeated lyophilizations resulted in a denser powder with reduced susceptibility to collapse and improved the quality of lyophilized urine samples. Lyophilized urine mRMs could be stored at room temperature for one month or under refrigeration conditions (4 ℃) for six months.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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