Emerging procedures and solvents in biological sample pre-treatment

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2023-05-01 DOI:10.1016/j.sampre.2023.100066
Valentina Greco , Alessandro Giuffrida , Marcello Locatelli , Fabio Savini , Ugo de Grazia , Luigi Ciriolo , Miryam Perrucci , Abuzar Kabir , Halil Ibrahim Ulusoy , Cristian D'Ovidio , Antonio Maria Catena , Imran Ali
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引用次数: 3

Abstract

The treatment of biological samples, especially from complex matrices, has consistently challenged analytical operators. The classic problems to be faced for any analysis, regardless of the origin of the sample, such as for example contamination and loss of analyte, in biological samples, are particularly emphasized. In particular, the main cause of the error is due to the degradation of the analyte which in several cases due to biological interaction. Many factors can influence the stability of drugs, chief among them the physicochemical properties of the drug, characteristics of the matrix, the tendency to conjugation/deconjugation, sample collection procedure, container characteristics (e.g., oxidation, adsorption), and the use of preservatives or other additives. The problem is severe in the toxicological and forensic fields, especially for analyzes considered "non-repeatable." In this review, we will explore all the major problems in the pre-extraction phase for the chemical-analytical aspect in the pharmacotoxicological and forensic fields.

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生物样品预处理中的新兴程序和溶剂
生物样品的处理,特别是复杂基质的处理,一直对分析操作员提出挑战。特别强调了任何分析所面临的经典问题,无论样品的来源如何,例如生物样品中分析物的污染和损失。特别是,误差的主要原因是由于分析物的降解,在某些情况下是由于生物相互作用。许多因素会影响药物的稳定性,其中最主要的是药物的物理化学性质、基质的特性、结合/去结合的趋势、样品收集程序、容器特性(如氧化、吸附)以及防腐剂或其他添加剂的使用。该问题在毒理学和法医学领域非常严重,尤其是对于被认为“不可重复”的分析。在这篇综述中,我们将探讨药物毒理学和法医领域化学分析方面在提取前阶段的所有主要问题。
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