National Institute of Pharmaceutical Education and Research-Ahmedabad (NIPER-A), An Institute of National Importance, Government of India, Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Gandhinagar, Gujarat, India.
Crit Rev Anal Chem. 2023;53(7):1515-1530. doi: 10.1080/10408347.2022.2035210. Epub 2022 Feb 9.
Accurate quantification of biomarkers has always been a challenge for many bioanalytical scientists due to their endogenous nature and low concentration in biological matrices. Different analytical approaches have been developed for quantifying biomarkers including enzyme-linked immunosorbent assay, immunohistochemistry, western blotting, and chromatographic techniques assisted with mass spectrometry. Liquid chromatography-tandem mass spectrometry-based quantification of biomarkers has gained more attention over other traditional techniques due to its higher sensitivity and selectivity. However, the primary challenge lies with this technique includes the unavailability of a blank matrix for method development. To overcome this challenge, different analytical approaches are being developed including surrogate analyte and surrogate matrix approach. Such approaches include quantification of biomarkers in a surrogate matrix or quantification of an isotopically labeled surrogate analyte in an authentic matrix. To demonstrate the authenticity of the surrogate approach, it is mandatory to establish quantitative parallelism through validation employing respective surrogate analytes and surrogate matrices. In this review, different bioanalytical approaches for biomarker quantification and recent advancements in the field aiming for improvement in the specificity of the techniques have been discussed. Liquid chromatography-tandem mass spectrometry-based surrogate approaches for biomarker quantification and significance of parallelism establishment in both surrogate matrix and surrogate analyte-based approaches have been critically discussed. In addition, different methods for demonstrating parallelism in the surrogate method have been explained.
由于生物标志物的内源性和在生物基质中的低浓度,准确地定量分析一直是许多生物分析科学家面临的挑战。已经开发了不同的分析方法来定量分析生物标志物,包括酶联免疫吸附测定、免疫组织化学、蛋白质印迹和色谱技术与质谱联用。基于液相色谱-串联质谱的生物标志物定量分析由于其更高的灵敏度和选择性,比其他传统技术受到更多关注。然而,该技术的主要挑战在于缺乏用于方法开发的空白基质。为了克服这一挑战,正在开发不同的分析方法,包括替代物分析物和替代基质方法。这些方法包括在替代基质中定量生物标志物或在真实基质中定量同位素标记的替代物分析物。为了证明替代方法的真实性,必须通过使用相应的替代物分析物和替代基质进行验证来建立定量平行性。在这篇综述中,讨论了生物标志物定量的不同生物分析方法和该领域的最新进展,旨在提高技术的特异性。对基于液相色谱-串联质谱的生物标志物定量替代方法以及在替代基质和替代物分析物方法中建立平行性的重要性进行了批判性讨论。此外,还解释了在替代方法中证明平行性的不同方法。