Department of Pharmacy, National University of Singapore, 18 Science Drive 4, Singapore, 117543, Singapore.
School of Pharmacy, Monash University Malaysia, Level 5, Building 2, 47500, Bandar Sunway, Selangor Darul Ehsan, Malaysia.
Eur J Drug Metab Pharmacokinet. 2023 Sep;48(5):467-494. doi: 10.1007/s13318-023-00846-4. Epub 2023 Jul 26.
This review provides an overview on the current applications of dried blood spots (DBS) as matrices for therapeutic drug (TDM) and drug or disease response monitoring (DRM). Compared with conventional methods using plasma/serum, DBS offers several advantages, including minimally invasiveness, a small blood volume requirement, reduced biohazardous risk, and improved sample stability. Numerous assays utilising DBS for TDM have been reported in the literature over the past decade, covering a wide range of therapeutic drugs. Several factors can affect the accuracy and reliability of the DBS sampling method, including haematocrit (HCT), blood volume, sampling paper and chromatographic effects. It is crucial to evaluate the correlation between DBS concentrations and conventional plasma/serum concentrations, as the latter has traditionally been used for clinical decision. The feasibility of using DBS sampling method as an option for home-based TDM is also discussed. Furthermore, DBS has also been used as a matrix for monitoring the drug or disease responses (DRM) through various approaches such as genotyping, viral load measurement, assessment of inflammatory factors, and more recently, metabolic profiling. Although this research is still in the development stage, advancements in technology are expected to lead to the identification of surrogate biomarkers for drug treatment in DBS and a better understanding of the correlation between DBS drug levels and drug responses. This will make DBS a valuable matrix for TDM and DRM, facilitating the achievement of pharmacokinetic and pharmacodynamic correlations and enabling personalised therapy.
这篇综述概述了目前使用干血斑(DBS)作为治疗药物(TDM)和药物或疾病反应监测(DRM)基质的应用。与使用血浆/血清的传统方法相比,DBS 具有几个优势,包括微创性、需要的血量少、降低生物危害性风险以及提高样本稳定性。在过去十年中,文献中报道了许多利用 DBS 进行 TDM 的检测方法,涵盖了广泛的治疗药物。有几个因素会影响 DBS 采样方法的准确性和可靠性,包括红细胞压积(HCT)、血量、采样纸和色谱效应。评估 DBS 浓度与传统血浆/血清浓度之间的相关性至关重要,因为后者一直被用于临床决策。还讨论了将 DBS 采样方法用作基于家庭的 TDM 的替代方法的可行性。此外,DBS 还被用作通过各种方法监测药物或疾病反应(DRM)的基质,例如基因分型、病毒载量测量、炎症因子评估,以及最近的代谢组学。尽管这项研究仍处于开发阶段,但技术的进步有望在 DBS 中确定治疗药物的替代生物标志物,并更好地了解 DBS 药物水平与药物反应之间的相关性。这将使 DBS 成为 TDM 和 DRM 的有价值的基质,有助于实现药代动力学和药效学的相关性,并实现个体化治疗。