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利用体积吸收微采样和干血斑,通过液相色谱-串联质谱法定量儿科患者体内的抗真菌三唑类药物。

Utilization of volumetric absorptive microsampling and dried plasma spot for quantification of anti-fungal triazole agents in pediatric patients by using liquid chromatography-tandem mass spectrometry.

作者信息

Simeoli Raffaele, Cairoli Sara, Galaverna Federica, Becilli Marco, Boccieri Emilia, Antonetti Giacomo, Vitale Alessia, Mancini Alessandro, Rossi Chiara, Vici Carlo Dionisi, Goffredo Bianca Maria

机构信息

Division of Metabolic Diseases and Drug Biology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Department of Hematology/Oncology, Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

出版信息

J Pharm Biomed Anal. 2023 Nov 30;236:115688. doi: 10.1016/j.jpba.2023.115688. Epub 2023 Aug 29.

Abstract

BACKGROUND

Recently, increasing attention has been paid to the use of microsampling techniques for therapeutic drug monitoring (TDM) in neonatal and pediatric populations. Volumetric Absorptive Microsampling (VAMS) has been introduced in the market under the name Mitra® (Neoteryx). These devices consist of porous absorbent tips that allow collection of fixed blood volumes (10-30 µL) to overcome the DBS-related hematocrit effect. Here, the authors analyzed the concentrations of triazole agents (voriconazole, posaconazole, and isavuconazole) in VAMS and dried plasma spot (DPS) samples.

METHODS

Fifty whole blood samples were obtained from pediatric patients subjected to systemic anti-fungal therapy. VAMS were collected by dipping the tip into whole blood before centrifugation for plasma recovery. Then, 30 µL of plasma was carefully spotted on filter paper to obtain DPS. Anti-fungal concentrations were measured using a validated LC-MS/MS kit (MassTox® Antimycotic Drugs/EXTENDED) provided by Chromsystems (Chromsystems Instruments & Chemicals). Drug concentrations in VAMS and DPS samples were compared to those in fresh plasma using Passing-Bablok and Bland-Altman tests.

RESULTS

Plasma concentrations of voriconazole, posaconazole, and isavuconazole were positively and significantly correlated with those obtained in VAMS and DPS samples (Spearman r range, 0.82-0.94, p < 0.001). Data were further analyzed using the Bland-Altman test, which showed a % mean difference compared to fresh plasma of -15.06-10.98 (range). The stability of both VAMS and DPS was ensured for at least 14 d at room temperature.

CONCLUSIONS

These results demonstrate that VAMS and DPS can be used for the TDM of anti-fungal agents. Owing to their stability, both sampling devices can be easily stored and shipped, without the need for refrigeration, to TDM laboratories that facilitate remote TDM applications. Finally, VAMS could be particularly suitable for pediatric and neonatal patients because they allow the collection of a few microliters of blood, thus improving ethical and compliance limitations.

摘要

背景

近年来,新生儿和儿科人群中用于治疗药物监测(TDM)的微量采样技术越来越受到关注。体积吸收微量采样(VAMS)已以Mitra®(Neoteryx)的名称推向市场。这些装置由多孔吸收性尖端组成,可收集固定体积的血液(10 - 30微升),以克服与干血斑(DBS)相关的血细胞比容效应。在此,作者分析了VAMS和干血浆斑(DPS)样本中三唑类药物(伏立康唑、泊沙康唑和艾沙康唑)的浓度。

方法

从接受全身抗真菌治疗的儿科患者中采集了50份全血样本。在离心分离血浆前,将VAMS尖端浸入全血中进行采集。然后,将30微升血浆小心地滴在滤纸上以获得DPS。使用Chromsystems(Chromsystems Instruments & Chemicals)提供的经过验证的液相色谱 - 质谱/质谱试剂盒(MassTox®抗真菌药物/扩展版)测量抗真菌浓度。使用Passing - Bablok和Bland - Altman检验比较VAMS和DPS样本中的药物浓度与新鲜血浆中的药物浓度。

结果

伏立康唑、泊沙康唑和艾沙康唑的血浆浓度与VAMS和DPS样本中获得的浓度呈正相关且显著相关(Spearman相关系数范围为0.82 - 0.94,p < 0.001)。使用Bland - Altman检验进一步分析数据,结果显示与新鲜血浆相比,平均差异百分比为 - 15.06 - 10.98(范围)。VAMS和DPS在室温下至少14天的稳定性得到保证。

结论

这些结果表明,VAMS和DPS可用于抗真菌药物的TDM。由于它们的稳定性,这两种采样装置都可以轻松储存和运输,无需冷藏,可送至便于远程TDM应用的TDM实验室。最后,VAMS可能特别适合儿科和新生儿患者,因为它们允许采集几微升血液,从而改善了伦理和依从性方面的限制。

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