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一种使用容积吸收性微量采样装置Mitra同时定量测定他克莫司、环孢素A、犬尿氨酸、色氨酸和肌酐的离线固相萃取-液相色谱-串联质谱法。

An Offline SPE-LC-MS/MS Method for Simultaneous Quantification of Tacrolimus, Cyclosporine A, Kynurenine, Tryptophan, and Creatinine Using Volumetric Absorptive Microsampling Device Mitra.

作者信息

Nierychlewski Kajetan, Habler Katharina, Kemmner Stephan, Seibt Tobias, Fischereder Michael, Schwarz Markus

机构信息

Institute of Laboratory Medicine, LMU University Hospital, LMU Munich, Germany.

Transplant Center, LMU University Hospital, LMU Munich, Germany ; and.

出版信息

Ther Drug Monit. 2025 Oct 1;47(5):669-675. doi: 10.1097/FTD.0000000000001341. Epub 2025 May 22.

Abstract

BACKGROUND

Therapeutic drug monitoring of immunosuppressants is critical in balancing insufficient immunosuppression due to underdosing, and severe adverse effects due to overdosage. For a more comprehensive therapeutic drug monitoring and follow-up of transplant patients, the aim was to develop a liquid chromatography-tandem mass spectrometry method for the simultaneous quantification of tacrolimus, cyclosporine A, tryptophan, kynurenine, and creatinine using a volumetric absorptive microsampling device.

METHODS

Venous and capillary blood samples were simultaneously collected using a volumetric absorptive microsampling device called Mitra. The method involved protein precipitation followed by offline solid-phase extraction using a positive pressure manifold. Chromatographic separation was achieved by a formic acid-ammonium formate-methanol gradient on a Synergi Polar reversed-phase column. Multiple reaction monitoring in the positive ion mode and stable isotope-labeled internal standards were used for quantification. Validation was performed according to the European Medicines Agency and US Food and Drug Administration (FDA) guidelines.

RESULTS

Validation was successful, meeting European Medicines Agency and FDA guidelines. Investigation of selectivity, accuracy, and precision met the required criteria of a deviation <15%. Internal standards successfully compensated potential matrix effects. A comparison of 26 anonymized samples from transplant patients on Mitra with venous blood controls demonstrated the method's suitability.

CONCLUSIONS

For the first time, we herein describe a liquid chromatography-tandem mass spectrometry method for the simultaneous quantification of tacrolimus, cyclosporine A, tryptophan, kynurenine, and creatinine on Mitra. Self-collection of samples may facilitate therapeutic monitoring. Simultaneous determination of creatinine may help monitor kidney function, while tryptophan and kynurenine may serve as a biomarker for early detection of transplant rejection.

摘要

背景

免疫抑制剂的治疗药物监测对于平衡因剂量不足导致的免疫抑制不足和因过量导致的严重不良反应至关重要。为了对移植患者进行更全面的治疗药物监测和随访,目标是开发一种液相色谱-串联质谱法,使用体积吸收微采样装置同时定量测定他克莫司、环孢素A、色氨酸、犬尿氨酸和肌酐。

方法

使用一种名为Mitra的体积吸收微采样装置同时采集静脉血和毛细血管血样。该方法包括蛋白质沉淀,然后使用正压歧管进行离线固相萃取。在Synergi Polar反相柱上通过甲酸-甲酸铵-甲醇梯度进行色谱分离。采用正离子模式下的多反应监测和稳定同位素标记的内标进行定量。根据欧洲药品管理局和美国食品药品监督管理局(FDA)的指南进行验证。

结果

验证成功,符合欧洲药品管理局和FDA的指南。选择性、准确性和精密度的研究符合偏差<15%的要求标准。内标成功补偿了潜在的基质效应。对26份来自移植患者的匿名Mitra样本与静脉血对照样本的比较证明了该方法的适用性。

结论

我们首次在此描述了一种液相色谱-串联质谱法,用于在Mitra上同时定量测定他克莫司、环孢素A、色氨酸、犬尿氨酸和肌酐。自我采集样本可能有助于治疗监测。同时测定肌酐可能有助于监测肾功能,而色氨酸和犬尿氨酸可作为早期检测移植排斥反应的生物标志物。

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