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采用超高效液相色谱串联质谱法同时测定干血斑中环孢素 A 和他克莫司。

Simultaneous measurement of cyclosporin A and tacrolimus from dried blood spots by ultra high performance liquid chromatography tandem mass spectrometry.

机构信息

Department of Clinical Biochemistry, University Hospital of South Manchester, Wythenshawe, Manchester, United Kingdom.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Feb 1;883-884:102-7. doi: 10.1016/j.jchromb.2011.05.016. Epub 2011 May 20.

Abstract

Cyclosporin A (CsA) and tacrolimus are immunosuppressant drugs principally used in solid organ transplant recipients. Therapeutic drug monitoring (TDM) of both drugs is essential to avoid toxicity related to overdosage, and transplant rejection from underdosage. This necessitates frequent hospital visits to phlebotomy services. Capillary blood sampling onto dried blood spots (DBS) provides numerous advantages to venous whole blood sampling, including the ability for patients to send DBS to the laboratory by post, significantly reducing the number of unnecessary hospital visits. We have developed a novel, simple and rapid method for the extraction and simultaneous UPLC-MS/MS measurement of both CsA and tacrolimus from DBS. The extraction method involved a simple 30 min hot solvent extraction with ultrasonication. Extract (10 μL) was injected onto a Waters Acquity UPLC column filter unit security frit, coupled to a Waters Acquity BEH C18 UPLC column, with methanolic mobile phase gradient elution. Eluant was connected to a Waters Quattro Premier XE tandem mass spectrometer operating in ES+ mode. We detected multiple reaction monitoring (MRM) transitions of m/z 1220>1203 and 1231.9>1215.1 for CsA and d12 CsA respectively which co-eluted at 1.30min, and 821.6>768.5 and 809.6>756.5 for tacrolimus and ascomycin respectively which co-eluted at 1.17 min. Ion suppression was negligible. Mean recovery was 95.5% for CsA and 92.8% for tacrolimus. Limit of detection and limit of quantitation were both 8.5 μg/L for CsA, and 0.5 and 2.3 μg/L respectively for tacrolimus. The assay was linear up to 1500μg/L for CsA (r(2)=0.9999), and up to 50 μg/L for tacrolimus (r(2)=0.9994). Mean intra assay imprecision, inter assay imprecision and bias were all <10% for both CsA and tacrolimus. DBS were stable for at least 14 days at room temperature. Comparison of the DBS UPLC-MS/MS method and the routine venous whole blood LC-MS/MS assay demonstrated good agreement between the two methods for both drugs. We have developed a simple and robust method for the extraction and simultaneous measurement of CsA and tacrolimus from DBS. The method will allow TDM of transplant recipients to proceed at home using capillary blood sampling.

摘要

环孢素 A(CsA)和他克莫司是主要用于实体器官移植受者的免疫抑制剂药物。为避免因过量引起的毒性和因剂量不足引起的移植排斥反应,这两种药物的治疗药物监测(TDM)至关重要。这需要患者频繁前往医院的采血服务处进行静脉血样采集。采用毛细管血样点(DBS)进行检测具有许多优于静脉全血采样的优势,包括患者可以通过邮寄方式将 DBS 样本寄送至实验室,从而大大减少了不必要的医院就诊次数。我们开发了一种新颖、简单且快速的方法,可用于从 DBS 中同时提取和超高效液相色谱-串联质谱法(UPLC-MS/MS)测量 CsA 和他克莫司。该提取方法涉及使用超声辅助进行简单的 30 分钟热溶剂提取。从 10μL 提取液注入 Waters Acquity UPLC 柱过滤器单元安全 frit 中,与 Waters Acquity BEH C18 UPLC 柱相连,采用甲醇作为流动相梯度洗脱。洗脱液与 Waters Quattro Premier XE 串联质谱仪(采用电喷雾正离子模式)相连。我们检测到 m/z 1220>1203 和 1231.9>1215.1 的多重反应监测(MRM)跃迁,分别为 CsA 和氘代 CsA,两者在 1.30 分钟处共流出,以及 m/z 821.6>768.5 和 809.6>756.5 的跃迁,分别为他克莫司和 Aspergillus niger 衍生的 ascomycin,两者在 1.17 分钟处共流出。离子抑制可忽略不计。CsA 的平均回收率为 95.5%,他克莫司的平均回收率为 92.8%。CsA 的检测限和定量限均为 8.5μg/L,他克莫司的检测限和定量限分别为 0.5 和 2.3μg/L。该方法对 CsA 的线性范围高达 1500μg/L(r(2)=0.9999),对他克莫司的线性范围高达 50μg/L(r(2)=0.9994)。CsA 和他克莫司的批内精密度、批间精密度和偏差的平均误差均<10%。室温下 DBS 至少稳定 14 天。DBS 的 UPLC-MS/MS 方法与常规静脉全血 LC-MS/MS 测定方法的比较表明,两种方法对这两种药物的测定均具有良好的一致性。我们已经开发出一种简单而强大的方法,可用于从 DBS 中同时提取和同时测量 CsA 和他克莫司。该方法将允许使用毛细血管血样采集在家中进行移植受者的 TDM。

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