Centre for Pharmaceutical Innovation, UniSA: Clinical and Health Sciences, University of South Australia, GPO Box 2471, North Terrace, Adelaide, SA, 5000, Australia.
Royal Adelaide Hospital and The University of Adelaide, Adelaide Medical School, Adelaide, SA, Australia.
Anal Bioanal Chem. 2022 Aug;414(20):6029-6046. doi: 10.1007/s00216-022-04186-1. Epub 2022 Jul 7.
Low-dose methotrexate (MTX) plays a key role in treatment of rheumatoid arthritis. However, not all patients respond satisfactorily, and no therapeutic drug monitoring has been implemented in clinical practice, despite the fact that MTX therapy has now been available for decades. Analysis of individual intracellular MTX metabolites among rheumatoid arthritis (RA) patients is hampered by the low intracellular concentrations of MTX-PGs which require a highly sensitive method to quantify. Here, we present a rapid and highly sensitive LC (HILIC) MS/MS method with LLOQ 0.1 nM, 0.8 nmol/L for each metabolite of MTX-PG and MTX-PG respectively. Over a linear range of 0.1-100 nM, 0.8-100 nmol/L for each metabolite of MTX-PG and MTX-PG, respectively, the inter- and intra- accuracy and precision were within 15% of the nominal value for all MTX metabolites. The presented assay was used to assess and compare MTX metabolite concentrations extracted from four different matrices: red blood cells, plasma, peripheral blood mononuclear cells, and whole blood that have been collected either using traditional venepuncture or volumetric absorptive micro-sampling (VAMS) sampling techniques. The presented method not only improves analyte coverage and sensitivity as compared to other published methods; it also improves the greenness.
低剂量甲氨蝶呤(MTX)在治疗类风湿关节炎中起着关键作用。然而,并非所有患者的反应都令人满意,尽管 MTX 治疗已经有几十年的历史,但在临床实践中尚未实施任何治疗药物监测。分析类风湿关节炎(RA)患者个体细胞内 MTX 代谢物受到 MTX-PG 细胞内浓度低的限制,需要一种高度敏感的方法来定量。在这里,我们提出了一种快速且高度敏感的 LC(亲水作用色谱)MS/MS 方法,LLOQ 为 0.1 nM,MTX-PG 和 MTX-PG 的每种代谢物分别为 0.8 nmol/L。在 0.1-100 nM、0.8-100 nmol/L 的线性范围内,MTX-PG 和 MTX-PG 的每种代谢物的内、间精密度和准确度均在 15%以内。所提出的测定方法用于评估和比较从四种不同基质中提取的 MTX 代谢物浓度:使用传统静脉穿刺或体积吸收微采样(VAMS)采样技术采集的红细胞、血浆、外周血单核细胞和全血。与其他已发表的方法相比,所提出的方法不仅提高了分析物的覆盖率和灵敏度,而且提高了绿色度。