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开发一种灵敏的生化检测方法,用于检测托法替尼的依从性。

Development of a sensitive biochemical assay for the detection of tofacitinib adherence.

机构信息

Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology Medicine and Health, Core Technology Facility, The University of Manchester, Grafton Street, Manchester, M13 9NT, UK.

Centre for Epidemiology Versus Arthritis, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.

出版信息

Anal Methods. 2023 Apr 6;15(14):1797-1801. doi: 10.1039/d2ay01800d.

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease. Tofacitinib is a Janus Kinase inhibitor licensed for the treatment of RA that, unlike biologic anti-rheumatic drugs, is administered orally, but studies of long-term treatment adherence rates are lacking. The measurement of adherence, however, is challenging and there is currently no gold standard test for adherence. Here, we developed a novel HPLC MS/MS assay for the quantification of tofacitinib. The assay demonstrated a LLOQ for tofacitinib of 0.1 ng ml, within run accuracy was 81-85% at LLOQ and 91-107% at all other levels. To investigate the ability of the assay to detect adherence, tofacitinib was measured in a random selection of serum samples ( = 10) of tofacitinib treated RA patients who self-reported adherent behaviour. The assay measured tofacitinib in all samples above the LLOQ demonstrating the potential of the assay to sensitively measure biochemical adherence in real-world patient samples. This method for detection of adherence has the potential to be a more objective measure that could be used in the future in the clinic but will require further studies to explore factors that may influence measurement of drug levels, such as clinical characteristics of patients.

摘要

类风湿关节炎(RA)是一种慢性自身免疫性炎症性疾病。托法替布是一种 Janus 激酶抑制剂,已获得治疗 RA 的许可,与生物类抗风湿药物不同,它是口服给药的,但缺乏长期治疗依从性率的研究。然而,对依从性的测量具有挑战性,目前没有用于依从性的金标准测试。在这里,我们开发了一种新的 HPLC-MS/MS 测定法来定量测定托法替布。该测定法显示托法替布的LLOQ 为 0.1ng/ml,在LLOQ 时的日内精密度为 81-85%,在所有其他水平时的精密度为 91-107%。为了研究该测定法检测依从性的能力,我们对随机选择的托法替布治疗 RA 患者(n=10)的血清样本中的托法替布进行了测量,这些患者自我报告了依从性行为。该测定法在所有LLOQ 以上的样本中都测量到了托法替布,这表明该测定法有可能在真实世界的患者样本中灵敏地测量生化依从性。这种用于检测依从性的方法有可能成为一种更客观的衡量标准,未来可在临床中使用,但需要进一步研究来探索可能影响药物水平测量的因素,例如患者的临床特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dfb/10076935/af798319aad4/d2ay01800d-f1.jpg

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