Highly sensitive therapeutic drug monitoring of infliximab in serum by targeted mass spectrometry in comparison to ELISA data.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-02-29 DOI:10.1186/s12014-024-09464-x
Andreas Hentschel, Gina Piontek, Rob Dahlmann, Peter Findeisen, Roman Sakson, Phil Carbow, Thomas Renné, Yvonne Reinders, Albert Sickmann
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Abstract

Background: Presently, antibody concentration measurements for patients undergoing treatment are predominantly determined by ELISA, which still comes with known disadvantages. Therefore, our aim was to establish a targeted mass-spectrometric assay enabling the reproducible absolute quantification of peptides from the hypervariable and interaction regions of infliximab.

Methods: Peptides of infliximab were measured post-trypsin digestion and subsequent separation on a Vanquish Horizon UHPLC coupled to a TSQ Altis Triple-Quad mass spectrometer. Normalization and absolute quantification were conducted using stable isotope-synthesized peptides. Calibration curves covering a range of 0.25-50 µg/ml were employed for quantitation.

Results: We demonstrated the substantial influence of peptide selection, choice of hydrolase for digestion, and digestion time on absolute peptide yield (28-44% for peptide 1 and 64-97% for peptide 2). Furthermore, we showed that the generated calibration curves for absolute quantification were highly reproducible and robust (LLOQ1 0.72 µg/ml and LLOQ2 1.00 µg/ml) over several months. In comparison to ELISA values, the absolute values obtained by mass spectrometry often yielded lower results for both targeted peptides.

Conclusions: In this study, a semi-automated workflow was employed and tested with 8 patients and corresponding replicates (n = 3-4). We demonstrated the robust implementation of calibration curves for the absolute quantification of infliximab in patient samples, with coefficients of variation ranging from 0.5 to 9%. Taken together, we have developed a platform enabling the rapid (2 days of sample preparation and 30 min of measurement time per sample) and robust quantification of Infliximab antibody concentration in patients. The use of mass spectrometry also facilitates the straightforward expansion of the method to include additional antibody peptides.

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通过靶向质谱法对血清中的英夫利昔单抗进行高灵敏度治疗药物监测,并与酶联免疫吸附试验数据进行比较。
背景:目前,主要通过酶联免疫吸附法测定接受治疗的患者的抗体浓度,但这种方法仍存在众所周知的缺点。因此,我们的目标是建立一种有针对性的质谱检测方法,对英夫利昔单抗超变异区和相互作用区的肽段进行可重复的绝对定量:方法:英夫利昔单抗的肽段在胰蛋白酶消化后进行测定,随后在Vanquish Horizon超高效液相色谱仪和TSQ Altis三重四极杆质谱仪上进行分离。使用稳定同位素合成的肽进行归一化和绝对定量。定量采用的校准曲线范围为 0.25-50 µg/ml :我们证明了肽的选择、消化水解酶的选择和消化时间对肽绝对产量的重大影响(肽 1 为 28-44%,肽 2 为 64-97%)。此外,我们还发现所生成的绝对定量校准曲线在数月内具有高度的可重复性和稳健性(LLOQ1 为 0.72 µg/ml,LLOQ2 为 1.00 µg/ml)。与 ELISA 值相比,质谱法获得的两种目标肽的绝对值往往较低:本研究采用了半自动化工作流程,并对 8 名患者和相应的重复样本(n = 3-4)进行了测试。我们证明了校准曲线对患者样本中英夫利西单抗绝对定量的稳健实施,变异系数在 0.5% 到 9% 之间。综上所述,我们已经开发出一种平台,能够快速(2 天的样品制备时间和 30 分钟的每个样品测量时间)、稳健地定量检测患者体内的英夫利西单抗抗体浓度。质谱法的使用还有助于直接扩展该方法,以包括更多的抗体肽。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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