Development and validation of an HPLC-MS/MS method to simultaneously quantify brigatinib, lorlatinib, pralsetinib and selpercatinib in human K2-EDTA plasma

Biomed Chromatogr. 2023 Jun;37(6):e5628. doi: 10.1002/bmc.5628. Epub 2023 Apr 12.

Abstract

A liquid chromatography-tandem mass spectrometry method was developed and validated to quantify the small-molecule inhibitors (SMIs) brigatinib, lorlatinib, pralsetinib and selpercatinib, which are used in patients with oncogenic-driven non-small cell lung cancer. Chromatographic separation was performed on a HyPURITY® C18 analytical column with a gradient elution using ammonium acetate in water and in methanol, both acidified with formic acid 0,1%. Detection and quantification were performed using a triple quad mass spectrometer with an electrospray ionization interface. The assay was validated over a linear range of 50-2,500 ng/ml for brigatinib, 25-1,000 ng/ml for lorlatinib, 100-10,000 ng/ml for pralsetinib and 50-5,000 ng/ml for selpercatinib. All four SMIs were stable for at least 7 days under cool conditions (2-8°C), and at least 24 h at room temperature (15-25°C) in K2-EDTA plasma. Under freezing conditions (-20°C), all SMIs were stable for at least 30 days, except for the lowest quality control (QCLOW ) of pralsetinib. The QCLOW of pralsetinib was stable for at least 7 days at -20°C. This method provides an efficient and simple way to quantify four SMIs with a single assay in clinical practice.

Keywords: LC-MS/MS; non-small cell lung cancer; small-molecule inhibitors.

MeSH terms

  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Chromatography, High Pressure Liquid / methods
  • Edetic Acid
  • Humans
  • Lactams, Macrocyclic
  • Lung Neoplasms*
  • Reproducibility of Results
  • Tandem Mass Spectrometry / methods

Substances

  • selpercatinib
  • lorlatinib
  • pralsetinib
  • brigatinib
  • Edetic Acid
  • Lactams, Macrocyclic