4.5 Article

A Novel Method for Monitoring N-Nitrosamines Impurities Using NH2-MIL-101(Fe) Mediated Dispersive Micro-Solid Phase Extraction Coupled with LC-MS/MS in Biopharmaceuticals

Journal

JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 112, Issue 11, Pages 2783-2789

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.xphs.2023.07.017

Keywords

Nitrosamine; Antibody drug; LC-MS/MS; Dispersive micro-solid-phase extraction; Metal-organic framework; NH2-MIL-101(Fe)

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A highly efficient and convenient method using an amine-functionalized metal-organic framework as sorbent coupled with LC-MS/MS was developed for the simultaneous determination of 12 N-nitrosamines in biopharmaceuticals. The method was validated and showed good linearity, repeatability, and precision. The proposed adsorption mechanism on NH2-MIL-101(Fe) was supported by FTIR spectra. The method was successfully applied for the detection of trace nitrosamines in biopharmaceuticals.
A highly efficient and convenient method for the simultaneous determination of 12 N-nitrosamines (NAs) has been developed using an amine-functionalized metal-organic framework (NH2-MIL-101(Fe)) as sorbent for dispersive micro-solid phase extraction (D-mu SPE) coupled with LC-MS/MS in biopharmaceuticals. The experimental variables involved in the extraction process (i.e., amount of the sorbent, extraction time, desorption time, ionic strength, desorption solvent and volume) were optimized to achieve the best extraction efficiency of the target analytes. Under the optimum conditions, the method was successfully validated, showing good linearity in the range of 0.5-3.0 mu g/L with determination coefficients (R-2) higher than 0.990, repeatability (RSD <= 10.0%, spiked level at 2.0 mu g/L) and precision (RSD <= 8.2%). The limit of detection (LOD) and limit of quantitation (LOQ) were in the range of 0.005-0.025 mu g/L and 0.010-0.250 mu g/L, respectively. Satisfactory recoveries ranging from 82.4 to 116.8% were obtained by spiking standards at three different concentrations (0.5 mu g/L, 2.0 mu g/L and 3.0 mu g/L). Other validation parameters, including specificity, stability, and robustness, met the validation criteria. More importantly, the plausible adsorption mechanism on NH2-MIL-101(Fe) was proposed by Fourier-transform infrared (FTIR) spectra technique. Finally, this method was successfully applied to detect trace nitrosamines in biopharmaceuticals.(c) 2023 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.

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