Analysis of Oligonucleotide Impurities Using Single Quadrupole Mass Spectrometer
Applications | 2025 | ShimadzuInstrumentation
Oligonucleotide therapeutics represent an emerging class of drugs that demand rigorous impurity analysis to ensure safety and efficacy. Accurate detection and quantitation of sequence variants are essential in development and quality control stages.
This study demonstrates a workflow for identifying and quantifying n-1 and n-3 sequence impurities in a model oligonucleotide (FLP) using a Shimadzu LCMS-2050 single quadrupole mass spectrometer and LabSolutions Insight Biologics software.
The n-3 impurity was baseline separated, while the n-1 impurity co-eluted with the main peak but was successfully deconvoluted by MS data. FLP calibration (1–50 µmol/L) yielded r² ≥ 0.999. Both impurities were detected at ≥ 0.25% relative levels (0.05 µmol/L) with linearity r² ≥ 0.999.
Advances in high-throughput MS, AI-driven data processing, and integration with higher-resolution instruments will further improve sensitivity and throughput. Expansion to modified and larger oligonucleotides is anticipated.
The LCMS-2050 paired with LabSolutions Insight Biologics delivers a robust platform for impurity profiling in oligonucleotide therapeutics, achieving reliable detection and quantitation even for co-eluted sequence variants.
LC/MS, LC/SQ, Software
IndustriesPharma & Biopharma
ManufacturerShimadzu
Summary
Importance of the Topic
Oligonucleotide therapeutics represent an emerging class of drugs that demand rigorous impurity analysis to ensure safety and efficacy. Accurate detection and quantitation of sequence variants are essential in development and quality control stages.
Objectives and Study Overview
This study demonstrates a workflow for identifying and quantifying n-1 and n-3 sequence impurities in a model oligonucleotide (FLP) using a Shimadzu LCMS-2050 single quadrupole mass spectrometer and LabSolutions Insight Biologics software.
Methodology
- Reversed-phase ion-pair chromatography with 100 mmol/L HFIP and 10 mmol/L TEA gradient on a Shim-pack Scepter Claris C18 column.
- Mass detection in negative ESI/APCI mode over m/z 650–2000.
- Software-based sequence definition to combine multivalent and isotopic ions into single component chromatograms.
- Quantitation by correlating UV peak area with MS-derived component fractions through a defined calculation formula.
Instrumentation Used
- HPLC System: Nexera XS inert
- Mass Spectrometer: LCMS-2050 single quadrupole
- Column: Shim-pack Scepter Claris C18-120 (100 × 2.1 mm, 1.9 µm)
- Software: LabSolutions Insight Biologics
Main Results and Discussion
The n-3 impurity was baseline separated, while the n-1 impurity co-eluted with the main peak but was successfully deconvoluted by MS data. FLP calibration (1–50 µmol/L) yielded r² ≥ 0.999. Both impurities were detected at ≥ 0.25% relative levels (0.05 µmol/L) with linearity r² ≥ 0.999.
Benefits and Practical Applications
- Enables sensitive quantitation of well-separated and co-eluted oligonucleotide impurities.
- Simplifies QC workflows using a single-quadrupole MS.
- Combines UV and MS data for comprehensive purity assessment.
Future Trends and Applications
Advances in high-throughput MS, AI-driven data processing, and integration with higher-resolution instruments will further improve sensitivity and throughput. Expansion to modified and larger oligonucleotides is anticipated.
Conclusion
The LCMS-2050 paired with LabSolutions Insight Biologics delivers a robust platform for impurity profiling in oligonucleotide therapeutics, achieving reliable detection and quantitation even for co-eluted sequence variants.
Reference
- Ryutaro Takamine, Takao Yamaguchi, Challenges of Impurities Analysis in Manufacturing Therapeutic Oligonucleotides, J. Mass Spectrom. Soc. Jpn., 2023, 71(2), 51–54.
Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.
Similar PDF
Simple Analysis of Impurities in Oligonucleotide Therapeutics Using a Single Quadrupole Mass Spectrometer
2023|Shimadzu|Applications
Nexera™ XS inert High Performance Liquid Chromatograph LCMS-2050 Liquid Chromatograph Mass Spectrometer Application News Simple Analysis of Impurities in Oligonucleotide Therapeutics Using a Single Quadrupole Mass Spectrometer Takanari Hattori, Noriko Kato, and Junna Nakazono User Benefits Oligonucleotides and related…
Key words
flp, flpdcda, dcdaoligonucleotide, oligonucleotidetherapeutics, therapeuticsinert, inertoligonucleotides, oligonucleotidesnexera, nexeraimpurities, impuritiesrelated, relatedmass, massimpurity, impuritydozen, dozennews, newsscepter, scepterwithout
Efficient Method Development of Oligonucleotides by Reversed-Phase Ion-Pair Chromatography
2024|Shimadzu|Applications
Application News LabSolutions™ MD : Software for Efficient Method Development based on Analytical Quality by Design Efficient Method Development of Oligonucleotides by Reversed-Phase Ion-Pair Chromatography Shinichi Fujisaki and Risa Suzuki User Benefits LabSolutions MD can improve the efficiency of…
Key words
flp, flpcondition, conditionacetonitrile, acetonitrileoptimal, optimaloven, ovenratio, ratiomau, mautemp, tempdgda, dgdamethanol, methanolhfip, hfiplabsolutions, labsolutionsresolution, resolutiondesign, designseparation
Efficient Method Development of Oligonucleotides by Reversed-Phase Ion-Pair Chromatograph
2023|Shimadzu|Posters
Efficient Method Development of Oligonucleotides by Reversed-Phase Ion-Pair Chromatography P-BPHA13 Shin-ichi Fujisaki1, Risa Suzuki1, Kyoko Watanabe1, Junji Kawakami2, Takao Inoue3, Satoshi Obika4 1Shimadzu Corporation, Kyoto, Kyoto, Japan, 2Konan University, Kobe, Hyogo, Japan, 3National Institute of Health Sciences, Kawasaki, Kanagawa, Japan,…
Key words
flp, flpline, linemau, mauclaris, clarismin, mininert, inertmultiplied, multipliedgas, gaspump, pumpscouting, scoutingoligonucleotides, oligonucleotidesflowrate, flowrateoligonucleotide, oligonucleotidesystem, systeminertness
Impurity Profiling and Characterization of Therapeutic Oligonucleotides using Nominal Mass Spectrometry on a Single Quadrupole LC-UV-MS system
2024|Shimadzu|Posters
Impurity Profiling and Characterization of Therapeutic Oligonucleotides using Nominal Mass Spectrometry on a Single Quadrupole LC-UV-MS system Risa Suzuki1, 3, Kosuke Uchiyama1, Noriko Kato1, Simon Ashton2, Neil Loftus2, Yuka Fujito1 1Shimadzu Corporation, Kyoto, Japan; 2Shimadzu Corporation, Manchester, United Kingdom; 3Shimadzu…
Key words
flp, flpbiologics, biologicsnominal, nominalproduct, productinsight, insightmass, massimpurities, impuritiesabundance, abundanceimpurity, impurityoligonucleotide, oligonucleotidelength, lengthpda, pdarelated, relatedratio, ratiofull