Quality Control of Synthetic Biomolecules Using Rapid Methods with Serial Coupling of UV and MS Detectors
Posters | 2019 | Thermo Fisher Scientific | PittconInstrumentation
Quality control of synthetic biomolecules, including peptides and oligonucleotides, is essential for ensuring product purity, safety, and efficacy in pharmaceutical and biotechnology applications. Rapid analytical techniques that combine high-performance liquid chromatography with ultraviolet and mass spectrometric detection streamline impurity profiling and identity confirmation, supporting timely decision-making in research and manufacturing environments.
This work demonstrates a fast, integrated LC-UV-MS workflow for quality control of the human antimicrobial peptide LL-37 and several DNA oligomers. The goals were to achieve baseline separation of product and related impurities within minutes, to confirm component identities by accurate mass measurement, and to establish robust quantitative calibration for routine analysis.
Sample preparation involved 1 mg/mL peptide solutions in water+0.1% formic acid, spiked with LL-37 fragments at defined concentrations. DNA oligomers (29–40 mers) were reconstituted to 100 µM and diluted as required. Chromatographic conditions for peptides used an Acclaim 120 C18 column (50×2.1 mm, 2.2 µm), a 2 min gradient at 0.5 mL/min, UV detection at 214 nm, and positive-ion full-scan MS. Oligo analysis used a DNAPac RP column (2.1×10 mm, 4 µm), 15 min gradient, UV at 260 nm, and negative-ion MS. Key MS settings included HESI source, sheath gas ~50 psig, ion transfer tube 300 °C, and full-scan acquisition (m/z 500–2000).
Rapid peptide impurity profiling achieved baseline resolution of LL-37 and two synthetic fragments in under 2 min. Mass spectra enabled unambiguous peak assignment by matching observed charge-state distributions to theoretical masses, which would not be possible with UV alone. For DNA oligomers, UV calibration at 260 nm showed linearity from 0.05 to 50 µM. Mass confirmation of 29, 31, 37, and 40 mers delivered accuracy within ±0.1 Da and repeatability (%RSD ≤0.02%) across multiple injections. Extending column equilibration from 1 to 4.5 min improved peak area precision from 15.4% to 8.1% RSD when using ion-pair reagents.
Integration of fast LC-UV-MS methods into automated production lines could further reduce turnaround time for batch release testing. Advances in data-processing software may enable real-time identification of unknown impurities. Expansion of the approach to modified or conjugated biomolecules (e.g., peptides with PEGylation or nucleic acid therapeutics) will meet rising demands in drug development and personalized medicine.
The combination of rapid UHPLC separations, UV detection, and single-quadrupole MS provides a powerful, user-friendly platform for routine quality control of synthetic biomolecules. The method delivers fast impurity profiling, accurate mass confirmation, and reliable quantification, supporting efficient workflows in research and manufacturing laboratories.
1. Yufei Chen, Sidi Yang, Emmanuel A. Ho. Rapid Quantitation of Peptides Used in Microbicide Formulations. Chromatographia. 77(23-24), 1713–1720 (2014).
2. Thermo Fisher Scientific. Application note 72818: Impurity profiling of the synthetic peptide LL-37 using high-performance liquid chromatography with combined UV and single quadrupole mass spectrometric detection.
3. Thermo Fisher Scientific. Application note 72820: Oligonucleotide characterization for quality control and increased productivity by single quadrupole mass spectrometer with extended mass range.
HPLC, LC/MS, LC/SQ
IndustriesPharma & Biopharma
ManufacturerThermo Fisher Scientific
Summary
Significance of the Topic
Quality control of synthetic biomolecules, including peptides and oligonucleotides, is essential for ensuring product purity, safety, and efficacy in pharmaceutical and biotechnology applications. Rapid analytical techniques that combine high-performance liquid chromatography with ultraviolet and mass spectrometric detection streamline impurity profiling and identity confirmation, supporting timely decision-making in research and manufacturing environments.
Objectives and Study Overview
This work demonstrates a fast, integrated LC-UV-MS workflow for quality control of the human antimicrobial peptide LL-37 and several DNA oligomers. The goals were to achieve baseline separation of product and related impurities within minutes, to confirm component identities by accurate mass measurement, and to establish robust quantitative calibration for routine analysis.
Used Instrumentation
- Vanquish Flex Binary UHPLC system
- Thermo Scientific ISQ EM single quadrupole mass spectrometer (m/z 50–2000)
- Variable wavelength UV detector
- Chromeleon 7.2.9 chromatography data system with Autospray smart method setup
Methodology
Sample preparation involved 1 mg/mL peptide solutions in water+0.1% formic acid, spiked with LL-37 fragments at defined concentrations. DNA oligomers (29–40 mers) were reconstituted to 100 µM and diluted as required. Chromatographic conditions for peptides used an Acclaim 120 C18 column (50×2.1 mm, 2.2 µm), a 2 min gradient at 0.5 mL/min, UV detection at 214 nm, and positive-ion full-scan MS. Oligo analysis used a DNAPac RP column (2.1×10 mm, 4 µm), 15 min gradient, UV at 260 nm, and negative-ion MS. Key MS settings included HESI source, sheath gas ~50 psig, ion transfer tube 300 °C, and full-scan acquisition (m/z 500–2000).
Results and Discussion
Rapid peptide impurity profiling achieved baseline resolution of LL-37 and two synthetic fragments in under 2 min. Mass spectra enabled unambiguous peak assignment by matching observed charge-state distributions to theoretical masses, which would not be possible with UV alone. For DNA oligomers, UV calibration at 260 nm showed linearity from 0.05 to 50 µM. Mass confirmation of 29, 31, 37, and 40 mers delivered accuracy within ±0.1 Da and repeatability (%RSD ≤0.02%) across multiple injections. Extending column equilibration from 1 to 4.5 min improved peak area precision from 15.4% to 8.1% RSD when using ion-pair reagents.
Benefits and Practical Applications
- Accelerated QC workflows with sub-2 min impurity profiling for peptides
- Mass-based identity confirmation and impurity detection without additional experiments
- Extended mass range allowing detection of multiple charge states of mid-sized biomolecules
- Robust performance under challenging ion-pairing conditions with minimal cleaning
Future Trends and Potential Applications
Integration of fast LC-UV-MS methods into automated production lines could further reduce turnaround time for batch release testing. Advances in data-processing software may enable real-time identification of unknown impurities. Expansion of the approach to modified or conjugated biomolecules (e.g., peptides with PEGylation or nucleic acid therapeutics) will meet rising demands in drug development and personalized medicine.
Conclusion
The combination of rapid UHPLC separations, UV detection, and single-quadrupole MS provides a powerful, user-friendly platform for routine quality control of synthetic biomolecules. The method delivers fast impurity profiling, accurate mass confirmation, and reliable quantification, supporting efficient workflows in research and manufacturing laboratories.
References
1. Yufei Chen, Sidi Yang, Emmanuel A. Ho. Rapid Quantitation of Peptides Used in Microbicide Formulations. Chromatographia. 77(23-24), 1713–1720 (2014).
2. Thermo Fisher Scientific. Application note 72818: Impurity profiling of the synthetic peptide LL-37 using high-performance liquid chromatography with combined UV and single quadrupole mass spectrometric detection.
3. Thermo Fisher Scientific. Application note 72820: Oligonucleotide characterization for quality control and increased productivity by single quadrupole mass spectrometer with extended mass range.
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