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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Development and validation of SEC-UV/HRMS procedure for simultaneous determination of BSA and its association products</dc:title><dc:creator>Hodnik,	Blaž	(Avtor)
	</dc:creator><dc:creator>Čamič,	Žiga	(Avtor)
	</dc:creator><dc:creator>Pompe,	Matevž	(Avtor)
	</dc:creator><dc:subject>size exclusion chromatography</dc:subject><dc:subject>proteins</dc:subject><dc:subject>high-resolution mass spectrometry</dc:subject><dc:description>Monitoring peptide and protein self-association is essential for understanding biological function, formulation stability, and aggregation mechanisms. While size-exclusion chromatography (SEC) is routinely used to quantify protein-size variants under native conditions, its hyphenation to high-resolution mass spectrometry (HRMS) for simultaneous structural characterization remains limited. Here, we report the development and validation of a robust SEC-UV/HRMS method optimized for native-like analysis of bovine serum albumin (BSA) monomers and higher-order oligomers using standard-flow electrospray ionization. Systematic evaluation of source parameters, mobile-phase composition, and chromatographic conditions enabled retention of native BSA structure, minimized in-source unfolding, and enhanced MS sensitivity, allowing detection of oligomers up to the heptamer. A short, narrow-bore 200 Å UHPLC SEC separation column was used. Low-flow separations (~0.05 mL/min) enabled efficient ionization and 10 min run times. An accelerated 60 °C stress-testing protocol demonstrated that SEC-MS can semi-quantitatively monitor oligomerization dynamics, complementing UV-based quantification and revealing transient species not resolved by UV alone. The method showed acceptable linearity, precision, and sample stability, and comparison with SEC-RALS/LALS confirmed molecular-weight trends across aggregation states. Overall, the developed SEC-UV/HRMS workflow provides a rapid, sensitive, and widely accessible approach for UV-based quantification of monomer- and HRMS-based characterizing protein aggregation in research and quality control in pharmaceutical laboratories.</dc:description><dc:date>2026</dc:date><dc:date>2026-03-20 12:11:44</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>180956</dc:identifier><dc:identifier>UDK: 543.544:543.51</dc:identifier><dc:identifier>ISSN pri članku: 1420-3049</dc:identifier><dc:identifier>DOI: 10.3390/molecules31061001</dc:identifier><dc:identifier>COBISS_ID: 272258051</dc:identifier><dc:language>sl</dc:language></metadata>
