Enhancing Selectivity in Reversed-Phase Analysis Through Effective Utilization of Mobile Phase pH
Technical notes | 2025 | ShimadzuInstrumentation
The pH of the mobile phase critically influences ionization states of analytes in reversed-phase liquid chromatography. Proper pH control enhances peak shape, retention, and selectivity, while minimizing undesirable interactions with silanol sites. Recent advances in column chemistry extend usable pH ranges, enabling robust separation of acidic, neutral and basic compounds under both acidic and alkaline conditions.
This report evaluates the performance of two organic–silica hybrid columns (Shim-pack Scepter and Shim-pack NovaCore) across a wide pH spectrum. It aims to demonstrate their high-pH durability, improved selectivity through pH adjustment, and compatibility with LC-MS/MS applications.
The study employed continuous high-pH mobile phase flow tests, retention experiments for model acidic (naproxen), neutral (butyrophenone) and basic (amitriptyline) compounds across pH 2.5–10.1, and application examples under acidic and alkaline gradients. Performance metrics included theoretical plate count, peak shape, retention time shifts, and reproducibility.
Continuous exposure to pH 11.5 mobile phase showed that both hybrid columns maintained plate counts (>80 % of initial) over 400 h, outperforming a conventional silica column. Ionization studies confirmed that adjusting pH relative to analyte pKa effectively controls retention and peak symmetry: acidic compounds eluted faster at higher pH, while basic compounds exhibited stronger retention in alkaline media. Application examples under acidic conditions provided sharp peaks for antihistamines and mixed compound mixtures, whereas alkaline gradients on NovaCore columns enabled efficient separation of β-blockers with clear resolution and reduced analysis time.
Ongoing development of organic-inorganic hybrid and core-shell materials will further improve high-pH stability, speed, and resolution. Integration with ultra-high-performance systems and automated method scouting platforms will streamline method development for complex matrices. Emerging areas include biotherapeutic analysis, metabolomics profiling, and green chromatography employing lower organic solvent consumption.
Organic–silica hybrid columns such as Shim-pack Scepter and NovaCore deliver robust performance across a broad pH range, enabling superior selectivity and durability compared to traditional silica or polymer columns. Their compatibility with LC-MS/MS and high-speed separations makes them versatile tools for modern analytical challenges.
Consumables, LC columns
IndustriesOther
ManufacturerShimadzu
Summary
Significance of the Topic
The pH of the mobile phase critically influences ionization states of analytes in reversed-phase liquid chromatography. Proper pH control enhances peak shape, retention, and selectivity, while minimizing undesirable interactions with silanol sites. Recent advances in column chemistry extend usable pH ranges, enabling robust separation of acidic, neutral and basic compounds under both acidic and alkaline conditions.
Objectives and Study Overview
This report evaluates the performance of two organic–silica hybrid columns (Shim-pack Scepter and Shim-pack NovaCore) across a wide pH spectrum. It aims to demonstrate their high-pH durability, improved selectivity through pH adjustment, and compatibility with LC-MS/MS applications.
Methodology
The study employed continuous high-pH mobile phase flow tests, retention experiments for model acidic (naproxen), neutral (butyrophenone) and basic (amitriptyline) compounds across pH 2.5–10.1, and application examples under acidic and alkaline gradients. Performance metrics included theoretical plate count, peak shape, retention time shifts, and reproducibility.
Instrumentation Used
- Shimadzu HPLC systems equipped with Shim-pack Scepter C18-120 and Shim-pack NovaCore C18-HB columns
- Mobile phases: buffers (formic, acetate, phosphate, carbonate) adjusted to pH 2.5–11.5 with organic modifiers (acetonitrile, methanol)
- UV detection at 230 nm or 254 nm; MS-compatible volatile buffers evaluated
Main Results and Discussion
Continuous exposure to pH 11.5 mobile phase showed that both hybrid columns maintained plate counts (>80 % of initial) over 400 h, outperforming a conventional silica column. Ionization studies confirmed that adjusting pH relative to analyte pKa effectively controls retention and peak symmetry: acidic compounds eluted faster at higher pH, while basic compounds exhibited stronger retention in alkaline media. Application examples under acidic conditions provided sharp peaks for antihistamines and mixed compound mixtures, whereas alkaline gradients on NovaCore columns enabled efficient separation of β-blockers with clear resolution and reduced analysis time.
Benefits and Practical Applications
- Extended pH range (1–12) allows method flexibility from strongly acidic to alkaline conditions
- Enhanced selectivity by tuning ionization state for acidic, neutral and basic analytes
- High mechanical strength and reproducibility support prolonged use with harsh mobile phases
- Compatibility with LC-MS/MS using volatile buffers facilitates bioanalytical and pharmaceutical workflows
Future Trends and Potential Applications
Ongoing development of organic-inorganic hybrid and core-shell materials will further improve high-pH stability, speed, and resolution. Integration with ultra-high-performance systems and automated method scouting platforms will streamline method development for complex matrices. Emerging areas include biotherapeutic analysis, metabolomics profiling, and green chromatography employing lower organic solvent consumption.
Conclusion
Organic–silica hybrid columns such as Shim-pack Scepter and NovaCore deliver robust performance across a broad pH range, enabling superior selectivity and durability compared to traditional silica or polymer columns. Their compatibility with LC-MS/MS and high-speed separations makes them versatile tools for modern analytical challenges.
References
- Snyder LR, Kirkland JJ, Glajch JL. Practical HPLC Method Development. Wiley-Interscience; 1997.
- Bradshaw TP. Introduction to Protein and Peptide HPLC. Phenomenex; 1998.
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