Primesep - Separation of Ions
Brochures and specifications | 2004 | SIELCInstrumentation
Ion chromatography is widely used for inorganic and charged organic species but requires specialized equipment, aqueous-only mobile phases, multiple dilution/cleanup steps and cannot simultaneously analyze neutral analytes or both anions and cations in one run. Mixed-mode HPLC expands analytical capabilities by combining hydrophobic and ion-exchange interactions on the same stationary phase.
This work introduces PrimesepTM mixed-mode stationary phases as a versatile alternative to classical ion chromatography. It demonstrates simultaneous separation of inorganic ions and organic counter-ions or polar molecules in a single HPLC method without ion-pairing reagents, using standard reversed-phase equipment augmented with an evaporative light scattering detector (ELSD).
Primesep columns (A, 100, 200, 300 for cation exchange; B for anion exchange; C for complexation; SWITCH for pH-dependent behavior) were paired with mobile phases composed of water, acetonitrile or methanol and acidic or buffering modifiers (trifluoroacetic, acetic, formic acids; ammonium acetate/formate; triethylamine acetate). Analyses employed standard HPLC pumps, Primesep columns (dimensions 50–250 × 4.6 mm, particle sizes 5–10 µm), ELSD and optional UV detection. Retention was tuned via organic modifier ratio, acid concentration and mobile phase pH.
• Simultaneous separation of organic drug molecules and their inorganic counter-ions (Na+, K+, Zn2+, Ni2+) in a single run with ELSD quantitation.
• Effective retention of highly polar species—including underivatized amino acids, glycine derivatives, pheromones, glyphosate, quaternary amines—without ion-pair reagents.
• Rapid column re-equilibration (2–3 column volumes) using acid gradients.
• Unique selectivity: Primesep C reverses classical ion-exchange elution orders (e.g., tertiary to primary amines; K+ < Na+ < Li+), controlled by pH in the 3–7 range.
• High peak symmetry and efficiency compared to conventional C18 or dedicated ion-exchange columns.
Advances may include tailored mixed-mode phases for complex biological and environmental matrices, high-throughput screening, deeper integration with mass spectrometry for trace analysis and the design of next-generation pH-switchable and selective hosting phases for targeted ion separations.
PrimesepTM mixed-mode HPLC combined with ELSD provides a versatile, cost-effective alternative to traditional ion chromatography and reversed-phase methods. It enables one-step analysis of diverse polar and hydrophobic, organic and inorganic species using standard equipment and simple, MS-compatible mobile phases.
Ion chromatography, Consumables, LC columns
IndustriesOther
ManufacturerSIELC
Summary
PrimesepTM Mixed-Mode HPLC as an Alternative to Ion Chromatography
Importance of the Topic
Ion chromatography is widely used for inorganic and charged organic species but requires specialized equipment, aqueous-only mobile phases, multiple dilution/cleanup steps and cannot simultaneously analyze neutral analytes or both anions and cations in one run. Mixed-mode HPLC expands analytical capabilities by combining hydrophobic and ion-exchange interactions on the same stationary phase.
Study Objectives and Overview
This work introduces PrimesepTM mixed-mode stationary phases as a versatile alternative to classical ion chromatography. It demonstrates simultaneous separation of inorganic ions and organic counter-ions or polar molecules in a single HPLC method without ion-pairing reagents, using standard reversed-phase equipment augmented with an evaporative light scattering detector (ELSD).
Methodology and Instrumentation
Primesep columns (A, 100, 200, 300 for cation exchange; B for anion exchange; C for complexation; SWITCH for pH-dependent behavior) were paired with mobile phases composed of water, acetonitrile or methanol and acidic or buffering modifiers (trifluoroacetic, acetic, formic acids; ammonium acetate/formate; triethylamine acetate). Analyses employed standard HPLC pumps, Primesep columns (dimensions 50–250 × 4.6 mm, particle sizes 5–10 µm), ELSD and optional UV detection. Retention was tuned via organic modifier ratio, acid concentration and mobile phase pH.
Main Findings and Discussion
• Simultaneous separation of organic drug molecules and their inorganic counter-ions (Na+, K+, Zn2+, Ni2+) in a single run with ELSD quantitation.
• Effective retention of highly polar species—including underivatized amino acids, glycine derivatives, pheromones, glyphosate, quaternary amines—without ion-pair reagents.
• Rapid column re-equilibration (2–3 column volumes) using acid gradients.
• Unique selectivity: Primesep C reverses classical ion-exchange elution orders (e.g., tertiary to primary amines; K+ < Na+ < Li+), controlled by pH in the 3–7 range.
• High peak symmetry and efficiency compared to conventional C18 or dedicated ion-exchange columns.
Benefits and Practical Applications
- Direct injection of complex samples without dilution or cleanup.
- Compatibility with standard HPLC systems and multiple detectors (ELSD, UV, MS).
- No need for separate ion chromatography instruments or mobile phase ion-pairing additives.
- Broad solvent compatibility supports simultaneous analysis of neutral, charged organic and inorganic analytes.
- Flexible method development by tuning pH and organic composition.
- Suits analytical and preparative scales in pharmaceutical, environmental, food and industrial quality control.
Future Trends and Applications
Advances may include tailored mixed-mode phases for complex biological and environmental matrices, high-throughput screening, deeper integration with mass spectrometry for trace analysis and the design of next-generation pH-switchable and selective hosting phases for targeted ion separations.
Conclusion
PrimesepTM mixed-mode HPLC combined with ELSD provides a versatile, cost-effective alternative to traditional ion chromatography and reversed-phase methods. It enables one-step analysis of diverse polar and hydrophobic, organic and inorganic species using standard equipment and simple, MS-compatible mobile phases.
References
- No references were cited in the original text.
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