| NUCLEODUR® HILIC · NUCLEOSHELL HILIC |
Separation science is always looking for new and effective strategies to accomplish the tasks of modern analytics. Especially for polar compounds reversed phase HPLC – the most common analytical method – is often limited. Here, hydrophilic stationary phases provide an additional tool for the separation of polar analytes in HPLC.
The expression HILIC (Hydrophilic Interaction Chromatography) was firstly published by Andrew Alpert in 1990 – since then it took quite some efforts to develop robust and reproducible hydrophilic HPLC phases for HILIC chromatography [A. Alpert, J. Chromatography 499 (1990), 177–196]. |
| HILIC combines the characteristics of the 3 major methods in liquid chromatography – reversed phase (RPC), normal phase (NPC) and ion chromatography (IC): |
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Stationary phases (adsorbents) are mostly polar modifications of silica or polymers (SiOH, Amino, Diol, (zwitter) ions, …) – like in NPC.
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Mobile phases (eluents) are mixtures of aqueous buffer systems and organic modifiers like acetonitrile or methanol – like in RPC.
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Fields of application include quite polar compounds as well as organic and inorganic ions – like in IC.
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| ”HILIC is NP chromatography of polar and ionic compounds under RP conditions.” |
| NUCLEODUR® HILIC and NUCLEOSHELL HILIC are special zwitterionic modified stationary phases based on ultra spherical NUCLEODUR® particles and core-shell NUCLEOSHELL particles, respectively. The betaine character of the ammonium-sulfonic acid ligands results in total charge equalization and in an overall neutrally charged but highly polar surface. |
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| Retention characteristics |
Commonly HILIC is described as partition chromatography or liquid/liquid extraction system between the mobile and stationary phase. Versus a water-poor layer of mobile phase a water-rich layer on the surface of the polar stationary phase is formed. Thus, a distribution of the analytes between these two layers will occur.
Furthermore HILIC includes weak electrostatic mechanisms as well as hydrogen donor interactions between neutral polar molecules under high organic elution conditions. This distinguishes HILIC from ion exchange chromatography - main principle for HILIC separation is based on compound’s polarity and degree of solvation.
More polar compounds will have stronger interaction with the stationary aqueous layer than less polar compounds – resulting in a stronger retention.
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Nonpolar compounds exhibit faster elution profiles due to minor hydrophobic interactions. Thus, as shown for the separation of uracil and naphthalene the elution order is quite often inverse on HILIC columns compared to RP columns.
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| Stability features |
Due to an advanced and unique surface modification procedure (pat. pend.) NUCLEODUR® and NUCLEOSHELL HILIC columns provide short equilibration times – after just 5 min equilibration already the 2nd injection shows stable and reproducible results.
Beyond this, NUCLEODUR® and NUCLEOSHELL HILIC columns are characterized by an outstanding column life time – even after nearly 800 runs the columns show no loss of pristine performance – peak shape and retention are still immaculate. |
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| Fields of application of HILIC phases |
Due to its high loadability NUCLEODUR® HILIC is also absolutely suitable for preparative and semi-preparative applications, while NUCLEOSHELL HILIC is recommended for rapid high-efficiency analytical separations.
Based on their special interaction and retention features HILIC columns are ideal for analysis of medium-polar and polar compounds, especially since this group of substances is gaining an increasing interest.
The examples below show separations on NUCLEODUR®
HILIC. Many of the separations have also been run on NUCLEOSHELL HILIC. These examples as well as further applications for both phases can be found in our application data base.
Determinations of polar compounds in food, such as melamine in milk or acrylamide in bakery products as well as separations of vitamins and organic acids in foodstuff and pharmaceutical products are efficiently performed on HILIC columns.
Stable and effective application notes were developed on NUCLEODUR® HILIC also for pharmaceutical and physiological substances, like the chemotherapeutic agent 5-fluorouracil, the energy carrier of muscle metabolism creatine, of catecholamines and amino acids.
In bioanalysis nucleotides, as well as pyrimidine and purine bases can be determinated efficiently.
In comparison with medium polar aminopropyl phases or modification with less balanced charge equalization NUCLEODUR®
HILIC and NUCLEOSHELL HILIC show superb separation and peak shape for
critical compounds like adenosine and its phosphate derivatives.
Because well-biodegradable, but more and more polar pesticides have to be analyzed, the determination of chlormequat, mepiquat, paraquat and diquat gains increasing importance.
Determinations of hydrocarbons, peptides and glycolised or phosphorylized compounds are other successful applications of HILIC phases. |
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| Advantages of NUCLEODUR® HILIC and NUCLEOSHELL HILIC |
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NUCLEODUR® HILIC and NUCLEOSHELL HILIC are outstandingly suited for the chromatography of medium-polar, polar and ionic compounds.
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They stand out due to short equilibration time and good lifetime.
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Besides the established detection systems UV and fluorescence an application with highly sensitive LC-MS, LC-MS/MS and light scattering detectors is possible.
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They are the alternative to RP-18 and further RP phases, to NP and ion exchanger phases for a reliable analysis. |