SHARC HPLC columns separate by hydrogen bonding.
SHARC HPLC Columns Separation Mechanism
SHARC columns are the first commercially available columns with separation based primarily on hydrogen bonding. SHARC stands for Specific Hydrogen-bond Adsorption Resolution Chromatography.
Hydrogen bonding is an interaction between hydrogen atom bound to electronegative atoms in a molecule, such as oxygen, nitrogen, fluorine. This is typically a weak interaction, especially when separation is performed in aqueous solutions. Liquid chromatography techniques evolved as tool for separation of different molecules based on their physico-chemical properties.
Most common techniques of the separation are:
• Hydrophobic separation based on degree of hydrophobicity of the molecule
• Ion-exchange separation based on number, nature, and distribution of charges in the molecule.
• Normal phase separation based on hydrophilic properties of the molecules including molecule dipoles value and dipoles position
• Size exclusion separation (SEC) based on molecule size and shape
Stationary phases based on these techniques never perform purely with one type of interaction. Hydrogen bonding is omnipresent in every one of these techniques with minor contribution to retention and selectivity. However, in some cases, especially in normal phase chromatography, the contribution of hydrogen bonding can be significant.
Why should I buy Shark HPLC Columns?
SHARC 1 is the first column specifically design to perform a separation based entirely on the interaction of the molecules capable providing hydrogen atom (donor) or attract hydrogen atom (acceptor) to the stationary phase with special properties.
SHARC 1 column operation conditions are unique. A mixture of acetonitrile (MeCN), a weak solvent, and methanol (MeOH), a strong solvent, are used as the mobile phase. Pure MeCN has very insignificant amount of hydrogen bonding with the SHARC stationary phase, while MeOH interacts strongly with SHARC stationary phase, which reduces the retention of analytes based on it’s capacity to hydrogen bond. By changing ratio of MeCN/MeOH the optimum retention profile can be obtained for many types of molecules with high selectivity, peak shape, efficiency, and speed.
Hydrogen bonding interaction H bonding chromatography
Surface interaction within the column with hydrogen bonding capable analytes with acetonitrile as the mobile phase. Surface interaction within the column with hydrogen bonding capable analytes with methanol as the mobile phase.
Hydrogen bonding energy is usually in range of 30 kJ/mol or less and depends strongly on the nature of the functional groups and their orientation within the molecule. This energy difference is the basis for selectivity of the interaction between the stationary phase and the molecule of different structure and chemical characteristics.
A given molecule can retain on the stationary phase with more than one hydrogen bond, while also performing as a donor or acceptor of a hydrogen atom.
Analytes can be retained on the stationary phase by more than one hydrogen bond and act as a donor or acceptor of the stationary phase hydrogen atom. Retention, therefore, strongly depends on the chemical nature of the stationary phase surface.
The presence of a polarized hydrogen atom is not always enough to gain retention by hydrogen bonding mechanisms. An analyte may form intramolecular as opposed to intermolecular hydrogen bonds which preclude the stationary phase interaction.
The SHARC 1 column is a hydrogen atom acceptor type stationary phase showing increased retention toward molecules with higher numbers of polar X-H bonds such as alcohols, amines, acids, amides, phenols etc.
Presence of a polarized hydrogen atom is not always enough to observe retention by hydrogen bond mechanism. Sometimes a compound can form intramolecular interactions, as oppose to intermolecular hydrogen bonding, and does not participate in stationary phase interaction.
SHARC 1 column is a hydrogen acceptor type stationary phase showing higher retention characteristics toward molecules with higher number of polar X-H bonds such as alcohols, amines, acids, amides, phenols etc.
Advantages of SHARC HPLC Columns
MeCN/MeOH mixture has 2-3 times lower viscosity than water/MeOH or water/MeCN mixture (fig. 5). As result smaller particles for column packing can be used without increasing the working pressure. UPLC-like conditions can be easily obtained on regular HPLC instrument with 2-3 times higher velocity with a shorter column with small particles. This can increase the speed of analysis up to 5 times. Using UPLC (RRLC, UHPLC) equipment allows to increase speed of analysis by another factor of 5 or 6.
MeOH is one of the most universal solvent for organic compounds. Combination of MeOH with MeCN allows to dissolve almost any molecules with high or low polarity. Hydrophobic molecules such as surfactants, lipids, and oil soluble vitamins, are soluble in this solvent combination. Very polar molecules such as sugars, di-ols, salts of amino compounds, carboxylic acids also dissolve in this solvent system.
Since hydrogen bonds formation is very specific in the interaction energy and strongly depends on molecule geometry, number of functional groups and the position of the functional groups, the selectivity of resolution of molecule of similar nature such as isomers, related impurities, product of oxidation or reduction can be achieved with SHARC separation very efficiently.
MeCN/MeOH mixture has low boiling point and much easier to evaporate than water. As result this solvent system is much friendlier for preparative type chromatography. The additional benefit of low viscosity allows SHARC to perform prep separation with higher throughput. This mobile system is MS friendly and allows implementation of MS-driven sample collection. In most cases isocratic method can be used due to high selectivity of the column which allows to recycle most of the mobile phase minimizing solvent consumption.
WIDE RANGE OF COMPOUNDS
Wide range of molecules can be analyzed with SHARC technique. Practically any molecule with functional group which contains oxygen and nitrogen can be retained and separate from similar compounds in this technology. Hydrocarbons is one class of compounds that will be retained poorly in this system, but they are typically well separated in reverse phase HPLC or GC.
Hydrogen-bonding interaction offers unique selectivity based on number of “interaction points” available for hydrogen bonding. One of the useful characteristics to determine retention patterns in hydrogen-bonding mode is the molecular polar surface area (PSA). This calculated parameter is usually used for prediction of drug transport properties, but we successfully applied it to hydrogen-bonding interactions. Polar surface area is defined as a sum of surfaces of polar atoms (usually oxygens, nitrogens and attached hydrogens) in a molecule. Since those polar atoms can participate in hydrogen-bonding interaction, estimation of elution order can often be made based on PSA. While PSA is a good indicator of elution time, it must be noted that polar surface area does not account for the accessibility of hydrogen-interaction sites. Not every polar surface participates in intermolecular hydrogen interactions with the stationary phase.
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