HPLC COLUMN
Contents:
1. Ion Exchange Column
2. Ion Chromatography Column
2.1 Suppressor Type Ion Chromatography Column
2.2 Non-Suppressor Type Ion Chromatography Column
2.3 Other Columns
3. Ion Exclusion Column
4. Ligand Exchange Column
5. Affinity Column
6. Chiral Column
7. Preparative Size Column
8. Guard Column
2. Ion Chromatography Column
2.1 Suppressor Type Ion Chromatography Column
2.2 Non-Suppressor Type Ion Chromatography Column
2.3 Other Columns
3. Ion Exclusion Column
4. Ligand Exchange Column
5. Affinity Column
6. Chiral Column
7. Preparative Size Column
8. Guard Column
1. Ion Exchange Column
The N and S ends on the magnet attract each other while N and N or S and S ends will repeal each other. The similar phenomenon occurs for electronics: Positive charge and negative charge attract each other while positive and positive or negative and negative charges repeal each other. When compounds dissociate and become ions, they will have electronic charges. Positive ion is called cation and negative ion is called anion.
Ion exchange mode uses ionic attraction and repulsion forces. What is different from magnet is that N end of magnet is always N, but molecular ion like protein can be an anion or a cation depending on the surrounding conditions (mobile phase). By changing the electronic characteristics of the mobile phase, the electronic charge of each component in the sample also changes. They may change from cation to anion (or vice versa) and this creates the interaction between the component and the packed gel. One time it may cause attraction and other time it may cause repulsion. Since the components that experience repulsion will be eluted out (and attraction causes retention) from the column, each component is separated based on their ionic strengths.
It is common to change the mobile phase during an analysis for ion exchange mode. Such method (changing mobile phase) is called gradient method. Most frequent method used for gradient elution is to prepare two mobile phases and change the ratio of two solvents over a time. Contrast to gradient method, the method uses single solvent throughout the run is called isocratic method.
Packed gel for ion exchange column is modified with either anion or cation functional groups. Commonly used functional groups are followings.
The N and S ends on the magnet attract each other while N and N or S and S ends will repeal each other. The similar phenomenon occurs for electronics: Positive charge and negative charge attract each other while positive and positive or negative and negative charges repeal each other. When compounds dissociate and become ions, they will have electronic charges. Positive ion is called cation and negative ion is called anion.
Ion exchange mode uses ionic attraction and repulsion forces. What is different from magnet is that N end of magnet is always N, but molecular ion like protein can be an anion or a cation depending on the surrounding conditions (mobile phase). By changing the electronic characteristics of the mobile phase, the electronic charge of each component in the sample also changes. They may change from cation to anion (or vice versa) and this creates the interaction between the component and the packed gel. One time it may cause attraction and other time it may cause repulsion. Since the components that experience repulsion will be eluted out (and attraction causes retention) from the column, each component is separated based on their ionic strengths.
It is common to change the mobile phase during an analysis for ion exchange mode. Such method (changing mobile phase) is called gradient method. Most frequent method used for gradient elution is to prepare two mobile phases and change the ratio of two solvents over a time. Contrast to gradient method, the method uses single solvent throughout the run is called isocratic method.
Packed gel for ion exchange column is modified with either anion or cation functional groups. Commonly used functional groups are followings.
Quaternary ammonium (QA) : Strong anion exchanger
Diethyl aminoethyl (DEAE) : Weak anion exchanger
Sulfopropyl (SP) : Strong cation exchanger
Carboxylmethyl (CM) : Weak cation exchanger
Gels generally used are porous gel
(having pores on the surface). However for the ion-exchange gel, small-sized
gel (2.0-2.5 um) without pores is sometimes used. Gels without pores are called
non-porous gel and it is effective for fast analysis. Both polymer-based and
silica-based columns are used for ion-exchange columns. Though unlike RP
columns that mainly uses silica base, ion-exchange columns requires use of
alkali conditions sometimes, so importance of polymer-based materials is higher
with ion-exchange columns than RP columns. Ion exchange is frequently used in
biochemistry area such as separation of protein, peptide, and nucleic acids.
2. Ion Chromatography Column
There are two types of Ion Chromatography methods: The suppressor method and non-suppressor method. Shodex carries columns suitable for both types. As the name tells, the suppressor method uses a suppressor which removes ions that interfere with analytes measurement. The suppressor system is expensive, but some say the sensitivity of suppressor method is superior to non-suppressor method. In contrast, system required for non-suppressor method is cheaper, but the useable solvent is limited to the ones with low conductivity such as phthalic acid.
2.1 Suppressor Type Ion Chromatography Column
Shodex IC SI-90 and SI-50 are the suppressor type anion chromatography columns. SI-50 is the higher performance type of SI-90. SI-52 is another suppressor type column suitable for the separation of oxyhalides.
2.2 Non-Suppressor Type Ion Chromatography Column
Shodex IC I-524A and NI-424 are the non-suppressor type anion chromatography columns. NI-424 is the higher performance type of I-524A. Shodex IC YK-421 and YS-50 are the non-suppressor type cation chromatography columns. YS-50 is the higher performance type of YK-421. They can separate both monovalent and divarent cations simultaneously.
2.3 Other Columns
There are other columns available for specific applications, such as for separation of transition metal and rare earth metal ions.
There are two types of Ion Chromatography methods: The suppressor method and non-suppressor method. Shodex carries columns suitable for both types. As the name tells, the suppressor method uses a suppressor which removes ions that interfere with analytes measurement. The suppressor system is expensive, but some say the sensitivity of suppressor method is superior to non-suppressor method. In contrast, system required for non-suppressor method is cheaper, but the useable solvent is limited to the ones with low conductivity such as phthalic acid.
2.1 Suppressor Type Ion Chromatography Column
Shodex IC SI-90 and SI-50 are the suppressor type anion chromatography columns. SI-50 is the higher performance type of SI-90. SI-52 is another suppressor type column suitable for the separation of oxyhalides.
2.2 Non-Suppressor Type Ion Chromatography Column
Shodex IC I-524A and NI-424 are the non-suppressor type anion chromatography columns. NI-424 is the higher performance type of I-524A. Shodex IC YK-421 and YS-50 are the non-suppressor type cation chromatography columns. YS-50 is the higher performance type of YK-421. They can separate both monovalent and divarent cations simultaneously.
2.3 Other Columns
There are other columns available for specific applications, such as for separation of transition metal and rare earth metal ions.
3. Ion Exclusion Column
Compared to ion-exchange column that uses attractive force between anion and cation, ion-exclusion mode uses repulsive force between the anion of analyte and packed gel. Ion-exclusion mode is not use solely: Generally it is a fine balance used with other separation modes such as partition/adsorption mode. For an example, partition/adsorption mode will work to retain the analyte while ion-exclusion will try to exclude analytes. Ion-exclusion mode is often used for organic acid analysis.
Compared to ion-exchange column that uses attractive force between anion and cation, ion-exclusion mode uses repulsive force between the anion of analyte and packed gel. Ion-exclusion mode is not use solely: Generally it is a fine balance used with other separation modes such as partition/adsorption mode. For an example, partition/adsorption mode will work to retain the analyte while ion-exclusion will try to exclude analytes. Ion-exclusion mode is often used for organic acid analysis.
4. Ligand Exchange Column
The packed gel used for a ligand-exchange column is modified with substances with ionic functional group. The modifier contains metal cation, which is called "counter ion". The ligand exchange mode is often used for the separation of saccharides using the interaction between positive charge of metal cation and negative charge of hydroxyl group (OH-) on saccharide. The number of OH- as well as their configurations influences the strength of interaction. Counter ions used include calcium, lead, zinc, and sodium. Often the separation works under combinations of size exclusion and ligand exchange and partition/adsorption and ligand exchange modes.
The packed gel used for a ligand-exchange column is modified with substances with ionic functional group. The modifier contains metal cation, which is called "counter ion". The ligand exchange mode is often used for the separation of saccharides using the interaction between positive charge of metal cation and negative charge of hydroxyl group (OH-) on saccharide. The number of OH- as well as their configurations influences the strength of interaction. Counter ions used include calcium, lead, zinc, and sodium. Often the separation works under combinations of size exclusion and ligand exchange and partition/adsorption and ligand exchange modes.
5. Affinity Columns
The separation mode of affinity column is different from other separation modes explained earlier. The packed gel is modified with so called ligands – similar to the functional groups. The ligand captures only a specific compound. It is similar to key and lock: Among many keys, only one specific key can open the lock. When sample containing mixed components is injected into an affinity column, only a specific component is retained by the ligand and all other components are going to be eluted. By changing the mobile phase, trapped component can be removed from the ligand and eluted. Figure below illustrates the affinity mode separation.  |
6. Chiral Column
Frequently compounds used for pharmaceutical material production has optical isomers. Optical isomerism is one type of stereoisomerism that two molecules have the same arrangement of atoms, but they have different orientations in space. One has a mirror image of the other and cannot be superimposed. Another familiar example is right and left hands. They have same shape, but cannot be superimposed. The asymmetric molecule is called chiral. When a beam of light is emitted to the pair of chiral compounds, one rotates the light to clockwise (dextrorotatory isomer, designated d or +) and the other rotates into counterclockwise (levorotatory isomer, designated l or -).
One famous story of chiral compound is thalidomide incident in late 1950s. Thalidomide was sold as a sedative drug and was thought that it does not give much side effect to pregnancy, thus was taken frequently by pregnant women. However it resulted in many severe birth defects. This is due to the chiral compounds; one has sedative effect while other is a potent teratogen. Chiral pairs are very alike but once they are taken by human (animals), their biological activities may be totally different from each other. A problem is that it is difficult to produce only one type of chiral compound during the production of pharmaceutical materials. As mentioned, leaving non-target chiral compound may cause another incident as thalidomide, and thus it is important to separate chiral compounds.
When separating two components by HPLC, the larger the difference in components' characteristics, the easier the separation. Thus, since chiral pair is very similar, it is extremely difficult to separate. Shodex provides optical isomer separation columns using different ligands: α-, β-, and γ- cyclodetrin derivatives, L-amino acids derivatives, and bovine serum albumin ligands. Each works under different mechanisms. For example, one uses conformational compatibility differences while other uses metal complex formation capacity differences of the isomers.
Frequently compounds used for pharmaceutical material production has optical isomers. Optical isomerism is one type of stereoisomerism that two molecules have the same arrangement of atoms, but they have different orientations in space. One has a mirror image of the other and cannot be superimposed. Another familiar example is right and left hands. They have same shape, but cannot be superimposed. The asymmetric molecule is called chiral. When a beam of light is emitted to the pair of chiral compounds, one rotates the light to clockwise (dextrorotatory isomer, designated d or +) and the other rotates into counterclockwise (levorotatory isomer, designated l or -).
One famous story of chiral compound is thalidomide incident in late 1950s. Thalidomide was sold as a sedative drug and was thought that it does not give much side effect to pregnancy, thus was taken frequently by pregnant women. However it resulted in many severe birth defects. This is due to the chiral compounds; one has sedative effect while other is a potent teratogen. Chiral pairs are very alike but once they are taken by human (animals), their biological activities may be totally different from each other. A problem is that it is difficult to produce only one type of chiral compound during the production of pharmaceutical materials. As mentioned, leaving non-target chiral compound may cause another incident as thalidomide, and thus it is important to separate chiral compounds.
When separating two components by HPLC, the larger the difference in components' characteristics, the easier the separation. Thus, since chiral pair is very similar, it is extremely difficult to separate. Shodex provides optical isomer separation columns using different ligands: α-, β-, and γ- cyclodetrin derivatives, L-amino acids derivatives, and bovine serum albumin ligands. Each works under different mechanisms. For example, one uses conformational compatibility differences while other uses metal complex formation capacity differences of the isomers.
7. Preparative Column
The columns mentioned so far were "analytical columns" with column internal diameter (ID) of 4.6 ~ 8.0 mm. Purpose of using preparative column is collecting target substances after separating from other substances. Analysis column can separate these substances, but treating amount per column is not so much. On the other hand, preparative columns, larger diameter than analytical columns, can increase treating amount per column. Generally large particle size of packing materials is applied for preparative column, but there are cases the same packing materials are used.
There are mainly two reasons for collecting components: (1) to use in other analysis and (2) to use for industrial products.
(1) By using HPLC separation, chromatogram obtained shows the peaks corresponding to the components in the sample. For unknown analyte, the position of peak does not tell any information about the composition of the peak. Thus it requires to collect the unknown peak (analyte) and by using other technique to find out the composition of the analyte. Often mass spectrometer (MS) is used for the identification. Coupling HPLC and MS online is becoming common and the unit system is also commercially available. Also in some research, a certain components of the sample may be required to be used in next experimental sample. By using a preparative column, the specific component can be obtained.
(2) Use in a large scale collection and/or purification.
For preparation of certain products (often for the production of pharmaceutical products), it requires to separate and collect a certain components of raw material in a large scale. The preparative column will be used as a production tool.
For (1), the amount collected will not be so large, thus 20 mm ID preparative column is used. If concentration of target compound in the sample is relatively high, smaller ID column might be sufficient for the purpose. For (2), use in production, the larger ID column such as 50, 100, or 200 mm is generally used.
The columns mentioned so far were "analytical columns" with column internal diameter (ID) of 4.6 ~ 8.0 mm. Purpose of using preparative column is collecting target substances after separating from other substances. Analysis column can separate these substances, but treating amount per column is not so much. On the other hand, preparative columns, larger diameter than analytical columns, can increase treating amount per column. Generally large particle size of packing materials is applied for preparative column, but there are cases the same packing materials are used.
There are mainly two reasons for collecting components: (1) to use in other analysis and (2) to use for industrial products.
(1) By using HPLC separation, chromatogram obtained shows the peaks corresponding to the components in the sample. For unknown analyte, the position of peak does not tell any information about the composition of the peak. Thus it requires to collect the unknown peak (analyte) and by using other technique to find out the composition of the analyte. Often mass spectrometer (MS) is used for the identification. Coupling HPLC and MS online is becoming common and the unit system is also commercially available. Also in some research, a certain components of the sample may be required to be used in next experimental sample. By using a preparative column, the specific component can be obtained.
(2) Use in a large scale collection and/or purification.
For preparation of certain products (often for the production of pharmaceutical products), it requires to separate and collect a certain components of raw material in a large scale. The preparative column will be used as a production tool.
For (1), the amount collected will not be so large, thus 20 mm ID preparative column is used. If concentration of target compound in the sample is relatively high, smaller ID column might be sufficient for the purpose. For (2), use in production, the larger ID column such as 50, 100, or 200 mm is generally used.
8. Guard Column
The presence of impurities in the sample may cause alternation of column by being deposited inside the column permanently. To prevent such problems, it is necessary to pre-treat the sample by centrifugion and/or filtration. However, there are components that cannot be removed by centrifugion/filtration. If those samples were injected, it may break the column.
The guard column is effective preventing the analytical column from being alternated by those impurities. The guard column is a smaller version of the analytical column; packed with the same type of gels as that is in analytical column. The guard column is placed before the analytical column, thus any potential impurities that may cause damages is trapped inside the guard column before it reaches the analytical column. The price of a guard column is generally about one third to one tenth of the analytical column. By using the guard column, it can enhance the analytical column life and thus can be more economical. Although for the relatively low-priced analytical columns, the price of guard column compared to the analytical column could be high. Thus for those columns, the corresponding guard column may not be available. Moreover, the use of guard column is more effective for the polymer-based columns that have expected long column lives compared to silica-based columns.
The presence of impurities in the sample may cause alternation of column by being deposited inside the column permanently. To prevent such problems, it is necessary to pre-treat the sample by centrifugion and/or filtration. However, there are components that cannot be removed by centrifugion/filtration. If those samples were injected, it may break the column.
The guard column is effective preventing the analytical column from being alternated by those impurities. The guard column is a smaller version of the analytical column; packed with the same type of gels as that is in analytical column. The guard column is placed before the analytical column, thus any potential impurities that may cause damages is trapped inside the guard column before it reaches the analytical column. The price of a guard column is generally about one third to one tenth of the analytical column. By using the guard column, it can enhance the analytical column life and thus can be more economical. Although for the relatively low-priced analytical columns, the price of guard column compared to the analytical column could be high. Thus for those columns, the corresponding guard column may not be available. Moreover, the use of guard column is more effective for the polymer-based columns that have expected long column lives compared to silica-based columns.
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