Showa Denko Shodex ORpak CDBS-453 User manual

Operation Manual Shodex ORpak CDBS-453 Version 211214E
Operation Manual
Shodex™ ORpak CDBS-453
Europe, Middle East, Africa, Russia
www.shodex.de
Sales Office:
Showa Denko Europe GmbH
Shodex Business
Konrad-Zuse-Platz 3
81829 Munich
Germany
Technical Support:
[email protected]
+49 (0)89 / 93 99 62 37
Quotes and Orders:
[email protected]
+49 (0)89 / 93 99 62 34

Operation Manual Shodex ORpak CDBS-453 Version 211214E
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Operation Manual
Shodex ORpak CDBS-453
(Please read this manual carefully to achieve the best and consistent column performance for a long time)
Important Handling Instructions
Caution! • Please consult the Safety Data Sheet (SDS) of reagents and solvents used with the
column and understand their proper handling methods to prevent potential health
hazards or death from occurring.
• Please wear appropriate personal protective equipment such as lab goggles and
gloves when handling organic solvents and acid and alkaline reagents. Avoid any direct
physical contact to prevent chemical injuries.
Before Using the Column
(1) Please visually inspect the package and outside of the column for any damage.
(2) Please check if product name and serial number written on the column package, column name tag,
and enclosed Certificate of Analysis (CoA) are matching and correct.
1. Introduction
Thank you for purchasing the Shodex™product. Shodex ORpak CDBS-453 is a chiral separation column
filled with spherical porous particles of silica modified with β-cyclodextrin group. Optical isomers are
separated by β-cyclodextrin's host-guest inclusion capability.
2. Column Components
3. Column Specifications
Product Code
Product Name
Column Size ID x Length
Particle Size
Theoretical Plate
Number (Per Column)
F7146003
ORpak CDBS-453
4.6 x 150 mm
3 µm
≥6,000
Base Material: Spherical porous particles of silica modified with β-cyclodextrin group
Column Housing: SUS-316 (stainless steel)
Screw Type: Internally-threaded type No.10-32 UNF
Shipping Solvent: 0.05 % Acetic Acid + 0.2 M Sodium Chloride Solution/Acetonitrile = 95/5
Recommended Storage:Fridge 4-8°C

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4. Usable Conditions
Product Name
Flow Rate (mL/min)
Maximum Pressure
(MPa) (Per Column)
pH
Range
Temperature (°C)
Recommended
Maximum
Recommended*
Range
ORpak CDBS-453
0.3 - 0.8
1.2
20
2 - 7
10 - 30
5 - 60
* In general, lower temperature setting is more suitable for the separations of optical isomers.
Usable solvents are listed below.
(1) A mixture of water and an organic solvent, such as acetonitrile, of any ratio can be used. Up to
100% water and organic solvents can be used.
(2) Ethanol, 2-propanol (IPA), and tetrahydrofuran (THF) can be used.
(3) Various buffer and aqueous salt solutions can be used instead of water. They include phosphate,
or acetate buffers, and sodium chloride solution. Please keep total concentration of salt under 1 M.
(4) Acetic acid can also be added. Please keep its concentration under 6.0 % (w/v).
Attention! • Use the column within above stated flow rate, pressure, and temperature ranges.
Using the column outside the given range may damage the column and lower its
performance.
• When using a mixture of buffer (or aqueous solution of salt) and organic solvent,
make sure there is no precipitation of salt.
• Column pressure is influenced by the eluent composition, flow rate, and column
temperature. When changing the eluent compositions, adjust the flow rate and
column temperature so that the column pressure remains below the usable maximum
pressure.
5. Eluent Preparation
(1) Degas the eluent fully to prevent the formation of air bubbles.
(2) Presence of small debris or insoluble substances may result in deterioration of the column and/or
they appear as noise on the chromatograms. Filter the eluent with a 0.45 μm disposable filter to
prevent the problems.
Attention! • Whenever water is required, use ultra-pure water freshly generated by a water
purification system or water from a newly opened HPLC grade distilled water bottle.
Use HPLC grade organic solvent whenever possible. Solvents left in an opened bottle
for a long time should not be used. The content may have been changed, absorbed
moisture, or has been contaminated.
• Always use freshly prepared solvents. Solvents stored for a long time may have
changed their compositions and may influence elution patterns and/or damage the
column.
Note • Use of on-line degasser is recommended.
6. Sample Preparation
(1) If possible, use the eluent for analysis to dissolve or dilute samples. If this is difficult, use a solvent
which has a composition that is as close as possible to the eluent's composition, but which fully
dissolves or dilutes the sample. When gradient elution is used, it is recommended to use the initial
eluent to prepare the sample.
(2) Filler the sample solution using disposable 0.45 μm filter to prevent the column from clogging or
deteriorating.
(3) Recommended sample injection volume is less than 20 μL per column.
(4) For the samples containing proteins, remove the proteins prior to the sample injection.

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7. Column Usage Procedure
7.1. HPLC System Preparation
Wash entire LC system prior to the column installation, including all flow-lines and sample loop by
switching the valve, and then replace the washing solution with the eluent to be used. If desired new
eluent has low miscibility/solubility to the eluent of previous analysis, first use the eluent that is
miscible/soluble to both eluents, and then replace it with the desired eluent.
e.g. When replacing chloroform to water first run methanol and then replace it with water.
e.g. When replacing highly concentrated buffer solution or salt solution to water/acetonitrile, first run
water and then replace it with water/acetonitrile.
Attention! • If the eluent left in the system is not compatible with the column to be used, it may
damage the column.
• A drastic change in the eluent compositions may remove substances adsorbed on
the system and they may enter and deteriorate the column.
7.2. Column Installation
(1) Connect the column to LC system by following the “flow direction arrow” () indicated on the
name tag. If guard column is used, position the guard column in front (before the inlet) of the analytical
column.
(2) Make sure to insert the tubing all the way to the end fitting and secure it with the male nut. It is
important that there is no extra space between the tubing and the column side of the end fitting.
Presence of an extra space will let the sample to spread out and may result in wide peaks.
(3) Set the initial flow rate at less than 0.2 mL/min and start the system. If using the column at an
elevated temperature, keep a low flow rate until the temperature of the column reaches to the set
temperature, and then gradually increase the flow rate to the desired.
Caution! • Verify that there is no solvent leak. It may cause electronic leakage, rust, and/or
chemical injury.
Attention! • Make sure not to let air bubbles enter the column while installing the column. The
air bubbles may damage the column.
• When restarting the system after column installation or after holding the eluent
flow, start the system at less than 0.2 mL/min. A rapid increase in pressure can damage
the column.
• If the column was used at an elevated temperature, lower the flow rate to less than
0.2 mL/min at the end of analysis. Then, turn off the column oven, and let the column
temperature return to room temperature before stopping the pump. If the pump was
stopped while the eluent inside the column was still hot, as the eluent temperature
decreases, its volume also decreases. This may result in creating an empty space in the
column and deteriorates the column.
Note •It is recommended to set the pump limiter to avoid exceeding the maximum
pressure.

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7.3. Solvent Exchange
(1) Start the system at less than 0.2 mL/min when replacing the solvent and continue for 60 minutes.
(2) Check miscibility/solubility of the desired new solvent and the solvent currently filled in the column.
(3) When replacing the current solvent with a solvent with low miscibility/solubility to the current
solvent, first use a solvent that is miscible/soluble to both eluents, and then replace it with the new
solvent.
(4) When using a gradient method, changes in the eluent compositions may increase the column
backpressure. Adjust the flow rate and column temperature so that the column backpressure remains
below the usable maximum pressure.
Attention! • After solvent replacement, it may take some time for the sample retention time to
stabilize. Before starting the measurement, inject the same sample repeatedly and
make sure the retention time is stable.
7.4. Column Cleaning
Problems in peak shapes and elution time changes or elevated column pressure etc. are often caused
by insoluble or adsorbing components present in the eluent and reagents being deposited inside the
column. These problems may be resolved by cleaning the column.
When washing the column, let the washing solution flow from the column outlet go directly into the
waste container and not let the solution go through the detector.
<Cleaning Method>
(1) Insoluble components that block the column inlet may be removed by reversing the flow direction,
i.e., introducing the eluent from the column outlet, with flow rate at less than half of the recommended
flow rate.
(2) Follow below cleaning steps for adsorbing components. For an efficient cleaning, reverse the flow
direction.
Introduce 50 mL of acetonitrile or methanol at 0.5 mL/min.
8. Column Storage
Remove the column from the system keeping the solvent used for the analysis. Securely tighten the
end caps and store the column at a location with stable temperature (a cool and dark space is
recommended).
It is recommended to store the column before and after use in the fridge at 4-8°C to improve the shelf
life.
Attention! • Never allow inside of the column to dry. It can damage the column.

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9. Column Inspection
Inspection method is described in the Certificate of Analysis (CoA).
Theoretical Plate Number (N) and Asymmetry Factor (Fas) were calculated using the below equations.
(1) Theoretical Plate Number (N)
(2) Asymmetry Factor (Fas)
10. Additional Warnings
(1) Do not remove end fittings.
(2) Do not make a strong impact on the column. Do not drop or hit the column on a hard surface.
Refer to the Shodex website (www.shodex.de) for product details and their applications.
For additional assistance, contact the distributor from whom you purchased the column or contact
your regional Shodex support office.

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11. Warranty (Version 4)
(1) Showa Denko K.K. warrants that the Shodex™product, at the time of delivery to the user, will
conform to the specification of the attached CERTIFICATE OF ANALYSIS, if the Shodex product is used
in accordance with the attached operating manual. The foregoing warranty is exclusive and is in lieu
of all other warranties with respect to the Shodex product, whether written, oral, implied, statutory or
otherwise. No warranties by Showa Denko K.K. are implied or otherwise created, including, but not
limited to, the warranty of merchantability and fitness for particular purposes.
(2) Any claim of inconformity to the specification must be notified to Showa Denko K.K. within ten (10)
days after delivery to the user. User’s exclusive remedy and Showa Denko K.K.‘s exclusive liability for
such claim are limited to the replacement of the Shodex product in question. In no event is Showa
Denko K.K. liable for any indirect, incidental or consequential damage arising out of in connection with
the Shodex Column, whether or not such damage is allegedly based on breach of warranty, negligence
or otherwise.
(3) No warranty is made in any of the following cases:
3-1 If the Shodex product is not used in accordance with the operating manual
3-2 If the Shodex product is remodelled by anyone other than person or firm designated by
Showa Denko K.K.
3-3 If the Shodex product is disposed of
3-4 If the Shodex product is resold by the user without giving prior written notice to Showa
Denko K.K.
3-5 If the performance of the Shodex product is not conform to the specification of the
attached CERTIFICATE OF ANALYSIS due to any of the reasons below:
a) Computer virus
b) Impurities contained in the sample, reagent, gas air or cooling water provided by
the user
c) Breakdown or malfunction of equipment, apparatus or component used in
combination with the Shodex product
d) Force majeure such as fire, earthquake, flood, other natural disaster, crime, riot, act
of terrorism, war or radioactive contamination
(4) In no event is Showa Denko K.K. liable for
4-1 the results of analyses or preparations using the Shodex product or any portion of the
same, including, but not limited to, the reliability, accuracy, efficacy and safety of said results,
and
4-2 the occupational hazard in the use of the Shodex product, whether or not such use is made
in accordance with the attached Conditions for use.
(5) The Shodex Column is for laboratory use only. It must not be used for clinical diagnosis. Showa
Denko K.K. is not liable for any use of the Shodex product except laboratory use.