LC6000 Good Practice Handbook
To ensure long term reliability and efficiency of the SCION Instruments LC6000 it is vital that considerations are taken when operating the HPLC system. SCION Instruments have now released their LC6000 Good Practice Handbook, a necessity for any HPLC user. The following handbook will provide guidelines for instrument preparation and routine operation recommendations to maintain the outstanding life-time performance of the LC6000.
The LC6000 Good Practice Handbook is designed for all users of SCION Instruments LC6000, High
Performance Liquid Chromatography (HPLC) systems. The below set of guidelines will ensure reliability and efficiency of the LC6000.
A. Mobile Phase
Optimisation of the mobile phase is critical to not only any HPLC application but for maintaining the health of your LC6000. Careful consideration is needed during mobile phase selection.
A1. Solvent Quality
Any solvents as mobile phase should be of the highest HPLC or MS grade quality. The solvents should
not contain any impurities which could lead to contamination, ghost peaks visible in results and pressure fluctuations within the LC6000. Aqueous solvents should always be deionised and purified.
A2. Solvent Selection
Solvent selection is an intrinsic part of method development and optimisation. The elution strength of
selected solvents will determine the separation of both target compounds and method run time. By choosing a solvent with a strong elution strength, typically Acetonitrile, a lower solvent to aqueous ratio is required, thus reducing cost. However, consideration must be taken as interactions between
functional groups of a target compound and both the stationary phase / mobile phase can occur.
Additionally, when using an Ultra-Violet detector, Diode Array Detector or Fluorescence Detector, the
specific absorbance of the solvent must also be considered. If the absorbance of the solvent is similar to that of the target compound, then the solvent is not suitable for use as mobile phase.
A3. Use of Buffers
Mobile phases containing a buffered solution should be prepared fresh daily. Buffers should be
homogeneous, fully dissolved and pH adjusted accordingly. Poor pH control can lead to damage of the
LC6000 and analytical column. When using a buffered mobile phase, always use a plunger wash on the
6100 Pump as this will eliminate the build-up of any salts within the buffer. At the end of the day always flush the system with water and solvent. This will prevent salt precipitation, damage to the instrument seals and leaks within the system.
A4. Filtering of Mobile Phase
Offline filtering of the mobile phase is recommended especially when buffered solutions have been
prepared, by using a 0.45µm filter. This will remove any particulates from the mobile phase, preventing
blockages of the LC6000. Solvent bottle filtering (online) is always recommended, especially when a
highly aqueous mobile phase is used. The LC6000 is supplied with online mobile phase filters, connected to the mobile phase PTFE tubing. It is good practice to regularly change these filters from the solvent bottle.
A5. Degassing of Mobile Phase
Degassing of the mobile phase is critical to any HPLC setup. Degassing removes air from the mobile
phase, preventing blockages within the LC6000. If air is introduced into the 6100 pump, unstable flow
and pressure fluctuations will be observed. Remove air from the LC6000 by purging the system. It is
always recommended to use the 6-Channel Degassing Unit with the 6100 pump, however offline manual degassing is also recommended.
A6. Other Mobile Phase Considerations
When choosing your optimum mobile phase for the analysis, be sure to consider the pH limitations of
your analytical column. Incorrect pH of the mobile phase can damage the stationary phase of the
column, resulting in poor chromatography and shorter lifespan of the column. When using an aqueous
mobile phase, regularly flush the column with solvent to prevent microbial growth. It is good practice
that when storing a column, it is thoroughly flushed with organic solvent and correctly capped at each
B. Sample Preparation
The removal of interferences and sample matrices is vital prior to any analysis being completed on the
LC6000. This process is done through sample preparation. Alongside the removal of any interferences,
sample preparation is also completed to dilute or concentrate samples. Sample preparation techniques
such as Liquid-Liquid Extract, Solid Phase Extraction and sample filtering, ensure clean samples are
introduced into the HPLC which also protects the stationary phase of the column.
B1. Solubility of the Sample
To eliminate split or broadened peaks, the sample must be completely soluble in the chosen solvent.
The chemical and physical properties of target compounds should be used to determine their solubility.
If the solubility of the sample is unknown, a solubility test must be performed. Dissolve the sample in
different solvents an observe the solubility behaviour during each test. If the sample is soluble in a
solvent, the end solution will be clear and free from particles.
B2. Solvent Selection for Sample Preparation
When preparing a sample for analysis, it is important to ensure that the sample is dissolved or prepared in the same solvent as the mobile phase. In particular, if a gradient mobile phase method is used, the sample should be prepared in the same composition as the start of a method. For example: If a gradient method begins at 15% methanol: 85% water, the sample should also be dissolved in 15% methanol: 85% methanol.
C. Instrument Preparation
Before performing an injection on the LC6000, ensure that the instrument is ready for use.
C1. Instrument Warmup
Before beginning an analysis, ensure that the lamps of the detectors are turned on and have had
sufficient time to heat up. The lamps are ready to use when the baseline of the LC6000 is stable. Flush
the LC6000 with solvent to ensure that there is no air in the system. If fluctuating pressure or flow is
observed then use the Purge function within the Maintenance Tool. Once the system is free of air, set
the pump to a flow of 1mL/min and observe for any leaks. Continue flow through the column to ensure
the column is equilibrated with the current mobile phase (flush the column with 10 to 20 times the
column volume for proper equilibration).
C2. Instrument Checklist
Before beginning an analysis ensure that all of the below requirements are met
- All LC6000 modules are connected in series to the organiser
- All tubing and connections are secure with no leaks
- The instrument is configured within Compass Configuration Manager and communication has been established
- Detectors are turned on, lamps are heated before use• Fresh mobile phase has been prepared including degassing
- The LC6000 has been properly purged with new mobile phase
- Purging of the LC6000 has been performed correctly and no air is in the system
- The autosampler syringe is free from air
- HPLC column has been installed and flushed thoroughly with fresh mobile phase
If the above steps have been completed, the instrument is ready for use.
D. Instrument Shut Down
When an instrument is to be shut down, it is critical that it is done in a manner that the instrument will
not be damage.
D1. Shut Down Procedure
- Ensure that all analyses have been completed
- Flush the column with solvent to ensure removal of contaminants
- Disconnect the column and install a backpressure device
- Remove all samples from the autosampler tray
- Flush the system with water if a buffered solution was previously used
- Replace the mobile phase with 100% Methanol or Isopropanol
- Purge the pump with the above solvent before flushing the system at 1mL/min (ensure no
column is installed)
- Wash the needle two to three times
- Disconnect the system from CompassCDS control and close CompassCDS
If the above steps have been completed, the instrument is ready for switch off. Always turn off the power to each individual module before turning off the power to the Organiser.
For more information contact Ashleigh Mellor, LC Product Manager.
Download the complete handbook: LC6000 Good Practice Handbook
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