Retention Time Variability in HPLC

In High-Performance Liquid Chromatography (HPLC), retention time variability is an important aspect to consider. It is crucial for ensuring the reliability and accuracy of chromatographic data. This variability can have significant implications for the quality of analytical results and the consistency of chromatographic separations.

In this article, we will explore the factors that contribute to retention time variability in HPLC, methods for controlling and minimizing these fluctuations, and the implications for analytical method development and quality control.

I’m sure we have all experienced it – that sinking feeling when you realize your analyte retention times have drifted outside the software ‘window’ and you have a pile of chromatograms with no quantitative results. Or you are trying to get that system suitability result to begin your batch of analyses as you really need to get out of the door fast but your retention times just won’t settle down. Or you are trying to reproduce Bob from the R&D centers method and his retention times (or chromatogram..!) look nothing like yours. Or you are trying to validate your method and the three-column lots you are trying to give different retention behavior to the column that you just developed your method on. Or every time you do an injection the retention time of the analyte changes just a little – it doesn’t cause anything to fall over, but you just don’t understand why.

Yes – there are a whole bunch of retention time issues that cause problems in HPLC. A lot of the underlying causes we can do something about – others we just need to be aware of the cause and put our minds to rest. The remainder of this technical tip will outline how to overcome, or better control, all of the situations outlined above.

Factors Influencing Retention Time Variability

Retention time variability in HPLC can be influenced by various factors:

• Column Age and Condition: Over time, HPLC columns may become worn or fouled, leading to changes in retention times.
• Mobile Phase Composition: Variations in the composition of the mobile phase can lead to fluctuations in retention times.
• Flow Rate: Changes in flow rate can directly impact retention time.
• Temperature: Fluctuations in the temperature of the column can affect retention time.
• Injection Volume: Variability in the injection volume can lead to inconsistent retention times.
• Sample Matrix: The complexity and characteristics of the sample matrix can impact retention time.

ALSO READ: Troubleshooting Leaks in HPLC

Controlling Retention Time Variability

To minimize retention time variability, several strategies can be employed:

• Column Maintenance: Regular maintenance and proper care of HPLC columns can help reduce variability.
• Mobile Phase Preparation: Consistent preparation and use of mobile phases with appropriate pH and ionic strength can minimize fluctuations.
• Flow Rate Calibration: Regularly checking and calibrating the flow rate can help maintain consistency.
• Temperature Control: Using a column oven can help regulate and maintain a constant temperature.
• Sample Preparation: Ensuring consistent sample preparation methods can reduce variability.
• System Calibration: Regular calibration of the HPLC system can help ensure stable and reliable performance.

Overarching rules on retention time variability:

• If the void (hold-up) time (t0) and analyte retention time (tR) vary together, suspect a flow rate change. In this scenario, the analyte capacity factor (k) will remain constant.
• If only the analyte retention time varies, with the void (hold-up) time remaining constant, then k will also change. In this scenario suspect a change in the selectivity or retentivity of the separation system

Drifting Retention Times

• This is typically due to a change in mobile phase composition, which can be caused when pre-mixed mobile phases lose some of the organic solvents through evaporation as the run progresses. Ever noticed this seems to happen more towards the end of a run? Well of course the organic solvent is being continually lost to the atmosphere – or as the eluent in the sealed bottle depletes there is more headspace for the more volatile component to evaporate into - and of course, a small amount of evaporation makes a bigger overall composition change in the ever diminishing volume of liquid.
• This is typically why we see elution times becoming longer rather than shorter. What to do? Mix eluents (even isocratic ones) online or at the very least ensure the reservoir you are using is capped. We may also experience a change in the pH of the aqueous component of the eluent over time which is caused by the ingress of CO2; lowering the eluent pH and changing the retention and perhaps even the selectivity of the separation….so again, cap your bottle.
• Do not use lab film to cover eluent reservoirs – especially when using MS detection (watch out for ions at 142 Da as you leach the plasticizer from the film!).
• Another related note on eluents here – if we de-gas pre-mixed mobile phases using a vacuum, the very act of sucking the mobile phase through the filter under the vacuum can cause loss of the more volatile component which will lead to irreproducible changes in eluent composition from batch to batch of eluent.
• The same is also true when degassing premixed phases using ultrasonic baths; the warming of the eluent in the sonic bath can lead to loss of the organic modifier and, hence, change retention characteristics.

• Temperature is another variable that can alter retention time, changing not only the viscosity of the eluent but also the kinetics of the retention mechanism. Ionizable compounds tend to be affected by temperature more than non-ionogenic compounds; therefore, selectivity may also change. Most systems come with column heaters/chillers these days, but if yours doesn’t, and you get large temperature variations in the lab, this can cause retention time variability (especially when the system is placed directly below your air-con). Even systems that do have column heaters work in different ways – some pre-warm the eluent before entry into the column for example and these systems may well give different retention times to those that heats the column only.

ALSO READ: SOP for Verification of System Suitability Test

Variable Retention Times

• Equilibrating or priming a column when beginning an analysis can also show some strange retention time shifts and variability. Without going into too much detail, this is due to the stationary phase surface being modified by your eluent or sample components. Primarily it’s the ‘wetting’ of the surface (especially with more hydrophobic phases such as C18) as the bonded phase takes on a layer of hydration - a slightly crass description but one which will do for this short tip.
• Furthermore, the polar or ionized silanol (Si-OH) groups on the silica surface can irreversibly bind with polar analyte components or buffer ions to change the overall surface polarity. What to do – well you can try to inject 10x more concentrated samples than you normally would to try and achieve the equilibration in a shorter time (fewer injections).
• In this category, we must also consider the more esoteric issue of the sample diluent. For reasons that are too detailed to enter into here, the eluotropic strength and ionic strength of the sample diluent can sometimes have a big effect on analyte retention time and peak shape – yes that’s the sample diluent, the thing you dissolve the sample in – not the HPLC eluent.
• You should always strive to match the aqueous/organic ratio of the eluent (at the start of the gradient if doing gradient elution) as well as the buffer strength of the eluent. If the diluent is more highly organic than the eluent (for solubility reasons) – try to restrict your injection volume to 10 μL or less.

Column to Column Retention Time Irreproducibility

• And what of the situation in which the column you used to develop your method doesn’t behave like the new shiny ones you just bought to do your validation? This is the same as the previous situation really. Everything you put down the column (eluent and samples) modifies the surface – sometimes irreversibly, and the same goes for all of the stuff your colleague also put down the column before you used it to develop your method.
• What to do – buy a new column for method development and let it equilibrate properly before using it. If you have an ion pair reagent (and remember TFA is an ion pair reagent) and you remove it, use a different pairing reagent, or switch to a different eluent modifier – you should contact your column supplier before continuing with method development – it may well be that you need a new column.

Retention Time Issues in Method Transfer

• Matching retention times with Bob from R&D’s method is another tricky situation. You must make sure that you are preparing the eluent in the same way – including weighing solid buffers, taking care with volumetric work, adding organic to aqueous portions, and adjusting the pH using the same acid or base and doing so with a properly calibrated pH meter. Further, the use of the same buffer is important – and just a note to all users of phosphate buffers – monosodium dihydrogen phosphate is not the same as disodium monohydrogen phosphate and neither of them has real buffering capacity between pH 3 and 6.
• Crucially, if the method involves gradient elution, you REALLY MUST know the gradient dwell volume for each system and adjust for any differences before repeating the method. If Bob’s dwell volume is shorter than yours then you need to use an instrument capable of injection delay (injection occurring after the gradient has started) and if his dwell volume is larger than yours, add an isocratic hold at the start of the method equal to the difference in volume x flow rate. If he was smart when he developed the method, then he would have inserted an isocratic portion at the start of the gradient which you can adjust to make sure the gradient dwell volume differences are catered for.

Hardware-Related Retention Time Problems

Pump at a fixed flow rate – until they leak or break. In the majority of cases, poor pump performance will be accompanied by other symptoms such as low, high, or cycling back pressure – but not always. The easiest way to check your flow rate accuracy is to run the eluent into a 10 mL volumetric cylinder and time it. If you get 10 mL in 10 min when operating at 1 mL/min then all is well – if not – all is bad and you need to get the system checked out.

Methods for Measuring Retention Time Variability

Measuring retention time variability can be done through:

• Reproducibility Tests: Conducting tests to evaluate the consistency of retention times across multiple injections.
• Retention Time Ranges: Monitoring the range of retention times for specific compounds over multiple runs.
• Statistical Analysis: Analyzing data for trends and patterns in retention time variations.

Implications of Retention Time Variability

Retention time variability can have several implications for analytical chemistry:

• Accuracy: Inaccurate retention times can lead to errors in compound identification and quantification.
• Reproducibility: High variability can compromise the reproducibility of chromatographic results.
• Quality Control: Consistent retention times are essential for maintaining the quality of analytical methods.

Best Practices for Managing Retention Time Variability

Here are some best practices to manage retention time variability effectively:

• Standard Operating Procedures (SOPs): Implementing SOPs for HPLC analysis can help standardize methods and reduce variability.
• Regular System Checks: Conducting regular maintenance checks on HPLC equipment can identify and address potential issues early.
• Use of Reference Standards: Using high-quality reference standards can help ensure consistent calibration and performance.
• Continuous Training: Ongoing training for laboratory personnel can improve understanding and adherence to best practices.
• Data Analysis: Continuously analyzing data for trends and patterns can help identify and correct issues promptly.

Conclusion

Managing retention time variability in HPLC is critical for maintaining the reliability and accuracy of analytical results. By understanding the factors that influence variability and implementing effective strategies for control, laboratory professionals can achieve greater consistency and precision in their chromatographic analyses.

ALSO READ: Why Degassing of HPLC Mobile Phase is Necessary?