With a sound understanding of chromatography principles, and taking some time to properly understand the variables within each method (all of the variables, not just the ‘headlines’) as well as considering those variables which are not stated in the method, we can save ourselves a lot of trouble once we don our lab coats and cross the laboratory threshold. Of course, it takes time to build the knowledge and experience necessary to spot these potential issues, but once we are aware of the possible pitfalls within a method, we can pay close attention to them during the implementation of the method, or even change those parameters, where the client or regulatory guidance allows.
The sources of ‘problems’ within chromatographic methods are too numerous to list here, however, the starting point in any method-detective work is a thorough reading of the method to gain a sense if it stacks up against our previous experience and knowledge. In this series, I’ll be covering some typical examples from problematic methods to highlight specific issues and areas to focus on, but also expanding upon these a little, to give some general guidance on what does or doesn’t, in my experience, constitute a clue that may be worthy of further investigation.
I’m going to start with an HPLC method and we will concentrate on the mobile phase and HPLC column combination. I will consider the issues with column geometry and stationary phase chemistry again in later blogs, so this example will serve as an illustration of what we might look for when investigating mobile phase conditions.
I recently came across this information in a method that was being transferred.
- Sample diluent: Dilute sulphuric acid (approximately pH 2.8) : Methanol 50:50
- Column: end-capped ethylene-bridged octadecylsilyl silica gel for chromatography (hybrid material) R (1.7 µm)
- Buffer solution: Dissolve 1.36 g of potassium dihydrogen phosphate R in 900 mL of water for chromatography R. Add 0.15 g of sodium heptanesulfonate R, adjust to pH 7.0 with triethylamine R and dilute to 1000 mL with water for chromatography R.
- Mobile phase A: methanol R, buffer solution (10:90 v/v)
- Mobile phase B: buffer solution, methanol R (15:85 v/v)
- Detection: spectrophotometer at 254 nm.
Figure 2: Representations of various silica surface species (note C8 ligands shown in the figure – C18 ligands are recommended in the Pharmacopeial method
Species 5 in Figure 2 represents an acidic silanol group that has not been effectively treated with an end-capping reagent (such as that shown in species 8) which will be anionic under the mobile phase conditions of our method (species 5 will have a pKa of around 4). If left untreated, these silanol anions will form electrostatic attractions with cationic analyte molecules and unwanted secondary interactions can lead to issues with peak broadening and tailing as well as extended column equilibration times and possible issues with peak area reproducibility. Therefore, ionogenic masking reagents such as triethylamine were traditionally added to mobile phases to effectively ‘end-cap' anionic surface sites, as the triethylamine, which is fully protonated below pH 7.2, is electrostatically attracted to the ionised surface silanol residues.
Let’s now look at the column being used.
The so-called bridged ethylene hybrid columns were introduced by Waters in around 2004 in order to fulfil several requirements including, improved peak shape for charged (especially cationic) analytes, increased ruggedness under UHPLC conditions and increased resistance to extremes of eluent pH (especially high pH), using organic / inorganic hybrid substrates.
However, we must go back even further to highlight some of the issues with the method under consideration. The lone (acidic) silanol groups which are masked using the triethylamine additive, were particularly prevalent when manufacturers used Type A silica as stationary phase substrate materials. This silica contained metal ions which are known to ‘activate’ surface silanol groups towards interaction with basic analytes and was typically not treated to avoid the presence of lone silanol groups. The later development of Type B silica effectively reduced silanol activity by removing target metal ions from the silica matrix and used surface treatments to reduce the number of lone silanols and promote the amount of inter-hydrated or vicinal silanol groups (species 2 in Figure 2). These developments were very effective at reducing the interactions between basic analytes and surface silanol species, effectively negating the requirement for masking reagents such as triethylamine. The bridged ethylene phases (species 1 in Figure 2) are known to further reduce the number of inherent silanol species capable of interaction with basic analytes in their ionised state.
One must therefore question, given the fact that due to these new stationary phase materials the use of silanol masking reagents have not been required for over 20 years now, why triethylamine is included in this method?
Further, triethylamine is relatively volatile and will be lost from the mobile phase to the atmosphere on standing, causing drift in analyte retention over time as the inherent pH of the mobile phase will change as the triethylamine concentration lowers. In my own experience, it is also possible for the triethylamine to ‘settle’ within the eluent, again leading to drifting or changing analyte retention. Further problems with this reagent also exist. As it inherently alters the stationary phase surface, one has to be mindful when equilibrating the HPLC column as extended flushing of the phase is often necessary to obtain reproducible retention times for the first injections of a sequence. One also must question the possible interaction between the anionic ion-pairing reagent and the triethylamine cation. The possibility of this interaction, forming a neutral complex, may render the masking reagent ineffective and one needs to wonder what robustness issues this may create.
Let’s now consider the role of the ion-pairing reagent in this separation. Modern stationary phases such as those used in this method, are capable of withstanding high pH mobile phase environments and as such we must also call into question the use of this type of buffer in the method. In this separation, the analytes have several basic functional groups ranging from 7.25 to 10.0 and therefore it is conceivable that, by adjusting the mobile phase pH to pH 10.5 or 11, the degree of ionisation of some of the analyte basic moieties will be reduced and therefore retention may be gained, even using the more hydrophobic C18 stationary phase. Further, there are many stationary phases available which contain more polar functional chemistry or are designed to work with very little or no organic modifier within the mobile phase at the beginning of the mobile phase gradient to facilitate retention of more polar or ionised analytes. The use of ion-pairing reagents such as sodium heptane sulphonate has not been necessary for many years, since the introduction of higher quality silica, combined with more polar (so-called Polar Embedded) and more pH resistant stationary phases can be used to gain sufficient reversed-phase retention, even for more polar analytes.
The column contains 1.7mm particles which are designed for use with UHPLC systems, given the higher inherent back-pressure created when using such small diameter particles. Intrinsically, these systems have very small internal volumes and very narrow internal diameter tubing and connectors, to reduce the effects of extra column (bed) band broadening on the separation. The use of a solid, involatile buffer with UHPLC systems is to be avoided, as any precipitation of the buffer through the use of highly organic eluents or via evaporation of the mobile phase on standing, will lead to significant problems with system blockages and overpressure situations. Further, the column end frits used with UHPLC columns containing 1.7mm particles typically have a porosity of around 0.2 mm which renders them even more susceptible to blockages with solid particles. It is possible to filter the eluent solution to remove any particulate materials initially present in the eluent system, however one must again be very mindful that the triethylamine additive is relatively volatile and therefore this may be partially lost if filtration is achieved using vacuum apparatus. The target eluent pH of 7.0 is also relatively problematic, given that the pKa of at least one of the ionogenic analyte functional groups in each of the analytes was close to 7.0, we might expect a relatively large change in the ionic character of the analyte, and therefore its retention, unless the pH of the mobile phase is very accurately controlled each time it is made. To ensure the method is robust, it would have been better to quote a volume or weight of triethylamine required to achieve the desired pH, which could be controlled much more reproducibly.
It should be further noted that the detection is at a fixed wavelength of 254nm and this can be problematical when the ionic strength of the mobile phase changes to such a large extent during the analysis, as is the case here, where the aqueous component ranges from 90% to 15% during the course of the analysis. Without the judicious set-up of the detector, for example, by employing an appropriate reference wavelength to account for differences in the refractive index of the eluent, such changes in ionic strength might well give rise to retention time shifts, peak shape changes and unstable and rising baselines during the gradient, unless sufficient time is given to allow re-equilibration of the column between sample injections. It may be far more judicious to use a ternary system in which the ionic strength is maintained using a third eluent system which contains the buffer and additives at a higher concentration (i.e. all reagents at 10x concentration and added at a constant 10% of mobile phase composition during the analysis).
From this brief review, it would very much appear that the current method has been ‘stitched together’ using a very traditional mobile phase with a modern stationary phase which should not require any of the now ‘exotic’ mobile phase additives to achieve a suitable separation. Without the requisite experience in critical evaluation of chromatography methods, this combination may be baffling and the resulting problems are very difficult to interpret or overcome.
Let’s summarise some of the detective work that we have undertaken to start building our investigative toolkit.
1) The use of phosphate or other solid buffers suggest that the method is ‘older’ and these buffers usually preclude the use of MS detection and present issues with system blockages under high organic strength mobile phases.
2) The use of ion-pairing reagents such the sulphonic acids or alkyl amines again suggest the method is older. These reagents were typically used in conjunction with older stationary phase types and their need can often be negated by judicious selection of a more modern stationary phase that is capable of retaining ionised analytes. Further, the use of ion-pairing reagents can present real challenges with column equilibration.
3) By studying the physicochemical parameters of the analyte, it may be possible to suppress analyte ionisation using pH control and modern stationary phases exist which will withstand eluent pH values between (approximately) 2 and 11.
4) The use of ‘exotic’ additives within mobile phases such as triethylamine should ring alarm bells in terms of the robustness of the method and the potential issues with peak tailing, due to their association with older, less inert, stationary phase chemistries and substrates.
5) One should always consider the analyte structure and the polarity (LogP, LogD) and the pKa of any ionogenic functional groups with respect to the mobile phase being used. It is a real skill to be able to visualise the degree of ionisation of each analyte and anticipate any issues with retention and resolution under the mobile phase conditions specified.
6) Eluent pH values that closely approach the pKa of any ionogenic groups will present potential robustness issues with retention and resolution of the separation. Further, methods that specify the eluent components volumetrically rather than gravimetrically should, where possible, be converted to gravimetric specification to enable more accurate mobile phase preparation.
7) The ionic strength of the eluent additives can give clues into the quality of the method and where high ionic strength (above 25mM) is required, this highlights several possible issues in implementation. High ionic strength can indicate that robustness can only be achieved by significantly altering the nature of the stationary phase and there may issue with a mismatch between the analyte diluent and the mobile phase. These phases will also require significantly extended column equilibration times. High ionic strength mobile phases which use solid buffers can present significant issues with system blockage, especially where eluent conditions reach >60% acetonitrile or >95% methanol during the gradient.
8) Eluent gradients that present a significant change in ionic strength can present issues with baseline stability, especially when using UV detection. These problems can be minimised through careful optimisation of the reference wavelength; however, the general principle should be to minimise the ionic strength of the eluent and the change in ionic strength throughout the gradient.