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September 1, 2014

John W. Dolan**LCGC Europe**, LCGC Europe-09-01-2014, Volume 27, Issue 9

John W. Dolan

John Dolan has been writing "LC Troubleshooting" for **LCGC** for over 25 years. One of the industry's most respected professionals, John is currently a principal instructor for LC Resources, Walnut Creek, California He is also a member of **LCGC's** editorial advisory board.

LCGC Europe

Pages: 480–485

*How can resolution be determined when peak width cannot be measured?*

**How can resolution be determined when peak width cannot be measured?**

I have had several reader inquiries lately regarding how to estimate resolution between two peaks in a liquid chromatography (LC) separation when the traditional calculation doesn't work. An example of this is shown for peak pairs A, B, and C in the chromatogram of Figure 1. In each case, the valley between the peaks does not dip below 50% of the height of the smaller peak, making it impossible to measure the peak width at the baseline or half-height. In this month's "LC Troubleshooting" instalment, I would like to share a simple technique to estimate resolution that has been in use for many years (for example, see reference 1), but may not be well known because of our dependence on automatic data processing systems today.

Figure 1: An example of poorly resolved peak pairs A, B, and C.

Most of us use the method of equation 1 or 2 to calculate the resolution, *R*_{s}, of a pair of peaks with retention times *t*_{1} and *t*_{2}:

where *w*_{b1} and *w*_{b2} are the baseline peak widths between tangents drawn to the sides of the peaks, and *w*_{h1} and *w*_{h2} are the corresponding peak widths measured at half the peak height. That is, the resolution is the difference in retention times divided by the average baseline peak width (thus the factor of 2 in equation 1). The peak width at the baseline for a Gaussian peak is 4 σ (4 standard deviations), whereas at the half-height, it is 2.354 σ, so the factor in equation 2 is (2 × 2.354/4) = 1.18. Because the half-height peak width is easier to measure (no tangent drawing involved), most data systems use the half-height method (equation 2) to calculate resolution.

The technique of equations 1 and 2 works well when the peaks are well separated, as with Figure 2(a), where *R*_{s} = 1.3. When the resolution drops much below this, it will be difficult to measure the baseline peak width, but it may be possible to measure the half-height width. However, as the resolution drops, the valley between the two peaks rises, and at some point it becomes no longer possible to measure the half-width, either (for example, Figure 2[b]). Unfortunately, as the amount of peak overlap increases, measurement of resolution becomes more important. This is because it is more difficult to accurately measure peak areas when resolution drops below ~1.2, so system suitability tests often have minimum resolution requirements for partially separated peaks.

Figure 2: Simulated chromatograms for peak-height ratios of 2:1. (a) Rs = 1.3; (b) Rs = 0.9, h1, h2, and hv are heights of the first peak, second peak, and valley, respectively; (c) Rs = 0.75.

One way to estimate resolution for overlapping peaks is to measure the relative height of the valley between the peaks. The ideal chromatographic peak is Gaussian in shape, so we can generate Gaussian peaks (for example, in Excel) and sum their peak heights across a two-peak chromatogram. By changing the amount of resolution (overlap) and the peak heights, we can generate a simple tool to estimate resolution based on the relative height of the valley.

The Gaussian function is as follows:

where *y* is the peak height at point *x* and *x* is the retention time measured from the band centre (*t* = 0) in units of the standard deviation of the peak (σ). All the peaks I generated for Figures 2 and 3 range from times of -4σ to + 9σ relative to the centre of the first peak. Recall that the width of a peak between tangents drawn to baseline is 4σ. The chromatogram for the first peak of each pair is shown in red, the second in blue, and the sum of the two in green. In all cases, the second peak is of constant height, and the height of the first peak is varied (for example, in Figure 2, peak 1 is always twice the height of peak 2). Note that all the chromatograms of Figures 2–4 are computer-generated simulations; real peaks are likely to tail somewhat.

Figure 3: Simulated chromatograms for various peak-height ratios. (a) peak-height ratio = 1:1, Rs = 0.6; (b) ratio = 10:1, Rs = 0.9; (c) ratio = 100:1, Rs = 0.9.

Now, I have the ability to generate chromatograms as in Figures 2 and 3 for any desired resolution and any relative peak height. I have used such data to construct Table 1. The resolution (left-hand column) is known from the inputs. From the data in the spreadsheet (not shown) or the chromatograms, I can determine the peak height (which may be increased by overlap from the other peak) as *h*_{1} and *h*_{2} for the two peaks and the peak-height ratio (always *h*_{1}:*h*_{2} in Figures 2 and 3 because the second peak is smaller). The height of the valley (green line) is *h*_{v}/*h*_{2} (always the smaller of the two peaks). Each column of data is for one peak-height ratio, with the %-height of the valley shown below for each value of resolution. (I have done some rounding of numbers for presentation simplicity, so if you try to repeat my calculations, your results may vary slightly.) It should be obvious that if peak 2 is larger than peak 1, the data of Table 1 still apply — just remember to use the smaller of the two peaks for the valley-height ratio.

Figure 4: Simulated chromatograms showing effect of peak tailing factors (TF) (for peaks 1 and 2, respectively), on resolution for peak-height ratios of 1:1. (a) TF1 = TF2 = 1.0; (b) TF1 = 1.5, TF2 = 1.0; (c) TF1 = 1.0, TF2 = 1.5.

Next, let's see when it is appropriate to use Table 1 to estimate resolution and when it is not very useful. First, consider the chromatogram of Figure 2(a). In this case, *R*_{s} = 1.3 and the first peak is twice the height of the second (*h*_{1}:*h*_{2} = 2:1). In this example, either the baseline or half-height peak widths can be measured easily, so there is no need to use Table 1 for help. A calculation using either equation 1 or equation 2 will give better results when one of them can be applied. You can see from Table 1 (*R*_{s} = 1.3, ratio = 2:1) that the height of the valley is 10%. My suggestion is not to use Table 1 if the valley is less than ~10%, so I have not even shown valley heights < 10%.

Table 1: The valley-height technique of estimating resolution.

For the chromatogram of Figure 2(b) (*R*_{s} = 0.9, ratio = 2:1), the valley height is 54%. This means that it is not possible to measure the peak width, even at the half-height, so the method of Table 1 will be quite useful.

Table 1 works quite nicely when the peak-height ratios and the valley heights correspond to values in the table. When this is not the case, some interpolation will be necessary. In the example of Figure 2(c), the peak-height ratio is 2:1 and valley is 86% of the height of the second peak. In the 2:1 ratio column of Table 1, 86% falls roughly midway between a valley of 75% (*R*_{s} = 0.8) and 96% (*R*_{s} = 0.7), so we can assign *R*_{s} = 0.75 to this chromatogram (which is the resolution I selected to generate the data). Because of the rather coarse nature of the data intervals in Table 2 and other uncertainties, I suggest that you don't refine your estimates of resolution by more than 0.05 units using this technique.

I mentioned above that whenever you can measure the peak width at baseline or half-height, you are better off using the traditional resolution calculation of equation 1 or 2. Let's look at some other examples where the valley-height technique is limited. In the chromatogram of Figure 3(a), you can see that there is barely any valley between the peaks for the case of equal height peaks and *R*_{s} = 0.6 — the valley height is 91%. You can also see that the peak heights (green) of both peaks are greater than the individual peaks (red and blue) because of severe overlap. I don't think it is worthwhile trying to estimate the resolution with the valley-height technique if the valley height is more than ~90%. I have left a few values with valleys > 90% in Table 1 to help with interpolation with smaller valley ratios.

As the peak height difference between the two peaks gets larger, the valley-height technique still works, but a larger difference in retention times is required to obtain a reasonable valley. For example, in Figure 3(b) with a peak height ratio of 10:1, *R*_{s} = 0.9 is required to get the same 91% valley as with a 1:1 peak height ratio where resolution of only 0.6 was required (Figure 3[a]). When a peak height ratio of 100:1 is encountered (Figure 3[c]), *R*_{s} = 0.9 produces only a small bump on the tail of the first peak. At some point when the peak size ratio becomes too large, even with symmetric peaks, it will not be possible to observe two peaks, whereas with the same retention times and equal sized peaks, the separation would be obvious. Compare the chromatograms of Figures 2(b), 3(b), and 3(c) to see this trend for peaks with *R*_{s} = 0.9.

Peak tailing of the first peak of a peak pair will always reduce the resolution, whether the calculations of equations 1 or 2, or the valley-height technique of Table 1 is used. This is illustrated with Figure 4, where Figure 4(a) has *R*_{s} = 1.5 and both peaks are symmetric, so the tailing factor (TF) is 1.0. In Figure 4(b), the peaks have the same retention times, but the first peak has TF = 1.5. My measurements show a valley height of 19%, so for a 1:1 peak height ratio this equates to *R*_{s} ≈ 1.1. On the other hand, tailing only for the second peak, as in Figure 4(c), will not affect the resolution. It is only the case where the peak tails into the valley that resolution is reduced.

All of the chromatograms in Figures 2–4 are simulated; so what happens when we try to apply the valley-height technique to a real example? Let's go back to the chromatogram of Figure 1, where the reader was unable to determine resolution between peak pairs A, B, and C using direct calculations. I expanded the chromatogram and measured the peak and valley heights for each pair. For peak pair A, the peak height ratio is 1.36:1 and the valley height is 64%. The height ratio is closest to the 1.33:1 data set in Table 1, so I would estimate *R*_{s} ≈ 0.8. For pair B, the height ratio is 2.17:1 and the valley is 50%. Using the 2:1 column in Table 1, *R*_{s} ≈ 0.9. For pair C, the peak height ratio cannot be determined, but my guess is that it is at least 100:1 and the valley is 69% of the smaller peak, so this gives *R*_{s} ≈ 1.2. You could interpolate more carefully between the data points in Table 1, but as I mentioned above, I would not try to get closer than ~0.05 resolution units using Table 1. I don't know the nature of the sample in Figure 1, but it is typical of what might be observed for an impurities analysis of a pharmaceutical product. In such cases it may not be essential, or even possible, to separate all peaks to baseline, but it would be nice to be able to put a number on the resolution of the various peak pairs. Using the valley-height technique, we can do just that, when the traditional approach of equations 1 and 2 was not possible.

When chromatographic peaks are well separated, the traditional technique of calculating resolution based on retention time differences and average peak widths, as in equations 1 and 2, is the preferred way to determine resolution. This would generally apply over the range of peak height ratios of approximately 1:1 to 1:10 and resolution of at least 1.3. When resolution drops below ~1.3, it becomes more difficult to determine peak widths, so an estimate of resolution using the valley-height technique is more convenient. When the valley height exceeds ~40% of the height of the smaller peak, even the width at half height cannot be determined with confidence, so the valley-height method is the best choice. In the real chromatogram of Figure 1, we were able to estimate the resolution of three peak pairs using the valley-height technique when it was not possible to make the corresponding calculations with equation 1 or 2.

Peak tailing for the first peak of a peak pair will always reduce resolution. In such cases, the valley-height technique may give more realistic values of resolution, as was illustrated with the chromatograms of Figure 4.

From a system suitability standpoint, the valley-height technique can be useful to assess separation quality when a marginal separation is the best that can be obtained, as in Figure 1 for peak pairs A, B, and C. For the example of Figure 2(b), there is very little peak overlap at the peak centres, so peak-height measurements may be more appropriate for quantification; alternatively, peak-area measurements, using a perpendicular drop at the valley to separate the peak areas, should also give acceptable results for this example. You could specify in the system suitability requirements that *R*_{s} > 0.9 should be obtained. However, for routine work it may be more convenient just to set a limit on the valley height that corresponded to *R*_{s} = 0.9. For example, you could require that the valley be no more than 55% of the height of the second peak and have the same result without the added step of looking up the resolution in Table 1.

There is an interesting paradox here: As chromatographers, we are usually more concerned with peak separation when resolution drops below *R*_{s} ≈ 1.5, at which point we must rely more on estimates than more exact calculations. Conversely, when *R*_{s} > 1.5, calculations become easier, but once baseline resolution is obtained, accurate measurements of resolution are of less interest. So when accuracy is important, we can't get it, and when it is not as important, it is easy to obtain.

**John W. Dolan** is vice president of LC Resources, Walnut Creek, California, USA. He is also a member of *LCGC Europe*'s editorial advisory board. Direct correspondence about this column should go to the editor-in-chief, Alasdair Matheson, at amatheson@advanstar.com

(1) L.R. Snyder and J.J. Kirkland, *An Introduction to Modern Liquid Chromatography, 2nd edition* (Wiley-Interscience, New York, USA, 1979), Chapter 2.