System suitability is to prove
that system is working perfectly before the analysis on HPLC,
GC, TOC analyser or any other system. It is required to done before every
sample analysis. HPLC, short for High-performance liquid chromatography is
a technique used for separating the components in a mixture.
HPLC chromatographic technique is used in
pharmaceutical industries for analysis. System suitability testing limits are acceptance
criteria that must met before starting the analysis.
There are some System suitability parameters which
can be used to check the system before starting the sample analysis are listed
below.
1. Retention
time
2. Resolution
3. Repeatability
4. Plate
Count
5. Tailing
Factor
6. Signal-to-noise
ratio
7. Pressure
Retention
Time:
In liquid chromatography
and gas chromatography, the retention time, tR, is defined as the time elapsed
between the injection of the sample and the appearance of the maximum peak
response of the eluted sample zone. tR may be used as a parameter for
identification. Chromatographic retention times are characteristic of the
compounds they represent but are not unique. Coincidence of retention times of
a sample and a reference substance can be used as a partial criterion in
construction of an identity profile but may not be sufficient on its own to
establish identity. Absolute retention times of a given compound may vary from
one chromatogram to the next.
Resolution (Rs):
Resolution is a measure
for the ratio of the distance of two adjacent peak maxima and their widths. For
complex sample mixtures Rs should be determined for the critical pairs of components
to characterize their separation.
Resolution is calculated
by following formula,
RS
= 2(tR2 − tR1) / (W1 + W2)
Where, tR2 and
tR1 are retention times of two compounds, W2 and W1
are the corresponding widths at the bases of the peaks obtained by
extrapolating the relatively straight sides of the peaks to the baseline.
Repeatability/Precision:
Replicate injections of a
standard preparation are used to demonstrate the system performance when it
gets exposed to some specified column usage, environment, and plumbing
conditions. Data from five or six replicate injections are used if
requirement of relative standard deviation is less than 2%.
Plate
Count/ Column Efficiency:
The Column Efficiency is
measured by following formula,
N
= 16(tR/W)2
where tR is
the retention time of the substance, and W is the peak width at its base, obtained
by extrapolating the relatively straight sides of the peak to the baseline. The
value of N depends upon the substance being chromatographed as well as the
operating conditions, such as the flow rate and temperature of the mobile phase
or carrier gas, the quality of the packing, the uniformity of the packing
within the column, and, for capillary columns, the thickness of the stationary
phase film and the internal diameter and length of the column.
Tailing
Factor/Symmetry Factor:
Tailing Factor is
calculated by following formula,
AS = W0.05/2f
where W0.05 is the width
of the peak at 5% height and f is the distance from the peak maximum to the
leading edge of the peak, the distance being measured at a point 5% of the peak
height from the baseline.
Signal-to-noise
ratio:
This parameter is used
for the lower-end calculation of the performance of the system.
Noise: It is measured between two specific lines that bracket
the baseline.
Signal: It is measured starting from the baseline’s middle and
ending to the peak’s top.
Once calculating both
these factors, the ratio can be measured by dividing the signal value by the
noise value. With this, generally, the noise value has to be reduced using one
of the following methods:
- Signal Averaging
- Reagent and Solvent Purity
- Column Flushing and Sample Clean-Up
- Temperature Control
- Additional Pulse Damping and Mixing
The signal-to-noise ratio
(S/N) is a useful system suitability parameter. The S/N is calculated as
follows:
S/N
= 2H/h
where H is the height of
the peak measured from the peak apex to a baseline extrapolated over a distance
≥5 times the peak width at its half-height; and h is the difference between the
largest and smallest noise values observed over a distance ≥5 times the width
at the half-height of the peak and, if possible, situated equally around the
peak of interest
System
Pressure:
System suitability tests
must be performed under controlled pressure limit. Monitor the pressure
variation throughout the analysis.
Conclusion:
The above mentioned
system suitability parameters are not must. These parameters and acceptance
criteria are performed during the method validation and fixed based on the
method development outcome results. But system suitability should meet the
acceptance criteria before starting the sample analysis.
0 Comments