GAS LIQUID CHROMATOGRAPHY (GLC)
One of the most difficult and frustrating problems ever
encountered in the domain of pharmaceutical analysis is that of the
simultaneous separation, identification and above all the quantitation of more
than one compound from a complex mixture in a pharmaceutical product.
A good of sophisticated chromatographic techniques of
separation have been put forward since early fifties that may be categorized
into the following four groups,
namely :
(a) Gas-Solid
adsorption Chromatography (GSC),
(b) Gas-Liquid
partition Chromatography, (GLC),
(c)
Liquid-Solid adsorption Chromatography (LSC), and
(d)
Liquid-Liquid partition Chromatography (LLC).
The first two groups have been collectively termed as ‘Gas Chromatography’. Its phenomenal
growth at almost logarithmic pace may be attributed to its unparalleled
potential in resolving components of a complex mixture. Gas chromatography fundamentally is a separation technique that not
only essentially provides prima facie indentification
of a compound but also caters for quantitative estimation after due
calibration.
Gas chromatography makes use, as the stationary
phase, a glass or metal column filled either with a powdered adsorbent or a non-volatile liquid coated on a
non-adsorbent powder. The mobile-phase consists of an inert-gas loaded with the
vapourised mixture of solutes flowing through the stationary phase at a
suitable temperature. In the course of the passage of the vapour of the sample
through the column, separation of the components of the sample occurs in two
ways, namely :
(a) due to adsorption effects-i.e., when the prepared column consists
of particles of adsorbent only, and
(b) due to partition effects-i.e., when the particles of adsorbent
are coated with a liquid that forms a stationary phase.
Martin and Synge in 1952, became the Nobel Laureates for
their excellent, innovative research work on the development of partition chromatography.
It is, however, pertinent to mention here that GLC has a
much greater application in the field of pharma-ceutical analysis which extends
over to most organic constituents that have a measurable vapour present at the
temperature employed.
The principal advantages of GC are enumerated below,
namely :
·
It has high frequency of separation and even complex
mixtures may be adequately resolved into constituents,
·
It has a very high degree of sensitivity in detection of
components i.e., only a few mg of
sample is enough for complete analysis,
·
Speed of analysis is quite rapid,
·
Gives reasonably good accuracy and precision,
·
The technique is fairly suitable for routine analysis
because its operation and related calculations do not require highly skilled
personnel, and
The overall cost of equipment is comparatively low and
its life is generally long.
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