Instrument
discussed above are general purpose instruments which provide useful information
regarding physicochemical properties and microbiological analysis of milk and
milk products (proximate analysis). However, development of more sophisticated
instruments has enabled the estimation of pesticide residues, toxins, antibiotic
residues etc in part per billion (ppb) levels which was impossible with classical
instruments. Some of these instruments are discussed below in brief.
i.
Flame Photometer: Flame photometer is used for the quantative chemical analysis
for the determination of alkali and alkaline earth metals (Sodium and Potassium
etc.) present in solution. Flame photometer is must when concentration of the
element is very low, say of the order of 1ppm as ordinary method, such as gravimetric
or volumetric will not respond. The principle of flame photometer is based on
the fact that different eliments emits light of different wave length on burning
in a flame. This characteristics wave length by a particular element isolated to
the characteristics wave band by an optical filter is allowed to fall on a
photocell whose output is measured by a suitable deflection for instant an
electronic amplifier and a meter or glavnometer. The intensity of the emitted
light is proportional to the concentration of the element in the solution. Thus
the concentration of an eliment can be determined in the solution through
determination of the intensities of solutions of different but known
concentrations and preparation of a standard curve.
ii.
Atomic Absorption Spectrophotometer: This instrument employ
special light source (hollow cathode lamps) constructed for the specific
element to be analyzed. A sample is dissolved in a solvent and burnt for
atomization and light from the specific cathode lamp is passed through the
flame. The proportion of light absorbed is proportional to the concentration of
the element in the sample.
Thus by comparison
of the extent of absorbed light of the unknown sample and a series of standard
solutions it is possible to calculate the concentration of the element in the
unknown sample. The instrument is widely used and accepted technique for
determining trace (hg/ml) or ultra trace (sub-hg/ml) levels of an element in a
wide variety of samples.
iii.
High Precision Thin Tayer Chromatography (HPTLC): In
chromatography the solution are resolved by differential rates of elution as
they passes through the plate or column. Their separation is governed by their
distribution between the stationary and mobile phases. HPTLC is a more
sensitive, adaptable and rapid technique than paper chromatography. It has wide
application in quantifying as well as qualitative analysis of various
biomolecular. It is the cheapest and the
best method for isolating and identifying minor components of food.
iv.
Gas Liquid Chromatography (GLC): It is the most elegant and
useful method in analytical chemistry. It is a form of partition chromatography
in which the stationary phase is a film held in place on a solid support and
the mobile phase is a carrier gas flowing over the surface of a liquid film in
a controlled fashion. The vaporized sample is fractionated as a consequences of
being partioned between the mobil gas phase and liquid stationary phased held
in a column. Analysis of food using GLC is concerned with the assay of lipid,
proteins, carbohydrates, preservatives, flavours, colorants and texture modifiers.
It is particularly suitable for determination of fatty acid profile of the food
lipids and flavours compounds of a food. It is also usefull in the analysis
of vitamins,
steroids drugs and pesticide residues.
v.
High Pressure liquid chromatography (HPLC): This is a very fine
and high precision technique but the successful use of the techniques for a
given problem requires the right combination of a variety of operating
conditions such as the type of column, packing and mobile phase, column length
and diameter, flow rate, column temperature and sample size. In fact newer
columns and packing materials offer high performance at moderate pressure
(although still high relative to gravity flow). HPCL methods have been
developed in a variety of areas including organics, biological, small
molecules, macromolecules, pollutants, polymers, and many others.
Chromatography can be done in a number of modes. The best mode for a particular
separations depends on the structural characteristics of the solutes to be
separated and the analysis requirements. HPLC methods can be selected based on
the molecular weight and the solubility of the substance. In many samples
separation can be achieved by reverse phase chromatography using a bonded
silica, stationary phase.Reverse phase HPLC is the first choice because it is
often faster, cheaper and easier than other alternatives.
vi.
Rancimate: This is a modern, PC-controlled instrument which is used to determine
the oxidative stability of a fatty food. The determination of the oxidative
stability in natural fat and oils is a method of quality control in food industry.
This method has been developed as an automated version of the extremely
demanding AOM method (active oxygen method) for the determination of
the induction time of fats and oils. In this method the highly volatile organic
acids produced by oxidation are absorbed in water and used to indicate the
induction time.
vii.
Liquid Chromatography Mass Spectrophotometer (LCMS): Its
an indispensable tool for problems solving in virtually all analytical fields
requiring “information rich” chemical analysis. Its use is must when the
concentration of residues and contaminants is in PPB levels.
viii.Gas
Chromatography Mass Spectrophotometer (GCMS): It
involves high resolution capillary gas chromatography with mass spectral
detection,aids in the analysis of residual volatiles in polymers,
pharmaceuticals and packing materials. It is must for the pesticide analysis.
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