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INTRODUCTION: are yellow or orange carotenoids known as

xanthophylls.
Lipids are substances found in living
life forms that are insoluble in water yet Column chromatography is one of the
dissolvable in nonpolar solvents and most useful methods for the separation and
solvents of low polarity. This absence of purification of both solids and liquids when
dissolvability in water is an essential carrying out small-scale experiments.
property because our body chemistry is so Column chromatography is another solid-
firmly based on water. Most body liquid technique in which the two phases are
constituents including carbohydrates which a solid (stationary phase) and a liquid
are dissolvable in water. In any case, the (moving phase). The theory of column
body likewise needs insoluble mixes for chromatography is analogous to that of thin-
some purposes, including the partition of layer chromatography. The most common
compartments containing watery adsorbents - silica gel and alumina - are the
arrangements from each other, that is the same ones used in TLC. The sample is
place lipids come in. The water-insolubility dissolved in a small quantity of solvent (the
of lipids is because of the way that the polar eluent) and applied to the top of the column.
groups they contain are significantly smaller The eluent, instead of rising by capillary
than their alkane-like (nonpolar) segments. action up a thin layer, flows down through
These nonpolar portions give the water- the column filled with the adsorbent. Just as
repellent, or hydrophobic property. An in TLC, there is an equilibrium established
important use for lipids, particularly in between the solute adsorbed on the silica
animals, is storage of energy. Plant store gel or alumina and the eluting solvent
energy in form of starch. Animals including flowing down through the column.
people think that its more efficient to utilize
lipids (fats). In spite of the fact that our The stationary phase or adsorbent in
bodies do store a few carbohydrates as column chromatography is a solid. The most
glycogen for quick energy when we require common stationary phase for column
it, energy stored as fats is significantly more chromatography is silica gel, followed by
important. The reason is essentially that the alumina. Cellulose powder has often been
consuming of fats creates more than twice used in the past. Also possible are ion
as much energy as consuming of an equal exchange chromatography, reversed-phase
weight of carbohydrates. chromatography (RP), affinity
The yolk makes up about 33% of the chromatography or expanded bed
liquid weight of the egg; it contains adsorption (EBA). The stationary phases
approximately 60 calories, three times the are usually finely ground powders or gels
caloric content of the egg white. and/or are microporous for an increased
surface, though in EBA a fluidized bed is
One large egg (50 grams in weight, 17 used.
gram yolk) contains approximately: 2.7g
protein, 210 mg cholesterol, 0.61g The mobile phase or eluent is either a
carbohydrates and 4.51g total fat. (USDA pure solvent or a mixture of different
National Nutrient Database) solvents. It is chosen so that the retention
factor value of the compound of interest is
All of the fat soluble vitamins, (A, D, E and roughly around 0.2 - 0.3 in order to minimize
K) are found in the egg yolk. Egg yolks are the time and the amount of eluent to run the
one of the few foods naturally containing chromatography. The eluent has also been
vitamin D. chosen so that the different compounds can
Egg yolk is a source of lecithin, an be separated effectively. The eluent is
emulsifier and surfactant. The yellow color optimized in small scale pretests, often
is caused by lutein and zeaxanthin, which
using thin layer chromatography (TLC) with
the same stationary phase.

The objectives of the experiment are as


follows: (1) to extract total lipids from
chicken egg yolk, (2) to analyze the lipids
present in the crude extract using column
chromatography

Conclusion:
Extraction of Total Lipids from Chicken
Egg Yolk. Lipids are dissolvable in organic
solvents, however sparingly solvent or
insoluble in water. The current techniques
for the extraction of lipids from source
material ordinarily include specific solvent
extraction and the beginning material might
be subjected to drying before extraction.
Solubility of lipids is an important criterion
for their extraction from source material and
depends intensely on the type of lipid
present, and the proportion of nonpolar
(basically triacylglycerols) and polar lipids
(fundamentally phospholipids and
glycolipids) in the specimen; accordingly, a
few solvent system may be considered,
depending upon the kind of sample and its
component. The solvents of choice are
generally hexane, chloroform, methanol or
chloroform, methanol or water.

Complex lipids were isolated from


the egg yolk and were separated into
phosphorylated and non-phosphorylated
lipids. Non-phosphorylated lipid and
cholesterol gave a positive result for
Liebermann-Burchard and Salkowski tests
which means that cholesterol is present in
the non-phosphorylated lipid sample.
Phosphorylated lipid and lecithin reacted
positively for both Krauts and Ninhydrin
tests which means that lecithin is present in
the phosphorylated lipid sample. For
Molisch test, both non-phosphorylated lipid
and galactocerebroside yielded a positive
result which means that they contain a
carbohydrate.

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