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The plants based medicine has served the mankind
in the treatment of various ailments since times
immemorial. In India around 25000 effective plant based
formulations are used in traditional and folk medicine.
There is a need of scientific investigations to prove the
rationale of using these formulations in healthcare and
such research have accelerated with a great pace in
recent years. Some major pharmaceutical companies
are currently conducting extensive research on plant
materials for possible new pharmaceuticals. Plants
have given some novel pharmaceuticals like opium,
aspirin, digitalis, quinine which are in a great demand.
The Sacred Fig, Ficus religiosa L (family moracea) is a
multipurpose forest tree with great religious holdings,
native to India, Bangladesh, Nepal, Pakistan, Sri
Lanka and southwest China. Ficus religiosa is used in
traditional medicine for about 50 types of disorders
including asthma, diabetes, diarrhea, epilepsy, gastric
problems, bacterial infections, diabetes, gonorrhea, skin
diseases, inflammatory disorders, infectious, sexual
disorders and many more. Despite its diverse medicinal
properties, the tree has not been exploited commercially
for pharmaceuticals purpose. The religious holdings
and social values associated with this tree restrict its
use for isolation, identification, characterization and
commercial supply of secondary metabolites. Hence,
there is an urgent need for alternative source. Plant
cell cultures were introduced as an important tool for
studying and producing plant secondary metabolites in
the mid 1960s. Till now there is no report of production of
any secondary metabolite from the callus tissue of Ficus
religiosa L. We aimed at optimizing the conditions for
producing the callus cultures from the nodal segments
of 45-50 years old tree of Ficus religiosa L. The callus so
produced was continuously propagated and proliferated
remarkably for a span of six months. Various extracts
of the callus tissue and the stem segments of the tree
were prepared using the different solvents in decreasing
order of solvents. A comparative analysis of various
phytochemicals was carried out between aqueous
extract of callus and aqueous extract of stem. Various
qualitative tests for different phyto-chemicals showed
the remarkable presence in callus tissue as indicated
by dark intense color reactions whereas in stem extract
faint colour reactions appeared for some. Total phenolic
content was many folds more in callus cultures as
compared to in vivo source, as indicated by quantitative
tests. A discussion will be presented regarding various
factors for production of various secondary metabolites
in callus cultures.
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