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Cards (346)
Pharmacognosy
Applied science that deals with the biological, biochemical and economic features of drugs or biological origin and their constituents
Crude drugs
Plant exudates
Natural
substances
No
molecular
modification had been made
Derivatives
or extractives
Chief
principles
or constituents of crude
drugs
Solvent / menstruum
Liquid
or
liquid
mixture
Marc
Undissolved
portion
Indigenous
plants
Native countries
Naturalized plants
Foreign
land
Rinorea
niccolifera
Metal eating plant
(more on nickel)
Geographic
source & Habitat
Region in which the plant or
animal
yielding the drug
grows
Infusion
Hot water (ex. Tea); short contact action -
3-5
minutes only
Maceration
Soaked in solvent for
long periods
of time
Percolation
Filtering
of fluids through porous materials; passage through
percolate
(ex. Simple Syrup USP)
Digestion
Not boiling (low heat); <35 - 40⁰ C
Decoction
Boiling
water
Liquid-Liquid Extraction
1.
Portioning
2.
Distillation
Distillation
Purifying liquid by
heating
and
cooling
Collection
Small scale
Improper collection results to partial or complete substitution
Collection time -
Flower
- best to harvest at dawn
Bark
- spring and summer
Root crops - when upper ground portion is about to wither
Harvesting
Large
scale
Manual labor vs.
mechanical
devices
Mechanical
devices: pickers, mowers, binders, swath, steel
Manual - for
potent
constituents
Drying
Air
drying and
artificial
drying
Prevent
bacterial, fungal growth and enzymatic degradation
Facilitates
grinding
and
milling
Curing
- special drying process
Garbling
Final step in the
preparation
of crude drugs
Removal of
extraneous
matter (other parts of the plant, dirt, added adulterants)
Packaging
, storage & preservation
To avoid insect attacks: Expose drug to
65°c
Fumigation
with
methyl bromide
Add a drop of
chloroform
or
carbon tetrachloride
Evaluation of Drugs
Quality
(inherent/descriptive in nature) and purity
Qualitative
and quantitative assays
Quality
- intrinsic property of drug; type of medicinal principles
Quantity
- amount
Organoleptic
/Morphological evaluation
1. Evaluate
macroscopic
appearance of drug:
Shape
2.
Size
3.
Color
4.
Fracture
&
internal
color
5.
Odor
6.
Taste
Microscopic evaluation
1. Identity and
purity
of the
drug
substance
2.
Adulterant
can also be detected
microscopically
3.
Staining
techniques and
reagents
Pharmacologic
evaluation
1.
Preclinical
or
Bioassay
2.
Living organism
or their
isolated
living tissues are used
3.
Antibiotics
, toxins and toxoids and
vitamins
Chemical
evaluation
1. Qualitative and
quantitative
determination of their
active
principles
2.
Assay
- titration is the best method for determining official potency
3.
Preliminary Phytochemical Screening
Physical evaluation
1.
Physical characteristic
or parameters with the use if
physico-chemical techniques
2. Solubility, sp. Gr.,
optical rotation
, congealing point, refractive index,
melting point
Classification
of Drugs
Morphology
Taxonomy
Pharmacologic
Chemical
Alphabetical
Constituent
Mixture of
substance
Secondary
plant substance
Extracted
,
crystallized
and purified
Inert
matter
Active
Constituent
Secondary
metabolites
Isolated
constituent that is either
pharmacologically active
or pharmaceutically active
Pharmaceutically
active
Cause chemical changes in the
preparation
Pharmacologically
active
Responsible
for the
therapeutic
activity
Inert
constituents
No definite
pharmacologic
activity
Drug
Biosynthesis/Biogenesis is Influenced by
Ontogeny or
Stage
of
Development
(stage of development)
Heredity
(genetic composition)
Environment (soil, climate, associated flora and
method
of
cultivation
)
Biosynthesis
of Glycosides
1.
Condensation
products of
sugar
and the acceptor unit called as aglycone
2. Sugar phosphates +
uridine triphosphate
(UTP) → uridine diphosphate
sugar complex
3.
Uridine diphosphate sugar complex
+
acceptor
units → glycoside production
Glycosides
and their biosynthesis
Anthracene
glycosides
Phenol
Glycosides
Steroid
Glycosides
Flavonoid
Glycosides
Cyanogenetic
Glycosides
Thioglycosides/
Isothiocyante
Glycosides
Saponin Glycosides
Aldehyde Glycosides
Biosynthesis
of Phenylpropanoids
Shikimic
Acid biosynthetic pathway → phenylalanine and tyrosine →
phenylpropanoids
Phenylpropanoids
Phenolic
in character; devoid of
nitrogen
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