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Speaker
Prof. (Dr.) Ashwani Kumar
Professor, Guru Gobind Singh College of Pharmacy, Yamuna Nagar
Topic: Medicinal and Aromatic Plants I 03.09.2022
Medicinal and Aromatic
Plants
{औषधीय और सुगंधधत पौधे }
Dr. Ashwani Kumar
Professor
Guru Gobind Singh College of Pharmacy
ashwani1683@gnkgei.ac.in
Learning
Outcomes
Concepts of Herbal Drug Development
Extraction Technologies of Herbal
Drugs
Chemical Characterization of Herbal
Drugs
In-vitro & in-vivo evaluation of herbal
drugs
Herbal Formulation Development
Introduction
• Medicinal and aromatic plants (MAPs) play
an important role in the healthcare of people
around the world.
• Until the advent of modern medicine, man
depended on plants for treating diseases.
Teerth (1998) listed 85 commonly used herbs
in Ayurveda since past.
• Indian systems of medicine ‘Ayurveda,’
‘Sidha’ and ‘Unani’ (arabic) entirely, and
homeopathy to some extent, depend on plant
materials or their derivatives for treating
human ailments
• India has long time legacy of plant-based
medicines since vedic era.
PLANTS AS SOURCE OF BIOACTIVE MOLECULES
60,000 years ago
Plant-derived products have dominated the human pharmacopoeia for thousands
of years ………until the synthesis of aspirin ushered in an era dominated by the
pharmaceutical industry
The history of drugs
1897
towards the scientific validation of
medicinal plants from all over the world and
the isolation of bioactive molecules from
natural sources
Unit
Operations
in
Extraction
1. Size reduction
2. Extraction
Cold aqueous percolation
Hot aqueous extraction (decoction)
Solvent extraction (cold or hot)
3. Filtration
4. Concentration
5. Drying
Commonly used methods in the
extraction of medicinal plants
• Hydro-distillation method:
Soxhlet extraction
Clevenger extraction
Microwave-assisted extraction
Ultrasound-assisted extraction
• Enfleurage method
• Ecuelle method
Clevenger apparatus Soxhlet apparatus
Ecuelle Method
Percolation Method Decoction
Maceration Enfleurage
EXTRACTION OF BIOACTIVE COMPOUNDS FROM PLANTS
The case of Curcuma longa L.
curcumin
demethoxycurcumin
(DMC)
bisdemethoxycurcumin
(BDMC)
FROM CONVENTIONAL METHODS……
Ethanol: highest yield of extract, very low
content in curcuminoids
Acetone/ethyl acetate: more appropriate,
but more toxic!
……….TO THE INNONATIVE ONES
 Microwaves assisted-extraction (MAE)
 Ultrasound assisted-extraction (UAE)
 Pulsed electric field (PEF) extraction
 Ionic liquid-assisted extraction (ILAE)
 Supercritical fluid extraction (SFE)
Rhizome contents: curcuminoids (2–6%), volatile oil (3–7%),
fiber (2–7%), mineral matter (3–7%), protein (6–8%), fat (5–
10%), moisture (6–13%), and carbohydrate (60–70%)
undesirable impacts
toward the
environment and food
components
Supercritical fluid extraction (SFE) of C. longa L.
CO2
 inexpensive, environmentally friendly and generally
recognized as safe
 easily tunable solvent strength
 gaseous at room temperature and pressure, which makes
extract recovery very simple and provides solvent-free
extracts.
Oleoresin of C. longa
SFE-CO2
Soxhelet CO2
CO2 + EtOH
350 bar
65°C
scCO2 + 30% EtOH s
sufficient to achieve
convincible amount of
curcumin yield
Chemical Characterization of Herbal Drugs
• Phytochemicalscreening:Alkaloids,Flavonoids,Tannins,Glycosides etc.
• Qualitative&QuantitativeAnalysis:Thinlayerchromatography,HPLC,GCetc.
• IsolationofMarkerCompounds:
ColumnChromatography
Flashchromatography
• CharacterizationofMarkerCompound:FTIR,NMR,Mass
QUALITY
CONTROL
METHODS
FOR HERBAL
DRUGS
• Powder fineness and sieve size
• Determination of foreign matter
• Macroscopic and microscopic examination
• Thin-layer chromatography
• Determination of ash
• Determination of extractable matter
• Determination of water and volatile matter
• Determination of volatile oils
• Determination of bitterness value, swelling
index and foaming index.
DETERMINATION OF PESTICIDE RESIDUES
Medicinal plant materials are liable to contain pesticide residues which
accumulate from agricultural practices, such as spraying and
administration of fumigants during storage.
WhereADL=Acceptable dailylimit
W= body weight
E=Extraction factor
MDI=Mean daily intake of drug
Maximum residue limit =
ADLx W x E
MDI X (100 X Safety factor)
DETERMINATION
OF ARSENIC AND
HEAVYMETALS
Contamination of medicinal plant materials with
arsenic and heavy metals can be attributed to many
causes including environmental pollution and traces
of pesticides.
• Limit test for arsenic
The amount of arsenic in the medicinal plant
material is estimated by matching the depth of colour
with that of a standard stain.
• Limit test for cadmium and lead
The method of determination is left to the analyst.
Nevertheless, the determination must be consistent
and sensitive enough to allow comparison with a
reference material.
RADIOACTIVE CONTAMINATION
A certain amount of exposure to ionizing radiation cannot be avoided
since there are many sources, including radionuclides occurring naturally in
the ground and the atmosphere.
Since radionuclides from accidental discharges vary with the type of
facility involved, a generalized method of measurement is so far not
available.
However, should such contamination be of concern, suspect samples can
be analysed by a competent laboratory. Details of laboratory techniques
are available from the International Atomic Energy Agency (IAEA).
• Preparation of sample solution
(plant extract)
• Preparation of culture
media Sample added to the
culture media
• Incubate for 24hrs to 48hrs at
aseptic condition
• Growth of microorganisms can
be identified by
turbidity/staining with suitable
reagents
DETERMINATIONOFMICRO-ORGANISMS
Ex-vivo studies
DRUG DISCOVERY PROCESS
AFTER ISOLATION OF METABOLITES FROM PLANTS, THE EVALUATION OF THE BIOLOGICAL ACTIVITY CAN BE PERFORMED
From basic research to the market?
Some natural compounds failed at the preclinical phase
DRUG DISCOVERY AND NATURAL PRODUCTS
What challenges
Major drawbacks
 Solubility
 Stability
 Selectivity
oImproving solubility
oImproving stability
o Improving the bioavailability and effects of NP
o Reducing the toxicity by loading them into
different types of delivery systems
BIO-TECHONOLOGY CAN HELP IN
Factors affecting
stability of
Herbal
medicinal
products
Plant Tissue Culture
Plant tissue culture is a technique of
growing plant cells, tissues, organs,
seeds or other plant parts in a sterile
environment on a nutrient medium
How?
Adult plant cells are totipotent,
meaning they have the ability to give rise
to a fully differentiated plant. Because of
this, it is possible to collect cells from a
mature plant and use those cells to
produce clones of that plant.
Plant tissue Culture Basics
 Modern plant tissue culture is performed under aseptic conditions
 Living plant materials from the environment are naturally contaminated on
their surfaces (and sometimes interiors) with microorganisms, so surface
sterilization of starting material (explants) in chemical solutions (usually
alcohol and sodium or calcium hypochlorite is required).
 Explants are then usually placed on the surface of a solid culture medium, but
are sometimes placed directly into a liquid medium, when cell suspension
cultures are desired.
 Culture media are generally composed of inorganic salts plus a few organic
nutrients, vitamins and plant hormones.
Plant tissue Culture Basics
 As cultures grow, pieces are typically sliced off and transferred to new
media (subcultured) to allow for growth or to alter the morphology of
the culture.
Plant Tissue Culture Applications
 Availability of raw material
 Fluctuation in supplies and quality
 Patent Rights
 Easy purification of the compound
 Modifications in chemical structure
 Disease free plants
 Crop improvement
 Biosynthetic Pathways
 Immobilization of cells
CSIR-Central Institute of Medicinal and
Aromatic Plants, Lucknow (UP).
CSIR-Institute of Himalayan BioresourceTechnology,
Palampur (HP)
CONCLUSIONS
Bioactive compounds of plant origin possess desired health/wellness benefit effects
in humans. So we should work together for the maintaining of sustainability of
plants.
Continuously growing interest in natural compounds has led to the development of
innovative extraction techniques, more sustainable and eco-friendly allowing
higher yields in a shorter time, significant reduction in solvent consumption and
energy consumption.
To overcome phytochemical drawbacks (instability, low solubility and poor
absorption) NDDS (nanoencapsulation, using biodegradable and biocompatible
material), is a way to formulate them in order to enhance the therapeutic efficacy.
Medicinal and Aromatic Plants.pptx

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Medicinal and Aromatic Plants.pptx

  • 1. Speaker Prof. (Dr.) Ashwani Kumar Professor, Guru Gobind Singh College of Pharmacy, Yamuna Nagar Topic: Medicinal and Aromatic Plants I 03.09.2022
  • 2. Medicinal and Aromatic Plants {औषधीय और सुगंधधत पौधे } Dr. Ashwani Kumar Professor Guru Gobind Singh College of Pharmacy ashwani1683@gnkgei.ac.in
  • 3.
  • 4. Learning Outcomes Concepts of Herbal Drug Development Extraction Technologies of Herbal Drugs Chemical Characterization of Herbal Drugs In-vitro & in-vivo evaluation of herbal drugs Herbal Formulation Development
  • 5. Introduction • Medicinal and aromatic plants (MAPs) play an important role in the healthcare of people around the world. • Until the advent of modern medicine, man depended on plants for treating diseases. Teerth (1998) listed 85 commonly used herbs in Ayurveda since past. • Indian systems of medicine ‘Ayurveda,’ ‘Sidha’ and ‘Unani’ (arabic) entirely, and homeopathy to some extent, depend on plant materials or their derivatives for treating human ailments • India has long time legacy of plant-based medicines since vedic era.
  • 6.
  • 7. PLANTS AS SOURCE OF BIOACTIVE MOLECULES 60,000 years ago Plant-derived products have dominated the human pharmacopoeia for thousands of years ………until the synthesis of aspirin ushered in an era dominated by the pharmaceutical industry The history of drugs 1897 towards the scientific validation of medicinal plants from all over the world and the isolation of bioactive molecules from natural sources
  • 8.
  • 9.
  • 10. Unit Operations in Extraction 1. Size reduction 2. Extraction Cold aqueous percolation Hot aqueous extraction (decoction) Solvent extraction (cold or hot) 3. Filtration 4. Concentration 5. Drying
  • 11. Commonly used methods in the extraction of medicinal plants • Hydro-distillation method: Soxhlet extraction Clevenger extraction Microwave-assisted extraction Ultrasound-assisted extraction • Enfleurage method • Ecuelle method
  • 13. Ecuelle Method Percolation Method Decoction Maceration Enfleurage
  • 14. EXTRACTION OF BIOACTIVE COMPOUNDS FROM PLANTS The case of Curcuma longa L. curcumin demethoxycurcumin (DMC) bisdemethoxycurcumin (BDMC) FROM CONVENTIONAL METHODS…… Ethanol: highest yield of extract, very low content in curcuminoids Acetone/ethyl acetate: more appropriate, but more toxic! ……….TO THE INNONATIVE ONES  Microwaves assisted-extraction (MAE)  Ultrasound assisted-extraction (UAE)  Pulsed electric field (PEF) extraction  Ionic liquid-assisted extraction (ILAE)  Supercritical fluid extraction (SFE) Rhizome contents: curcuminoids (2–6%), volatile oil (3–7%), fiber (2–7%), mineral matter (3–7%), protein (6–8%), fat (5– 10%), moisture (6–13%), and carbohydrate (60–70%) undesirable impacts toward the environment and food components
  • 15. Supercritical fluid extraction (SFE) of C. longa L. CO2  inexpensive, environmentally friendly and generally recognized as safe  easily tunable solvent strength  gaseous at room temperature and pressure, which makes extract recovery very simple and provides solvent-free extracts. Oleoresin of C. longa SFE-CO2 Soxhelet CO2 CO2 + EtOH 350 bar 65°C scCO2 + 30% EtOH s sufficient to achieve convincible amount of curcumin yield
  • 16. Chemical Characterization of Herbal Drugs • Phytochemicalscreening:Alkaloids,Flavonoids,Tannins,Glycosides etc. • Qualitative&QuantitativeAnalysis:Thinlayerchromatography,HPLC,GCetc. • IsolationofMarkerCompounds: ColumnChromatography Flashchromatography • CharacterizationofMarkerCompound:FTIR,NMR,Mass
  • 17. QUALITY CONTROL METHODS FOR HERBAL DRUGS • Powder fineness and sieve size • Determination of foreign matter • Macroscopic and microscopic examination • Thin-layer chromatography • Determination of ash • Determination of extractable matter • Determination of water and volatile matter • Determination of volatile oils • Determination of bitterness value, swelling index and foaming index.
  • 18. DETERMINATION OF PESTICIDE RESIDUES Medicinal plant materials are liable to contain pesticide residues which accumulate from agricultural practices, such as spraying and administration of fumigants during storage. WhereADL=Acceptable dailylimit W= body weight E=Extraction factor MDI=Mean daily intake of drug Maximum residue limit = ADLx W x E MDI X (100 X Safety factor)
  • 19. DETERMINATION OF ARSENIC AND HEAVYMETALS Contamination of medicinal plant materials with arsenic and heavy metals can be attributed to many causes including environmental pollution and traces of pesticides. • Limit test for arsenic The amount of arsenic in the medicinal plant material is estimated by matching the depth of colour with that of a standard stain. • Limit test for cadmium and lead The method of determination is left to the analyst. Nevertheless, the determination must be consistent and sensitive enough to allow comparison with a reference material.
  • 20. RADIOACTIVE CONTAMINATION A certain amount of exposure to ionizing radiation cannot be avoided since there are many sources, including radionuclides occurring naturally in the ground and the atmosphere. Since radionuclides from accidental discharges vary with the type of facility involved, a generalized method of measurement is so far not available. However, should such contamination be of concern, suspect samples can be analysed by a competent laboratory. Details of laboratory techniques are available from the International Atomic Energy Agency (IAEA).
  • 21. • Preparation of sample solution (plant extract) • Preparation of culture media Sample added to the culture media • Incubate for 24hrs to 48hrs at aseptic condition • Growth of microorganisms can be identified by turbidity/staining with suitable reagents DETERMINATIONOFMICRO-ORGANISMS
  • 23. DRUG DISCOVERY PROCESS AFTER ISOLATION OF METABOLITES FROM PLANTS, THE EVALUATION OF THE BIOLOGICAL ACTIVITY CAN BE PERFORMED From basic research to the market? Some natural compounds failed at the preclinical phase
  • 24. DRUG DISCOVERY AND NATURAL PRODUCTS What challenges Major drawbacks  Solubility  Stability  Selectivity oImproving solubility oImproving stability o Improving the bioavailability and effects of NP o Reducing the toxicity by loading them into different types of delivery systems BIO-TECHONOLOGY CAN HELP IN
  • 26.
  • 27.
  • 28. Plant Tissue Culture Plant tissue culture is a technique of growing plant cells, tissues, organs, seeds or other plant parts in a sterile environment on a nutrient medium
  • 29. How? Adult plant cells are totipotent, meaning they have the ability to give rise to a fully differentiated plant. Because of this, it is possible to collect cells from a mature plant and use those cells to produce clones of that plant.
  • 30. Plant tissue Culture Basics  Modern plant tissue culture is performed under aseptic conditions  Living plant materials from the environment are naturally contaminated on their surfaces (and sometimes interiors) with microorganisms, so surface sterilization of starting material (explants) in chemical solutions (usually alcohol and sodium or calcium hypochlorite is required).  Explants are then usually placed on the surface of a solid culture medium, but are sometimes placed directly into a liquid medium, when cell suspension cultures are desired.  Culture media are generally composed of inorganic salts plus a few organic nutrients, vitamins and plant hormones.
  • 31. Plant tissue Culture Basics  As cultures grow, pieces are typically sliced off and transferred to new media (subcultured) to allow for growth or to alter the morphology of the culture.
  • 32. Plant Tissue Culture Applications  Availability of raw material  Fluctuation in supplies and quality  Patent Rights  Easy purification of the compound  Modifications in chemical structure  Disease free plants  Crop improvement  Biosynthetic Pathways  Immobilization of cells
  • 33. CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow (UP). CSIR-Institute of Himalayan BioresourceTechnology, Palampur (HP)
  • 34.
  • 35. CONCLUSIONS Bioactive compounds of plant origin possess desired health/wellness benefit effects in humans. So we should work together for the maintaining of sustainability of plants. Continuously growing interest in natural compounds has led to the development of innovative extraction techniques, more sustainable and eco-friendly allowing higher yields in a shorter time, significant reduction in solvent consumption and energy consumption. To overcome phytochemical drawbacks (instability, low solubility and poor absorption) NDDS (nanoencapsulation, using biodegradable and biocompatible material), is a way to formulate them in order to enhance the therapeutic efficacy.