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- •Foreword
- •Contributors
- •Preface
- •Contents
- •1. General Pharmacology
- •2. Pharmacology of Peripheral Nervous System
- •3. Pharmacology of Cardiovascular System
- •4. Drugs Acting on Urinary System
- •5. Drugs Acting on Respiratory System
- •6. Pharmacology of Central Nervous System
- •7. Chemotherapy
- •8. Autacoids and their Antagonists
- •9. Pharmacology of Drug Acting on theGastrointestinal Tract
- •10. Immunopharmacology
- •11. Vitamin and Minerals
- •12. Hormones
- •1. Introduction to Pharmacognosy
- •2. Sources and Classification of Crude Drugs
- •3. Factors Influencing Quality of Crude Drugs
- •4. Techniques in Microscopy
- •5. Introduction of Phytoconstituents
- •6. Glycosides
- •7. Alkaloids
- •8. Terpenoids, Volatile Oils and Resins
- •9. Principles of Plant Classification
- •10. Pharmaceutical Aids
- •11. Plant Products
- •12. Toxic Drugs
- •13. Poisonous Plants
- •14. Enzymes
- •15. Quantitative Microscopy
- •16. Biogenetic Pathways
- •17. Herbarium
- •18. Herbal Formulation
- •19. Plant Tissue Culture
- •20. Herbal Cosmetics
- •21. Herbal Formulation
- •1. Cellular Components
- •2. Carbohydrates
- •3. Proteins
- •4. Lipids
- •5. Vitamins
- •6. Biological Oxidation and Reduction
- •7. Enzymes
- •8. Nucleic Acids
- •9. Hereditary Diseases
- •1. Plant Cell
- •3. Fermentation
- •4. Recombinant DNA Technology
- •5. Proteomics
- •1. Introduction to Microbiology
- •2. Microscopy
- •3. Staining Methods
- •4. Biology of Microorganisms
- •5. Fungi and Viruses

S. No Type of organ
culture
5. Ovary culture In vitro method to produce haploids. The
6. Embryo culture Embryo culture can be defined as in vitro
7. Anther and
pollen culture
Description Applications
nature of growth of ovaries under the
influence of nutrients, vitamins and plant
growth regulators
development of isolated mature or immature
zygotic embryos from seeds in a suitable
culture medium to form seedlings. Plant cells
can also be induced to form embryos in plant
tissue culture; these embryos are called
somatic embryos. Two main steps in embryo
culture are removal or excision of the embryo
and taking care of nutritional requirement
Generally two procedures are followed to
obtain haploid plants in anther and pollen
culture: Direct culture of excised anthers on
liquid medium or on agar and by removal of
pollens from anther and its culture in a liquid
medium
Example: Unpollinated ovaries of Citrus
aurantifolia and C. sinensis produced
embryos and plantlets in culture regenerated
from the ovary wall
Provides a better and direct somatic
embryogenesis system. Embryo culture
may help shorten the breeding cycle, the
production of monoploids , testing for seed
viability, study of host pathogen interaction,
germination of seeds of parasitic plants
as well as rare plants, example: Musa
bulbisiona, where seed do not germinate in
nature but can be obtained through embryo
culture.
Used for the production of haploids,
which are of immense importance for the
improvement of some crop plants like
coffee, fruit trees where improvements of the
species is difficult due to their heterozygous
nature. Important for development of
mutants. Also useful material for studying
somatic cell genetics, especially for cell
modification by the introduction of foreign
organic matter. Applied in Datura innoxia and
rapeseed plant
HAIRY ROOT CULTURE
PROTOPLAST CULTURE
Thecell wall is thick made-up of cellulose andpectin.
Duringvarious proceses of crop improvementthrough
varioustypesofcultureitactsasabarriersoitisdissolved
bytheuseofcellulaseandpectinaseandanakedprotoplast
canbe freed. Protoplast (cell without cell wall)can be
developedinto individual plants orthey could be used
tofusewithnakedprotoplastofothervarietiesorspecies
to produce what are called somatic embryo. Crossing the
protoplastshasbeengreatlyfacilitatedbychemicalssuch
aspolyethyleneglycolorbyotherprocessessuchaselectro-
fusion.Suchhybridisationiscalledsomatichybridisation.
e.g.developingsomatichybridsbycrossingprotoplasts
oftwo species in crops: Brassica, Nicotiana, Petunia and
Solanum.
Isolation of Protoplast
By mechanical method
Plasmolyticum enzymatic method
Micropropagation
Thetissueculturepropagationprocesscanbedenedin
fourmainstages:
Section 2 Pharmacognosy
319

Stage.
No.
I Small pieces of plant material, called explants, are
II The cells of the explants multiply in one of two ways The cells may form a callus, are supplied with the correct
III The plantlets have developed and are ready for root
IV The plantlets are removed from the glass container They are divided, planted in a sterile medium, and placed
Stages of tissue culture propagation Description of stage
The explants are cleaned and placed on sterile agar
carefully removed from the parent plant. Explants are
obtained from the actively growing part (shoot tips,
sections of leaves, stems and roots, embryos, etc.) of
a desired plant
formation
medium in glass bottles or test tubes
The sterile agar medium is a gel that contains water,
sugars, nutrients, and plant hormones to support and
promote plant growth
Tiny leaves, stems and roots make tissue culture possible
hormones in the medium, these callus cells can develop
into a normal plant. The explant may produce many new
explants
Shoots are transplanted to another medium containing
auxins, a hormone that induces the growth of roots
The plantlets are also given higher light intensity in
preparation
in a greenhouse.
Care must be taken during this transition to acclimatise
the plant to their new environment
MULTIPLE CHOICE QUESTIONS
1. Select the media generally used in callus culture.
A. Liquid media B. Semi-solid media
C. Solid media D. None of these
2. The process of formation callus from meristmatic
state is known as ___________ .
A. Redifferentiation B. Cell division
C. Dedifferentiation D. Both A and B
3. Select the process by which culture can be
maintained for extended periods:
A. Primary culture
Section 2 Pharmacognosy
320
B. Totipotency
C. Proliferating media
D. Subculturing
4. In vivo callus culture can be occurred by:
A. Incorporating growth regulators
B. Result of wounding or cut
C. Incorporating cells in media
D. All of the above
5. In vivo callus culture can be done by:
A. By incorporating cells on growth media
B. Exogenous auxin
C. Both A and B
D. Endogenous auxin
6. Choose the method to induce in vitro callus
formation.
A. Totipotency
B. Endogenous auxin
C. Endogenous cytokinen
D. Incorporating auxin

7. Cytokinin in high ratio results in formation of:
A. Root B. Leaves
C. Shoot D. None of these
8. Auxin to cytokinin ratio if increases, it results in
formation of:
A. Shoot B. Root
C. Leaves D. None of the above
9. Media used in suspension culture is:
A. Solid media B. Agar media
C. Semi-solid media D. Broth media
10. Select the type of culture vessels used in
suspension culture.
A. Erlenmeyer flask B. Test tube
C. Petri dish D. None of these
11. Callus culture is similar to suspension culture
except addition of:
A. Tragacanth B. Agar
C. Gum acacia D. None of these
12. Name the type of callus formed in callus culture:
A. Hard callus B. Semi-solid callus
C. Stiff callus D. Soft callus
13. Incubation temperature of suspension culture is:
A. 50–55 ºC B. 20 ºC
C. 35–40°ºC D. 25 ºC
14. Generally cultures are sealed with:
A. Double aluminium foil
B. Single aluminium foil
C. Parafilms
D. Both A and B
15. Time duration to form cell suspension:
A. 4-6 weeks B. 3-4 days
C. 2-4 weeks D. 24 hrs
16. Types of cells formed in callus culture:
A. Colenchyma cells B. Sclerenchyma cells
C. Parenchyma cells D. None of these
17. Name the media used for callus culture:
A. Solid media B. Liquid media
C. Semi solid media D. None of these
18. Phenomenontogeneratewholeplantis known
as:
A. Dedifferentiation B. Cell division
C. Organogenesis D. Redifferentiation
19. Which type of light is used in suspension culture
during incubation?
A. Low intensity of light
B. High intensity of light
C. UV light
D. None of the above
20. Name the component necessary for suspension
culture.
A. High intensity light
B. Incubation at 45 ºC
C. Agar
D. Continous agitation
21. Throughout susupension culture continuous
agitation can be obtained at __________ rpm:
A. 10–20
B. 300–400
C. 100–200
D. No agitation needed
22. Select which one is type of suspension culture.
A. Continous culture B. Batch culture
C. Protoplast culture D. Both A and B
23. Name the process which occurs during incubation
period:
A. Cell differentiation
B. Cell division
C. Formation of primary metabolite
D. All of the above
24. Why growth of cells halts after sometime in
primary culture media?
A. Sufficient ingredient
B. Initiation of lag phase
C. Initiation of exponential phase
D. Formation of toxic metabolites
25. The process of transferring inoculum’s primary
media to secondary media is known as:
A. Primary culture B. Broth media
C. Subculture D. All of these
26. Phasediagramcurveisaplotbetween:
A. Cell colony vs time
B. Time vs size
C. Time vs cell size
D. Cell number vs time
27. The phase at which toxic metabolites accumulates
is:
A. Lag phase B. Exponential phase
C. Linear D. Stationary
28. Prolongationofstationaryphaseleadsto:
A. Lysis of cell B. Formation of toxic
C. Extensive death D. All of these
29. Select the cell doubling time of nicotiana tobacum:
A. 36 hr B. 48 hr
C. 22 hr D. 20 hr
30. What happens after addition of cellulose and
pectinase in culture media?
A. Cell lysis B. Callus formation
C. Cell dispersion D. Cell death
31. Select the disadvantage of batch cultures.
A. No period of steady state
B. Exponential growth achieved
C. Lage phase short time
D. All of the above
32. Select the culture used to overcome no period
steady state.
A. Batch culture
B. Zygotic embryo culture
C. Protoplast culture
D. Continuous culture
Section 2 Pharmacognosy
321

33. Open type and closed type cultures are:
A. Batch cultures
B. Zygote embryo cultures
C. Continuous cultures
D. Protoplast
34. Turbodiostat culture is a type of:
A. Open type continuous culture
B. Batch culture
C. Closed type continuous culture
D. Protoplast culture
35. Which type of culture is chemostat?
A. Batch type B. Closed type
C. Protoplast D. Open type
36. Select the main disadvantage(s) of continuous
culture due to which it is not used in large
scale:
A. Require lot of attraction
B. Equipment not available
C. No steady state period
D. Both A and B
37. Name the type of protoplast fusion in which after
enzymatic degradation protoplast fuse together
form homokaryons.
A. Cybridisation B. Totipotency
C. Spontaneous fusion D. Electrofusion
38. Select the option to reduce plasmodermatal
connection.
A. Charophyceae B. Plasmolyticum
C. Both A and B D. None of these
39. Solution of NaNO
used as:
3
A. Hypotonic B. Hypertonic
C. Isotonic D. None of these
40. Name the inventer(s) of NaNO
fusion:
3
A. Kuster B. Carlson
C. Pow et al D. Evans and Cocking
41. Therstsomatichybridinplantbyusingfusogen
was developed by:
A. Keller and Melcher B. Kuster
C. Carlson D. Evans and Cocking
42. Which method is not used in protoplast fusion?
A. Electroporation B. Chemical fusion
C. Electrofusion D. PEG treatment
43. Kellers and Melcher used for which treatment
A. High pH and high Ca
B. NaNo
treatment
3
2+
treatment
C. PEG treatment
D. Mechanism of fusion
44. Select the pH of protoplast fusion of tobacco:
A. Weak acid B. Highly alkaline
C. Neutral D. Weak base
45. Choose the concentration of Ca
Section 2 Pharmacognosy
322
protoplast fusion:
A. 1 mm B. 10 mm
C. 50 mm D. 20 mm
2+
used for
46. PEG acceptance asfusogen ofPlant protoplast
because
A. Formation of high frequency Hetrokaryons
B. Lowcytotoxicity
C. Both A and B
D. Low heterokaryons formation
47. In which fusion of technique high formation of
Binucleat , heterokaryons produced:
A. PEG treatment
B. High PH and Ca
2+
C. NaNO3 treatment
D. Electro fusion
48. Problemassociated with highly alkaline
solution
A. Protoplast lysis
B. Aggregration between two or three protoplast
C. Large clumps of protoplast
D. Low frequency heterokaryons
49. MainadvantagesofPEGtreatmentoverprotoplast
fusion
A. Large clumpot protoplast achieved
B. Aggregation between two or three protoplast
C. Toxic method
D. Low frequency heterokaryone
50. The widely used method for plant protoplast
fusion is:
A. High PEG and high Ca2+
B. NaNO3 treatment
C. Peg treatment
D. High Ca and PH
51. PEGperceutusedinprotoplastfusionare...
A. 10–15% B. 15–45%
C. 60–70% D. 95%
52. ChoosethecorrectopinionforPEGhigherthen
1000 mw causes
A. Adhesion
B. High frequency fusion of protoplast
C. Both A and B
D. Cohesion
53. ProlongationofincubationinPEGsolutionleads
to:
A. Cell lysis
B. Homokaryon formation
C. Decreased heterokaryon formation
D. Increased heterokaryon formation
54. Increase in Mechanism of fusion protoplast
adhesion is:
A. Temperature dependent
B. Temperature independent
C. pH independent
D. None of the baove
55. Select the nature of charge on plant protoplast.
A. Amphiphiles
B. Negative charge
C. Positive charge
D. No charge

56. Charge on protoplast vary up to:
A. +10 to +40 mv B. – 40 to – 60mv
C. 0 to – 10 mv D. –10 to – 30 mv
57. In mechanism of membrane fusion, the membrane
must have molecular distance of:
A. 20 Å B. 30 Å
C. 100 Å D. 80 Å
2+
58. Select the disadvantage of high pH, high Ca
ion
treatment:
A. Increase in negative charge
B. Neutralic charge
C. Tight adhesion
D. Reduces heterokaryon formation
59. Select the concentration which completely
removes the charges from tobacoo:
A. 10 mm CaCl
B. 30 mm CaCl
C. 60 mm CaCl
D. 100 mm CaCl
. 2H2O
2
. 2H2O
2
.2H2O
2
. 2H2O
2
60. SelectthebondwhichbindPEGmoleculeswith
protein bohydrate:
A. Hydrogen bond
B. Covalent bond
C. Ionic bond
D. Weak van der waal force
2+
61. In treatment with Ca
andPEG,Ca2+ works via:
A. Bridge between negative protein and PEG
B. Bridge between molecules of protoplast
C. Hydrogen bond
D. Strong covalent bond
62. PEGtreatmentusedinanimalcellculturescauses:
A. Hydrogen bond formation
B. Chemical charge
C. Structure alteration
D. None of the above
63. When PEG is used, the aggregation of
intramembranous protein occurs in:
A. Plant cell B. Animal cell
C. Both A and B D. None of these
64. Disadvantage(s) of chemical fusion:
A. Toxic fusogen
B. Produces random multiple cell aggregates
C. Fusogen must removed before culture
D. All of the above
65. Select the rapid method of fusion:
A. NaNO
B. High pH and high Ca
treatment
3
2+
C. Mechanism of fusion
D. Electrofusion
66. The time duration to complete electrofusion is:
A. 15 minutes B. 30 minutes
C. 1 hour D. 2 hours
67. Select themore benecialfusion for Solanum
tuberosum:
A. NaNO
treatment
3
B. Electrofusion
C. High PEG
D. All of the above
68. Solanun Brevidens produced more effectively by:
A. Nano
treatment
3
B. Electrofusion
C. PEG treatment
D. All of the above
69. Electrofusionofprotoplastwasrstdemonstrated
by:
A. Senda et al B. Zimmermann
C. Abkong D. Kao and Wetter
ANSWER KEY
1 B 2 C 3 D 4 B 5 D 6 D 7 C 8 B 9 D 10 A 11 B 12 D 13 D 14 D
15 A 16 C 17 C 18 D 19 A 20 D 21 C 22 D 23 B 24 D 25 B 26 D 27 D 28 D
29 B 30 C 31 A 32 D 33 C 34 A 35 D 36 D 37 C 38 B 39 A 40 D 41 C 42 A
43 A 44 B 45 C 46 C 47 A 48 C 49 B 50 D 51 B 52 C 53 C 54 B 55 B 56 D
57 A 58 B 59 A 60 A 61 A 62 C 63 B 64 D 65 D 66 A 67 B 68 B 69 A
Section 2 Pharmacognosy
323

20. Herbal Cosmetics
HERBAL PLANTS FOR SKIN CARE
Latin name Common name Part used Uses
Acorus calamus Sweet flag Rhizome Aromatic, dusting powders, skin lotions
Allium sativum Garlic Bulb Promotes skin healing, antibacterial controls sore, pimples
and acne
Aloe vera Aloe Leaf Moisturizer, sunscreen, emollient
Alpinia galanga Galanga Rhizome Aromatic, dusting powders
Avena sativa Oat Fruit Moisturizer, skin tonic
Asparagus
racemosus
Azadirachta indica Neem Leaf Antiseptic, reduce dark spots, antibacterial
Andropogon
muricates
Adhatoda vasica
Nees
Ailanthus excelsa Maharukh Leaf Check skin eruption and useful in skin creams and lotions
Buchanania lanzan Chironnji Seed Skin ointments, rashes, spots
Butea frondosa Dhak Leaf, seed Leaf used for pimples and seed used for fungal infection
Carica papaya Papaya Fruit Skin soft and remove blemishes
Cassia tora Panwar Leaf and seed Skin infection, ringworm and eruption
Citrus limon Nimbu Fruit Skin nourishment, useful as facial ingredients
Cocos nucifera Nariyal Oil Skin itches and rashes
Cucumis sativus Khira Fruit and seeds Protect skin from sunburn
Curcuma longa Haldi Rhizome Anti-inflammatory, antioxidant, enhances colour of skin
Curcuma amada Amhaldi Dry rhizome Face pack, acne and blemishes
Cuscuta refexa Akash Bhel Whole plant Dermatitis, itching and ringworm
Callicarpa
marcophylla
Echinacea
purpurea
Centella asiatica Gotu kola Plant Wound healing
Symphytum
officinale
Crocus sativus Kesar Flowering top Skin cleansing lotion
Eclipta alba Bhringraj Whole plant Skin diseases and eczema
Euphorbia
thymifolia
Jasminum
grandiflorum
Juniperus
communis
Section 2 Pharmacognosy
Lavendula vera Lavender Essential oil Antiacne cream
324
Shatavari Roots Used to wrinkle on the face
Khas Root Cure irrigated skin and allergies
Vasca Leaf Skin affection and control of scabies
Priyangu Dry fruits Treat acne, pimples and allergic skin patches
Echinacea Roots, stem, and
leaves
Comfrey Leaves Cell regeneration, stimulates the growth of new cells
Choti Dhudhi Whole plant Ringworm and skin infections
Chameli Flowers Skin diseases, protection from sunburn.
Aaraar Whole plant Skin rejuvenation
Skin regeneration
Contd...

Latin name Common name Part used Uses
Leucas aspera Hul Khusa Leaves Control scabies, skin psoriases, chronic skin, skin eruption
and eczema
Mallotus
Kamala Flower Controls scabies, ringworm
philippensis
Mangifera indica Mango Plant Antioxidant
Matricaria
Babuna Leaves Antiacne
chamomilla
Mimosa pudica Lajwanti Plant Skin cream and controls itching
Ocimum sanctum Tulsi Leaves Skin infection and rejuvenation
Phyllanthus
Amla Fruit Antioxidant
emblica
Prunus amygdalus Badam Fruit Skin beautification
Psoralea corylifolia Babchi Seed Skin diseases
Rosa damascena Lal Gulab Flowers Beautification, smoothness and protection from sunburns
Rubia cordifolia Manjit
Dry roots and stem
Dark spots on face
Santalum album Chandan Hardwood Skin beautification, protection of sunburn, antioxidant
properties
Saussurea lappa Kuth Root Treatment of chronic skin diseases
Sesamum indicum Til Seed Skin protection and rejuvenation
Swertia chirayita Til Bark Antioxidant
Withania somnifera Aswagandha Root Skin cleansing formulations and antioxidant
HERBAL PLANT FOR HAIR CARE
Latin name Common name Part used Uses
Emblica officinalis
Acacia concinna Ritha, Shikakai
Aloe barbadensis Aloe
Azadirachta indica Neems
Callicarpa
macrophylla
Eclipta prostrata Bhringraj
Lawsonia inermis Mehandi
Centella asiatica Brahmi
Eclipta alba Bhringraj Hair tonic
Cocos nucifera Coconut fruit Oil of coconut fruit is used in different hair formulations
Eucalyptus
globulus
Lawsonia inermis Henna Leaves Hair colour
Azadirachta indica Neem Leaves Hair tonic and conditioners
Hibiscus rosa
sinensis
Amla Dry fruits Hair care, hair tonic
Pods Hair growth, prevent hair splitting, hair falling and
dandruff
Leaves Hair falling, dandruff, sunburn
Whole plant Hair and scalp care
Priyangu
Fruits Prevent acne
Whole plant Keep hairs in their original colour
Leaves Colour the hairs
Herb
Maintains proper bodily environment that leads to
healthy hairs
such as shampoos and hair oil
Eucalyptus Fruit Prevents Dandruff
Gurhal Petal Prevents premature graying, hair loss and scalp
disorders.
Contd...
Section 2 Pharmacognosy
325

Latin name Common name Part used Uses
Nardostachys
jatamansi
Trigonella foenum
graecum
Juniperus
virginiana
Rosmarinus
officinale
Arnica montana Arnica Flower Tonic and stimulates hair follicles
Betula pendula Birch Leaves Antidandruff
Calendula
officinalis
Carthamus
tinctorius
Centella asiatica Mandukaparni Whole plant Growth and maintenance of hairs
Ficus racemosus Bargad Root Checks hair fall
Salvia officinalis Sage Whole plant Hair conditioner
Sapindus
mukorossi
Saussurea lappa Kuth Root Hair dyeing
Terminilia bellirica Behera Seed Hair dyeing preparations
Thymus serphyllum Banajwain Whole Herb Preparing hair tonic
Jatamansi Rhizomes Hair tonic and impart blackness to hairs.
Fenugreek Seeds Hair grow, preserves natural colour, keeps hair silky and
also cures dandruff
Cedar wood oil Woods Hair loss and dandruff
Rosemary OIl Promote hair growth and shining
Marigold Flowers Hair cream for smoothing effect
Safflower Whole plant Hair tonic
Ritha Fruit Natural shampoo and hair cleanser
Introduction
Intellectualproperty rights (IPRs) defined as ideas,
inventions,andcreativeexpressionsbasedonapublic
willingnesstobestowthestatusofproperty.
IPRsprovideexclusiverightstotheinventorsorcreatorsof
that property, in order to enable them to reap commercial
benetsfromtheircreativeeffortsorreputation.
Thereareseveraltypesofintellectualpropertyprotection
like patent, copyright, trademark, etc.
IPRsis prerequisite forbetter identication, planning,
commercialisation,rendering,andtherebyprotectionof
inventionorcreativity.Pharmaceuticalindustrycurrently
hasanevolvingIPRstrategyrequiringabetterfocusand
approach in the coming era.
Types of Intellectual Properties and their Description
Originally, only patent, trademarks, and industrial
designswere protected as ‘industrial property’, but
nowtheterm‘intellectualproperty’hasamuchwider
meaning.IPRenhancestechnologyadvancementinthe
followingways:
a. It provides a mechanismof handling infringement,
piracy, and unauthorized use.
b. Itprovidesapoolofinformationtothegeneralpublic
sinceallformsofIParepublishedexceptincaseoftrade
secrets.
Section 2 Pharmacognosy
IPprotection can be sought for a variety ofintellectual
326
effortsincluding:
I Patentsarerecognitionforaninvention,whichsatises
thecriteria of global novelty, non-obviousness, and
industrial application.
II Industrial designsrelates to featureof any shape,
conguration,surfacepattern,compositionoflinesand
coloursappliedtoanarticlewhether2-D,e.g.textile,
or3-D.
III Trademarks relate to unique mark, name or logo
underwhichtradeisconductedforanyproductor
serviceandbywhichthemanufacturerortheservice
provideris identied. It can bebought, sold, and
licensed,hasnoexistence apart fromthegoodwill
oftheproductorserviceitsymbolises.Atrademark
isamark(i.e.thenameoftheproductpresentedon
signs or packages) which can be used to protect an
herbalmedicine’sreputation.Manufacturersidentify
afederally registered trademark with acircled R
symbol,i.e.“®”.Trademarksareconsumer-oriented
offerstheenduser a guaranteeofquality,service,
and product image.
IV Copyright relates to expressionofideas in material
formandincludesliterary,musical,dramatic,artistic,
cinematography work, audio tapes, and computer
software.
V Geographicalindications are indications, which
identifyas good as originating in the territory ofa
country or a region or locality in that territory where
agivenquality,reputation,orothercharacteristicof
the goods is essentially attributable to its geographical
origin.

IPR Laws in India
Asa member of the variousinternational conventions
andagreements,Indiaisboundtoenact/amendrelevant
domesticlaws to gearup and face the challenges of
globalisation.Inordertoconrmtothestipulationsinthe
TRIPS(Trade-relatedAspectsofIntellectual Property Rights)
Agreement, IPRs related laws in India are undergoing
changes.
APatentAct(1970)whichwasoneofthemostimportant
milestonesinthehistoryofIPRlawsinIndiaamendments
bygovernmentin1999,2002and2005.Themainchanges
brought through the amendments do not substantially
affect traditional knowledge, farmers’ rights and
biodiversity.Therearealsofewprovisions,whichattempt
toreduce biopiracy. As an example,the scope ofan
‘invention’hasbeenexpandedtocoverallgroundsofnew
scienticcreations.Despite,newusesofknownsubstances,
includingtheduplicationoftraditionalknowledgehave
beenspecicallyexcludedfrompatentability.Inaddition,
thenondisclosureofthesourceofgeographicaloriginof
atraditionallyknownmaterialhasbeenmadeabasisfor
thechallengeofapatent.
TheBiologicalDiversityAct,2002wasadoptedfollowing
India’sraticationoftheBiodiversityConvention(CBD).
Itaims to conserve biodiversity, sustainableuse of
biologicalresourcesandequitablesharingofbenetsthat
arisefromtheiruseortraditionalknowledge.Itmandates
thesettingupofinstitutionsatnational,stateandlocal
levels,forthepurposeofregulationofbiologicaldiversity.
TheActattempts to regulate accessto biodiversity for
commercialpurposes,toghtbiopiracy,andrecognise
community rights overtraditional knowledge and
biodiversity.
Plant Varieties Protection and Farmers Rights (PVPFR)
Act, 2001 was enacted under the obligations set out in
AgreementonTrade-relatedIntellectualPropertyRights
(TRIPS)whichmandatestheprotectionofplantvarieties
either by patents. The Indian legislation on Plant Varieties
Protection (PVP) is being perceived as a progressive
legislation when compared to the PVP Acts adopted by
theother developing nations. The PVPFRAct of India,
inadditiontoofferingprotectiontoplantbreedersinthe
formofplantbreeder’srights,alsoprotectstherightsof
thefarmerstosave,use,sow,re-sow,exchange,shareor
sellfarmproduceincludingtheseedsofanyunprotected
variety,withanexemptiontopreventthesaleofbranded
seeds.This law incorporates some principlesof the
Conventionon Biological Diversity (CBD) likeprior
informedconsentandsharingofbenetswithfarmers.
PATENTS
Patentsmay provide the strongest IP protection, most
difculttoobtainfornaturalorherbalmedicines.Patents
providethe patentee the rights to exclude othersfrom
making,using,selling,offeringforsale,orimportingthe
patentedinvention.Itisagrantbyastatetoaninventor
orto his assignee,giving exclusive rights tomake, use,
exerciseandvendtheinventionsforalimitedperiod,in
exchangefordisclosureinapatentspecication.According
toPatentAct,1970,itisdenedasnewinventionwhich
shouldbeuseful,newandnon-obviousnotusedpreviously
inuseinIndiainvention.
Objectives
1. Giving a legalmonopoly to the patentee toreap the
economicbenetsfromhisinvention.
2. Facilitatingthe improvements or providing the
alternativeapproachestodevelopthenewideasorand
products.
3. Inventionofnewdrugs.
Objective of Patents
RATIONALE OF PATENT
Patentis recognition to the formof IP manifestedin
invention.Patentsaregrantedforpatentableinventions,
whichsatisfytherequirementsofnovelty and utility under
the stringent examination and opposition procedures
prescribed in the Indian Patents Act, 1970, but there is
noteven a prima-facie presumption as to the validity
ofthe patent granted. Most countries have established
nationalregimestoprovideprotectiontotheIPRwithinits
jurisdiction.Exceptinthecaseofcopyrights,theprotection
grantedtotheinventor/creatorinacountry(suchasIndia)
oraregion(suchasEuropeanUnion)isrestrictedtothat
territorywhere protection is sought and is notvalid in
other countries or regions. For example, a patent granted
inIndiaisvalidonly for India and notintheUSA.The
basicreasonforpatentinganinventionistomakemoney
throughexclusivity,i.e.,theinventororhisassigneewould
haveamonopolyif:
a. Inventorhasmadeanimportantinventionaftertaking
intoaccountthemodicationsthatthecustomer.
b. Patentagenthasdescribedandclaimedtheinvention
correctlyin the patentspecification drafted, then
theresultant patent would give the patent owner an
exclusivemarket.
Thepatentee can exercise his exclusivityeither by
marketingthepatentedinventionhimselforbylicensing
it to a third party.
PROCEDURE FOR PATENTING
1. FILLINGANAPPLICATION
A.Name,addressandnationalityoftheapplicant
B.Title,name,addressandnationalityoftheinventor,
ifheisnottheapplicantorco-applicant.
C.Specications(provisionalandcomplete)givingthe
detailsoftheinvention.
D.Claims,denitionandscopeoftheinvention.
Section 2 Pharmacognosy
327

2. EXAMINATIONOFTHEAPPLICATION
A.Priorapprovedpatentsorapplicationsled
B.Novelty
C.Usefulness
D.Natureofclaims
3. OPPOSITION
A 3-month timeperiod is given for any opposition.
Contraryclaimscanbeledandcontested.
4. GRANTING ANDSEALINGOFPATENT
Incaseofnooppositionorclearingsatisfactorilyallthe
objections by the applicant, patent is granted and sealed
bythepatentofcebypublishingintheofcialgazette.
5. REVOCATION
The validity ofthe patent canbe challenged inHigh
Courtunder specified grounds. The patent will be
revokedifthecourtupholdsthechallenge.
6. VALIDITYOFAPATENT
Patent for food and medicines and drugs produced
bychemicalprocesses5yearsperiodfromthedateof
grantingthepatentor7yearsperiodfromthedateof
lingapplicationorwhicheverisearlier.
Procedure of patent
Patentcanbeclaimedbythefollowing:
1. Anypersonclaimingtobethetrueandrstinventorof
theinvention.
2. Anypersonbeingtheassigneeofthepersonclaiming
tobethetrueandrstinventorinrespectoftheright
to make such application.
3. Anylegalrepresentativeofanydiseased person who
immediatelybeforehisdeathwasentitledtomakesuch
an application.
Thefollowingwouldnotqualifyaspatents:
1. Aninvention, which isfrivolous or whichclaims
anything obvious or contrary to the well-established
natural law.
2. An invention, the primary or intended useof which
would be contrary to law or morality or injurious to
public health.
z
A discovery, scientific theory, or mathematical method.
z
A mere discovery of any new property or new use
for a known substance or of the mere use of a known
process, machine, or apparatus unless such known
process results in a new product or employs at least
one new reactant.
z
A substance obtained by a mere admixture resulting only
in the aggregation of the properties of the components
thereof or a process for producing such substance.
z
A mere arrangement or re-arrangement or duplication
of a known device each functioning independently of
one another in its own way.
z
A method of agriculture or horticulture.
z
Any process for the medicinal, surgical, curative,
prophylactic diagnostic, therapeutic or other treatment
of human beings or any process for a similar treatment
of animals to render them free of disease or to increase
their economic value or that of their products.
z
An invention relating to atomic energy
z
An invention, which is in effect, is traditional
knowledge.
Section 2 Pharmacognosy
328
PATENTABLE
Newprocessofmanufacture
New chemical entities
Newformulationprocesses
Newcompositionofmatter
NONPATENTABLE
Discoveries
Methods of detection, diagnosis or
treatmentofdiseases
Analytical methods
Methodsofagriculture/cultivation
The products made by chemical synthesis
Animal,plant,andbiologicalmethodsfor
growing and rearing them.
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