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Mohammed N. Sabir

Pharmacognosy II Lecture 1

Lecture outlines…

Definition & Introduction…

Classification…

Physicochemical properties…

Isolation from nature…

Examples and medicinal uses…

Overview…

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Pharmacognosy II Lecture 1

TANNINS

Tannins are large phenolic non-nitrogenous biomolecules

having astringent properties.

Most are water-soluble, the multiple phenolic hydroxyls and carboxylic groups

are responsible for astringency and bitterness.

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They are broadly divided into two groups:

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1-The hydrolysable tannins, which are formed by the

esterification of sugars (e.g. glucose) with gallic acid.

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2-The non-hydrolysable tannins, (condensed tannins)

occur due to polymerization (condensation) reactions

between flavonoids.

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Pharmacognosy II Lecture 1

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Isolation

Both hydrolysable and condensed tannins are highly

soluble in water and alcohol but insoluble in organic

solvents such as ether, chloroform, and benzene.

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The general method for the extraction of tannic acid

from various galls is either with water-saturated ether,

or with mixture of water, alcohol, and ether.

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Acetone is added to the extraction procedure to inhibit

interaction between tannins and proteins or interfere

with the hydrogen bonding between them, thus

increasing the yield.

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After extraction, the aqueous and ethereal layers are

separately concentrated, dried, and subjected to

further isolation and purification by chromatography.

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The hydrolysable tannins are hydrolysed with bases to

simple acids and sugars.

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A key feature of tannins is their ability to bind to

proteins, and they have been used to tan leather, clarify

beer and as astringent preparations in pharmacy.

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They have a very wide distribution in plant kingdom

and may be produced by a plant as a feeding deterrent,

as their binding to proteins may reduce the dietary

value of the plant as a food.

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Some of these tannins are also plant pigments as

anthocyanidins.

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Some chemical tests for identification of tannins…

• Reaction with FeCl3.

• Goldbeater's skin test.

• Stiasny's method.

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Tannic acid is a mixture of gallic acid esters of glucose

and is obtained from nutgall, which is an abnormal

tissue growth of the tree Quercus infectoria (Fagaceae)

(ÁÁ�ÖÓd) as a response of larva inoculation of insects.

19 Andricus kollari مازوو

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The galls are harvested and extracted with solvents

(ether and water); the aqueous layer is collected and

evaporated to yield tannic acid, which is further

purified and used as a topical preparation for cold

sores.

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Epigallocatechin gallate (EGCG), epigallocatechin-3-

gallate, is the ester of epigallocatechin and gallic acid,

and is a type of catechin.

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EGCG is the most abundant catechin in tea and is a

potent antioxidant that have therapeutic applications in

(e.g. cancer). [It is found in green tea but not black tea].

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In black tea production, the catechins are converted to

theaflavins and thearubigins under high temperature,

an epimerization change is more likely to occur.

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Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41

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In addition to antioxidant and antiviral actions, tannins

also posses antimicrobial action.

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Tannin toxicity for fungi, bacteria and yeasts is due to

different mechanisms as been proposed include:-

Inhibition of extracellular microbial enzymes, deprivation of

the substrates required for microbial growth.

Direct action on microbial metabolism through inhibition of

oxidative phosphorylation.

Iron chelation is also proposed.

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Many microorganisms can overcome plant defenses

based on tannins through:-

Synthesis of tannin-complexing polymers.

Oxidation, tannin biodegradation.

Synthesis of siderophores.

See the reference… https://www.researchgate.net/publication/223084771_Antimicrobial_properties_of_tannin [accessed Apr 1, 2017].

Pharmacognosy II Lecture 1

The most important herbs rich with tannins used in

treatment of diarrhoea include:

- Sangisorba officinalis L.

- Acacia catechu Willd.

- Oak bark

- Quercus robur L.

- Potentilla erecta (L.) Rausch.

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Tannin-containing drugs are generally safe, but care

should be taken with concurrent administration of

other drugs since tannins are not compatible with

alkalis or alkaloids, and form complexes with proteins

and amino acids.

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Tannins in Herbal Medicine Punica garnatum (Lythraceae)

In the ancient Ayurveda system of medicine, the

pomegranate has extensively been used as a source of

traditional remedies for thousands of years.

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General uses of tannins

-Astringent (ppt. of Proteins).

-Hypolipidemic agents.

-Identification of Alkaloids.

-Tan leather.

-In Burns.

-Antidiarrheal agent.

-Antioxidant.

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Hamamelis Leaf (Witch hazel leaves)

Dried leaf of Hamamelis virginiana (Hamamelidaceae)

Hama = sametime

Melis = leaf

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Distilled witch hazel extract: prepared by steam

hydroalcoholic distillation of the dried leaves and twigs

of H. virginiana. Contains the volatile oil of the plant.

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Presence of tannins in fresh water

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Flavonoids and Flavonolignans

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•Introduction

-Are the largest group of naturally occurring phenolic compounds

-They occur in different plant parts (fruits, stem, barks, root, leaves, heartwood, flowers)

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Pharmacognosy II Lecture 1

•Introduction

-They are plant pigments or co-pigments (the yellow color of many fruits)

-They are found in different plant families (Rutaceae, Rosacea, Astraceae, Lamiaceae, Moraceae, Rubiaceae, and Myrtaceae)

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The biosynthesis of flavonoids I- Phenyl propanoids (4-hydroxy coumaric acid) II- MalonylCoA

Pharmacognosy II Lecture 1

Role of flavonoids in plants

1. Insect attractant (pollinating agents)

2. Plant pigments

3. Growth regulators

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Pharmacognosy II Lecture 1

Role of flavonoids in medicine •Antioxidants (free radical scavengers)

•Antimicrobial

•Mitochondrial adhesion inhibitors

•Antiulcers

•Estrogen receptor binding

•Cell cycle arrest

•Topoisomerase inhibitors

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Pharmacognosy II Lecture 1

Examples… 1-Naringin From Citrus paradisi Fam: Rutaceae

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Studies have shown that naringin has a cholesterol-lowering effect, reduces LDL oxidation and can help to prevent hypercholesterolemia.

Naringin is an aldose reductase inhibitor which means

that it can help to fight diabetic retinopathy.

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Pharmacognosy II Lecture 1

Naringin (and grapefruit) drug interactions

-Interfere

1. Calcium channel blockers

2. Sedatives

3. Cholesterol lowering drugs

4. Caffeine

5. Estrogen

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Metabolic interaction through interfering metabolism of these drugs and increasing their t1/2.

Pharmacognosy II Lecture 1

Naringin enhance our perception of taste by

stimulating the taste buds; that's why some people

consume a small amount of grapefruit juice before a

meal.

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Citrus aurantifolia Peels Fam: Rutaceae

Uses:- Capillary bleeding (membrane stabilizer) 03-Apr-17 Tannins & Flavonoids 47

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Flavonolignans

Silymarin (Silybum marianum L.) Milk Thistle Fam: Astraceae

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Hepatotoxic agents

•CCl4

•CHCl3

•Acetaminophen (Paracetamol©)

•Amanita phalloides

•Xenobiotics

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Fatty degeneration in Rat Liver after exposing to CCl4.

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Pharmacognostic Study of Silybum marianum, Mohammed Sabir, Lambert Academic Publishing, Germany, 1st Ed. 2014.

Pharmacognosy II Lecture 1

Mechanisms of action of Silybins

1. As antioxidant (inhibit lipid-peroxidation) through

free radical scavenging (antioxidant) Key

mechanism.

2. Regulators of intracellular content of glutathione.

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Pharmacognosy II Lecture 1

Mechanisms of action of Silybins 3. Cell membrane stabilizer and permeability

regulator that prevent entrance of toxins. 4. Promoters of ribosomal RNA synthesis and

stimulating liver regeneration (Hepatocytes protein synthesis).

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Pharmacognosy II Lecture 1

Mechanisms of action of Silybins 5. Inhibits transformation of stellate hepatocytes

into myofibroblasts.

6. Decrease the activity of tumor promoters.

7. Enhances apoptosis.

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Water solubility problems of silybin and methods of

enhancing its solubility…

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Water solubility affects bioavailability and its efficacy…

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JZS (2015) 17-3 (Part-A)

Bioavailability Enhancement of Silybin Through Carbon-23 Acid Derivatization Lena Nawzad Amin 1, Mohammed N. Sabir 2, Emad Manhal Al-Khafaji 3, Shwan Rachid 4

School of Pharmacy, Dept. of Pharmacognosy & Pharmaceutical Chemistry, Sulaimani University, Old campus, Sulaimaniyah Iraq Faculty of Science, Dept. of Chemistry University of Sulaimani, Qiliasan, Sulaimaniyah-Iraq Faculty of Sciences and Health, Koya University, Koya-Iraq.

Pharmacognosy II Lecture 1

Product Milk Thistle Herb Silybum marianum

Size - Mg. Silymarin Silybin Silymarin / Silybin

- Fruit referred to as seed one cap/tab Percent of product % in mg.

Maximum Milk Thistle (Siliphos) (Natural Wellness)

Dried extract (Siliphos)

240 mg.

33% 80 mg.

Thisilyn (Nature's Way)

Dried extract

175 mg. 80% 140 mg.

Legalon (Madaus, Germany)

Dried extract (40:1) 90 mg. 80%

70 mg.

Silymarin 80 (Planetary Formula)

Seed Extract plus Milk Thistle seed

210 mg. (plus 50 mg.)

80%

168 mg.

Milk Thistle (Kroeger)

Seed Extract plus Milk Thistle seed

175 mg. (plus 275 mg.)

80%

140 mg.

Silymarin (MediHerb, Australia)

Extract (70:1) 210 mg.

80% 168 mg.

Milk Thistle Seed (Gaia Herbs)

Liquid extract (1:1) 35 mg. 50%

17.5 mg.

Milk Thistle (generic) limited information

Extract 200 mg. 80%

160 mg.

Selected Milk Thistle Products

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Pharmacognosy II Lecture 1

NOTES : - Natural Wellness also has a product called UltraThistle that contains 360 mg

of silybin phytosome per capsule . - Thisilyn (distributed in the United States) uses the same ingredients as Legalon (Germany( - Silymarin 80 contains 50 mg of organically grown and processed milk thistle

seed. - Siliphos and Phytosome are registered trademarks of Indena (Italy.(

- Silybin Phytosome is also available from Enzymatic Therapy – 120 mg per

capsule.

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Lecture overview…

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Thanks for listening…

Any questions?

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