Extraction of Active Medicinal Principles from Natural Sources – PST05210 Basic Pharmacognosy

NTA Level 5 • Semester 2 • PST05210

Extraction of Active Medicinal Principles from Natural Sources

Basic Pharmacognosy • Source Session/Topic 14
Full source-text version: all educational wording from the extracted learning source is retained; only presenter/tutor metadata and web-layout noise are removed, while formatting is improved for readability.

Session 14: Extraction of Active Medicinal Principles from Natural Sources

Total Session Time: 120 minutes

Prerequisites

• None

Learning Tasks

By the end of this session students are expected to be able to:

• Definition of terms
• List types of extracts
• Explain factors affecting extraction process
• Explain Mechanism of solvent extraction
• Outline properties and types solvents
• Explain methods for extraction of active drugs

Resources Needed:

• Flip charts, marker pens, and masking tape
• Black/white board and chalk/whiteboard markers
• LCD Projector and laptop

SESSION OVERVIEW

|Step |Time |Activity/ |Content |

| | |Method | |

|1 |05 minutes |Presentation |Introduction, Learning |

| | | |Tasks |

|2 |10 minutes |presentation |Definition of terms |

|3 |05 minutes |Presentation |Types of extracts |

|4 |30 minutes |Presentation |Properties and types of |

| | |buzzing |solvents |

|5 |15 minutes |Presentation |Mechanism of Solvent |

| | | |Extraction |

|6 |05 minutes |Presentation |Factors affecting |

| | | |extraction |

|7 |40 minutes |Presentation |Methods of extraction |

| | |Small group Discussion| |

|8 |05 minutes |Presentation |Key Points |

|9 |05 minutes |Presentation |Evaluation |

SESSION CONTENTS

STEP 1: Presentation of Session Title and Learning Objectives (05 minutes)

READ or ASK students to read the learning objectives and clarify

ASK students if they have any questions before continuing.

STEP 2: Definition of terms (10 Minutes)

• Extraction is the method of removing active constituents from a solid or

liquid by means of liquid solvent.

o The separation of medicinally active portions of plant or animal

tissues from the inactive or inert components by using selective

solvents.

o In this method the wanted components are dissolved by the use of

selective solvents known as menstrum & undissolved part is a marc,

after the extraction unwanted matter is removed.

• Extract: Extracts can be defined as preparations of crude drugs which

contain all the constituents which are soluble in the solvent.

• Marc: Solid residue obtain after extraction Menstruum
• Solvent is a liquid substance capable to dissolve other substances

(solutes) without chemical changes.

o (The term “Solvents” refers to a class of chemical compounds described

by function – the term derives from Latin, meaning roughly to “loosen.”

In chemistry, solvents – which are generally in liquid form – are used

to dissolve, suspend or extract other materials, usually without

chemically changing either the solvents or the other materials

Step 3: Types of Extracts (05 minutes)

• Type of extracts

o Dry extract (Tab, cap.) E.g. belladonna extract

o Soft (Ointment, suppository) E.g. glycerrhiza extract.

o Liquid: As tincture.

STEP 4: Properties and Types of Solvents (30 minutes)

|Activity: Buzzing (10 minutes) |

| |

|DIVIDE students into small manageable groups |

| |

|ASK students to discuss on the following question |

| |

|What are types of solvents? |

| |

|ALLOW students to discuss for 15 minutes |

| |

|ALLOW few groups to present and the rest to add points not |

|mentioned |

| |

|CLARIFY and SUMMARIZE by using the contents below |

• Types of Solvent

o Molecular structure of solvents

o Inorganic solvents

o Organic solvents

• Molecular structure of solvents

o Molecular structure of solvents, Ability of a substance to dissolve

another substance is determined by compatibility of their molecular

structures (like dissolves like).

▪ Types of molecular structures of the solvents are as follows:
• Polar protic solvents

o A polar protic molecule consists of a polar group OH and a non-

polar tail. The structure may be represented by a formula R-OH.

Polar protic solvents dissolve other substances with polar protic

molecular structure. Polar protic solvents are miscible with water

(hydrophilic).

Examples of polar protic solvents:

▪ Water (H-OH),
▪ Acetic acid (CH3CO-OH)
▪ Methanol (CH3-OH),
▪ Ethanol (CH3CH2-OH),
▪ n-propanol (CH3CH2CH2-OH),
▪ n-butanol (CH3CH2CH2CH2-OH).
• Dipolar aprotic solvent

o Dipolar aprotic molecules possess a large bond dipole moment (a

measure of polarity of a molecule chemical bond). They do not

contain OH group.

Examples of dipolar aprotic solvents:\

▪ Acetone ((CH3)2C=O),
▪ Ehyl acetate (CH3CO2CH2CH3),
▪ Dimethyl sulfoxide ( (CH3)2SO ),
▪ Acetonitrile (CH3CN),
▪ Dimethylformamide ( (CH3)2NC(O)H ).
• Non-polar solvents

o Electric charge in the molecules of non-polar solvents is evenly

distributed, therefore the molecules have low dielectric

constant. Non-polar solvents are hydrophobic (immiscible with

water). Non-polar solvents are liphophilic as they dissolve non-

polar substances such as oils, fats, greases.

Examples of non-polar solvents:

▪ carbon tetrachloride (CCl4),
▪ benzene (C6H6),
▪ and diethyl ether ( CH3CH2OCH2CH3),
▪ hexane (CH3(CH2)4CH3),
▪ methylene chloride (CH2Cl2).
• Inorganic solvents

o The most popular inorganic (not containing carbon) solvents are

o water (H2O) and aqueous solutions containing special additives

(surfacants, detergents, PH buffers, inhibitors).

o Other inorganic solvents are liquid anhydrous

▪ Ammonia (NH3),
▪ concentrated sulfuric acid (H2SO4),
▪ sulfuryl chloride fluoride (SO2ClF).
• Organic solvents

o Oxygenated solvent is an organic solvent, molecules of which contain

oxygen. Oxygenated solvents are widely used in the paints, inks,

pharmaceuticals, fragrance sectors, adhesives, cosmetics, detergents,

food industries.

Examples of oxygenated solvents:

▪ Alcohols,
▪ Glycol ethers,
▪ Methyl acetate,
▪ Ethyl acetate,
▪ Ketones,
▪ Esters,
▪ Glycol ether/esters

STEP 5: Mechanism of Solvent Extraction (15 minutes)

• Mechanism of solvent extraction

o Dissolution of extractive substances out of disintegrated cells.

o Dissolution of extractive substances out of intact plant cell by

diffusion (requires steeping and swelling)

o Penetration of the solvent into the plant cells and swelling of the

cells.

o Diffusion of the dissolved extractive substances out of the cell.

o Plant constituents are usually contained inside the cells.

o Therefore, the solvent used for extraction must diffuse into the cell

to dissolve the desired compounds whereupon the solution must pass the

cell wall in the opposite direction and mix with the surrounding

liquid.

o An equilibrium is established between the solute inside the cells and

the solvent surrounding the fragmented plant tissues

STEP 6: Factors Affecting Extraction Process (05 Minutes)

• Nature of drug
• Solvent
• Temperature
• pH
• Particle size

STEP 7: Methods of extraction (45 minutes)

• Types of extractions are: Infusion, Decoction, Digestion, Maceration,

Percolation, Continues hot extraction, Supercritical fluid extraction,

counter current extraction, Microwave assisted extraction, Ultra

sonication-Assisted Extraction:

o Infusion

▪ Infusion: Fresh infusions are prepared by macerating the crude

drug for a short period of time with cold or boiling water. These

are dilute solutions of the readily soluble constituents of crude

drugs.

• Types of Infusion:

o Fresh Infusion: e.g. Infusion of orange (

o Concentrated Infusion: e.g. concentrated infusion of Quassia

o Decoction

▪ Decoction: In this process, the crude drug is boiled in a specified

volume of water for a defined time; it is then cooled and strained or

filtered. This procedure is suitable for extracting water-soluble,

heat stable constituents. e.g. Tea , Coffee

o Digestion

▪ This is a form of maceration in which gentle heat is used during

the process of extraction. It is used when moderately elevated

temperature is not objectionable. The solvent efficiency of the

menstruum is thereby increased. e.g. Extraction of Morphine

o Maceration

▪ Maceration: In this process solid ingredients are placed in a

stoppered container with the whole of the solvent and allowed to

stand for a period of at least 3 days (3 – 7 days) with frequent

agitation, until soluble matter is dissolved. The mixture is then

strained (through sieves / nets), the marc pressed and the combined

liquids clarified (cleaned by filtration) or by decantation, after

standing.

• Types of maceration

o Simple maceration: for organized and unorganized Crude drug e.g.

i) Tincture of Orange ii) Tincture of Lemon iii) Tincture of

Squill

o Double maceration: Concentrated infusion of orange

o Triple maceration: The maceration process may be carried out with

help of heat or stirring e.g. i) Concentrated infusion of Quassia

ii) Concentrated infusion of Senna

STEP 8: Key Points (5 minutes)

• Extraction is essential for isolation of different chemical constituent

from crude drug material.

• Depends on properties of material to be extracted.
• Hence it is necessary to study extraction methods in detail.

STEP 9: Evaluation (5 minutes)

• What are solvents used in extractions?
• What are the methods of extractions?

References

Trease, G. E., Evans, W. C., & Evans, D. (2009). Trease and Evans

pharmacognosy. London: Saunders.

Joanne Barnes et al (2002), Herbal medicines 3rd Edition: Pharmaceutical

Press

Wallis, T. E. (2005). Textbook of pharmacognosy. New Delhi: CBS.

Robbers, J. E., Speedie, M. K., Tyler, V. E., & Tyler, V. E. (1996).

Pharmacognosy and pharmacobiotechnology. Baltimore: Williams &

Wilkins.

Heinrich, M., Kinghorn, A. D., Maizels, D., Gibbons, S., & Phillipson, J.

D. (2012). Fundamentals of pharmacognosy and phytotherapy. Edinburgh:

Churchill Livingstone/Elsevier.

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