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