Liposomes-Classification, methods of preparation and application
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The document provides an overview of liposomes, which are microscopic vesicles made from phospholipids resembling cell membranes and used primarily for drug delivery. It details their preparation methods, including mechanical dispersion, solvent dispersion, and other techniques, as well as the various applications of liposomes in enhancing drug efficacy and targeting in medical treatments. Additionally, the document discusses the advantages of liposomes in protecting drugs from enzymatic degradation and improving drug solubility and absorption.
Liposomes-Classification, methods of preparation and application
- 1. LIPOSOMES Methods of preparation & Applications VIJAY GIT Bengaluru
- 2. PhospholipidsPhospholipids Polar Head Groups Three carbon glycerol
- 3. What is a liposome?What is a liposome? – Spherical (concentric) vesicles with a phospholipid bilayer Hydrophilic Hydrophobic
- 4. LIPOSOMES • The name liposome is derived from two Greek words: 'Lipos' meaning fat and 'Soma' meaning body. • Liposomes were first described by British haematologist Dr Alec D Bangham FRS in 1961, at the Babraham Institute, in Cambridge. • They were discovered when Bangham and R. W. Horne were testing the institute's new electron microscope by adding negative stain to dry phospholipids. • A liposome is a tiny bubble (vesicle), made out of the same material as a cell membrane. • Liposomes are simple microscopic vesicles in which an aqueous phase is entirely enclosed by membrane composed by lipid molecule. • Liposomes can be composed of naturally-derived phospholipids with mixed lipid chains (like egg phosphatidylethanolamine), or of pure surfactant components like DOPE(dioleoylphosphatidylethanolamine).
- 5. TYPES OF LIPOSOMES • Liposomes are classified on the basis of • - Structural parameters • - Method of preparation • - Composition and applications
- 10. Methods Of Liposomes Preparations • The correct choice of liposome preparation method depends on the following parameters: • 1) physicochemical characteristics of the material to be entrapped and those of the liposomal ingredients; • 2) the nature of the medium in which the lipid vesicles are dispersed; 3) the effective concentration of the entrapped substance and its potential toxicity; • 4) additional processes involved during application/ delivery of the vesicles; • 5) optimum size, polydispersity and shelf-life of the vesicles for the intended application. • 6) batch-to-batch reproducibility and possibility of large-scale production of safe and efficient liposomal products.
- 11. Handling Of Liposomes • The lipids used in the preparation of liposomes are unsaturated and hence susceptible to oxidation. • Also volatile solvents such as chloroform which are used will tend to evaporate from the container. • Thus liposomes must be stored in an inert atmosphere of nitrogen, and in the dark, in glass vessels with a securely fastened cap.
- 13. • General method of loading: • water soluble (hydrophilic) materials are entrapped by using aqueous solution of these materials as hydrating fluid or by the addition of drug/drug solution at some stage during manufacturing of the liposomes. • lipid soluble (lipophilic) materials are solubilized in the organic solution of the constitutive lipid and then evaporated to a dry drug containing lipid film followed by its hydration. • Passive Loading : involve the loading of the entrapped agents before or during the manufacturing procedure . • Remote Loading Or Active Loading: compounds with ionizable groups, and those which display both lipid and water solubility, can be introduced into the liposomes after the formation of intact vesicles.
- 14. MECHANICAL DISPERSION METHODS: Preparation of liposomes by lipid film hydration: • For preparing liposomes with mixed lipid composition, the lipids must first be dissolved and mixed in an organic solvent to assure a homogeneous mixture of lipids. • Organic solvents used are chloroform or chloroform:methanol mixtures. • Once the lipids are thoroughly mixed in the organic solvent, the solvent is removed to yield a lipid film. • For removal of small volume of organic solvents, dry nitrogen is used, for large volumes, rotary evaporator is used. • The lipid film is thoroughly dried to remove residual organic solvent by placing the vial or flask on a vacuum pump overnight. • Lipid solution frozen by placing the containers on a block of dry ice or swirling the container in a dry ice-acetone or alcohol.
- 15. Sizing of Lipid Suspension: Sonication • Disruption of LMV suspensions using sonic energy (sonication) typically produces small, unilamellar vesicles (SUV) with diameters in the range of 15-50nm. • The most common instrumentation for preparation of sonicated particles are bath and probe tip sonicators. • Sonication of an LMV dispersion is accomplished by placing a test tube containing the suspension in a bath sonicator (or placing the tip of the sonicator in the test tube) and sonicating for 5-10 minutes.
- 16. French Pressure Cell Method • The method involves the extrusion of MLV at 20,000 psi at 4°C through a small orifice. • The method has several advantages over sonication method. • The method is simple, rapid, reproducible and involves gentle handling of unstable materials. • Drawbacks of this method are that the temperature is difficult to achieve and the working volumes are relatively small (about 50 mL maximum).
- 18. SOLVENT DISPERSION METHODS Ether Injection Method • A solution of lipids dissolved in diethyl ether or ether/methanol mixture is slowly injected to an aqueous solution of the material to be encapsulated at 55-65°C or under reduced pressure. • The subsequent removal of ether under vacuum leads to the formation of liposomes. • The main drawbacks of the method are population is heterogeneous (70-190 nm) and the exposure of compounds to be encapsulated to organic solvents or high temperature.
- 19. Ethanol Injection Method • A lipid solution of ethanol is rapidly injected to a vast excess of buffer. • The MLVs are immediately formed. • The drawbacks of the method are that the population is heterogeneous (30-110 nm), liposomes are very dilute, it is difficult to remove all ethanol because it forms azeotrope with water and the possibility of various biologically active macromolecules to inactivation in the presence of even low amounts of ethanol.
- 21. Reverse Phase Evaporation Method • First water in oil emulsion is formed by brief sonication of a two phase system containing phospholipids in organic solvent (diethylether or isopropylether or mixture of isopropyl ether and chloroform) and aqueous buffer. • The organic solvents are removed under reduced pressure, resulting in the formation of a viscous gel. • The liposomes are formed when residual solvent is removed by continued rotary evaporation under reduced pressure. • With this method high encapsulation efficiency up to 65% can be obtained in a medium of low ionic strength for example 0.01M NaCl. • The method has been used to encapsulate small and large macromolecules. • The main disadvantage of the method is the exposure of the materials to be encapsulated to organic solvents and to brief periods of sonication
- 23. DETERGENT REMOVAL METHOD • The detergents at their critical micelles concentrations have been used to solubilize lipids. • As the detergent is removed the micelles become progressively richer in phospholipid and finally combine to form LUVs. • The detergents can be removed by dialysis. • The advantages of detergent dialysis method are excellent reproducibility and production of liposome populations which are homogenous in size. • The main drawback of the method is the retention of traces of detergent(s) within the liposomes.
- 25. Applications of liposomes • Liposomes are used for drug delivery due to their unique properties. • A liposome encapsulates a region on aqueous solution inside a hydrophobic membrane; dissolved hydrophilic solutes cannot readily pass through the lipids. • Hydrophobic chemicals can be dissolved into the membrane, and in this way liposome can carry both hydrophobic molecules and hydrophilic molecules. • There are three types of liposomes – MLV (multilamillar vesicles) SUV (Small Unilamellar Vesicles) and LUV (Large Unilamellar Vesicles) used to deliver different types of drugs. • Liposomes are used as models for artificial cells. • Liposomes can also be designed to deliver drugs in other ways.
- 26. • Liposomes that contain low (or high) pH can be constructed such that dissolved aqueous drugs will be charged in solution. • As the pH naturally neutralizes within the liposome (protons can pass through some membranes), the drug will also be neutralized, allowing it to freely pass through a membrane. • These liposomes work to deliver drug by diffusion rather than by direct cell fusion. • Another strategy for liposome drug delivery is to target endocytosis events. • Liposomes can be made in a particular size range that makes them viable targets for natural macrophage phagocytosis. • These liposomes may be digested while in the macrophage's phagosome, thus releasing its drug. • Liposomes can also be decorated with opsonins and ligands to activate endocytosis in other cell types. • The use of liposomes for transformation or transfection of DNA into a host cell is known as lipofection
- 27. • Protection against enzyme degradation of drugs • Liposomes are used to protect the entrapped drug against enzymatic degradation whilst in circulation. • The basis is that the lipids used in their formulation are not susceptible to enzymatic degradation; the entrapped drug is thus protected while the lipid vesicles are in circulation in the extracellular fluid. • Drug targeting • The approach for drug targeting via liposomes involves the use of ligands (e.g., antibodies, sugar residues, apoproteins or hormones), which are tagged on the lipid vesicles. • The ligand recognises specific receptor sites and, thus, causes the lipid vesicles to concentrate at such target sites. • By this approach the otherwise preferential distribution of liposomes into the reticuloendeothelial system RES (liver, spleen and bone marrow) is minimized.
- 28. • Topical drug delivery • The application of liposomes on the skin surface has been proven to be effective in drug delivery into the skin. • Liposomes increase the permeability of skin for various entrapped drugs and at the same time diminish the side effect of these drugs. • Enhanced antimicrobial efficacy • Antimicrobial agents have been encapsulated in liposomes for two reasons. • First, they protect the entrapped drug against enzymatic degradation. For instance, the penicillins and cephalosporin are sensitive to the degradative action of β-lactamase, which is produced by certain microorganisms. • Secondly, the lipid nature of the vesicles promotes enhanced cellular uptake of the antibiotics into the microorganisms, thus reducing the effective dose and the incidence of toxicity as exemplified by the liposomal formulation of amphotericin B.
- 29. Modes of liposome action • (i) Improved solubility of lipophilic and amphiphilic drugs. Examples include Porphyrins, Amphotericin B, Minoxidil. • (ii) Passive targeting to the cells of the immune system, especially cells of the mononuclear phagocytic system (in older literature reticuloendothelial system). • Examples are antimonials, Amphotericin B, porphyrins and also vaccines, immunomodulators or (immuno)supressors; • (iii) Sustained release system of systemically or locally administered liposomes. • Examples are doxorubicin, cytosine arabinose, cortisones, biological proteins or peptides such as vasopressin; • (iv) Site-avoidance mechanism: liposomes do not dispose in certain organs, such • as heart, kidneys, brain, and nervous system and this reduces cardio-, nephro-, • and neuro-toxicity. • Typical examples are reduced nephrotoxicity of Amphotericin B, and reduced cardiotoxicity of Doxorubicin liposomes.
- 30. • (v) Site specific targeting: in certain cases liposomes with surface attached ligands can bind to target cells (‘key and lock’ mechanism), or can be delivered into the target tissue by local anatomical conditions such as leaky and badly formed blood vessels, their basal lamina, and capillaries. • Examples include anticancer, antiinfection and antiinflammatory drugs • (vi) Improved transfer of hydrophilic, charged molecules such as chelators, antibiotics, plasmids, and genes into cells; and • (vii) Improved penetration into tissues, especially in the case of dermally applied liposomal dosage forms. • Examples include anaesthetics, corticosteroids, and insulin.