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a brief presentation on hydrogels

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  1. 1. Presented By: SANDEEP MOLLIDAIN M.Pharmacy (pharmaceutical technology) Dept. of pharmaceutical technology. Vsp.
  2. 2. C O N T E N T S <ul><li>Introduction </li></ul><ul><li>Classification of Hydrogels </li></ul><ul><li>Advantages of Hydrogels </li></ul><ul><li>Disadvantages of Hydrogels </li></ul><ul><li>Types of Hydrogels </li></ul><ul><li>Monomers Used In The Synthesis of Synthetic Hydrogels </li></ul><ul><li>Method of Preparation of Hydrogels </li></ul><ul><li>Characterization of Hydrogels </li></ul><ul><li>Common Uses For Hydrogels </li></ul><ul><li>Pharmaceutical Applications of Hydrogels </li></ul><ul><li>Summary and conclusions </li></ul><ul><li>References </li></ul><ul><li>Acknowledgement </li></ul>
  3. 3. Introduction: <ul><li>Hydrogel is a network of polymer chains that are </li></ul><ul><li>hydrophilic, water insoluble, sometimes found as a </li></ul><ul><li>colloidal gel in which water is the dispersion medium. </li></ul><ul><li>Hydrogels are highly absorbent natural or synthetic </li></ul><ul><li>polymers. </li></ul>Definition:
  4. 4. Introduction: <ul><li>Hydrogels are crosslinked polymer networks that absorb </li></ul><ul><li>substantial amounts of aqueous solutions. </li></ul><ul><li>Hydrogels can contain over 99.9% water. </li></ul><ul><li>Hydrogels are three-dimensional, hydrophilic, polymeric </li></ul><ul><li>networks capable of imbibing large amounts of water or </li></ul><ul><li>biological fluids. </li></ul>
  5. 5. Introduction: <ul><li>The networks are composed of homopolymers or </li></ul><ul><li>copolymers, and are insoluble due to the presence of </li></ul><ul><li>chemical crosslinks (tie-points, junctions), or physical </li></ul><ul><li>crosslinks, such as entanglements or crystallites. </li></ul><ul><li>The high water content of the materials contributes to </li></ul><ul><li>their biocompatibility. </li></ul>
  6. 6. Introduction: <ul><li>These crosslinks provide the network structure and </li></ul><ul><li>physical integrity. </li></ul><ul><li>These hydrogels exhibit a thermodynamic </li></ul><ul><li>compatibility with water which allows them to swell in </li></ul><ul><li>aqueous media. </li></ul>
  7. 7. Classification Of Hydrogels:
  8. 8. Advantages of Hydrogels : <ul><li>Hydrogels possess a degree of flexibility very similar </li></ul><ul><li>to natural tissue, due to their significant water content. </li></ul><ul><li>Entrapment of microbial cells within Hydrogel </li></ul><ul><li>beads has the advantage of low toxicity. </li></ul><ul><li>Environmentally sensitive Hydrogels have the </li></ul><ul><li>ability to sense changes of pH, temperature, or the </li></ul><ul><li>concentration of metabolite and release their load as </li></ul><ul><li>result of such a change. </li></ul>
  9. 9. Advantages of Hydrogels: <ul><li>Timed release of growth factors and other nutrients </li></ul><ul><li>to ensure proper tissue growth. </li></ul><ul><li>Hydrogels have good transport properties. </li></ul><ul><li>Hydrogels are Biocompatible. </li></ul><ul><li>Hydrogels can be injected. </li></ul><ul><li>Hydrogels are easy to modify. </li></ul>
  10. 10. Disadvantages of Hydrogels: <ul><li>Hydrogels are expensive. </li></ul><ul><li>Hydrogels causes sensation felt by movement of the </li></ul><ul><li>maggots. </li></ul><ul><li>Hydrogels causes thrombosis at Anastomosis sites. </li></ul><ul><li>The surgical risk associated with the device </li></ul><ul><li>implantation and retrieval. </li></ul><ul><li>Hydrogels are non-adherent; they may need to be </li></ul><ul><li>secured by a secondary dressing. </li></ul>
  11. 11. Disadvantages of Hydrogels: <ul><li>Hydrogels used as contact lenses causes lens </li></ul><ul><li>deposition,hypoxia, dehydration and red eye </li></ul><ul><li>reactions. </li></ul><ul><li>Hydrogels have low mechanical strength </li></ul><ul><li>Difficulty in handling. </li></ul><ul><li>Difficulty in loading. </li></ul><ul><li>Difficulty in Sterilization </li></ul>
  12. 12. Types of Hydrogels : Natural Polymers <ul><ul><li>e.g.: Dextran, Chitosan, Collagen, Dextran Sulfate </li></ul></ul><ul><ul><li>Disadvantages: </li></ul></ul><ul><ul><ul><li>Low mechanical Strength. </li></ul></ul></ul><ul><ul><ul><li>Batch variation. </li></ul></ul></ul><ul><ul><ul><li>Animal derived materials may pass on viruses. </li></ul></ul></ul>
  13. 13. Types of Hydrogels : Synthetic Polymers <ul><ul><li>e.g.:Poly (vinyl alcohol) </li></ul></ul><ul><ul><li>Disadvantages: </li></ul></ul><ul><ul><ul><li>Low biodegradability </li></ul></ul></ul><ul><ul><ul><li>Can include toxic substances </li></ul></ul></ul>
  14. 14. <ul><li>Hydrogels can be used in different types of </li></ul><ul><li>controlled release systems. </li></ul><ul><li>These are classified according to the mechanism </li></ul><ul><li>controlling the release of drug from the device as </li></ul><ul><li>- Diffusion controlled systems. </li></ul><ul><li>- Swelling controlled system. </li></ul><ul><li>- Chemically controlled system. </li></ul><ul><li>- Environmental responsive systems. </li></ul>Classification Of Hydrogel Based Systems:
  15. 15. <ul><li>Diffusion is the most common mechanism controlling release. </li></ul><ul><li>In hydrogel based drug delivery system. </li></ul><ul><li>There two types : </li></ul><ul><li>-Reservoir devices. </li></ul><ul><li>-Matrices devices </li></ul>Diffusion Controlled Release Systems:
  16. 16. <ul><li>Reservoir devices: </li></ul><ul><li>They consists of polymeric membrane </li></ul><ul><li>surrounding a core containing a drug . </li></ul><ul><li>Typically reservoir devices are capsules, cylinders, slabs or spheres. </li></ul><ul><li>Rate limiting step for drug release is diffusion through the outer membrane of the device. </li></ul>Diffusion Controlled Release Systems:
  17. 17. <ul><li>Draw backs: </li></ul><ul><li>In the event that the outer membrane ruptures the entire content of the device are delivered instantaneously . </li></ul><ul><li>While preparing these device care must taken to ensure that the device doesn't contain pin holes or defects that may lead to rupture. </li></ul>Diffusion Controlled Release Systems:
  18. 18. <ul><li>Matrix devices: </li></ul><ul><li>In matrix devices the drug is dispersed through out the 3D structure of the hydrogel. </li></ul><ul><li>Release occur due to diffusion of the drug through out the macro molecular mesh or water filled pores. </li></ul>Diffusion Controlled Release Systems:
  19. 19. <ul><li>In these release drug systems the drug is dispersed within a glassy polymer . </li></ul><ul><li>Up on contact with biological fluid, the polymer begins to swell. </li></ul><ul><li>As the penetrant enters the glassy polymer, the glass transition temperature of the polymer is lowered allowing for relaxations of the macro molecular chains. </li></ul>Swelling Controlled Release Systems:
  20. 20. <ul><li>They are of two types: </li></ul><ul><li>Erodible drug delivery system </li></ul><ul><li>-In erodible system drug release occurs due to degradation or dissolution of the hydrogel. </li></ul><ul><li>Pendent chain system </li></ul><ul><li>-In pendent chain system drug is affixed to the polymer back bone through degradable linkages. </li></ul><ul><li>-As these linkages degrade drug is released </li></ul>Chemically Controlled Release Systems
  21. 21. <ul><li>It is also known as degradable or absorbable release system, can be either matrix or reservoir type. </li></ul><ul><li>In reservoir type devices the membrane erodes significantly and drug is released by diffusion mechanism. </li></ul><ul><li>Zero order release can be obtained by this system. </li></ul>Erodible Drug Delivery System
  22. 22. <ul><li>This system consists of linear homo/co-polymers with drug attached to the back bone chains. </li></ul><ul><li>The drug is released from the polymer by hydrolysis or enzymatic degradation of these linkages. </li></ul>Pendent Chain System
  23. 23. Stimuli-sensitive Swelling-controlled Release Systems <ul><li>Environmentally-sensitive hydrogels have the ability </li></ul><ul><li>to respond to changes in their external environment. </li></ul><ul><li>They exhibit dramatic changes in their swelling </li></ul><ul><li>behavior, network structure, permeability or </li></ul><ul><li>mechanical strength in response to changes in the </li></ul><ul><li>pH or ionic strength of the surrounding biological </li></ul><ul><li>fluid, or temperature. </li></ul>
  24. 24. Stimuli-sensitive Swelling-controlled Release Systems <ul><li>Other hydrogels have the ability to respond to </li></ul><ul><li>applied electrical or magnetic fields, or to changes </li></ul><ul><li>in the concentration of glucose. </li></ul><ul><li>Because of their nature, these materials can be used </li></ul><ul><li>in a wide variety of applications, such as separation </li></ul><ul><li>membranes, biosensors, artificial muscles, chemical </li></ul><ul><li>valves and drug delivery devices. </li></ul>
  25. 25. pH-Sensitive Hydrogels: <ul><li>Hydrogels exhibiting pH-dependent swelling </li></ul><ul><li>behavior contain ionic networks contain either </li></ul><ul><li>acidic or basic groups. </li></ul><ul><li>In aqueous media of appropriate pH and ionic </li></ul><ul><li>strength, these groups ionize, and develop fixed </li></ul><ul><li>charges on the gel. </li></ul>
  26. 26. pH-Sensitive Hydrogels: <ul><li>As a result of the electrostatic repulsions, the </li></ul><ul><li>uptake of solvent in the network is increased. </li></ul><ul><li>Ionic groups, such as carboxylic or sulfonic acid, </li></ul><ul><li>show sudden or gradual changes in their dynamic </li></ul><ul><li>and equilibrium swelling behavior as a result of </li></ul><ul><li>changing the external pH. </li></ul>
  27. 27. pH-Sensitive Hydrogels: <ul><li>In these gels, ionization occurs when the pH of the </li></ul><ul><li>environment is above the pKa of the ionizable group. </li></ul><ul><li>As the degree of ionization increases (increased </li></ul><ul><li>system pH), the number of fixed charges increases, </li></ul><ul><li>resulting in increased electrostatic repulsions between </li></ul><ul><li>the chains. </li></ul><ul><li>This, in turn, results in an increased hydrophilicity of </li></ul><ul><li>the network, and greater swelling ratios. </li></ul>
  28. 28. pH-Sensitive Hydrogels: <ul><li>Conversely, cationic materials contain groups such </li></ul><ul><li>as amines. </li></ul><ul><li>These groups ionize in media which are at a pH </li></ul><ul><li>below the pKb of the ionizable species. </li></ul><ul><li>Thus, in a low pH environment, ionization </li></ul><ul><li>increases, causing increased electrostatic repulsions. </li></ul><ul><li>The hydrogel becomes increasingly hydrophilic and </li></ul><ul><li>will swell to an increased level. </li></ul>
  29. 29. Temperature-sensitive Hydrogels: <ul><li>Temperature-sensitive hydrogels have gained </li></ul><ul><li>considerable attention due to the ability of the </li></ul><ul><li>hydrogels to swell or deswell as a result of </li></ul><ul><li>changing the temperature of the surrounding fluid. </li></ul><ul><li>Widely used in on±off drug release regulations, </li></ul><ul><li>biosensors and intelligent cell culture dishes. </li></ul>
  30. 30. Temperature-sensitive Hydrogels: <ul><li>Thermosensitive hydrogels can be classified as </li></ul><ul><li>positive or negative temperature-sensitive systems. </li></ul><ul><li>A positive temperature-sensitive hydrogel has an </li></ul><ul><li>upper critical solution temperature (UCST). </li></ul><ul><li>Such hydrogels contract upon cooling below the </li></ul><ul><li>UCST. </li></ul>
  31. 31. Temperature-sensitive Hydrogels: <ul><li>Negative temperature-sensitive hydrogels </li></ul><ul><li>have a lower critical solution temperature (LCST). </li></ul><ul><li>These hydrogels contract upon heating above the </li></ul><ul><li>LCST. </li></ul>
  32. 32. Other Stimuli-sensitive Hydrogels: <ul><li>Several stimuli, other than pH and temperature, can </li></ul><ul><li>trigger drug release from a depot. </li></ul><ul><li>These include physical stimuli, such as light, </li></ul><ul><li>magnetic field , electric current and ultrasound , </li></ul><ul><li>which can be applied to the systems externally. </li></ul><ul><li>Chemical stimuli, like ionic species , certain </li></ul><ul><li>chemical substances and biological compounds. </li></ul>
  33. 33. Monomers Used In The Synthesis Of Synthetic Hydrogels: Monomer abbreviation Monomer HEMA Hydroxyethyl methacrylate HEEMA Hydroxyethoxyethyl methacrylate HDEEMA Hydroxydiethoxyethyl methacrylate MEMA Methoxyethyl methacrylate MEEMA Methoxyethoxyethyl methacrylate
  34. 34. Monomers Used In The Synthesis Of Synthetic Hydrogels: Monomer abbreviation Monomer EG Ethylene glycol EGDMA Ethylene glycol dimethacrylate NVP N-vinyl-2-pyrrolidone AA Acrylic acid PEGMA PEG methacrylate
  35. 35. Method Of Preparation Of Hydrogels: <ul><li>Crosslinking </li></ul><ul><li>Isostatic Ultra High Pressure </li></ul><ul><li>Nucleophilic Substitution Reaction </li></ul><ul><li>Using Gelling Agents </li></ul><ul><li>Use Of Irradiation </li></ul><ul><li>Freeze Thawing </li></ul>
  36. 36. Crosslinking: Linear polymers Crosslinking Chemical compounds Irradiation Monomers used in the preparation of the ionic polymer network contain an ionizable group, gets ionized, or undergoes substitution after the polymerization is completed.
  37. 37. By using Cross Linkers: Purpose <ul><li>To impart sufficient mechanical strength to these polymers </li></ul>Examples <ul><li>Cross linkers prevent burst release of the medicaments. </li></ul><ul><li>Glutaraldehyde, Calcium chloride </li></ul><ul><li>Presence of residue. </li></ul>Advantage Drawbacks
  38. 38. Isostatic Ultra High Pressure : ultrahigh pressure of 300-700 MPa gelatinization of starch molecules occur. IUHP brings about changes in the morphology of the polymer. Where as heat-induced gelatinization (40 to 52°C) causes a change in ordered state of polymer. Suspension of natural biopolymers (starch) 5or 20 min
  39. 39. Nucleophilic Substitution Reaction: Methacyloyl chloride 2-dimethylamino ethylamine. Nucleophilic substitution. N-2-dimethyl amino ethyl-methacryalmide (DMAEMA) (a pH and temperature sensitive.)
  40. 40. By Using Gelling Agents: Examples <ul><li>Glycophosphate. </li></ul><ul><li>1-2 Propanediol. </li></ul><ul><li>Glycerol. </li></ul><ul><li>Mannitol. </li></ul>Drawbacks <ul><li>Turbidity. </li></ul><ul><li>Presence of negative charged moieties pose problem of interaction with the drug. </li></ul>
  41. 41. Use Of Irradiation: <ul><li>Irradiation method processing is costly </li></ul><ul><li>Mechanical strength of such Hydrogels is less. </li></ul>Advantages Drawbacks <ul><li>Irradiation method is convenient. </li></ul><ul><li>Hydrogels prepared by microwave irradiation are more porous than conventional methods. </li></ul>
  42. 42. Freeze Thawing: <ul><li>Opaque in appearance </li></ul><ul><li>Little swelling capacity. </li></ul>Advantage Drawbacks <ul><li>Sufficient mechanical strength. </li></ul><ul><li>Good Stability. </li></ul>
  43. 43. Characterization Of Hydrogels:
  44. 44. Atomic Force Microscope Atomic Force Microscopy (AFM): <ul><li>A Multimode Atomic Force Microscope form Digital </li></ul><ul><li>Instrument is used to study the surface morphology of </li></ul><ul><li>the hydrogels. </li></ul>
  45. 45. X-ray Diffraction: <ul><li>Used to understand whether the polymers retain their </li></ul><ul><li>crystalline structure or they get deformed during the </li></ul><ul><li>pressurization process </li></ul>
  46. 46. FTIR (Fourier Transform Infrared Spectroscopy) <ul><li>Formation of coil or helix which is indicative of cross linking is evident by appearance of bands near 1648 cm -1 </li></ul>FTIR <ul><li>Any change in the morphology of Hydrogels changes their IR absorption spectra. </li></ul>
  47. 47. Rheology : <ul><li>Hydrogels are evaluated for viscosity under constant temperature (4°C) by using Cone Plate viscometer. </li></ul>Cone plate viscometer
  48. 48. Swelling Behavior: <ul><li>The Hydrogels are allowed to immerse in aqueous </li></ul><ul><li>medium or medium of specific pH to know their </li></ul><ul><li>swellability. of these polymeric networks. </li></ul><ul><li>These polymers show increase in dimensions related </li></ul><ul><li>to swelling. </li></ul>
  49. 49. <ul><li>Swelling degrees (SDs) of hydrogels were measured </li></ul><ul><li>at 37 0 C. The fresh made samples (wet) were weighted </li></ul><ul><li>and immersed in buffer solutions with different pH </li></ul><ul><li>values. These samples were gently wiped with filter </li></ul><ul><li>paper to remove the surface solution when taken out </li></ul><ul><li>from the solutions, then weighted and returned to the </li></ul><ul><li>Same container at pre-determined time intervals. </li></ul>Swelling Behavior:
  50. 50. Swelling Behavior: The SD was calculated as follows: W0 = Weight of the original Hydrogel Wt = is the weight of hydrogel at various swelling times SD (%)= (Wt/Wo)×100 Picture of a swollen Hydrogel
  51. 51. In-vitro Release Study For Drugs: <ul><li>Since Hydrogels are the swollen polymeric networks, </li></ul><ul><li>interior of which is occupied by drug molecules, </li></ul><ul><li>therefore, release studies are carried out to understand </li></ul><ul><li>the mechanism of release over a period of application </li></ul>
  52. 52. In-vitro Release Study For Drugs: <ul><li>Dissolution media: </li></ul><ul><li>Buffer solution with various pH </li></ul><ul><li>values. </li></ul><ul><li>R.P.M: 90 rpm. </li></ul><ul><li>Temperature : 37 0 C. </li></ul><ul><li>Sink condition is maintained by </li></ul><ul><li>replacing the buffer periodically. </li></ul>Dissolution apparatus
  53. 53. Physical, Chemical And Toxicological Properties Of Hydrogels: <ul><li>Factors affecting swelling of hydrogels. </li></ul><ul><li>Mechanical properties. </li></ul><ul><li>Cytotoxicity and in-vivo toxicity. </li></ul>
  54. 54. Factors Affecting Swelling Of Hydrogels: <ul><li>It is defined as the ratio of moles of crosslinking </li></ul><ul><li>agent to the moles of polymer repeating units. </li></ul><ul><li>The higher the crosslinking ratio, the more </li></ul><ul><li>crosslinking agent is incorporated in the hydrogel </li></ul><ul><li>structure. </li></ul>Crosslinking ratio
  55. 55. Factors Affecting Swelling Of Hydrogels: <ul><li>Highly crosslinked hydrogels have a tighter </li></ul><ul><li>structure, and will swell less compared to the </li></ul><ul><li>same hydrogels with lower crosslinking ratios. </li></ul><ul><li>Crosslinking hinders the mobility of the polymer </li></ul><ul><li>chain, hence lowering the swelling ratio. </li></ul>Crosslinking ratio
  56. 56. Factors Affecting Swelling Of Hydrogels: <ul><li>The chemical structure of the polymer may also </li></ul><ul><li>affect the swelling ratio of the hydrogels. </li></ul><ul><li>Hydrogels containing hydrophilic groups swell to a </li></ul><ul><li>higher degree compared to those containing </li></ul><ul><li>hydrophobic groups.. </li></ul>Chemical Structure
  57. 57. Factors Affecting Swelling Of Hydrogels: <ul><li>Hydrophobic groups collapse in the presence of </li></ul><ul><li>water, thus minimizing their exposure to the water </li></ul><ul><li>molecule. </li></ul><ul><li>As a result, the hydrogels will swell much less </li></ul><ul><li>compared to hydrogels containing hydrophilic </li></ul><ul><li>groups. </li></ul>Chemical Structure
  58. 58. Factors Affecting Swelling Of Hydrogels: <ul><li>Swelling of environmentally-sensitive hydrogels </li></ul><ul><li>can be affected by specific stimuli. </li></ul><ul><li>Swelling of temperature-sensitive hydrogels can be </li></ul><ul><li>affected by changes in the temperature of the </li></ul><ul><li>swelling media. </li></ul>Chemical Structure
  59. 59. Factors Affecting Swelling Of Hydrogels: <ul><li>Ionic strength and pH affect the swelling of ionic </li></ul><ul><li>strength- and pH-sensitive Hydrogels, respectively. </li></ul><ul><li>There are many other specific stimuli that can affect </li></ul><ul><li>the swelling of other environmentally-responsive </li></ul><ul><li>Hydrogels. </li></ul>Chemical Structure
  60. 60. Mechanical properties: <ul><li>Mechanical properties of hydrogels are very </li></ul><ul><li>important for pharmaceutical applications. </li></ul><ul><li>The integrity of the drug delivery device during </li></ul><ul><li>the lifetime of the application is very important to </li></ul><ul><li>obtain FDA approval, unless the device is </li></ul><ul><li>designed as a biodegradable system. </li></ul>
  61. 61. Mechanical properties: <ul><li>A drug delivery system designed to protect a </li></ul><ul><li>sensitive therapeutic agent,such as protein, must </li></ul><ul><li>maintain its integrity to be able to protect the protein </li></ul><ul><li>until it is released out of the system. </li></ul><ul><li>Changing the degree of crosslinking has been </li></ul><ul><li>utilized to achieve the desired mechanical property </li></ul><ul><li>of the hydrogel. </li></ul>
  62. 62. Mechanical properties: <ul><li>Increasing the degree of crosslinking of the system </li></ul><ul><li>will result in a stronger gel. </li></ul><ul><li>However, a higher degree of cross-linking creates a </li></ul><ul><li>more brittle structure. </li></ul><ul><li>Hence, there is an optimum degree of crosslinking </li></ul><ul><li>to achieve a relatively strong and yet elastic </li></ul><ul><li>hydrogel. </li></ul>
  63. 63. Mechanical properties: <ul><li>Copolymerization has also been utilized to achieve </li></ul><ul><li>the desired mechanical properties of hydrogels. </li></ul><ul><li>Incorporating a co-monomer that will contribute </li></ul><ul><li>to H-bonding can increase the strength of the </li></ul><ul><li>hydrogel. </li></ul>
  64. 64. Cytotoxicity And In-vivo Toxicity: <ul><li>Cell culture methods, also known as cytotoxicity </li></ul><ul><li>tests, can be used to evaluate the toxicity of </li></ul><ul><li>hydrogels. </li></ul><ul><li>Three common assays to evaluate the toxicity of </li></ul><ul><li>hydrogels include </li></ul><ul><li>-extract dilution. </li></ul><ul><li>-direct contact. </li></ul><ul><li>-agar diffusion. </li></ul>
  65. 65. Cytotoxicity And In-vivo Toxicity: <ul><li>Most of the problems with toxicity associated with </li></ul><ul><li>hydrogel carriers are the unreacted monomers, </li></ul><ul><li>oligomers and initiators that leach out during </li></ul><ul><li>application. </li></ul><ul><li>So, a good understanding the toxicity of the </li></ul><ul><li>monomers and initiators used is very important. </li></ul>
  66. 66. Cytotoxicity And In-vivo Toxicity: <ul><li>Approaches to solve this problem: </li></ul><ul><li>Modifying the rate of polymerization in order to </li></ul><ul><li>achieve a higher conversion </li></ul><ul><li>Extensive washing of the resulting hydrogel. </li></ul><ul><li>Formation of hydrogels without any initiators to </li></ul><ul><li>eliminate the problem of the residual initiator. </li></ul>
  67. 67. Cytotoxicity And In-vivo Toxicity: <ul><li>Commonly used technique to eliminate the problem </li></ul><ul><li>of the residual initiator is by using gamma irradiation. </li></ul><ul><li>Hydrogels can be made without the presence of </li></ul><ul><li>initiators by using thermal cycle to induce </li></ul><ul><li>crystallization. The crystals formed act as physical </li></ul><ul><li>crosslinks and are able to absorb the load applied to </li></ul><ul><li>the hydrogels. </li></ul>
  68. 68. Common Uses For Hydrogels:
  69. 69. Pharmaceutical Applications Of Hydrogels: <ul><li>Peroral Drug Delivery </li></ul><ul><li>Drug Delivery In The Oral Cavity </li></ul><ul><li>Drug Delivery in the G.I.T </li></ul><ul><li>Ocular Delivery </li></ul><ul><li>Transdermal Delivery </li></ul><ul><li>Subcutaneous Drug Delivery </li></ul><ul><li>Hydrogels To Fix Bone Replacements </li></ul><ul><li>Tissue Engineering </li></ul><ul><li>Protein Drug Delivery </li></ul><ul><li>Topical Drug Delivery </li></ul>
  70. 70. <ul><li>Drug delivery through the oral route has been the </li></ul><ul><li>most common method in the pharmaceutical </li></ul><ul><li>applications of hydrogels. </li></ul><ul><li>In peroral administration, hydrogels can deliver </li></ul><ul><li>drugs to four major specific sites; mouth, stomach, </li></ul><ul><li>small intestine and colon. </li></ul>Peroral Drug Delivery:
  71. 71. <ul><li>By controlling their swelling properties or </li></ul><ul><li>bio-adhesive characteristics in the presence of a </li></ul><ul><li>biological fluid, hydrogels can be a useful device </li></ul><ul><li>for releasing drugs in a controlled manner at these </li></ul><ul><li>desired sites. </li></ul>Peroral Drug Delivery:
  72. 72. <ul><li>Additionally, they can also adhere to certain specific </li></ul><ul><li>regions in the oral pathway, leading to a locally </li></ul><ul><li>increased drug concentration, and thus, enhancing </li></ul><ul><li>the drug absorption at the release site. </li></ul>Peroral Drug Delivery:
  73. 73. <ul><li>Drug delivery to the oral cavity can have versatile </li></ul><ul><li>applications in local treatment of diseases of the </li></ul><ul><li>mouth, such as periodontal disease, stomatitis, </li></ul><ul><li>fungal and viral infections,and oral cavity cancers. </li></ul><ul><li>Long-term adhesion of the drug containing hydrogel </li></ul><ul><li>against copious salivary flow, which bathes the oral </li></ul><ul><li>cavity mucosa, is required to achieve this local drug </li></ul><ul><li>delivery. </li></ul>Drug Delivery In The Oral Cavity:
  74. 74. Drug Delivery in the G.I.T: <ul><li>Ease of administration of drugs. </li></ul><ul><li>Availability of large surface area for drug absorption </li></ul><ul><li>High patient compliance. </li></ul><ul><li>First pass metabolism. </li></ul><ul><li>Pre-systemic metabolism. </li></ul>Advantages with oral route Drawbacks with oral route
  75. 75. Drug Delivery in the G.I.T: <ul><li>Hydrogel-based devices can be designed to deliver </li></ul><ul><li>drugs locally to specific sites in the GI tract. </li></ul><ul><li>E.g.,: Specific antibiotic drug delivery systems for the </li></ul><ul><li>treatment of H.pylori infection in peptic ulcer disease </li></ul><ul><li>These Hydrogels protect the insulin in the harsh, acidic </li></ul><ul><li>environment of the stomach before releasing the drug </li></ul><ul><li>in the small intestine. </li></ul>
  76. 76. Ocular Delivery : <ul><li>Effective tear drainage; blinking &Low permeability </li></ul><ul><li>of the cornea. </li></ul><ul><li>Limited absorption due to rapid elimination leading </li></ul><ul><li>to poor ophthalmic bioavailability. </li></ul><ul><li>Due to the short retention time, a frequent dosing </li></ul><ul><li>regimen is necessary for required therapeutic </li></ul><ul><li>efficacy. </li></ul>Drawbacks with ocular route
  77. 77. Ocular Delivery : <ul><li>Silicone rubber Hydrogel composite ophthalmic </li></ul><ul><li>inserts extended the duration of the Pilocarpine to </li></ul><ul><li>10 hr, compared to 3 hr when Pilocarpine nitrate was </li></ul><ul><li>dosed as a solution. </li></ul>Hydrogels in Ocular Delivery
  78. 78. Ocular Delivery : <ul><li>In-situ forming Hydrogels are attractive as an ocular </li></ul><ul><li>drug delivery system because of their facility in </li></ul><ul><li>dosing as a liquid,and long term retention property as </li></ul><ul><li>a gel after dosing. </li></ul>Hydrogels in Ocular Delivery
  79. 79. Ocular Delivery : <ul><li>Swollen Hydrogels can deliver drugs for long </li></ul><ul><li>duration. </li></ul><ul><li>Easy to remove. </li></ul><ul><li>Patient compliance is high. </li></ul>Advantages
  80. 80. Transdermal Delivery : <ul><li>Drug delivery to the skin has been generally </li></ul><ul><li>used to treat skin diseases or for disinfections </li></ul><ul><li>of the skin. </li></ul><ul><li>Transdermal route is employed for systemic </li></ul><ul><li>delivery of drugs. </li></ul>Purpose
  81. 81. Transdermal Delivery : <ul><li>The possible benefits of transdermal drug delivery </li></ul><ul><li>are - drugs can be delivered for a long duration. </li></ul><ul><li>- drugs can be delivered at a constant rate. </li></ul><ul><li>- drug delivery can be easily interrupted on </li></ul><ul><li>demand by simply removing the devices. </li></ul><ul><li>- drugs can bypass hepatic first-pass </li></ul><ul><li>metabolism. </li></ul>
  82. 82. Transdermal Delivery : <ul><li>Furthermore, because of their high water content, </li></ul><ul><li>swollen hydrogels can provide a better feeling for </li></ul><ul><li>the skin in comparison to conventional ointments </li></ul><ul><li>and patches. </li></ul>
  83. 83. Subcutaneous delivery: <ul><li>Subcutaneously inserted exogenous materials may </li></ul><ul><li>more or less evoke potentially undesirable body </li></ul><ul><li>responses, such as inflammation, carcinogenecity </li></ul><ul><li>and immunogenecity. </li></ul><ul><li>Therefore, biocompatibility is a prerequisite that </li></ul><ul><li>makes materials implantable. </li></ul>
  84. 84. Subcutaneous delivery: <ul><li>Due to their high water content, hydrogels are </li></ul><ul><li>generally considered as biocompatible materials. </li></ul><ul><li>They also provide several promising properties: </li></ul><ul><li>* minimal mechanical irritation upon in-vivo </li></ul><ul><li> implantation, due to their soft, elastic </li></ul><ul><li> properties. </li></ul>
  85. 85. Subcutaneous delivery: * Prevention of protein adsorption and cell adhesion arising from the low interfacial tension between water and hydrogels; * Broad acceptability for individual drugs with different hydrophilicities and molecular sizes * Unique possibilities to manipulate the release of incorporated drugs by crosslinking density and swelling.
  86. 86. Hydrogels To Fix Bone Replacements: <ul><li>Provided orthopedic fasteners and replacements </li></ul><ul><li>hip and knee replacements, etc. are coated with </li></ul><ul><li>Hydrogels which expand in the presence of liquids. </li></ul><ul><li>Swelling of such coatings causes the fastener or </li></ul><ul><li>replacement to be securely fixed into position once </li></ul><ul><li>inserted into bone material. </li></ul>
  87. 87. Hydrogels To Fix Bone Replacements:
  88. 88. Protein Drug Delivery: <ul><li>Interleukins are conventionally given as injection. </li></ul><ul><li>Hydrogels have the following advantages </li></ul><ul><li>-Better patient compliance. </li></ul><ul><li>-Hydrogels form insitu and release proteins </li></ul><ul><li> slowly </li></ul><ul><li> -They are biodegradable and biocompatible. </li></ul>
  89. 89. Topical Drug Delivery: <ul><li>Hydrogels are used to deliver drugs like Desonide </li></ul><ul><li>(synthetic corticosteroid) usually used as an anti- </li></ul><ul><li>inflammatory. </li></ul><ul><li>Hydrogels with their moisturizing properties avoids </li></ul><ul><li>scaling and dryness and has better patient </li></ul><ul><li>compliance. </li></ul>
  90. 90. Topical Drug Delivery: <ul><li>Antifungal formulations like Cotrimazole has been </li></ul><ul><li>developed as Hydrogel formulation for vaginitis and </li></ul><ul><li>shows better absorption than conventional cream </li></ul><ul><li>formulations. </li></ul>
  91. 91. Tissue Engineering: <ul><li>Microgels (micronized Hydrogels) can be used to </li></ul><ul><li>deliver macromolecules like phagosomes in to </li></ul><ul><li>cytoplasm of antigen-presenting cells. </li></ul><ul><li>The release is because of acidic conditions. Hydrogels </li></ul><ul><li>mold themselves to the pattern of membranes of the </li></ul><ul><li>tissues and have sufficient mechanical strength. </li></ul><ul><li>This property is also used in cartilage repairing </li></ul>
  92. 92. In The Treatment Lower Extremity Diabetic ulcers: <ul><li>Diabetic ulcers are the primary cause of amputations </li></ul><ul><li>of the leg, foot,or toe. </li></ul><ul><li>NanoDOX™ </li></ul><ul><li>A topical doxycycline Hydrogel for chronic wounds </li></ul><ul><li>NanoDOX™ contains 1% Doxycycline Monohydrate </li></ul><ul><li>Hydrogel. </li></ul><ul><li>Improve the topical delivery to increase local efficacy </li></ul>
  93. 93. Rectal Delivery: <ul><li>This route has been used to deliver many types of </li></ul><ul><li>drugs for treatment of diseases associated with the </li></ul><ul><li>rectum, such as hemorrhoids. </li></ul><ul><li>ADVANTAGES: </li></ul><ul><li>This route is an ideal way to administer drugs </li></ul><ul><li>suffering heavy first-pass metabolism. </li></ul>
  94. 94. Rectal Delivery: <ul><li>DRAWBACKS: </li></ul><ul><li>Patients compliance is less due to discomfort </li></ul><ul><li>arising from given dosage forms. </li></ul><ul><li>Substantial variability in patient’s acceptance of </li></ul><ul><li>treatment. this leads to variation of availability of </li></ul><ul><li>drugs. </li></ul>
  95. 95. Summary & Conclusion: <ul><li>Recent developments in the field of polymer </li></ul><ul><li>science and technology has led to the development </li></ul><ul><li>of various stimuli sensitive hydrogels like pH, </li></ul><ul><li>temperature sensitive, which are used for the targeted </li></ul><ul><li>delivery of proteins to colon, and chemotherapeutic </li></ul><ul><li>agents to tumors. </li></ul>
  96. 96. Summary & Conclusion: <ul><li>Some environmental variables, such as low pH and </li></ul><ul><li>elevated temperatures, are found in the body. </li></ul><ul><li>For this reason, either pH-sensitive and/or </li></ul><ul><li>temperature sensitive hydrogels can be used for </li></ul><ul><li>site-specific controlled drug delivery. </li></ul>
  97. 97. Summary & Conclusion: <ul><li>Hydrogels that are responsive to specific molecules, </li></ul><ul><li>such as glucose or antigens, can be used as </li></ul><ul><li>biosensors as well as drug delivery systems. </li></ul><ul><li>The hydrogels may be suitable as a wound </li></ul><ul><li>substitutes and can be used in wound healing. </li></ul>
  98. 98. Summary & Conclusion: <ul><li>New synthetic methods have been used to prepare </li></ul><ul><li>homo- and co-polymeric hydrogels for a wide </li></ul><ul><li>range of drugs, peptides, and protein delivery </li></ul><ul><li>applications. </li></ul><ul><li>Hydrogels are also used in regenerating </li></ul><ul><li>human tissue cells. </li></ul>
  99. 99. References: 1.Remington: The Science and Practice of Pharmacy. Published by Lippincott Williams & Wilkins, 2005. Twenty-First Editions. P.NO. 294,756,867,868. 2. Handbook of Pharmaceutical Excipients, A. Wade and P.J. Weller ed., The Pharmaceutical Press, London, 1994, pp. 229–232. 3. British Pharmacopoeia 2002, the Stationary Office, London, 2002, p. 2092–2094.
  100. 100. Thank You
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