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Name: Sayyad Ali
 Presented To Dr. Taos Khan

 Topic # Hydrogel

 Dated 27/02/1202

 COMSATS ABBOTTABAD.
                               1
Hydrogel
 Introduction

 The method by which a drug is delivered can
 have a significant effect on its efficacy. Some
 drugs have an optimum concentration range
 within which maximum benefit is derived, and
 concentrations above or below this range can
 be toxic or produce no therapeutic benefit at
 all.

                                                   2
• To minimize drug degradation and
  loss, to prevent harmful side-effects and
  to increase drug bioavailability and the
  fraction of the drug accumulated in the
  required zone, various drug delivery and
  drug targeting systems are currently
  under development



                                              3
• Among drug carriers one can name soluble
  polymers, micro particles made of insoluble
  or biodegradable natural and synthetic
  polymers, Microchips, microcapsules, cells,
   cell ghosts,lipoproteins, liposome’s, and
  micelles. The carriers can be made slowly
  degradable, stimuli-reactive (e.g., pH or
  temperature-sensitive), and even targeted.




                                                4
• Hydrogels are water-swollen polymeric
  materials that maintain a distinct three-
  dimensional structure. Their
  classification may be based on the source:
  natural, synthetic, or hybrid hydrogels
  (composed of synthetic and natural
  molecules); on the basis of nature of the
  crosslinking: covalent or non-covalent
  (physical) gels;

                                               5
• On the basis of nature of the network:
  homopolymer, copolymer, interpenetrating, or
  double networks; physical structure: (optically
  transparent), microporous, and macroporous
  hydrogels, and on their fate in the organism:
  degradable and non-degradable hydrogels.
  Due to their high water content, most
  hydrogel structures possess excellent
  biocompatibility.


                                                6
• There is a wide variety of the design options
  for the preparation of hydrogels of different
  structures and properties. The traditional
  methods of hydrogel synthesis were limited
  in the control of their detailed structure, but
  novel approaches based on genetic
  engineering and hybrid hydrogels, have
  considerably enhanced this research.



                                                7
• As a result, the application potential
  of hydrogels, in addition to
  traditional areas such as
  biomaterials and drug delivery
  systems, has expanded to other
  fields, such as microfluidics and
  nanotechnology.



                                           8
DISCOVERY
• In the early 1950s Otto and Lím from the
  Prague(Czechoslovakia) Institute of
  Chemical Technology initiated a research
  program to design polymers for medical
  use. Some merchandised polymers had been
  applied in humans use previously, but this
  was the first attempt to design polymers for
  human use with properties to fulfill the
  criteria of biocompatibility.


                                                 9
• The target was the design of new biomaterials
  for applications in ophthalmology. The main
  features of their design were (included in their
  grant proposal in 1952 which stated as
• (a)shape stability and softness similar to that
  of the soft surrounding tissue;
• (b) chemical and biochemical stability;



                                                 10
• c) high permeability for water-soluble
  nutrients and metabolites across the
  biomaterial tissue-interface.
• It is amazing that these hypotheses are
  still valid for soft contact lenses.




                                            11
• Based on this validation, Lím started
  efforts to synthesize new hydrogels.
  First, he considered polymerization of
  N-vinylpyrrolidone. However, it was not
  available, so Lim’s first experiments
  focused on partially methacryloylation of
  polyvinylalcohol. Polyvinylalcohol was
  chosen due to its previous use in human
  implants (Ivalon et al).


                                              12
• Methacryloyl esters were chosen
  because the structure of the polymer
  reflects a pivalic (trimethyl acetic
  acid) acid structure. The latter was
  known to be stable to pure hydrolysis.




                                       13
• The polyvinyl alcohol route produced
  optically clear hydrogels containing
  80–90% water but these hydrogels did
  not show mechanical properties
  necessary for use in contact lenses.




                                         14
gelatine hydrogels crosslinked with partially
oxidised dextrans.



                                                15
16
• One year later, Lím by chance identified
  a novel hydrogel material. He was
  synthesizing the tri ethylene glycol di
  methacrylate monomer by acid
  catalyzed trans esterification of methyl
  methacrylate with tri ethylene glycol.




                                         17
•   At the end of the reaction he come
    across with the neutralization of the
    acid, dilution with water to isolate the
    water-insoluble tri ethylene glycol di
    methacrylate, washing the organic layer
    with water, drying and isolating the pure
    product by distillation.




                                                18
•    (One day Lím had to catch the train to
    his home, so he stopped the reaction
    early, and managed to add water to
    separate the layers before leaving. In
    the morning, he noticed that the water
    layer turned into a clear hydrogel
    overnight).



                                              19
• Obviously, it was a copolymer of tri-
  ethylene-glycol, mono-methacrylate
  with tri-ethylene-glycol di-
  methacrylate led to the final
  selection of a hydrogel.



                                          20
• So the existence of hydrogels dates back to
  1960, when Otto and Lim first proposed the
  use of hydrophilic networks of poly-
  hydroxyl-ethyl methacrylate (PHEMA) in
  contact lenses.
• Since then, the use of hydrogels has
  extended to various biomedical and
  pharmaceutical applications.



                                            21
• In comparison to other synthetic
  biomaterials, hydrogels resemble living
  tissues closely in their physical properties
  because of their relatively high water
  content , soft and rubbery consistency.
• Hydrogels show minimal tendency to
  adsorb proteins from body fluids because
  of their low interfacial tension.


                                                 22
• Further, the ability of molecules of
  different sizes to diffuse into (drug
  loading) and out of (drug release)
  hydrogels allows the possible use of dry or
  swollen polymeric networks as drug
  delivery systems for
  oral, nasal, buccal, rectal, vaginal, ocular
  and parenteral routes of administration.


                                                 23
Hydrogel can be delivered by any of the following routs




                                                     24
• Because of these qualities it gained
  different names like ‘intelligent gels’ or
  ‘smart hydrogels. The smartness of any
  material is the key to its ability to
  receive, transmit or process a
  stimulus, and respond by producing a
  useful effect.




                                               25
Hydrogels are ‘smart’ or ‘intelligent’ in the
sense that they can recognize the
predominant stimuli and respond by
displaying changes in their physical or
chemical behavior, resulting in the release of
entrapped drug in a controlled manner.




                                                 26
• Some hydrogels undergo continuous or
  discontinuous changes in swelling that are
  mediated by external stimuli such as changes
  in pH, temperature, ionic strength, solvent
  type, electric and magnetic elds, light, and
  the presence of chelating species.




                                              27
• The majority of stimuli responsive
  hydrogels were created using conventional
  (traditional) methods of synthesis of a
  relatively small number of synthetic
  polymers, especially (meth) acrylate
  derivatives and their copolymers.



                                         28
• In 1968, Dusek and Patterson
  theoretically predicted that changes in
  external conditions might result in abrupt
  changes of the hydrogel’s degree of
  swelling.
• Indeed, 10 years later, Tanaka and others
  have veried the theory by experimental
  observations

                                           29
Pathways of solid polymer degradation(General)




                                             30
Cont.… pathways of degradation




                                 31
Basic difference in gel and hydrogel

• Both gels and hydrogels might be similar
   chemically, but they are physically distinct.
• D. Jordan suitably described gels as ‘The colloidal
   condition, the gel, is one which is easier to recognize
   than to define
 • Technically, gels are semi-solid systems
    comprising small amounts of solid, dispersed in
    relatively large amounts of liquid, having more
    solid-like than liquid-like character.
    Sometimes, hydrogels are also described as
    aqueous gels because of the prefix ‘hydro’.
                                                        32
• Although the term ‘hydrogel’ implies a
  material already swollen in water, while in a
  true sense hydrogel is a cross-linked network
  of hydrophilic polymers. They possess the
  ability to absorb large amounts of water and
  swell, while maintaining their three-
  dimensional (3D) structure.




                                                  33
• hydrogels display swelling in aqueous
  media for the same reasons that an
  analogous linear polymer dissolves in
  water to form an ordinary polymer
  solution. Thus, the feature central to the
  functioning of a hydrogel is its inherent
  cross-linking.
• Conventional gels can also develop small
  levels of cross-links as a result of a gain in
  energy under the influence of shear
  forces, but these are reversible
                                                   34
• Because of the above quality hydrogels is a
  polymer network, these polymers produce
  systems that extend a range of
  rigidities, beginning with a sol and
  increasing to jelly, gel and hydrogel.
  Thus, hydrogel, sometimes referred to as
  xerogel, is a more rigid form of gel




                                                35
Future perspectives

• An interesting characteristic about many
  responsive hydrogels is that the mechanism
  causing changes in network structure can be
  entirely reversible in nature.
• This conveys elastic deformability with
  ‘shape-memory’ behaviors so that hydrogels
  return back to their original shape at the
  end of initiating stimuli.


                                           36
• Keeping in view this quality The Jiang’s
  laboratory developed a tunable
  (adjustable) liquid lens that permits
  autonomous focusing. The design was
  based on a temperature-sensitive
  hydrogel.




                                             37
• All the scientific evidences seem to indicate
  that the basic and translational research in
  hydrogels has a bright future.
• Numerous new designs, e.g. involving protein
  domains containing non-recognized amino
  acids, successful attempts has done to control
  the morphology of self-assembling peptide
  bers, articial glycoproteins for controlling
  cell responses , hydrogels play a key role in
  the building material for the
  microchemotaxis and for all the above
  phenomena.
                                              38
• It has a role in the enhancement of the
  use of DNA recognition motifs, and an
  improved synthetic method can be
  established with hydrgel(Genetic
  Engineering).
• An outstanding example of the
  potential of stimuli-sensitive hydrogels
  in the development of
  bionanotechnology products is the
  design of optical systems that do not
  require mechanical components.

                                             39
Application of hydrogel
• New researchers have demonstrated that a gel
  composed of small, woven protein fragments
  can successfully carry and release proteins of
  different sizes to different targets in the body.

• It is enabling the delivery of drugs such as
  insulin and trastuzumab (A monoclonal
  antibody (protein) often used to treat breast
  and ovarian cancer), hormones, growth factors
  as well as eye medications.

                                                      40
• Furthermore, one can control the rate of release of
  active ingredients from hydrogel by changing the
  density of the gel, allowing for continuous drug
  delivery over a specific period of time.

• A newly introduced gel, known as a "nanofiber
  hydrogel scaffold," enables, over hours, days or even
  months, a gradual release of the proteins from the
  gel, and the gel itself is eventually broken down into
  harmless amino acids (the building blocks of
  proteins).


                                                        41
• Peptide hydrogels are ideally suited for drug
  delivery as they are pure, easy to design and
  use, non-toxic, bio-absorbable, and can be locally
  applied to a particular tissue.

• Depending on the size and density of the mesh, it
  can carry protein molecules between 14,000 and
  150,000 daltons (a unit of molecular weight).

• Earlier work showed that the hydrogels could also
  carry smaller molecules, between 300 and 900
  daltons. " So it can deliver both small molecules
  and big molecules,".
                                                       42
REFERENCES
1. Kopeček J, Yang J. Polymer Int. 2007;56:1078–1098.
2. Dušek K, Prins W. Adv Polym Sci. 1969;6:1–102.
3. Wichterle O. Encyclopedia of Polymer Science and Technology. In: Mark HF, Gaylord NG, Bikales N, editors. Interscience. Vol. 15.
New York, NY: 1971. pp. 273–291.
4. Andrade JD, editor. Hydrogels for Medical and Related Applications. ACS Symposium Series. Vol. 31. Washington D.C: 1976.
5. Ratner BD, Hoffman A. Hydrogels for Medical and Related Applications. In: Andrade JD, editor. ACS Symposium Series. Vol. 31.
Washington D.C: 1976. pp. 1–36.
6. KĹŻdela V. In: Encyclopedia of Polymer Science and Engineering. Mark HF, Kroschwitz J, editors. Wiley; New York, NY: 1987. pp.
783–807.
7. Peppas NA, editor. Hydrogels in Medicine and Pharmacy. I–III. CRC Press; Boca Ratyon, FL: 1987.
8. Brøndsted H, Kopeček J. Polyelectrolyte Gels. In: Harland RS, Prud’homme RK, editors. ACS Symposium Series. Vol. 480.
Washington D.C: 1992. pp. 285–304.
9. Kamath KR, Park K. Adv Drug Delivery Rev. 1993;11:59–83.
10. Osada Y, Gong J. Prog Polym Sci. 1993;18:187–226.
11. Peppas NA, Bures P, Leobandung W, Ichikawa H. Eur J Pharmaceutics Biopharm. 2000;50:27–46.
12. Hoffman AS. Adv Drug Delivery Rev. 2002;54:3–12.
13. Nayak S, Lyon LA. Angew Chem Int Ed. 2005;44:7686–7708.
14. LĂ­m, D., Personal communication, 2001.
15. LĂ­m D. RNDr Thesis. Technical University Prague; 1953.
16. Grindlay JH, Clagett OT. Proc Staff Meet Mayo Clin. 1949;24:538.
17. Wichterle O, Lím D. Nature. 1960;185:117–118.
18. Kopeček J, Lím DJ. Polym Sci Part A-1. 1971;9:147–154.
19. Dreifus M, Klenka L. Československá oftalmologie (in Czech) 1959;15:95–101.
20. Dreifus M, Wichterle O, Lím D. Československá oftalmologie (in Czech) 1960;16:154–159.
21. Dreifus M, Herben T, Lím D, Wichterle O. Sb Lék (In Czech) 1960;62:212–218.



                                                                                                                              43
22. Wichterle O. Original Czech version (“Vzpomínky”) in 1992. 1994. Recollections.
23. Wichterle O. Czechoslovak Academy of Sciences. U.S. Patents. 3,660,545; 3,408,429; 3,496,254;
3,499,862
24. Wichterle O. In: Soft Contact Lenses. Ruben M, editor. Wiley; New York: 1978. pp. 3–5.
25. Wichterle O. Czechoslovak Academy of Sciences. U.S. Patents. 3,361,858; 3,497,577; 3,542,907
26. It was an interesting time to be a graduate student in the early 60s at IMC Prague. In addition to
being exposed to an exciting new research field, it was possible to witness soccer and movie stars
visiting Prof. Wichterle and trying to get a free sample of soft contact lenses that were not commercially
available at that time.
27. Kolařík J, Migliaresi CJ. Biomed Mater Res. 1983;17:757–767.
28. Tighe BJ. In: Hydrogels in Medicine and Pharmacy. Peppas NA, editor. III. CRC Press; Boca
Raton, Florida: 1987. pp. 53–82.
29. Nicolson PC, Vogt J. Biomaterials. 2001;22:3273–3283. [PubMed]
30. Krejčí L, Harrison R, Wichterle O. Arch Ophthal. 1970;84:76–80. [PubMed]
31. Křístek A, König B, Wichterle O. Klin Abl Augenheilk (in German) 1966;149:219–227.
32. Kresa Z, Rems J, Wichterle O. Arch Otholaryngol. 1973;17:360–365.
33. Hubáček J, Wichterle O, Kliment K, Hubáček Jar, Dušek J. Československá otolaryngologie (in
Czech) 1968;17:211–215.
34. Šprincl L, Vacík J, Kopeček J, Lím D. J Biomed Mater Res. 1971;5:197–205. [PubMed]
35. Kopeček J, Šprincl L, Bažilová H, Vacík J. J Biomed Mater Res. 1973;7:111–121. [PubMed]



                             Thank you
                                                                                                       44

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Presentation: Hydrogel

  • 1. Name: Sayyad Ali  Presented To Dr. Taos Khan  Topic # Hydrogel  Dated 27/02/1202  COMSATS ABBOTTABAD. 1
  • 2. Hydrogel  Introduction  The method by which a drug is delivered can have a significant effect on its efficacy. Some drugs have an optimum concentration range within which maximum benefit is derived, and concentrations above or below this range can be toxic or produce no therapeutic benefit at all. 2
  • 3. • To minimize drug degradation and loss, to prevent harmful side-effects and to increase drug bioavailability and the fraction of the drug accumulated in the required zone, various drug delivery and drug targeting systems are currently under development 3
  • 4. • Among drug carriers one can name soluble polymers, micro particles made of insoluble or biodegradable natural and synthetic polymers, Microchips, microcapsules, cells, cell ghosts,lipoproteins, liposome’s, and micelles. The carriers can be made slowly degradable, stimuli-reactive (e.g., pH or temperature-sensitive), and even targeted. 4
  • 5. • Hydrogels are water-swollen polymeric materials that maintain a distinct three- dimensional structure. Their classification may be based on the source: natural, synthetic, or hybrid hydrogels (composed of synthetic and natural molecules); on the basis of nature of the crosslinking: covalent or non-covalent (physical) gels; 5
  • 6. • On the basis of nature of the network: homopolymer, copolymer, interpenetrating, or double networks; physical structure: (optically transparent), microporous, and macroporous hydrogels, and on their fate in the organism: degradable and non-degradable hydrogels. Due to their high water content, most hydrogel structures possess excellent biocompatibility. 6
  • 7. • There is a wide variety of the design options for the preparation of hydrogels of different structures and properties. The traditional methods of hydrogel synthesis were limited in the control of their detailed structure, but novel approaches based on genetic engineering and hybrid hydrogels, have considerably enhanced this research. 7
  • 8. • As a result, the application potential of hydrogels, in addition to traditional areas such as biomaterials and drug delivery systems, has expanded to other fields, such as microfluidics and nanotechnology. 8
  • 9. DISCOVERY • In the early 1950s Otto and LĂ­m from the Prague(Czechoslovakia) Institute of Chemical Technology initiated a research program to design polymers for medical use. Some merchandised polymers had been applied in humans use previously, but this was the first attempt to design polymers for human use with properties to fulfill the criteria of biocompatibility. 9
  • 10. • The target was the design of new biomaterials for applications in ophthalmology. The main features of their design were (included in their grant proposal in 1952 which stated as • (a)shape stability and softness similar to that of the soft surrounding tissue; • (b) chemical and biochemical stability; 10
  • 11. • c) high permeability for water-soluble nutrients and metabolites across the biomaterial tissue-interface. • It is amazing that these hypotheses are still valid for soft contact lenses. 11
  • 12. • Based on this validation, LĂ­m started efforts to synthesize new hydrogels. First, he considered polymerization of N-vinylpyrrolidone. However, it was not available, so Lim’s first experiments focused on partially methacryloylation of polyvinylalcohol. Polyvinylalcohol was chosen due to its previous use in human implants (Ivalon et al). 12
  • 13. • Methacryloyl esters were chosen because the structure of the polymer reflects a pivalic (trimethyl acetic acid) acid structure. The latter was known to be stable to pure hydrolysis. 13
  • 14. • The polyvinyl alcohol route produced optically clear hydrogels containing 80–90% water but these hydrogels did not show mechanical properties necessary for use in contact lenses. 14
  • 15. gelatine hydrogels crosslinked with partially oxidised dextrans. 15
  • 16. 16
  • 17. • One year later, LĂ­m by chance identified a novel hydrogel material. He was synthesizing the tri ethylene glycol di methacrylate monomer by acid catalyzed trans esterification of methyl methacrylate with tri ethylene glycol. 17
  • 18. • At the end of the reaction he come across with the neutralization of the acid, dilution with water to isolate the water-insoluble tri ethylene glycol di methacrylate, washing the organic layer with water, drying and isolating the pure product by distillation. 18
  • 19. • (One day LĂ­m had to catch the train to his home, so he stopped the reaction early, and managed to add water to separate the layers before leaving. In the morning, he noticed that the water layer turned into a clear hydrogel overnight). 19
  • 20. • Obviously, it was a copolymer of tri- ethylene-glycol, mono-methacrylate with tri-ethylene-glycol di- methacrylate led to the final selection of a hydrogel. 20
  • 21. • So the existence of hydrogels dates back to 1960, when Otto and Lim first proposed the use of hydrophilic networks of poly- hydroxyl-ethyl methacrylate (PHEMA) in contact lenses. • Since then, the use of hydrogels has extended to various biomedical and pharmaceutical applications. 21
  • 22. • In comparison to other synthetic biomaterials, hydrogels resemble living tissues closely in their physical properties because of their relatively high water content , soft and rubbery consistency. • Hydrogels show minimal tendency to adsorb proteins from body fluids because of their low interfacial tension. 22
  • 23. • Further, the ability of molecules of different sizes to diffuse into (drug loading) and out of (drug release) hydrogels allows the possible use of dry or swollen polymeric networks as drug delivery systems for oral, nasal, buccal, rectal, vaginal, ocular and parenteral routes of administration. 23
  • 24. Hydrogel can be delivered by any of the following routs 24
  • 25. • Because of these qualities it gained different names like ‘intelligent gels’ or ‘smart hydrogels. The smartness of any material is the key to its ability to receive, transmit or process a stimulus, and respond by producing a useful effect. 25
  • 26. Hydrogels are ‘smart’ or ‘intelligent’ in the sense that they can recognize the predominant stimuli and respond by displaying changes in their physical or chemical behavior, resulting in the release of entrapped drug in a controlled manner. 26
  • 27. • Some hydrogels undergo continuous or discontinuous changes in swelling that are mediated by external stimuli such as changes in pH, temperature, ionic strength, solvent type, electric and magnetic elds, light, and the presence of chelating species. 27
  • 28. • The majority of stimuli responsive hydrogels were created using conventional (traditional) methods of synthesis of a relatively small number of synthetic polymers, especially (meth) acrylate derivatives and their copolymers. 28
  • 29. • In 1968, Dusek and Patterson theoretically predicted that changes in external conditions might result in abrupt changes of the hydrogel’s degree of swelling. • Indeed, 10 years later, Tanaka and others have veried the theory by experimental observations 29
  • 30. Pathways of solid polymer degradation(General) 30
  • 31. Cont.… pathways of degradation 31
  • 32. Basic difference in gel and hydrogel • Both gels and hydrogels might be similar chemically, but they are physically distinct. • D. Jordan suitably described gels as ‘The colloidal condition, the gel, is one which is easier to recognize than to define • Technically, gels are semi-solid systems comprising small amounts of solid, dispersed in relatively large amounts of liquid, having more solid-like than liquid-like character. Sometimes, hydrogels are also described as aqueous gels because of the prefix ‘hydro’. 32
  • 33. • Although the term ‘hydrogel’ implies a material already swollen in water, while in a true sense hydrogel is a cross-linked network of hydrophilic polymers. They possess the ability to absorb large amounts of water and swell, while maintaining their three- dimensional (3D) structure. 33
  • 34. • hydrogels display swelling in aqueous media for the same reasons that an analogous linear polymer dissolves in water to form an ordinary polymer solution. Thus, the feature central to the functioning of a hydrogel is its inherent cross-linking. • Conventional gels can also develop small levels of cross-links as a result of a gain in energy under the influence of shear forces, but these are reversible 34
  • 35. • Because of the above quality hydrogels is a polymer network, these polymers produce systems that extend a range of rigidities, beginning with a sol and increasing to jelly, gel and hydrogel. Thus, hydrogel, sometimes referred to as xerogel, is a more rigid form of gel 35
  • 36. Future perspectives • An interesting characteristic about many responsive hydrogels is that the mechanism causing changes in network structure can be entirely reversible in nature. • This conveys elastic deformability with ‘shape-memory’ behaviors so that hydrogels return back to their original shape at the end of initiating stimuli. 36
  • 37. • Keeping in view this quality The Jiang’s laboratory developed a tunable (adjustable) liquid lens that permits autonomous focusing. The design was based on a temperature-sensitive hydrogel. 37
  • 38. • All the scientic evidences seem to indicate that the basic and translational research in hydrogels has a bright future. • Numerous new designs, e.g. involving protein domains containing non-recognized amino acids, successful attempts has done to control the morphology of self-assembling peptide bers, articial glycoproteins for controlling cell responses , hydrogels play a key role in the building material for the microchemotaxis and for all the above phenomena. 38
  • 39. • It has a role in the enhancement of the use of DNA recognition motifs, and an improved synthetic method can be established with hydrgel(Genetic Engineering). • An outstanding example of the potential of stimuli-sensitive hydrogels in the development of bionanotechnology products is the design of optical systems that do not require mechanical components. 39
  • 40. Application of hydrogel • New researchers have demonstrated that a gel composed of small, woven protein fragments can successfully carry and release proteins of different sizes to different targets in the body. • It is enabling the delivery of drugs such as insulin and trastuzumab (A monoclonal antibody (protein) often used to treat breast and ovarian cancer), hormones, growth factors as well as eye medications. 40
  • 41. • Furthermore, one can control the rate of release of active ingredients from hydrogel by changing the density of the gel, allowing for continuous drug delivery over a specific period of time. • A newly introduced gel, known as a "nanofiber hydrogel scaffold," enables, over hours, days or even months, a gradual release of the proteins from the gel, and the gel itself is eventually broken down into harmless amino acids (the building blocks of proteins). 41
  • 42. • Peptide hydrogels are ideally suited for drug delivery as they are pure, easy to design and use, non-toxic, bio-absorbable, and can be locally applied to a particular tissue. • Depending on the size and density of the mesh, it can carry protein molecules between 14,000 and 150,000 daltons (a unit of molecular weight). • Earlier work showed that the hydrogels could also carry smaller molecules, between 300 and 900 daltons. " So it can deliver both small molecules and big molecules,". 42
  • 43. REFERENCES 1. Kopeček J, Yang J. Polymer Int. 2007;56:1078–1098. 2. DuĹĄek K, Prins W. Adv Polym Sci. 1969;6:1–102. 3. Wichterle O. Encyclopedia of Polymer Science and Technology. In: Mark HF, Gaylord NG, Bikales N, editors. Interscience. Vol. 15. New York, NY: 1971. pp. 273–291. 4. Andrade JD, editor. Hydrogels for Medical and Related Applications. ACS Symposium Series. Vol. 31. Washington D.C: 1976. 5. Ratner BD, Hoffman A. Hydrogels for Medical and Related Applications. In: Andrade JD, editor. ACS Symposium Series. Vol. 31. Washington D.C: 1976. pp. 1–36. 6. KĹŻdela V. In: Encyclopedia of Polymer Science and Engineering. Mark HF, Kroschwitz J, editors. Wiley; New York, NY: 1987. pp. 783–807. 7. Peppas NA, editor. Hydrogels in Medicine and Pharmacy. I–III. CRC Press; Boca Ratyon, FL: 1987. 8. Brøndsted H, Kopeček J. Polyelectrolyte Gels. In: Harland RS, Prud’homme RK, editors. ACS Symposium Series. Vol. 480. Washington D.C: 1992. pp. 285–304. 9. Kamath KR, Park K. Adv Drug Delivery Rev. 1993;11:59–83. 10. Osada Y, Gong J. Prog Polym Sci. 1993;18:187–226. 11. Peppas NA, Bures P, Leobandung W, Ichikawa H. Eur J Pharmaceutics Biopharm. 2000;50:27–46. 12. Hoffman AS. Adv Drug Delivery Rev. 2002;54:3–12. 13. Nayak S, Lyon LA. Angew Chem Int Ed. 2005;44:7686–7708. 14. LĂ­m, D., Personal communication, 2001. 15. LĂ­m D. RNDr Thesis. Technical University Prague; 1953. 16. Grindlay JH, Clagett OT. Proc Staff Meet Mayo Clin. 1949;24:538. 17. Wichterle O, LĂ­m D. Nature. 1960;185:117–118. 18. Kopeček J, LĂ­m DJ. Polym Sci Part A-1. 1971;9:147–154. 19. Dreifus M, Klenka L. ČeskoslovenskĂĄ oftalmologie (in Czech) 1959;15:95–101. 20. Dreifus M, Wichterle O, LĂ­m D. ČeskoslovenskĂĄ oftalmologie (in Czech) 1960;16:154–159. 21. Dreifus M, Herben T, LĂ­m D, Wichterle O. Sb LĂŠk (In Czech) 1960;62:212–218. 43
  • 44. 22. Wichterle O. Original Czech version (“VzpomĂ­nky”) in 1992. 1994. Recollections. 23. Wichterle O. Czechoslovak Academy of Sciences. U.S. Patents. 3,660,545; 3,408,429; 3,496,254; 3,499,862 24. Wichterle O. In: Soft Contact Lenses. Ruben M, editor. Wiley; New York: 1978. pp. 3–5. 25. Wichterle O. Czechoslovak Academy of Sciences. U.S. Patents. 3,361,858; 3,497,577; 3,542,907 26. It was an interesting time to be a graduate student in the early 60s at IMC Prague. In addition to being exposed to an exciting new research field, it was possible to witness soccer and movie stars visiting Prof. Wichterle and trying to get a free sample of soft contact lenses that were not commercially available at that time. 27. Kolařík J, Migliaresi CJ. Biomed Mater Res. 1983;17:757–767. 28. Tighe BJ. In: Hydrogels in Medicine and Pharmacy. Peppas NA, editor. III. CRC Press; Boca Raton, Florida: 1987. pp. 53–82. 29. Nicolson PC, Vogt J. Biomaterials. 2001;22:3273–3283. [PubMed] 30. Krejčí L, Harrison R, Wichterle O. Arch Ophthal. 1970;84:76–80. [PubMed] 31. Křístek A, KĂśnig B, Wichterle O. Klin Abl Augenheilk (in German) 1966;149:219–227. 32. Kresa Z, Rems J, Wichterle O. Arch Otholaryngol. 1973;17:360–365. 33. Hubáček J, Wichterle O, Kliment K, Hubáček Jar, DuĹĄek J. ČeskoslovenskĂĄ otolaryngologie (in Czech) 1968;17:211–215. 34. Ĺ princl L, VacĂ­k J, Kopeček J, LĂ­m D. J Biomed Mater Res. 1971;5:197–205. [PubMed] 35. Kopeček J, Ĺ princl L, BaĹžilovĂĄ H, VacĂ­k J. J Biomed Mater Res. 1973;7:111–121. [PubMed] Thank you 44