Department of Hydrogels for Medical and Technical Practice
Characterization of Dept. Hydrogels for medical and
technical practice
The development of synthetic hydrogels for biomedical use as
well as contact and intraocular lenses is the typical topic for
department. The research has been advanced continuously from the
period of the eighties when our department was closely associated
with the Academician Otto Wichterle DSc, one of the leading
pioneers of polymer science.
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Figure 1: Academician Otto Wichterle DSc in front
of a machine for contact lenses producing |
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Fig 2: All operations in preparation of medical grade
articles are carried out in a clean room of type A |
New polymeric materials are tested
using physical and chemical methods. The material properties
(swelling, mechanical, transport and optical properties) are
studied including their biocompatibility and interaction with
living tissue.
In the last year we developed
polymer materials facilitating wound healing, which are capable
of removing reactive oxygen and nitrogen species. The wound-cover
material is characteristic in that it consists of a polymer
carrier based on slightly crosslinked hydrophilic polymers or
copolymers and physiological bioactive substances with radical
scavenger properties, selected from the group of vitamins A,
carotenoids, vitamins E, ubiquinones, flavonoids, nicotinamide,
uric acid, bilirubin, lipoic acid, glutathione, and melatonin.
The material is successfully used in veterinary medicine.
New hydrophilic polymer supports
for cultivation and subsequent transplantation of keratinocytes
designed for treatment of burns and large skin defects have also
been prepared. We continued the research by testing low-hydrated
materials containing ether groupings. We prepared copolymers of
glycerol monomethacrylate and 2-ethoxyethyl methacrylate
crosslinked with glycerol dimethacrylate and compared them with
copolymers of glycerol mono- and dimethacrylate. Following our
present and previous results, it is evident that one of the main
factors determining keratinocyte adhesion is the equilibrium
swelling of hydrogel. Low-hydrated hydrogels show enhanced
sorption of proteins important for cell adhesion (e.g.
fibronectin and its active adhesive sequences). Thus, we started
preparation of polymer carriers based on 2-ethoxyethyl
methacrylate (possibly with a low admixture of 2-hydroxyethyl
methacrylate) crosslinked with hexane-1,6-diyl dimethacrylate
and containing modified adhesive amino acid sequences derived
from fibronectin (e.g. RGD with synergic sequence PHSRN). We
prepared 6-methacrylamidohexanoyl-PHSRNamide and
6-methacrylamidohexanoyl-RGD-amide by a method of solid-phase
synthesis of peptides. Both the prepared amides were
copolymerized with 2-ethoxyethyl methacrylate. Now we are
working on optimization of the length and type of flexible spacer
between methacrylate chain and adhesive sequences.
In
the framework of the research on implants for the central nervous
system, we continued in the research of macroporous hydrogels
based on copolymers of 2-hydroxyethyl methacrylate, methacrylic
acid and [2-(methacryloyloxy)ethyl]trimethylamonium
chloride and their polyelectrolyte complexes. Previous results
have demonstrated the possibility of obtaining controlled pore
size, pore communication, and suitable biological response. Our
hydrogels show predominantly communicating pores and quite a
narrow pore size distribution as follows from confocal and
electron microscopy.
From
the viewpoint of mechanical properties, the 10 mol% concentration
of ionic monomers is an optimum (properties of the resulting
polymer are similar to those of the nervous tissue). As most
polymer - living tissue interactions are localized in the protein
layer at the interface, we prepared a layer of selected proteins
on surfaces of the materials. The described macroporous hydrogels
were used for immobilization of model proteins: albumin (low pI,
4.9) and avidin (high pI, 10.5). The protein adsorption capacity
was measured and kinetic studies were carried out. The protein -
polymer complex is stable, desorption of proteins is minimal.
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Fig 3: AquaSEM picture of a macroporous hydrogel
prepared by a copolymerization of 2-hydroxyethyl
methacrylate and sodium methacrylate (11.3 mol %) in the
presence of NaCl (particle size 50 - 90 um). After
polymerization NaCl was washed out by water. This
material is tested in vivo and vitro as
potential implant in the central nervous system. |
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Fig 4: AFM picture of 1% poly(HEMA) deposited
onto a fused silica as a polymer layer for capillary
electrophoretic separations of biologically active
compounds |
In
the framework of the research on new hydrogel materials for
contact lenses, we prepared copolymers of diethylene glycol
methacrylate with new types of perfluorinated vinyl monomers.
They are transparent gels with promising properties. The
mentioned structures enhance oxygen permeability of resulting
hydrophilic gels.
We also participate in the development of novel separation
techniques, e.g. in syntheses of imprinted polymers for
high-performance liquid chromatography or capillary
electrochromatography and in the study of permanent hydrogel
coatings of fused-silica columns for capillary electrophoresis.
The biomedical properties of
prepared polymers are evaluated by long-standing and successful
collaboration with the teams of co-workers at the Institute of
Anatomy, the First Faculty of Medicine at Charles University,
Prague, and Burn center, the Third Faculty of Medicine at Charles
University, Prague as well as at the Department of Eye
Histochemistry, the Institute of Experimental Medicine, Academy
of Sciences, Prague.
In cooperation with the Charles
University of Prague, the Institute of Chemical Technology of
Prague our department educates several PhD. and diploma students
and generates the opportunity to evolve both pure and applied
research.
Further our department makes use
of long tradition in coactions with the Czech Contact Lens
Society and we profess at the Second Faculty of Medicine at
Charles University, Prague as external lecturers.
Send your comments to:
jiri@imc.cas.cz
Last modified: 04.06.2004
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