Polymer networks applied in clinical dentistry can be divided into two
groups: (i) hard, solid two-and threedimensional crosslinked structur
es formed during photo-curing of dental polymeric filling compositions
, and (ii) soft, hydrogel-type of networks based on polymeric ionic co
mplexes, used for the tightening of microchannels in teeth. The first
group is based on crosslinked di- and trifunctional monomers, and on s
olid poly(acrylic acid) - inorganic glasses (''glass - ionomer cements
'') This group has found wide clinical applications, in spite of many
disadvantages such as susceptibility towards hydrolytic, mechanical. b
io- and enzymatic degradations, and contents of toxic, allergenic and
mutagenic components. The second group, the soft-hydrogel type of netw
orks, has been investigated and developed at our institute in order to
tighten channels in teeth. The microchannels, with a diameter of 30-2
00 Angstrom in enamel and 1-3 mu m in dentine, are filled with a loose
, native biohydrogel of protein origin. Hydrogels have the ability to
swell in water of biological fluids present in the oral cavity, and ca
n retain a significant fraction of fluid within the structure. Decreas
ing pH below 5.5 causes a slow dissolution of the hydroxyapatite cryst
al in the walls of the microchannels with a consequent widening of the
ir lumens. Metabolites and toxins from microorganisms, which are alway
s present in the oral cavity, can penetrate into these enlarged channe
ls and cause inflammatory reactions in the underlying pulp tissue. In
order to decrease fluid flow and inhibit penetration of microorganisms
, but still allow diffusion of ions and water, we have developed and t
ested polymeric hydrogels based on poly(acrylic acid) and metal salts,
and chitosan, which can be formed directly in the microchannels of de
ntal hard tissues.