Hyaluronan (Hyal) was modified by the insertion of sulphate to hydroxyl gro
ups. A series of heparin-like compounds with controllable properties was ob
tained. The physicochemical and biological behaviours of all these sulphate
d hyaluronan acids (HyalS(x)) and their complexes with heavy metal ions (Cu
2+ and Zn2+) were investigated. HyalS(x) derivatives showed a good anticoag
ulant activity and low platelet aggregation which increased with increasing
degree of sulphation. Moreover HyalS(x) and their Cu2+ complexes were demo
nstrated to favour the growth of human endothelial cells. However, the util
isation of HyalS(x) as a material is hindered by its high solubility in phy
siological solution. Our approach to improve its stability was directed to
the synthesis of new HyalS(x)-based hydrogels and on the preparation of new
biocompatible polymeric surfaces obtained through covalent photoimmobilisa
tion of HyalS(x). The reaction of primary ovine chondrocytes and B10D2 endo
thelial cells was studied on both matrices in terms of cell number, F-actin
and CD44 receptor immunostaining. Analysis of cell movement showed that th
e cells respond to HyalS(x) showing good adhesion and spreading. These resu
lts suggest that HyalS(x) containing materials could be used as biomaterial
s to aid cartilage repair and vessel endothelisation. (C) 2000 Elsevier Sci
ence Inc. All rights reserved.