New cross-linked and sulfated derivatives of partially deacetylated hyaluronan: Synthesis and preliminary characterization

✍ Scribed by Vittorio Crescenzi; Andrea Francescangeli; Davide Renier; Davide Bellini

• Publisher: Wiley (John Wiley & Sons)
• Year: 2002
• Tongue: English
• Weight: 155 KB
• Volume: 64
• Category: Article
• ISSN: 0006-3525
• DOI: 10.1002/bip.10131

✦ Synopsis

Partial chemical deacetylation of hyaluronan (HA) has been carried out using known procedures and carefully controlled experimental conditions in order to minimize chain degradation. The sample described herein (deHA) has a degree of deacetylation of about 17%, which corresponds to what required for its further use, but a molecular weight of about 1/25 with respect to the native, starting material. Chemical gels have been prepared with different degrees of cross-linking by means of a Ugi multicomponent condensation reaction involving aqueous deHA, formaldehyde, and cyclohexylisocyanide: the gels are mechanically stable and exhibit good water uptake strongly dependent on the extent of cross-linking, as expected. deHA samples have also been selectively N-sulfated or O-sulfated: the former exhibit anticoagulant properties well exceeding those of the latter and not too inferior to heparin.