Trimethylammonium-2-hydroxypropyl-(TMAHP) spacer was introduced into heparin (H) and theprepared films were characterized by elemental analysis, NMR, SEC-MALS, TG/DTG/DTA, AFM andmechanical tester. When quaternized at the ratio of H/NaOH/alkylating agent/H2O = 0.1-1/0-2/0.1-1/50-500 mmol, H was substituted at A6 and A3 positions. The formation of double-substituted structuresby substitution of free hydroxyl group of the previously introduced TMAHP substituent is evident. Inthe absence of NaOH (H/GTMAC/H2O = 1:1:500) the most drastic decrease of Mnto 8.639 kg/mol andMw/Mnat 1.48 was observed in comparison to H (Mn= 9532 g/mol with Mw/Mn= 1.38). The film mechan-ical properties were better on H (E = 4030 MPa; ?b= 65 MPa; ?b= 4.6%) than on quaternized specimens(? = 2500-3340 MPa; ?b= 25-40 MPa; ?b= 1.7-1.8%). The AFM images did not prove relation betweenmechanical properties and surface shape.
Cationization of heparin for film applications
Mendichi Raniero;
2015
Abstract
Trimethylammonium-2-hydroxypropyl-(TMAHP) spacer was introduced into heparin (H) and theprepared films were characterized by elemental analysis, NMR, SEC-MALS, TG/DTG/DTA, AFM andmechanical tester. When quaternized at the ratio of H/NaOH/alkylating agent/H2O = 0.1-1/0-2/0.1-1/50-500 mmol, H was substituted at A6 and A3 positions. The formation of double-substituted structuresby substitution of free hydroxyl group of the previously introduced TMAHP substituent is evident. Inthe absence of NaOH (H/GTMAC/H2O = 1:1:500) the most drastic decrease of Mnto 8.639 kg/mol andMw/Mnat 1.48 was observed in comparison to H (Mn= 9532 g/mol with Mw/Mn= 1.38). The film mechan-ical properties were better on H (E = 4030 MPa; ?b= 65 MPa; ?b= 4.6%) than on quaternized specimens(? = 2500-3340 MPa; ?b= 25-40 MPa; ?b= 1.7-1.8%). The AFM images did not prove relation betweenmechanical properties and surface shape.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
