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M Mauzac

Publications and source records attributed to M Mauzac.

8 recordsLinked to original sources
PubMed2005

Chiral molecular imprinting in liquid-crystalline network.

A cholesteric imprinted elastomer was obtained by cross-linking a nematic side-chain polysiloxane around a chiral template. The template was first linked to some functionalised groups of the polymer via hydrogen-bound interactions, then was removed by washing. The sample was macroscopically oriented during the synthesis; so, both a molecular chirality and a supramolecular phase chirality were topologically imprinted inside the network. Batch rebinding experiments, performed in the presence of the template or of the other enantiomer, showed that the imprinted polymer has a pronounced stereo-selectivity towards the template enantiomer. The rebinding capacity appeared to be greater than an unimprinted mesogenic network as well as than an imprinted non mesogenic one.

Journal Article↗
PubMed1987

Anticoagulant hydrogels derived from crosslinked dextran. Part I: Synthesis, characterization and antithrombic activity.

Hydrogels have been prepared by binding various amino acids to Sephadex derivatives bearing carboxymethyl and sulphonated benzylamide groups. Depending on the chemical nature and content of the amino acid substituent, these insoluble strongly hydrophilic materials may absorb 7 to 19 volumes of buffer per volume of dry material. These hydrogels present antithrombic activity in relation to their swelling ratio. The adsorption of thrombin might partially explain the anticoagulant effect as shown by the evaluated affinity constants between the hydrogels and the enzyme i.e. 1 to 2 X 10(6) I/M.

Anticoagulants↗
PubMed1987

Anticoagulant hydrogels derived from crosslinked dextran. Part II: Mechanism of thrombin inactivation.

Sephadex derivatives bearing carboxymethyl, sulphonated benzylamine and amino acid groups exhibit heparin-like behaviour as demonstrated by the kinetic study of the thrombin inactivation in the presence of antithrombin III. Furthermore, whatever the chemical composition of these hydrogels, the diffusion coefficient of thrombin remained approximately constant and could not be connected with the variation of the antithrombin activity of the resins. Hence, in the heparin-like mechanism, the diffusion rate of thrombin inside the beads of hydrogels was not the limiting step. In fact, the swelling ratio (varying according to the chemical composition of these biomaterials) was involved in the anticoagulant properties of the resins.

Anticoagulants↗
PubMed1985

Anticoagulant activity of dextran derivatives. Part II: Mechanism of thrombin inactivation.

The mechanism of anticoagulant activity of dextrans substituted with carboxylic and benzylamide sulphonate groups is studied by various coagulation tests. These derivatives exhibit a heparin-like antithrombic activity which requires the presence of antithrombin III; however they are less effective than heparin on a weight basis. They also exert a direct antithrombic activity by an antithrombic III independent pathway; but this action is negligible compared to the thrombin inhibition observed in the presence of antithrombin III. Dextran derivatives have been prepared with antithrombic properties similar to those of heparin.

Antithrombin III↗
PubMed1985

Anticomplementary activity of dextran derivatives.

Substitution with carboxylic and benzylamine sulphonated groups conferred on dextran both antithrombic activity and the capacity to inhibit formation of the amplification C3 convertase of complement. In dextrans substituted with carboxylic groups (greater than 40%), a high content of sulphonate (greater than 10%) resulted in both anticomplementary and antithrombic properties whereas a lower content of sulphonate resulted in high anticomplementary but weak antithrombic activity. The anticomplementary activity of highly substituted dextrans was similar to that of heparin, although anticoagulant activity was much lower than in heparin, confirming independent structural requirements for both activities in the heparin molecule.

Complement C3-C5 Convertases↗
PubMed1984

Anticoagulant activity of dextran derivatives. Part I: Synthesis and characterization.

Substituted dextrans bearing carboxymethyl and benzylsulphonate groups have been prepared. These materials exhibit an antithrombic activity correlated with the ratio of each substituent. The highest activity is obtained when the dextran derivative contains more than 50% of carboxylic acid groups and simultaneously about 15% of benzylsulphonate functions.

Anticoagulants↗
PubMed1982

Antithrombic activity of some polysaccharide resins.

Crosslinked dextrans (Sephadex) bearing essentially carboxymethyl, benzylsulphonate and alpha-amino acid groups have been synthesized. The antithrombic activity of the resins may be the result of a cooperative effect between the functional groups. The binding of benzylsulphonate to carboxymethylated Sephadex endows these materials with activity. However the highest activity is obtained when the resins contain simultaneously benzylsulphonate, alpha-amino acid and carboxylic acid groups.

Anticoagulants↗