Thermally driven formation of polyphenolic carbonized nanogels with high anticoagulant activity from polysaccharides

Biomater Sci. 2021 Jul 7;9(13):4679-4690. doi: 10.1039/d1bm00402f. Epub 2021 May 21.

Abstract

We have demonstrated that alginate with negligible anticoagulant activity can be converted into carbonized nanogels with potent anticoagulant activity through a solid-state heating process. The conversion of alginate into graphene-like nanosheet (GNS)-embedded polyphenolic-alginate nanogels (GNS/Alg-NGs) has been carried out through condensation and carbonization processes. The GNS/Alg-NGs exhibit much stronger anticoagulant activity (>520-fold) compared to untreated alginate, mainly because their polyphenolic structures have a high binding affinity [dissociation constant (Kd) = 2.1 × 10-10 M] toward thrombin. In addition, the thrombin clotting time delay caused by the GNS/Alg-NGs is 10-fold longer than that of natural polyphenolic compounds, such as quercetin, catechin, naringenin, caffeic acid, and ferulic acid. The thrombin- or kaolin-activated thromboelastography of whole-blood coagulation reveals that the GNS/Alg-NGs display a much stronger anticoagulant ability than that of untreated alginate and naturally sulfated polysaccharides (fucoidan). The GNS/Alg-NGs exhibit superior biocompatibility and anticoagulant activity, as observed with an in vivo rat model, revealing their potential as a blood thinner for the treatment of thrombotic disorders.

MeSH terms

  • Animals
  • Anticoagulants* / pharmacology
  • Blood Coagulation
  • Nanogels
  • Polysaccharides* / pharmacology
  • Rats
  • Thrombin / pharmacology

Substances

  • Anticoagulants
  • Nanogels
  • Polysaccharides
  • Thrombin