Rapid Hemostatic Biomaterial from a Natural Bath Sponge Skeleton

Mar Drugs. 2021 Apr 15;19(4):220. doi: 10.3390/md19040220.

Abstract

Uncontrolled bleeding is the main cause of mortality from trauma. Collagen has been developed as an important hemostatic material due to its platelet affinity function. A bath sponge skeleton is rich in collagen, also known as spongin. To understand the hemostatic effect of spongin, spongin materials, SX, SFM and SR were prepared from the bath sponge Spongia officinalis, and hemostatic experiments were performed. The SX, SFM and SR were significantly better than the positive control, type I collagen, in shortening the whole blood clotting time in vitro and hemostasis upon rat tail amputation. In a hemostatic experiment of rabbit common carotid artery injury, the hemostatic time and 3 h survival rate of the SFM group were 3.00 ± 1.53 min and 100%, respectively, which are significantly better than those of the commercial hemostat CELOX-A (10.33 ± 1.37 min and 67%, respectively). Additionally, the SFM showed good coagulation effects in platelet-deficient blood and defibrinated blood, while also showing good biocompatibility. Through a variety of tests, we speculated that the hemostatic activity of the SFM is mainly caused by its hyperabsorbency, high affinity to platelets and high effective concentration. Overall, the SFM and spongin derivates could be potential hemostatic agents for uncontrolled bleeding and hemorrhagic diseases caused by deficiency or dysfunction of coagulation factors.

Keywords: Spongia officinalis; biocompatibility; hemostasis; platelet; spongin.

MeSH terms

  • Animals
  • Blood Coagulation / drug effects
  • Blood Coagulation Tests
  • Carotid Artery Injuries / drug therapy*
  • Collagen / isolation & purification
  • Collagen / pharmacology*
  • Collagen / toxicity
  • Disease Models, Animal
  • Hemorrhage / prevention & control*
  • Hemostasis / drug effects*
  • Hemostatics / isolation & purification
  • Hemostatics / pharmacology*
  • Hemostatics / toxicity
  • Molecular Structure
  • Platelet Activation / drug effects
  • Platelet Function Tests
  • Porifera / metabolism*
  • Rabbits
  • Rats
  • Structure-Activity Relationship

Substances

  • Hemostatics
  • Collagen