TY - JOUR
T1 - A self-assembling hydrophobically modified chitosan capable of reversible hemostatic action
AU - Dowling, Matthew B.
AU - Kumar, Rakesh
AU - Keibler, Mark A.
AU - Hess, John R.
AU - Bochicchio, Grant V.
AU - Raghavan, Srinivasa R.
N1 - Funding Information:
This work was partially funded by grants from MIPS and TEDCO . MBD was supported by a Fischell Fellowship from the Department of Bioengineering. We thank Dr. Michael Kilbourne, Dr. Gerard DeCastro, and Dr. Ian Driscoll for assistance with rat and pig experiments, as well as the Thomas D. Morris Institute for Surgical Research for providing the facilities for animal studies. Undergraduate students Da-Tren Chou and Shelby Skoog assisted with some of the experiments performed during this project.
PY - 2011/5
Y1 - 2011/5
N2 - Blood loss at the site of a wound in mammals is curtailed by the rapid formation of a hemostatic plug, i.e., a self-assembled network of the protein, fibrin that locally transforms liquid blood into a gelled clot. Here, we report an amphiphilic biopolymer that exhibits a similar ability to rapidly gel blood; moreover, the self-assembly underlying the gelation readily allows for reversibility back into the liquid state via introduction of a sugar-based supramolecule. The biopolymer is a hydrophobically modified (hm) derivative of the polysaccharide, chitosan. When hm-chitosan is contacted with heparinized human blood, it rapidly transforms the liquid into an elastic gel. In contrast, the native chitosan (without hydrophobes) does not gel blood. Gelation occurs because the hydrophobes on hm-chitosan insert into the membranes of blood cells and thereby connect the cells into a sample-spanning network. Gelation is reversed by the addition of α-cyclodextrin, a supramolecule having an inner hydrophobic pocket: polymer hydrophobes unbind from blood cells and embed within the cyclodextrins, thereby disrupting the cell network. We believe that hm-chitosan has the potential to serve as an effective, yet low-cost hemostatic dressing for use by trauma centers and the military. Preliminary tests with small and large animal injury models show its increased efficacy at achieving hemostasis - e.g., a 90% reduction in bleeding time over controls for femoral vein transections in a rat model.
AB - Blood loss at the site of a wound in mammals is curtailed by the rapid formation of a hemostatic plug, i.e., a self-assembled network of the protein, fibrin that locally transforms liquid blood into a gelled clot. Here, we report an amphiphilic biopolymer that exhibits a similar ability to rapidly gel blood; moreover, the self-assembly underlying the gelation readily allows for reversibility back into the liquid state via introduction of a sugar-based supramolecule. The biopolymer is a hydrophobically modified (hm) derivative of the polysaccharide, chitosan. When hm-chitosan is contacted with heparinized human blood, it rapidly transforms the liquid into an elastic gel. In contrast, the native chitosan (without hydrophobes) does not gel blood. Gelation occurs because the hydrophobes on hm-chitosan insert into the membranes of blood cells and thereby connect the cells into a sample-spanning network. Gelation is reversed by the addition of α-cyclodextrin, a supramolecule having an inner hydrophobic pocket: polymer hydrophobes unbind from blood cells and embed within the cyclodextrins, thereby disrupting the cell network. We believe that hm-chitosan has the potential to serve as an effective, yet low-cost hemostatic dressing for use by trauma centers and the military. Preliminary tests with small and large animal injury models show its increased efficacy at achieving hemostasis - e.g., a 90% reduction in bleeding time over controls for femoral vein transections in a rat model.
KW - Amphiphilic biopolymer
KW - Chitosan
KW - Cyclodextrin
KW - Hemostasis
KW - Self-assembly
UR - http://www.scopus.com/inward/record.url?scp=79952041390&partnerID=8YFLogxK
U2 - 10.1016/j.biomaterials.2010.12.033
DO - 10.1016/j.biomaterials.2010.12.033
M3 - Article
C2 - 21296412
AN - SCOPUS:79952041390
SN - 0142-9612
VL - 32
SP - 3351
EP - 3357
JO - Biomaterials
JF - Biomaterials
IS - 13
ER -