A self-assembling hydrophobically modified chitosan capable of reversible hemostatic action

被引:209
作者
Dowling, Matthew B. [2 ]
Kumar, Rakesh [1 ]
Keibler, Mark A. [1 ]
Hess, John R. [3 ]
Bochicchio, Grant V. [4 ]
Raghavan, Srinivasa R. [1 ,2 ]
机构
[1] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20742 USA
[2] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[3] Univ Maryland, Sch Med, Dept Pathol, Baltimore, MD 21201 USA
[4] Univ Maryland, Sch Med, Dept Surg, Baltimore, MD 21201 USA
关键词
Chitosan; Hemostasis; Self-assembly; Cyclodextrin; Amphiphilic biopolymer; HEMORRHAGE; DRESSINGS; FIBRIN; MODEL; EFFICACY; INJURY; SWINE; MECHANISM; NETWORKS; POLYMERS;
D O I
10.1016/j.biomaterials.2010.12.033
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 alpha-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. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3351 / 3357
页数:7
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