Comparison of structural and hemostatic properties of the poly-N-acetyl glucosamine Syvek Patch with products containing chitosan

被引:64
作者
Fischer, TH
Connolly, R
Thatte, HS
Schwaitzberg, SS
机构
[1] Univ N Carolina, Dept Patholbiol & Lab Med, Chapel Hill, NC 27516 USA
[2] Tufts Univ New England Med Ctr, Dept Surg, Boston, MA 02111 USA
[3] Harvard Univ, Sch Med, Dept Surg, VA Boston Healthcare Syst, Boston, MA 02115 USA
关键词
hemostasis; N-acetyl glucosamine; hemostatic patches;
D O I
10.1002/jemt.20017
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Polysaccharides are becoming increasingly developed as therapeutics and medical products, as the new field of Glycomics expands. Glycosaminoglycans that contain N-acetyl glucosamine constituents have been the focus of research leading to medical devices. A new hemostatic bandage, the Syvek Patch, has been introduced in the recent past for the control of bleeding at vascular access sites in interventional cardiology and radiology procedures. This product consists of poly-N-acetyl glucosamine (pGlcNAc) isolated in a unique fiber crystalline structural form from the large-scale culture and processing of a marine diatom. The Syvek pGlcNAc fiber material has chemical, physical, and biological properties that result in its favorable performance as a hemostat. Two new products, the Clo-Sur PAD and ChitoSeal, have recently become available also as patch hemostats. These two products both use chitosan, another N-acetyl glucosamine containing glycosaminoglycan, as their active ingredient. Structural, chemical, and biological comparisons of Syvek pGlcNAc and chitosan reveal a number of important differences. Syvek pGlcNAc fibers contain similar to50 fully acetylated, high molecular weight pGlcNAc molecules in a crystalline, three-dimensional beta structure array, and are insoluble. Chitosan is a low molecular weight mixed amorphous cationic polymer with no regular structure as a solid, and is water-soluble taking on a random coil configuration when in solution. These structural dissimilarities result in differences in the hemostatic properties of the two materials. Syvek pGlcNAc is able to significantly reduce the in vitro fibrin clot formation time of platelet-rich plasma samples and has the ability to cause aggregation of red blood cells in vitro. Chitosan is no better than gauze or other controls in these in vitro assays. The Syvek Patch is able to control the bleeding and cause hemostasis in a coagulopathic swine spleen-bleeding animal model 100% of the time, whereas Clo-Sur PAD was completely unsuccessful (0%) and ChitoSeal (25%) was worse than a gauze pad control (50%) in the same model. Syvek pGlcNAc fibers have structural and chemical properties that provide a unique basis for their ability to interact with blood components to cause hemostasis. Chitosan does not have the same properties and capabilities.
引用
收藏
页码:168 / 174
页数:7
相关论文
共 24 条
[1]   STRUCTURE OF BETA-CHITIN OR PARALLEL CHAIN SYSTEMS OF POLY-BETA-(1-]4)-N-ACETYL-D-GLUCOSAMINE [J].
BLACKWEL.J .
BIOPOLYMERS, 1969, 7 (03) :281-&
[2]   CHITIN FIBRES OF DIATOMS THALASSIOSIRA FLUVIATILIS AND CYCLOTELLA CRYPTICA [J].
BLACKWELL, J ;
PARKER, KD ;
RUDALL, KM .
JOURNAL OF MOLECULAR BIOLOGY, 1967, 28 (02) :383-+
[3]   CHITOSAN - A NEW TOPICAL HEMOSTATIC AGENT FOR DIFFUSE CAPILLARY BLEEDING IN BRAIN-TISSUE [J].
BRANDENBERG, G ;
LEIBROCK, LG ;
SHUMAN, R ;
MALETTE, WG ;
QUIGLEY, H .
NEUROSURGERY, 1984, 15 (01) :9-13
[4]   Comparison of poly-N-acetyl glucosamine (P-GlcNAc) with absorbable collagen (Actifoam), and fibrin sealant (Bolheal) for achieving hemostasis in a swine model of splenic hemorrhage [J].
Chan, MW ;
Schwaitzberg, SD ;
Demcheva, M ;
Vournakis, J ;
Finkielsztein, S ;
Connolly, RJ .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2000, 48 (03) :454-457
[5]   A pilot study evaluating the efficacy of a fully acetylated poly-N-acetyl glucosamine membrane formulation as a topical hemostatic agent [J].
Cole, DJ ;
Connolly, RJ ;
Chan, MW ;
Schwaitzberg, SD ;
Byrne, TK ;
Adams, DB ;
Baron, PL ;
O'Brien, PH ;
Metcalf, JS ;
Demcheva, M ;
Vournakis, J .
SURGERY, 1999, 126 (03) :510-517
[6]  
DELVIN HB, 1969, BRIT J SURG, V56, P446
[7]   Intracellular function in rehydrated lyophilized platelets [J].
Fischer, TH ;
Merricks, EP ;
Russell, KE ;
Raymer, RA ;
White, GC ;
Bode, AP ;
Nichols, TC ;
Read, MS .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (01) :167-174
[8]  
FRY DE, 1980, AM SURGEON, V46, P28
[9]   REFINEMENT OF STRUCTURE OF BETA-CHITIN [J].
GARDNER, KH ;
BLACKWELL, J .
BIOPOLYMERS, 1975, 14 (08) :1581-1595
[10]   Separation technologies for glycomics [J].
Hirabayashi, J ;
Kasai, K .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2002, 771 (1-2) :67-87