Hemostatic action of polyurethane foam with 55% polyethylene glycol compared to collagen and gelatin

被引:15
作者
Broekema, Ferdinand I. [1 ]
van Oeveren, Wim [2 ,3 ]
Boerendonk, Andrea [1 ]
Sharma, Prashant K. [4 ]
Bos, Rudolf R. M. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Oral & Maxillofacial Surg, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiothorac Surg, Groningen, Netherlands
[3] Haemoscan, Stavangerweg 23-23, NL-9723 JC Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Engn FB 40, WJ Kolff Inst, POB 196, NL-9700 AD Groningen, Netherlands
关键词
Polyurethane; collagen; gelatin; hemostasis; viscoelastic properties; IN-VITRO ANALYSIS; FACTOR-XII; CROSS-LINKING; AGENTS; COAGULATION; ACTIVATION; THROMBOSIS; FILMS;
D O I
10.3233/BME-161578
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
BACKGROUND: For most topical hemostatic agents the mechanism of hemostatic action is not fully understood. OBJECTIVE: This work aimed to investigate the hemostatic mechanism of action and viscoelastic properties of polyurethane foam (PU) in comparison to the widely used collagen and gelatin. METHODS: The hemostatic mechanism of action of the materials was tested using human whole blood and platelet-poor plasma (PPP). The ability of the hemostatic agent to exert pressure on the wound was quantified in terms of its viscoelastic properties both under dry and wet conditions using a low load compression tester (LLCT). RESULTS: It has been shown that collagen and PU initiate hemostasis through both thrombocyte aggregation and contact activation of the coagulation cascade. Gelatin did not show improved thrombocyte aggregation or initiation of the coagulation cascade compared to the negative control group. PU is more firm under wet conditions and shows more springback than collagen and gelatin. CONCLUSIONS: We conclude that PU is promising as a topical hemostatic agent because it initiates both the coagulation cascade and thrombocyte aggregation. Furthermore, it has favorable viscoelastic properties compared to collagen and gelatin which leads to increased pressure on a wound.
引用
收藏
页码:149 / 159
页数:11
相关论文
共 25 条
[1]   A Comprehensive Review of Topical Hemostatic Agents Efficacy and Recommendations for Use [J].
Achneck, Hardean E. ;
Sileshi, Bantayehu ;
Jamiolkowski, Ryan M. ;
Albala, David M. ;
Shapiro, Mark L. ;
Lawson, Jeffrey H. .
ANNALS OF SURGERY, 2010, 251 (02) :217-228
[2]   Mechanical and thermal properties of gelatin films at different degrees of glutaraldehyde crosslinking [J].
Bigi, A ;
Cojazzi, G ;
Panzavolta, S ;
Rubini, K ;
Roveri, N .
BIOMATERIALS, 2001, 22 (08) :763-768
[3]  
Broekema F.I., 2012, CLIN ORAL INVESTIG
[4]   In vitro analysis of polyurethane foam as a topical hemostatic agent [J].
Broekema, Ferdinand I. ;
van Oeveren, Wim ;
Zuidema, Johan ;
Visscher, Susan H. ;
Bos, Rudolf R. M. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2011, 22 (04) :1081-1086
[5]   Crosslinking and composition influence the surface properties, mechanical stiffness and cell reactivity of collagen-based films [J].
Grover, Chloe N. ;
Gwynne, Jessica H. ;
Pugh, Nicholas ;
Hamaia, Samir ;
Farndale, Richard W. ;
Best, Serena M. ;
Cameron, Ruth E. .
ACTA BIOMATERIALIA, 2012, 8 (08) :3080-3090
[6]   Activated factor 12 (FXIIa) predicts recurrent coronary events after an acute myocardial infarction [J].
Grundt, H ;
Nilsen, DWT ;
Hetland, O ;
Valente, E ;
Fagertun, HE .
AMERICAN HEART JOURNAL, 2004, 147 (02) :260-266
[7]   Preparation and characterization of highly porous, biodegradable polyurethane scaffolds for soft tissue applications [J].
Guan, JJ ;
Fujimoto, KL ;
Sacks, MS ;
Wagner, WR .
BIOMATERIALS, 2005, 26 (18) :3961-3971
[8]   TOPICAL HEMOSTATIC AGENTS FOR DERMATOLOGIC SURGERY [J].
LARSON, PO .
JOURNAL OF DERMATOLOGIC SURGERY AND ONCOLOGY, 1988, 14 (06) :623-632
[9]  
Maas C, 2008, J CLIN INVEST, V118, P3208, DOI [10.1172/JC135424, 10.1172/JCI35424]
[10]   Role of tissue factor in hemostasis, thrombosis, and vascular development [J].
Mackman, N .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (06) :1015-1022