Development of a chitosan-based wound dressing with improved hemostatic and antimicrobial properties

被引:759
作者
Ong, Shin-Yeu [1 ]
Wu, Jian [1 ]
Moochhala, Shabbir M. [1 ]
Tan, Mui-Hong [1 ]
Lu, Jia [1 ]
机构
[1] DSO Natl Labs, Def Med & Environm Res Inst, Combat Care Lab, Singapore 117510, Singapore
关键词
Wound dressing; Chitosan; Hemostatic; Antimicrobial;
D O I
10.1016/j.biomaterials.2008.07.034
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hemorrhage remains a leading cause of early death after trauma, and infectious complications in combat wounds continue to challenge caregivers. Although chitosan dressings have been developed to address these problems, they are not always effective in controlling bleeding or killing bacteria. We aimed to refine the chitosan dressing by incorporating a procoagulant (polyphosphate) and an antimicrobial (silver). Chitosan containing different amounts and types of polyphosphate polymers was fabricated, and their hemostatic efficacies evaluated in vitro. The optimal chitosan-polyphosphate formulation (ChiPP) accelerated blood clotting (p = 0.011), increased platelet adhesion (p = 0.002), generated thrombin faster (p = 0.002), and absorbed more blood than chitosan (p < 0.001). Silver-loaded ChiPP exhibited significantly greater bactericidal activity than ChiPP in vitro, achieving a complete kill of Pseudomonas aeruginosa and a >99.99% kill of Staphylococcus aureus consistently. The silver dressing also significantly reduced mortality from 90% to 14.3% in a P. aeruginosa wound infection model in mice. Although the dressing exerted severe cytotoxicity against cultured fibroblasts, wound healing was not inhibited. This study demonstrated for the first time, the application of polyphosphate as a hemostatic adjuvant, and developed a new chitosan-based composite with potent hemostatic and antimicrobial properties. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4323 / 4332
页数:10
相关论文
共 46 条
[1]   Testing of modified zeolite hemostatic dressings in a large animal model of lethal groin injury [J].
Ahuja, Naresh ;
Ostomel, Todd A. ;
Rhee, Peter ;
Stucky, Galen D. ;
Conran, Richard ;
Chen, Zheng ;
Al-Mubarak, Ghada A. ;
Velmahos, George ;
deMoya, Marc ;
Alam, Hasan B. .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2006, 61 (06) :1312-1320
[2]   In harm's way: Infections in deployed American military forces [J].
Aronson, Naomi E. ;
Sanders, John W. ;
Moran, Kimberly A. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (08) :1045-1051
[3]   Blood protein adsorption onto chitosan [J].
Benesch, J ;
Tengvall, P .
BIOMATERIALS, 2002, 23 (12) :2561-2568
[4]  
Brett DW, 2006, OSTOMY WOUND MANAG, V52, P34
[5]   A comparative study of the cytotoxicity of silver-based dressings in monolayer cell, tissue explant, and animal models [J].
Burd, Andrew ;
Kwok, Chi H. ;
Hung, Siu C. ;
Chan, Hui S. ;
Gu, Hua ;
Lam, Wai K. ;
Huang, Lin .
WOUND REPAIR AND REGENERATION, 2007, 15 (01) :94-104
[6]   Chitosan enhances platelet adhesion and aggregation [J].
Chou, TC ;
Fu, E ;
Wu, CJ ;
Yeh, JH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 302 (03) :480-483
[7]  
Chung YC, 2004, ACTA PHARMACOL SIN, V25, P932
[8]   A retrospective cohort study of Acticoat™ versus Silvazine™ in a paediatric population [J].
Cuttle, Leila ;
Naidu, Sanjeev ;
Mill, Julie ;
Hoskins, Wendy ;
Das, Karina ;
Kimble, Roy M. .
BURNS, 2007, 33 (06) :701-707
[9]  
DIQUELOU A, 1994, BLOOD, V84, P2206
[10]  
Feng QL, 2000, J BIOMED MATER RES, V52, P662, DOI 10.1002/1097-4636(20001215)52:4<662::AID-JBM10>3.0.CO