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Recently, the market of medical devices shows serious need for wound dressings for first aid and temporary traumatic wounds. Such a wound dressing should show primarily the hemostatic effect and antibacterial activity allowing protection against infection. Tromboguard® topical wound dressing is a three-layer dressing with active layer. It contains chitosan, sodium alginate/calcium alginate with addition of silver salt. The wound dressing provides protective performance as well as is characterized by the ability to immediately stop bleeding and antibacterial activity allowing protection against infection and occurrence of secondary infection without the need for or with limited participation of antibiotics. Tromboguard® topical wound dressing is a firs aid dressing designed for the uniform services (military and homeland) and rescue.
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121 - 130
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Contributors
- Institute of Biopolymers and Chemical Fibres ul. M. Skłodowskiej-Curie 19/27, 90-570 Łódź, Poland, biomater@ibwch.lodz.pl
author
- Institute of Security Technologies “MORATEX”, mstruszczyk@moratex.eu
author
- Institute of Biopolymers and Chemical Fibers
author
- Institute of Biopolymer and Chemical Fibres
author
- Institute of Security Technologies “MORATEX”
author
- Institute of Security Technologies “MORATEX”
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- Institute of Security Technologies “MORATEX”
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- TRICOMED SA
author
- TRICOMED SA
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- TRICOMED SA
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- TRICOMED SA
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- TRICOMED SA
References
- PN-EN 13726-1:2005 „Test methods for primary wound dressings - Part 1: Aspects of absorbency”.
- PN-EN 13726-2:2005 „Test methods for primary wound dressings - Part 2: Moisture vapour transmission rate of permeable film dressings”.
- PN-EN 13726-3:2005 „Non-active medical devices - Test methods for primary wound dressings - Part 3: Waterproofness”.
- PN-EN 13726-4:2005 „Non-active medical devices - Test methods for primary wound dressings - Part 4: Conformability”.
- PN-EN ISO 14971:2009 “Medical devices - Application of risk management to medical devices”.
- JIS L 1902:2002 “Testing for antibacterial activity and efficacy on textile products”.
- ASTM 1980F:2002 “Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices”.
- PN-EN ISO 10993-1:2009 “Biological evaluation of medical devices - Part 1: Evaluation and testing”.
- PN-EN ISO 10993-5:2001 “Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity”.
- PN-EN ISO 10993-10:2003 “Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization”.
- PN-EN ISO 10993-4:2002 “Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood”.
- PN-EN ISO 10993-6:2007 “Biological evaluation of medical devices - Part 6: Tests for local effects after implantation”.
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article
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YADDA identifier
bwmeta1.element.psjd-dee1c687-1326-4d93-b84a-6e1b98be2cf2