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Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch

Two self-adhering hemostatic patches, based on either PEG-coated collagen (PCC) or PEG-coated oxidized cellulose (PCOC), are compared regarding to maximum burst pressure, mechanical stability, and swelling. In addition, the induction of tissue adhesions by the materials was assessed in a rabbit live...

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Autores principales: Slezak, Paul, Monforte, Xavier, Ferguson, James, Sutalo, Sanja, Redl, Heinz, Gulle, Heinz, Spazierer, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966486/
https://www.ncbi.nlm.nih.gov/pubmed/29796769
http://dx.doi.org/10.1007/s10856-018-6078-9
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author Slezak, Paul
Monforte, Xavier
Ferguson, James
Sutalo, Sanja
Redl, Heinz
Gulle, Heinz
Spazierer, Daniel
author_facet Slezak, Paul
Monforte, Xavier
Ferguson, James
Sutalo, Sanja
Redl, Heinz
Gulle, Heinz
Spazierer, Daniel
author_sort Slezak, Paul
collection PubMed
description Two self-adhering hemostatic patches, based on either PEG-coated collagen (PCC) or PEG-coated oxidized cellulose (PCOC), are compared regarding to maximum burst pressure, mechanical stability, and swelling. In addition, the induction of tissue adhesions by the materials was assessed in a rabbit liver abrasion model. Both materials showed comparable sealing efficacy in a burst pressure test (37 ± 16 vs. 35 ± 8 mmHg, P = 0.730). After incubation in human plasma, PCC retained its mechanical properties over the test period of 8 h, while PCOC showed faster degradation after the 2 h time-point. The degradation led to a significantly decreased force at break (minimum force at break 0.55 N during 8 h for PCC, 0.27 N for PCOC; p < 0.001). Further, PCC allowed significantly higher deformation before break (52% after 4 h and 50% after 8 h for PCC, 18% after 4 h and 23% after 8 h for PCOC; p = 0.003 and p < 0.001 for 4 h and 8 h, respectively) and showed less swelling in human plasma (maximum increase in thickness: ~20% PCC, ~100% PCOC). Faster degradation of PCOC was visible macroscopically and histologically in vivo after 14 days. PCC showed visible structural residues with little cellular infiltration while strong infiltration with no remaining structural material was seen with PCOC. In vivo, a higher incidence of adhesion formation after PCOC application was detected. In conclusion, PCC has more reliable mechanical properties, reduced swelling, and less adhesion formation than PCOC. PCC may offer greater clinical benefit for surgeons in procedures that have potential risk for body fluid leakage or that require prolonged mechanical stability. [Image: see text]
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spelling pubmed-59664862018-06-04 Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch Slezak, Paul Monforte, Xavier Ferguson, James Sutalo, Sanja Redl, Heinz Gulle, Heinz Spazierer, Daniel J Mater Sci Mater Med Biomaterials Synthesis and Characterization Two self-adhering hemostatic patches, based on either PEG-coated collagen (PCC) or PEG-coated oxidized cellulose (PCOC), are compared regarding to maximum burst pressure, mechanical stability, and swelling. In addition, the induction of tissue adhesions by the materials was assessed in a rabbit liver abrasion model. Both materials showed comparable sealing efficacy in a burst pressure test (37 ± 16 vs. 35 ± 8 mmHg, P = 0.730). After incubation in human plasma, PCC retained its mechanical properties over the test period of 8 h, while PCOC showed faster degradation after the 2 h time-point. The degradation led to a significantly decreased force at break (minimum force at break 0.55 N during 8 h for PCC, 0.27 N for PCOC; p < 0.001). Further, PCC allowed significantly higher deformation before break (52% after 4 h and 50% after 8 h for PCC, 18% after 4 h and 23% after 8 h for PCOC; p = 0.003 and p < 0.001 for 4 h and 8 h, respectively) and showed less swelling in human plasma (maximum increase in thickness: ~20% PCC, ~100% PCOC). Faster degradation of PCOC was visible macroscopically and histologically in vivo after 14 days. PCC showed visible structural residues with little cellular infiltration while strong infiltration with no remaining structural material was seen with PCOC. In vivo, a higher incidence of adhesion formation after PCOC application was detected. In conclusion, PCC has more reliable mechanical properties, reduced swelling, and less adhesion formation than PCOC. PCC may offer greater clinical benefit for surgeons in procedures that have potential risk for body fluid leakage or that require prolonged mechanical stability. [Image: see text] Springer US 2018-05-23 2018 /pmc/articles/PMC5966486/ /pubmed/29796769 http://dx.doi.org/10.1007/s10856-018-6078-9 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Biomaterials Synthesis and Characterization
Slezak, Paul
Monforte, Xavier
Ferguson, James
Sutalo, Sanja
Redl, Heinz
Gulle, Heinz
Spazierer, Daniel
Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
title Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
title_full Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
title_fullStr Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
title_full_unstemmed Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
title_short Properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
title_sort properties of collagen-based hemostatic patch compared to oxidized cellulose-based patch
topic Biomaterials Synthesis and Characterization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966486/
https://www.ncbi.nlm.nih.gov/pubmed/29796769
http://dx.doi.org/10.1007/s10856-018-6078-9
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