J Kurtz 1 , B Rael 2 , J Lerma 2 , C Wright 3 , T Khraishi 2 , E D Auyang 4 . Show Affiliations »
Abstract
BACKGROUND: Oxidative degradation by reactive oxygen species (ROS) from inflammation initiates cross-linking, depolymerization, and formation of a quasi-crystalline quality in polypropylene (PP) meshes that cause embrittlement (J Urol 188:1052, 2012). Embrittlement leads to change in tensile strength and is associated with post-operative complications that include pain, adhesion, dislodgment, and fragmentation. METHODS: A laboratory environment was constructed to study the relationship between concentration of ROS and change in tensile strength. Samples of Ethicon Ultrapro© PP mesh were exposed to 1 mM, 0.1 M, or 1 M hydrogen peroxide solutions for 6 months and were subjected to load displacement tensile testing (LDTT) and compared to unexposed (0 M) meshes of the same brand. RESULTS: Load at failure and elongation to failure after LDTT were determined with 95 % confidence interval. For unexposed (0 M) samples, tensile strength was 28.0 ± 2.4 lbf and elongation to failure was 2.0 ± 0.3 in. For samples exposed to 1 mM, tensile strength was 19.2 ± 1.1 lbf and the elongation to failure was 2.0 ± 0.1 in. For samples exposed to 0.1 M, tensile strength was 19.3 ± 1.6 lbf and elongation to failure was 1.9 ± 0.1 in. For samples exposed to 1 M, tensile strength was 20.7 ± 1.2 lbf and elongation to failure was 0.47 ± 0.02 in. CONCLUSION: The results demonstrated that a 6-month exposure to a physiologic range of ROS (1 mM) decreased tensile strength of PP mesh by 31 %. 1 mM and 0.1 M samples behaved similarly demonstrating properties of a quasi-crystalline nature. 1 M samples displayed qualities of extreme embrittlement. Scanning electron microscopy (SEM) observed fiber changes. 1 M meshes had features of brittle materials. Knowledge of changes in physical properties of PP meshes is useful for considerations for the development of a more biocompatible surgical mesh.
BACKGROUND: Oxidative degradation by reactive oxygen species (ROS ) from inflammation initiates cross-linking, depolymerization, and formation of a quasi-crystalline quality in polypropylene (PP) meshes that cause embrittlement (J Urol 188:1052, 2012). Embrittlement leads to change in tensile strength and is associated with post-operative complications that include pain , adhesion, dislodgment, and fragmentation. METHODS: A laboratory environment was constructed to study the relationship between concentration of ROS and change in tensile strength. Samples of Ethicon Ultrapro© PP mesh were exposed to 1 mM, 0.1 M, or 1 M hydrogen peroxide solutions for 6 months and were subjected to load displacement tensile testing (LDTT) and compared to unexposed (0 M) meshes of the same brand. RESULTS: Load at failure and elongation to failure after LDTT were determined with 95 % confidence interval. For unexposed (0 M) samples, tensile strength was 28.0 ± 2.4 lbf and elongation to failure was 2.0 ± 0.3 in. For samples exposed to 1 mM, tensile strength was 19.2 ± 1.1 lbf and the elongation to failure was 2.0 ± 0.1 in. For samples exposed to 0.1 M, tensile strength was 19.3 ± 1.6 lbf and elongation to failure was 1.9 ± 0.1 in. For samples exposed to 1 M, tensile strength was 20.7 ± 1.2 lbf and elongation to failure was 0.47 ± 0.02 in. CONCLUSION: The results demonstrated that a 6-month exposure to a physiologic range of ROS (1 mM) decreased tensile strength of PP mesh by 31 %. 1 mM and 0.1 M samples behaved similarly demonstrating properties of a quasi-crystalline nature. 1 M samples displayed qualities of extreme embrittlement. Scanning electron microscopy (SEM) observed fiber changes. 1 M meshes had features of brittle materials. Knowledge of changes in physical properties of PP meshes is useful for considerations for the development of a more biocompatible surgical mesh.
Entities: Chemical
Disease
Keywords:
Load displacement tensile testing (LDTT); Polypropylene (PP) surgical mesh; Reactive oxygen species (ROS); Scanning electron microscopy (SEM)
Mesh: See more »
Substances: See more »
Year: 2015
PMID: 26679171 DOI: 10.1007/s00464-015-4646-3
Source DB: PubMed Journal: Surg Endosc ISSN: 0930-2794 Impact factor: 4.584