FE analysis of aortoiliac bifurcation

This action is realized by the project NEXLIZ - CZ.1.07/2.3.00/30.0038, which is co-financed by the European social fund and the state budget of the Czech republic

Effects of Age and Loading Velocity on the Delamination Strength of the Human Aorta

Delamination strength is the mechanical property which plays a key role in the pathological process referred to as Arterial Dissection. This dissection, known especially for its occurrence in the thoracic aorta, is manifested by a separation of the layers of an artery wall, and may end with total rupture and internal haemorrhaging. Although its incidence is relatively rare, from 3 to 6 cases per 100 000 per year, it is a life-threating disease with a significant lethality [1-3]. The exact conditions under which the dissection is initiated, and as a crack propagates through the arterial wall, remain an open topic in computational as well as experimental mechanics. The aim of our study is to contribute to the deepening of our knowledge of Arterial Dissection, by collecting experimental data which is suitable for the purpose of showing how the delamination strength measured in the peeling experiments depends on age and anatomical location. In addition to the effects of age and location, our study also focuses on the effect of loading rate. The experimental branch of our research is complemented by a computational modelling of the delamination interface, in which we are looking for a numerical characterization of the material parameters describing discontinuity propagation. An XFEM model of the peeling experiment is built in Abaqus, which in our approach plays the role of the regression analysis, incorporating the cohesive zone (CZ) in order to model the delaminating arterial layers. The main objective is to obtain a detailed description of a set of constitutive parameters, which would be age- and location-specific. Our present data suggest that delamination strength strongly depends on age, and furthermore, the anatomical site also seems to be a significant factor. On the other hand, the loading velocity does not cause significant changes in results

Survival dimensionality reduction (SDR): development and clinical application of an innovative approach to detect epistasis in presence of right-censored data

Contains fulltext : 89126.pdf (publisher's version ) (Open Access)BACKGROUND: Epistasis is recognized as a fundamental part of the genetic architecture of individuals. Several computational approaches have been developed to model gene-gene interactions in case-control studies, however, none of them is suitable for time-dependent analysis. Herein we introduce the Survival Dimensionality Reduction (SDR) algorithm, a non-parametric method specifically designed to detect epistasis in lifetime datasets. RESULTS: The algorithm requires neither specification about the underlying survival distribution nor about the underlying interaction model and proved satisfactorily powerful to detect a set of causative genes in synthetic epistatic lifetime datasets with a limited number of samples and high degree of right-censorship (up to 70%). The SDR method was then applied to a series of 386 Dutch patients with active rheumatoid arthritis that were treated with anti-TNF biological agents. Among a set of 39 candidate genes, none of which showed a detectable marginal effect on anti-TNF responses, the SDR algorithm did find that the rs1801274 SNP in the Fc gamma RIIa gene and the rs10954213 SNP in the IRF5 gene non-linearly interact to predict clinical remission after anti-TNF biologicals. CONCLUSIONS: Simulation studies and application in a real-world setting support the capability of the SDR algorithm to model epistatic interactions in candidate-genes studies in presence of right-censored data. Availability: http://sourceforge.net/projects/sdrproject/

FE analysis of aortoiliac bifurcation

This action is realized by the project NEXLIZ - CZ.1.07/2.3.00/30.0038, which is co-financed by the European social fund and the state budget of the Czech republic

Surface modification of low-density polyethylene with poly(2-ethyl-2- oxazoline) using a low-pressure plasma treatment

Low-density polyethylene (LDPE) is a suitable polymer for biomedical applications due to its good physiochemical properties, but its insufficient biocompatibility is often an issue. Therefore, biocompatible substances such as those based on 2-ethyl-2-oxazoline seem to be a good choice to increase the LDPE biocompatibility. In this work, the surface modification of LDPE with poly(2-ethyl-2-oxazoline) with two different end-groups was investigated. This modification led to the improvement of surface and adhesion properties, which were investigated by several analytical methods. The low-temperature plasma treatment of the LDPE surface was sufficient to create binding sites for the permanent attachment of poly(2ethyl-2-oxazoline) chains. This was confirmed by infrared spectroscopy and X-Ray photoelectron spectroscopy. It was found that the polymer containing the acrylic end-group was well attached to the LDPE surface. 2013 Elsevier Ltd. All rights reserved.This work was supported by the Slovak Grant Agency VEGA for projects Nr. 2/0064/10 , Nr. 2/0151/12 , and Nr. 2/0185/10 ). The Center for Materials, Layers and Systems for Applications and Chemical Processes under Extreme Conditions was supported by the Research & Development Operational Program funded by the ERDF. Electron microscopy at IMC was performed with financial support through grant TACR TE01020118 .Scopu

Poly(2-ethyl-2-oxazoline) Conjugates with Salicylic Acid via Degradable Modular Ester Linkages

International audienceConjugation of drugs to polymers is a widely used approach to gain control over the release of therapeutics. In this contribution, salicylic acid, a multipurpose model drug, is conjugated to the biocompatible poly(2ethyl-2-oxazoline) (PEtOx). The drug is attached to the side chains of a polymer carrier through a hydrolytically cleavable ester linker, via a sequential postpolymerization modification. The chemical modulation of this ester, i.e., by primary or secondary alcohols, is demonstrated to greatly influence the ester hydrolysis rate. This crucial parameter allows us to tune the in vitro kinetics of the sustained drug release for periods exceeding a month in phosphate-buffered saline (PBS). The synthetic accessibility of the cleavable linker, together with the modularity of the drug release rate offered by this approach, highlights the utility of this class of polymers in the field of long-lasting drug delivery systems for persistent and chronic disease treatment