ArticleJournal of materials science. Materials in medicine2013
Self-assembling surfaces of blood-contacting materials.
Article in Journal of materials science. Materials in medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Biocompatibility testing of composite biomaterial designed for a new petal valve construction for pulsatile ventricular assist device.Journal of materials science. Materials in medicine · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The optimal scaffold should have the self-organising property of activating the appropriate tissues surrounding the re-population. The anti-bacterial property of the coating was obtained through surface pre-treatment with coatings a few nanometres in thickness deposited using vapour-based methods. The coating's anti-thrombogenic properties were obtained by the selective mobilisation of cellular functions, which was controlled by the structure of porous coatings deposited on bulk substrates and by the small biological agent-L-arginyl-glycyl-L-aspartic acid (tripeptide Arg-Gly-Asp-RGD) protein domains. Two tests simulating arterial flow conditions were performed: Impact-R, for examining platelet function under near physiological conditions, and radial flow chamber, a cell detachment test that gives an overview of cell behaviour and shear stresses that could appear between the cell and the biomaterial. Cell structures were analysed using laser scanning confocal microscopy and flow cytometry. The performed in vitro dynamic test for the haemo-compatibility revealed the most promising surface functionalization was based on porous extracellular-like structure covered with endothelium cells simultaneously. The antibacterial function was achieved by the appropriate phase composition of the coating used for the pre-treatment stage. The coating for the pre-treatment was selected on the basis of the blood-material and bacteria-material interaction.
Indexed as
Identifiers
23229573What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.