Evidence map›Paper›PMID 30440023›Full record

ArticlePloS one2018

Changes in chemical and ultrastructural composition of ameroid constrictors following in vitro expansion.

Thomas S Anderson, Graham A Rance, Long Jiang, Matthew J Piggott, Elinor J Field, Guillaume P Chanoit

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Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Thomas S AndersonBristol Veterinary School, Faculty of Health Sciences, University of Bristol, Langford, Bristol, United Kingdom.ORCID 0000-0002-5234-5516
Graham A RanceNanoscale and Microscale Research Centre, Faculty of Science, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0002-8325-1096
Long JiangAdvanced Materials and Healthcare Technologies, School of Pharmacy, Faculty of Science, University of Nottingham, Nottingham, United Kingdom.
Matthew J PiggottAdvanced Materials and Healthcare Technologies, School of Pharmacy, Faculty of Science, University of Nottingham, Nottingham, United Kingdom.ORCID 0000-0001-6165-6079
Elinor J FieldBristol Veterinary School, Faculty of Health Sciences, University of Bristol, Langford, Bristol, United Kingdom.
Guillaume P ChanoitBristol Veterinary School, Faculty of Health Sciences, University of Bristol, Langford, Bristol, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo (1) characterise the chemical and ultra-structural composition of ameroid constrictors, at a native state and during in vitro expansion and (2) determine the presence of irritant compounds at the surface or within the bulk of the constrictor.

methodsTwelve sterile, commercially packaged ameroid constrictors (3 repeats of 3.5 mm, 5 mm, 6 mm and 7 mm internal diameter) were analysed by time-of-flight secondary ion mass spectrometry, Raman spectroscopy, attenuated total reflectance Fourier transform infrared spectroscopy and scanning electron microscopy.

resultsAmeroid constrictors have a composition commensurate with casein with little-to-no intra- or inter- constrictor variation. Microscopic analysis indicated that the topographical features of the constrictor surfaces were consistent between all constrictors. Following in vitro expansion there was a reproducible decrease in Ca+ ion content, little-to-no variation in secondary protein structure and morphological changes including the presence of surface aggregates present only at the inner surface of the ameroid constrictor. The potential irritant polydimethylsiloxane was found on the constrictor surface. A trace quantity of an ion fragment assigned as formaldehyde was detected; however, the extremely low level is thought highly unlikely to play a role as an inflammatory trigger clinically. DISCUSSION: There is a high degree of inter- and intra-constrictor homogeneity from different batches, and reproducible ultrastructural changes following in vitro expansion. Variations occur in both the surface chemistry and topography of the device during closure, which can potentially affect the biomaterial-host interface. Ameroid constrictor closure mechanism is likely involving calcium-mediated inter-protein interactions rather than the imbibition of water only.

Indexed as

AnimalsBlood ProteinsCaseinsDogsFormaldehydeHydrogelsInflammationMicroscopy, Electron, ScanningProtein ConformationameroidBlood ProteinsCaseinsFormaldehydeHydrogels

Identifiers

PMID30440023
PMCPMC6237400

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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.