Thomas S. Anderson
Changes in chemical and ultrastructural composition of ameroid constrictors following in vitro expansion
Anderson, Thomas S.; Rance, Graham A.; Jiang, Long; Piggott, Matthew J.; Field, Elinor J.; Chanoit, Guillaume P.
GRAHAM RANCE Graham.Rance@nottingham.ac.uk
Senior Research Fellow
LONG JIANG Long.Jiang@nottingham.ac.uk
Surface Analytical Officer
Matthew J. Piggott
Elinor J. Field
Guillaume P. Chanoit
Andrew C. Gill
To (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.
Twelve 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.
Ameroid 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.
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.
|Journal Article Type||Article|
|Publication Date||Nov 15, 2018|
|Publisher||Public Library of Science|
|Peer Reviewed||Peer Reviewed|
|APA6 Citation||Anderson, T. S., Rance, G. A., Jiang, L., Piggott, M. J., Field, E. J., & Chanoit, G. P. (2018). Changes in chemical and ultrastructural composition of ameroid constrictors following in vitro expansion. PLoS ONE, 13(11), 1-13. https://doi.org/10.1371/journal.pone.0207471|
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