Bristol Veterinary School, Faculty of Health Sciences, University of Bristol, Langford, Bristol, United Kingdom.
Nanoscale and Microscale Research Centre, Faculty of Science, University of Nottingham, Nottingham, United Kingdom.
PLoS One. 2018 Nov 15;13(11):e0207471. doi: 10.1371/journal.pone.0207471. eCollection 2018.
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.
(1)描述缩窄环在自然状态下以及在体外扩张过程中的化学和超微结构组成,(2)确定在缩窄环的表面或内部是否存在刺激性化合物。
使用飞行时间二次离子质谱、拉曼光谱、衰减全反射傅里叶变换红外光谱和扫描电子显微镜对 12 个无菌、商业包装的缩窄环(3 次重复,内径分别为 3.5 毫米、5 毫米、6 毫米和 7 毫米)进行分析。
缩窄环的组成与酪蛋白相当,且在各缩窄环之间,无论是内部还是外部,其组成几乎没有差异。微观分析表明,所有缩窄环的表面形貌特征都一致。体外扩张后,钙离子含量可重复性下降,二级蛋白质结构几乎没有变化,形态学变化包括仅在缩窄环内部表面存在的表面聚集物。在缩窄环表面发现了潜在的刺激性聚二甲基硅氧烷。检测到一个被指定为甲醛的离子碎片的痕量,但由于其极低的水平,临床上认为其极不可能作为炎症触发物发挥作用。
不同批次的缩窄环之间具有高度的同质性和内聚性,并且在体外扩张后具有可重复的超微结构变化。在缩窄环闭合过程中,器械的表面化学和形貌都发生了变化,这可能会影响生物材料-宿主界面。缩窄环的闭合机制可能涉及钙介导的蛋白质间相互作用,而不仅仅是吸水。