首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Screening for extractables in additive-manufactured acrylonitrile butadiene styrene orthopedic cast
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Screening for extractables in additive-manufactured acrylonitrile butadiene styrene orthopedic cast

机译:添加剂制造丙烯腈丁二烯苯乙烯骨晶浇铸中的筛选物筛选

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摘要

The use of additive-manufactured components in medical applications, specifically medical devices (e.g., orthopedic casts), has increased in recent years. Such devices may be fabricated at the point of care using consumer-grade additive manufacturing. Limited studies have been conducted to evaluate the extractable substances of these devices. Chemical characterization followed by toxicological risk assessment is one means of evaluating safety of devices. This study was designed to determine the extractables profile of additive-manufactured materials according to filament grade and post-processing method. Feedstocks for additive manufacturing were tested as filament and manufactured casts, while the cast from consumer-grade filament (CGF) was post-processed. Samples were extracted using three solvents of varying polarities. Extracts were analyzed by gas chromatography/mass spectrometry (GC/MS) and liquid chromatography/mass spectrometry (LC/MS) techniques. In GC/MS analysis, isopropanol extracts generated fewer compound identifications for USP Class VI filament (USPF)-based casts (3) compared with the respective filament (17) while hexane generated the most compound identifications for the finished cast manufactured from CGF. CGF was found to have the highest number of nonvolatile extractables for isopropanol (15) and hexane (34) by positive ion LC/MS. Additionally, CGF produced more non-polar extractables in hexane than the USPF. A known polymer byproduct and potential genotoxicant, styrene acrylonitrile (SAN) trimer, was one of the compounds identified in both GC/MS and LC/MS at quantities ranging from 19 to 270 mu g g(-1). Overall these results suggested that the extractables profile was affected by the filament material, printing procedure, and post-processing method.
机译:近年来,在医疗应用中使用添加剂制造的组件,特别是医疗装置(例如,矫形铸造)。这种装置可以在使用消费者级添加剂制造的护理点来制造。已经进行了有限的研究以评估这些装置的可提取物质。化学表征随后毒理风险评估是评估装置安全的一种方法。本研究旨在根据长丝级和后处理方法确定添加剂制造材料的可提取物轮廓。添加剂制造的原料被测试为长丝和制造的铸件,而来自消费级灯丝(CGF)的铸造后处理。使用三种不同极性的三种溶剂来提取样品。通过气相色谱/质谱(GC / MS)和液相色谱/质谱(LC / MS)技术分析提取物。在GC / MS分析中,与相应的长丝(17)相比,异丙醇提取物为USP类VI长丝(USPF)的速率(3)产生了较少的化合物鉴定(3),而己烷产生由CGF制造的成品铸造的最复合鉴定。发现CGF通过正离子LC / MS具有最多的异丙醇(15)和己烷(34)的非挥发性萃取物。另外,CGF在己烷中产生了比USPF更多的非极性萃取物。已知的聚合物副产物和潜在的遗传毒剂,苯乙烯丙烯腈(SAN)三聚体,是在GC / MS和LC / MS中鉴定的化合物之一,其数量为19-270μmGg(-1)。总体而言,这些结果表明,可萃取物配置文件受细丝材料,印刷过程和后处理方法的影响。

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