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Biodegradability of Para-aramid Respirable-Sized Fiber-Shaped Particulates (RFP) in Human Lung Cells1

机译:人肺细胞中对位芳纶可吸入尺寸纤维状微粒(RFP)的生物降解性 1

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Using both in vivo (inhalation) and in vitro (cell culture) studies, we previously reported that p-aramid respirable fibers (RFP—defined as respirable-sized fiber-shaped particulates) are biodegraded in lungs and lung cells of rats following exposures. The current studies were undertaken to determine whether shortening mechanisms of p-aramid RFP biodegradability are also operative in human lung cells. Cultures of human A549 lung epithelial cells (A549), primary alveolar macrophages (HBAL) (collected via bronchoalveolar lavage [BAL]) from volunteers), and co-cultures (Co) of the A549 and HBAL were incubated with p-aramid RFP for either 1 h, 1 day, or 1 week to assess RFP shortening. Lengths of RFP were measured using scanning electron microscopy (SEM) following fixation, digestion of culture tissue components, and processing. Similar to findings using rat lung cells, only slight RFP shortening was measured in A549 cultures at 1-day and 1-week post-incubation. More importantly, in HBAL and Co groups, greater transverse cleavage of p-aramid RFP was measured at 1-day and 1-week postexposure compared to 1-h HBAL or Co groups, or in any A549 groups. In contrast, cellulose RFP, a biopersistent reference control fiber, were not measurably shortened under similar circumstances. Second, p-aramid RFP were incubated either with phosphate-buffered saline (PBS), or acellular BAL fluids from human volunteers or rats and processed for SEM analysis of RFP lengths. Mean lengths of p-aramid RFP incubated with human or rat BAL fluids were substantially decreased compared to PBS. Similar to our findings with rat lung cells, components of human lung fluids coat the p-aramid RFP as a prerequisite for subsequent enzymatic cleavage by human phagocytic lung cells and this finding reinforces the concept that inhaled p-aramid RFP are likely to be biodegradable in the lungs of humans.
机译:使用体内(吸入)和体外(细胞培养)研究,我们先前曾报道过暴露后,对位芳族聚酰胺可吸入纤维(RFP,定义为可吸入大小的纤维状颗粒)在大鼠的肺和肺细胞中被生物降解。进行了当前的研究以确定对位芳族聚酰胺RFP生物降解性的缩短机制在人肺细胞中是否也起作用。将人A549肺上皮细胞(A549),原发性肺泡巨噬细胞(HBAL)(通过志愿者的支气管肺泡灌洗[BAL]收集)以及A549和HBAL的共培养物(Co)与对位芳纶RFP孵育, 1小时,1天或1周以评估RFP缩短。固定,培养组织成分的消化和加工后,使用扫描电子显微镜(SEM)测量RFP的长度。与使用大鼠肺细胞的发现相似,在孵育后1天和1周时,在A549培养物中仅测到了轻微的RFP缩短。更重要的是,在HBAL和Co组中,与1小时HBAL或Co组或任何A549组相比,暴露后1天和1周测得的对位芳族聚酰胺RFP的横向切割更大。相反,纤维素RFP(一种生物持久性参比纤维)在类似情况下无法测量地缩短。其次,将对位芳族聚酰胺RFP与磷酸盐缓冲盐水(PBS)或人类志愿者或大鼠的脱细胞BAL液一起孵育,并进行RFP长度的SEM分析。与PBS相比,与人或大鼠BAL液温育的对位芳族聚酰胺RFP的平均长度显着减少。与我们对大鼠肺细胞的发现相似,人类肺液中的成分覆盖了p-芳族聚酰胺RFP,这是随后被人吞噬性肺细胞进行酶促裂解的前提条件,这一发现强化了吸入p-芳族聚酰胺RFP可能在体内被生物降解的概念。人类的肺部。

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