Lopes Viviana R, Sanchez-Martinez Carla, Strømme Maria, Ferraz Natalia
Nanotechnology and Functional Materials, Department of Engineering Sciences, Uppsala University, Box 534, 75121, Uppsala, Sweden.
Present affiliation: Ocular Biology and Therapeutics, UCL Institute of Ophthalmology, 11-43 Bath Street, EC1V 9EL, London, UK.
Part Fibre Toxicol. 2017 Jan 10;14(1):1. doi: 10.1186/s12989-016-0182-0.
Nanocellulose, and particularly nanofibrillated cellulose (NFC), has been proposed for a diversity of applications in industry and in the biomedical field. Its unique physicochemical and structural features distinguish nanocellulose from traditional materials and enable its use as an advance nanomaterial. However, its nanoscale features may induce unknown biological responses. Limited studies with NFC are available and the biological impacts of its use have not been thoroughly explored. This study assesses the in vitro biological responses elicited by wood-derived NFC gels, when human dermal fibroblasts, lung MRC-5 cells and THP-1 macrophage cells are exposed to the nanomaterial. Furthermore, whether the presence of surface charged groups (i.e. carboxymethyl and hydroxypropyltrimethylammonium groups) on NFC can induce distinct biological responses is investigated.
The introduction of surface charged groups resulted in individual nanofibrils, while fibril aggregates predominated in the unmodified NFC gel suspensions as observed by transmission electron microscopy. In the presence of proteins, the surface modified NFCs formed compact agglomerates while the agglomeration pattern of the unmodified NFC was similar in the presence of proteins and in physiological buffer. Unmodified and modified NFC gels did not induce cytotoxicity in human dermal fibroblasts, lung and macrophage cells. No significant ROS production by THP-1 macrophages was found and no cellular uptake was observed. However, an inflammatory response was detected when THP-1 macrophages were treated with unmodified NFC as assessed by an increase in TNF-α and IL1-β levels, an effect that was absent when surface charged groups were introduced into NFC.
Taken together, the data presented here show the absence of cytotoxic effects associated with the exposure to unmodified, carboxymethylated and hydroxypropyltrimethylammonium-modified NFCs. Unmodified NFC presented a pro-inflammatory effect which can be further moderated by introducing surface modifications such as carboxymethyl and hydroxypropyltrimethylammonium groups into the nanofibrils. The present findings suggest that the inflammatory response to NFC might be driven by the material surface chemistry, and thus open up for the possibility of designing safe nanocellulose materials.
纳米纤维素,尤其是纳米纤丝化纤维素(NFC),已被提出可用于工业和生物医学领域的多种应用。其独特的物理化学和结构特征使纳米纤维素有别于传统材料,并使其能够用作先进的纳米材料。然而,其纳米级特征可能会引发未知的生物学反应。关于NFC的研究有限,其使用的生物学影响尚未得到充分探索。本研究评估了木源NFC凝胶在人皮肤成纤维细胞、肺MRC-5细胞和THP-1巨噬细胞暴露于该纳米材料时引发的体外生物学反应。此外,还研究了NFC表面带电基团(即羧甲基和羟丙基三甲基铵基团)的存在是否能诱导不同的生物学反应。
通过透射电子显微镜观察,表面带电基团的引入导致了单个纳米纤丝,而在未改性的NFC凝胶悬浮液中,纤维聚集体占主导地位。在有蛋白质存在的情况下,表面改性的NFC形成紧密的团聚物,而未改性的NFC在有蛋白质和生理缓冲液存在时的团聚模式相似。未改性和改性的NFC凝胶在人皮肤成纤维细胞、肺细胞和巨噬细胞中均未诱导细胞毒性。未发现THP-1巨噬细胞产生显著的活性氧,也未观察到细胞摄取。然而,当用未改性的NFC处理THP-1巨噬细胞时,通过TNF-α和IL-β水平的升高评估发现有炎症反应,而将表面带电基团引入NFC时则没有这种效应。
综上所述,此处呈现的数据表明,暴露于未改性、羧甲基化和羟丙基三甲基铵改性的NFC不会产生细胞毒性作用。未改性的NFC呈现出促炎作用,通过将羧甲基和羟丙基三甲基铵基团等表面改性引入纳米纤丝中可进一步减轻这种作用。目前的研究结果表明,对NFC的炎症反应可能由材料表面化学驱动,从而为设计安全的纳米纤维素材料提供了可能性。