Mukherjee Sourav P, Lozano Neus, Kucki Melanie, Del Rio-Castillo Antonio E, Newman Leon, Vázquez Ester, Kostarelos Kostas, Wick Peter, Fadeel Bengt
Nanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Nanomedicine Laboratory, Faculty of Medical & Human Sciences and National Graphene Institute, University of Manchester, Manchester, United Kingdom.
PLoS One. 2016 Nov 23;11(11):e0166816. doi: 10.1371/journal.pone.0166816. eCollection 2016.
Nanomaterials may be contaminated with bacterial endotoxin during production and handling, which may confound toxicological testing of these materials, not least when assessing for immunotoxicity. In the present study, we evaluated the conventional Limulus amebocyte lysate (LAL) assay for endotoxin detection in graphene based material (GBM) samples, including graphene oxide (GO) and few-layered graphene (FLG). Our results showed that some GO samples interfered with various formats of the LAL assay. To overcome this problem, we developed a TNF-α expression test (TET) using primary human monocyte-derived macrophages incubated in the presence or absence of the endotoxin inhibitor, polymyxin B sulfate, and found that this assay, performed with non-cytotoxic doses of the GBM samples, enabled unequivocal detection of endotoxin with a sensitivity that is comparable to the LAL assay. FLG also triggered TNF-α production in the presence of the LPS inhibitor, pointing to an intrinsic pro-inflammatory effect. Finally, we present guidelines for the preparation of endotoxin-free GO, validated by using the TET.
纳米材料在生产和处理过程中可能被细菌内毒素污染,这可能会混淆这些材料的毒理学测试,尤其是在评估免疫毒性时。在本研究中,我们评估了传统的鲎试剂(LAL)检测法用于检测基于石墨烯的材料(GBM)样品中的内毒素,这些样品包括氧化石墨烯(GO)和少层石墨烯(FLG)。我们的结果表明,一些GO样品干扰了各种形式的LAL检测。为了克服这个问题,我们开发了一种TNF-α表达测试(TET),使用在有或没有内毒素抑制剂硫酸多粘菌素B的情况下培养的原代人单核细胞衍生巨噬细胞,并且发现该检测方法在使用无细胞毒性剂量的GBM样品时,能够明确检测内毒素,其灵敏度与LAL检测相当。在存在LPS抑制剂的情况下,FLG也会引发TNF-α的产生,表明其具有内在的促炎作用。最后,我们提出了通过使用TET验证的无内毒素GO的制备指南。