Monteiro-Riviere Nancy A, Inman Alfred O, Wang Yunyu Y, Nemanich Robert J
Center for Chemical Toxicology Research and Pharmacokinetics, North Carolina State University, Raleigh, North Carolina 27606, USA.
Nanomedicine. 2005 Dec;1(4):293-9. doi: 10.1016/j.nano.2005.10.007.
Interactions of multiwalled carbon nanotubes (MWCNTs) with human epidermal keratinocytes (HEKs) were studied with respect to the effect of surfactant on dispersion of MWCNT aggregates and cytotoxicity. Our earlier studies had shown that the unmodified MWCNTs were localized within the cytoplasmic vacuoles of HEKs and elicited an inflammatory response. However, MWCNTs in solution tend to aggregate and, therefore, cells are exposed to large MWCNT aggregates. The purpose of this study was to find a surfactant that prevents the formation of large aggregates of MWCNTs without being toxic to the HEKs. HEKs were exposed to serial dilutions (10% to 0.1%) of L61, L92, and F127 Pluronic and 20 or 60 Tween for 24 hours. HEK viability, proportional to surfactant concentration, ranged from 27.1% to 98.5% with Pluronic F127; viability with the other surfactants was less than 10%. Surfactants dispersed and reduced MWCNT aggregation in medium. MWCNTs at 0.4 mg/mL in 5% or 1% Pluronic F127 were incubated with HEKs and assayed for interleukin 8 (IL-8). MWCNTs were cytotoxic to HEKs independent of surfactant exposure. In contrast, MWCNT-induced IL-8 release was reduced when exposed to 1% or 5% Pluronic F127 (P < .05). However, both MWCNTs and surfactant, alone or in combination, increased IL-8 release compared with control exposures at 12 and 24 hours. These results suggest that the surfactant-MWCNT interaction is more complex than simple dispersion alone and should be investigated to determine the mode of interaction.
针对表面活性剂对多壁碳纳米管(MWCNTs)聚集体分散及细胞毒性的影响,研究了MWCNTs与人表皮角质形成细胞(HEKs)的相互作用。我们早期的研究表明,未修饰的MWCNTs定位于HEKs的细胞质空泡内并引发炎症反应。然而,溶液中的MWCNTs容易聚集,因此细胞会暴露于大的MWCNT聚集体中。本研究的目的是找到一种既能防止MWCNTs形成大聚集体又对HEKs无毒的表面活性剂。将HEKs暴露于L61、L92和F127普朗尼克以及20或60吐温的系列稀释液(10%至0.1%)中24小时。与表面活性剂浓度成正比,使用普朗尼克F127时HEK活力范围为27.1%至98.5%;使用其他表面活性剂时活力小于10%。表面活性剂可分散并减少培养基中MWCNT的聚集。将0.4 mg/mL的MWCNTs在5%或1%的普朗尼克F127中与HEKs孵育,并检测白细胞介素8(IL-8)。MWCNTs对HEKs具有细胞毒性,与是否暴露于表面活性剂无关。相比之下,当暴露于1%或5%的普朗尼克F127时,MWCNT诱导的IL-8释放减少(P < 0.05)。然而,与12小时和24小时的对照暴露相比,MWCNTs和表面活性剂单独或联合使用均增加了IL-8的释放。这些结果表明,表面活性剂与MWCNT的相互作用比单纯的分散更为复杂,应进行研究以确定相互作用模式。