Background: Increasing concern has been expressed regarding the potential adverse health effects that may be associated with human exposure to inhaled multi-walled carbon nanotubes (MWCNTs). Thus it is imperative that an understanding as to the underlying mechanisms and the identification of the key factors involved in adverse effects are gained. In the alveoli, MWCNTs first interact with the pulmonary surfactant. At this interface, proteins and lipids of the pulmonary surfactant bind to MWCNTs, affecting their surface characteristics. Aim of the present study was to investigate if the pre-coating of MWCNTs with pulmonary surfactant has an influence on potential adverse effects, upon both (i) human monocyte derived macrophages (MDM) monocultures, and (ii) a sophisticated in vitro model of the human epithelial airway barrier. Both in vitro systems were exposed to MWCNTs either pre-coated with a porcine pulmonary surfactant (Curosurf) or not. The effect of MWCNTs surface charge was also investigated in terms of amino (−NH₂) and carboxyl (−COOH) surface modifications. Results: Pre-coating of MWCNTs with Curosurf affects their oxidative potential by increasing the reactive oxygen species levels and decreasing intracellular glutathione depletion in MDM as well as decreases the release of Tumour necrosis factor alpha (TNF-α). In addition, an induction of apoptosis was observed after exposure to Curosurf pre-coated MWCNTs. In triple cell-co cultures the release of Interleukin-8 (IL-8) was increased after exposure to Curosurf pre-coated MWCNTs. Effects of the MWCNTs functionalizations were minor in both MDM and triple cell co-cultures. Conclusions: The present study clearly indicates that the pre-coating of MWCNTs with pulmonary surfactant more than the functionalization of the tubes is a key factor in determining their ability to cause oxidative stress, cytokine/chemokine release and apoptosis. Thus the coating of nano-objects with pulmonary surfactant should be considered for future lung in vitro risk assessment studies.

The past a few years have witnessed the wide use of metallic nanoparticles as ideal reporters for colorimetric detection, which generally involves an analyte-triggered alteration of aggregation degree of applied nanoparticles, and thus the change of colloidal color. However, these aggregation-based colorimetric probe are associated with a number of drawbacks, including poor stability of nanoaggregates, requirement of complicated functionalization and non-linearity of output signals. To address these problems, we herein employ mesoporous silica-coated gold nanorods (MS AuNRs) as novel nanocomposites for non-aggregation-based label-free colorimetric sensing relying on their chemical redox-modulated surface chemistry. In our sensing system, Hg²⁺ ions are reduced to Hg⁰ depositing on the surface of MS AuNPs and result in a great color change of MS AuNRs, while the subsequent introduction of S²⁻ leads to a reverse process owing to the extraction of Hg⁰ by S²⁻. The experimental results for colorimetric sensing of Hg²⁺ and S²⁻ imply considerable sensitivity and specificity, suggesting the high potential of our approach for rapid environmental monitoring and bioanalysis in the future.

Biomaterials that can drive stem cells to an appropriate differentiation level and decrease apoptosis of transplanted cells are needed in regenerative medicine. Nanomaterials are promising novel materials for such applications. Here we reported that carboxylated multiwalled carbon nanotube (MWCNT 1) promotes myogenic differentiation of mouse myoblast cells and inhibits cell apoptosis under the differentiation conditions by regulating basic helix-loop-helix transcription factors. MWCNT 1 attenuates bone morphogenetic protein receptor (BMPR) signaling activity by binding to BMPR2 and attenuating the phosphorylation of BMPR1. This molecular understanding allowed us to tune stem cell differentiation to various levels by chemical modifications, demonstrating human control of biological activities of nanoparticles and opening an avenue for potential applications of nanomaterials in regenerative medicine.