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1333 Tio2 and tio2-mesoporous silica nanoparticle toxicity evaluated on primary human peripheral blood mono/lymphocytes
  1. C Petrarca1,
  2. E Clemente1,
  3. G Zaccariello2,
  4. E Sabbioni3,
  5. M Di Gioacchino1
  1. 1University ‘G. d’Annunzio’ of Chieti-Pescara, Chieti, Italy
  2. 2University Ca’ Foscari of Venezia, Venezia-Mestre, Italy
  3. 3Italian Society of Nanotoxicology, Rome, Italy


Introduction TiO2-NPs are the most produced nanomaterial as UV filters. They are considered as nontoxic at the exposure levels of the occupational environments; nevertheless, potentially dangerous organic molecules can be formed due to photocatalysis. Mesoprous silica (SiO2) nanoparticles (MSN) incorporating Ti-nano were produced to improve their properties. We studied whether human lymphocytes/monocytes can be the target of a toxic action of all these NPs.

Methods Activated/quiescent huPBMCs were exposed ex-vivo to: TiO2-NPs (21 nm); MSN (100 nm); TiO2-MSN (4.4 nm TiO2 into MSN pores). They were characterised for: cell viability/apoptosis by MTT and Annexin-V; ROS by DCFH oxidation; nuclear morphology by fluorescence microscopy; cytokines by ELISA.

Results The viability of activated lymphocytes exposed to the highest doses all NPs was significantly reduced. All NPs induced apoptosis, but only TiO2-NPs induced ROS. IL-2, IL-17, IFN-g were downmodulated by all; MSNs were associated with increased IL-1β and IL-4 secretion; TiO2-NPs induced IL-10, TNF-α and IL-23.

Conclusion Different patterns of cytokine in response to the three different NPs tested: they are all immunosuppressive, but only TiO2-MSN seem to act as pro-inflammatory and pro-allergic agents. The presence of TiO2 in MSN appear to influence the effects of these larger NPs, possibly related to its pro-oxidative and pro-apoptotic effect.

  • nanoparticles
  • titanium
  • mesoporous silica
  • lymphocytes
  • cytokines

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