Behaviour of silver nanoparticles in simulated saliva and gastrointestinal fluids
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28506800
DOI
10.1016/j.ijpharm.2017.05.026
PII: S0378-5173(17)30438-6
Knihovny.cz E-zdroje
- Klíčová slova
- Dynamic light scattering, Reconstructed human tissue models, Saliva, Silver nanoparticles, Simulated gastrointestinal fluids, Transmission electron microscopy,
- MeSH
- kovové nanočástice chemie MeSH
- lidé MeSH
- pilotní projekty MeSH
- sliny chemie MeSH
- stříbro * MeSH
- techniky tkáňových kultur MeSH
- velikost částic MeSH
- žaludeční šťáva chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- stříbro * MeSH
Continuously increasing application of silver nanoparticles (AgNPs) requires information on their safety and performance under biological conditions. Assessment of AgNPs in biological systems is also related to availability of robust toxicological methods for evaluation of toxic potential of AgNPs and information on their physicochemical state. Silver nanoparticles were subjected to action of simulated saliva, gastric and intestinal fluids, appropriately supplemented with digestive enzymes pepsin or pancreatin. The behaviour of AgNPs was determined using dynamic light scattering and transmission electron microscopy, and their toxicity as well as capability to induce inflammatory reactions were assessed using reconstructed human tissue models (EpiOral, EpiGingival, EpiIntestinal). The study revealed that during exposure to the fluids, AgNPs size and morphology changed and depended on composition and pH of the respective fluid. If present, the change in terms of growth of AgNPs size occurred immediately after contact of AgNPs with the respective fluid and continued with prolonged time of contact. A pilot study on reconstituted human tissue models revealed low toxicity and inflammatory effects of AgNPs and confirmed the suitability of 3-D models for toxicological studies including bioavailability.
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