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Abstract
The increasing use of nanoparticles in products
likely results in increased exposure of both workers and
consumers. Because of their small size, there are concerns
that nanoparticles unintentionally cross the barriers of the
human body. Several in vivo rodent studies show that,
dependent on the exposure route, time, and concentration,
and their characteristics, nanoparticles can cross the lung,
gut, skin, and placental barrier. This review aims to evaluate
the performance of in vitro models that mimic the barriers
of the human body, with a focus on the lung, gut, skin,
and placental barrier. For these barriers, in vitro models
of varying complexity are available, ranging from singlecell-
type monolayer to multi-cell (3D) models. Only a few studies are available that allow comparison of the in vitro
translocation to in vivo data. This situation could change
since the availability of analytical detection techniques is
no longer a limiting factor for this comparison. We conclude
that to further develop in vitro models to be used in
risk assessment, the current strategy to improve the models
to more closely mimic the human situation by using cocultures
of different cell types and microfluidic approaches
to better control the tissue microenvironments are essential.
At the current state of the art, the in vitro models do not
yet allow prediction of absolute transfer rates but they do
support the definition of relative transfer rates and can thus
help to reduce animal testing by setting priorities for subsequent
in vivo testing.
Original language | English |
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Pages (from-to) | 1469-1495 |
Journal | Archives of Toxicology |
Volume | 89 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2015 |
Keywords
- titanium-dioxide nanoparticles
- plasma-mass spectrometry
- zinc-oxide nanoparticles
- field-flow fractionation
- air-liquid interface
- organs-on-chips
- pulmonary drug-delivery
- short-term inhalation
- m-cell model
- gold nanoparticles
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Dive into the research topics of 'Progress and future of in vitro models to study translocation of nanoparticles'. Together they form a unique fingerprint.Projects
- 1 Finished
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Risico's nanotechnologie biobeschikbaarheid en toxicologie contrafinanciering (KB-37-002-001, KB-23-002-005, KB-15-003-010)
Peters, R.
1/01/11 → 31/12/21
Project: EZproject