2023
DOI: 10.1016/j.fct.2023.114157
|View full text |Cite
|
Sign up to set email alerts
|

Inhalation toxicity of thermal transformation products formed from e-cigarette vehicle liquid using an in vitro lung model exposed at the Air–Liquid Interface

T. Ruth,
J. Daniel,
A. König
et al.
Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 45 publications
0
1
0
Order By: Relevance
“…Biological limitations include i) the use of the A549 human lung cell line. Despite its widespread use as in vitro lung model for ALI experiments [ 31 , 42 ], there are drawbacks compared to primary cells. For example, A549 cells lack the ability to form tight junctions [ 35 , 57 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Biological limitations include i) the use of the A549 human lung cell line. Despite its widespread use as in vitro lung model for ALI experiments [ 31 , 42 ], there are drawbacks compared to primary cells. For example, A549 cells lack the ability to form tight junctions [ 35 , 57 ].…”
Section: Discussionmentioning
confidence: 99%
“…Forty-eight hours before exposure, A549 cells were seeded on the apical side of 6-well-sized inserts (4.524 cm 2 area, pore size 0.4 μm, transparent membrane, Greiner Bio-One, Frickenhausen, Germany) at a density of 60.000 cells/cm 2 in 1 mL growth medium ( Fig 3 ), according to Ruth et al [ 42 ]. Before seeding, inserts without cells were placed into microplates (CytoOne, Starlab GmbH) filled with 1.5 mL growth medium in the basal compartment and were incubated for 30 min in the incubator to condition the membranes of the inserts.…”
Section: Methodsmentioning
confidence: 99%
“…Forty-eight hours before exposure, A549 cells were seeded on the apical side of 6-well-sized inserts (4.524 cm² area, pore size 0.4 µm, transparent membrane, Greiner Bio-One, Frickenhausen, Germany) at a density of 60.000 cells/cm² in 1 mL growth medium (Fig 3), according to Ruth et al [27]. Before seeding, inserts without cells were placed into microplates (CytoOne, Starlab GmbH) filled with 1.5 mL growth medium in the basal compartment and were incubated for 30 min in the incubator to condition the membranes of the inserts.…”
Section: Methodsmentioning
confidence: 99%