Evidence map›Paper›PMID 36786980›Full record

ArticleDrug delivery and translational research2023

The development of a 3D-printed in vitro integrated oro-pharyngeal air-liquid interface cellular throat model for drug transport.

Zara Sheikh, Antonella Granata, Ye Zhang, Hanieh Mohammad Gholizadeh Mahvizani, Dina Silva, Paul M Young, Luca Casettari, Hui Xin Ong, Daniela Traini

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In one paragraph

Article in Drug delivery and translational research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 3 countries.

Zara SheikhRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia.ORCID 0000-0002-2403-5772
Antonella GranataRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia.
Ye ZhangRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia.
Hanieh Mohammad Gholizadeh MahvizaniRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia.
Dina SilvaRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia.
Paul M YoungRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia.
Luca CasettariDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Hui Xin OngRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia. huixin.ong@mq.edu.au.
Daniela TrainiRespiratory Technology, The Woolcock Institute of Medical Research, Glebe, NSW, 2037, Australia. daniela.traini@mq.edu.au.
Woolcock Institute of Medical Research · AUUniversity of Urbino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To simulate the deposition of drugs in the oro-pharynx region, several in vitro models are available such as the United States Pharmacopeia-Induction Port (USP-IP) throat and the Virginia Commonwealth University (VCU) models. However, currently, there is no such in vitro model that incorporates a biological barrier to elucidate drug transport across the pharyngeal cells. Cellular models such as in vitro air-liquid interface (ALI) models of human respiratory epithelial cell lines are extensively used to study drug transport. To date, no studies have yet been performed to optimise the ALI culture conditions of the human pharyngeal cell line Detroit 562 and determine whether it could be used for drug transport. Therefore, this study aimed to develop a novel 3D-printed throat model integrated with an ALI cellular model of Detroit 562 cells and optimise the culture conditions to investigate whether the combined model could be used to study drug transport, using Lidocaine as a model drug. Differentiating characteristics specific to airway epithelia were assessed using 3 seeding densities (30,000, 60,000, and 80,000 cells/well (c/w), respectively) over 21 days. The results showed that Detroit 562 cells completely differentiates on day 18 of ALI for both 60,000 and 80,000 c/w with significant mucus production, showing response to bacterial and viral stimuli and development of functional tight junctions and Lidocaine transport with no significant differences observed between the ALI models with the 2 cell seeding densities. Results showed the suitability of the Low density (60,000 c/w or 1.8 × 10

Indexed as

Nebulizers and VaporizersPharynxCell LineEpithelial CellsHumansPrinting, Three-Dimensional3D printingAir–liquid interfaceDetroit 562In vitro throat modelLidocaineParacellular transport

Identifiers

PMID36786980
OpenAlexW4320709759

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.