Evidence map›Paper›PMID 36977814›Full record

ArticlePharmaceutical research2023

Improvement of Workflows and Assay Reproducibility by The Introduction of "Assay-Ready" Culturing of MDCK Cells for Transport Studies.

Patricia Muschong, Liang Jin, Jan Schejbal, Mario Mezler, Manuel Weinheimer

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Article in Pharmaceutical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Patricia MuschongQuantitative, Translational & ADME Sciences, AbbVie Deutschland GmbH & Co KG, Knollstr, 67061, Ludwigshafen, Germany.
Liang JinQuantitative, Translational & ADME Sciences, AbbVie Bioresearch Center, 100 Research Drive, Worcester, MA, 01605, USA.
Jan SchejbalQuantitative, Translational & ADME Sciences, AbbVie Bioresearch Center, 100 Research Drive, Worcester, MA, 01605, USA.
Mario MezlerQuantitative, Translational & ADME Sciences, AbbVie Deutschland GmbH & Co KG, Knollstr, 67061, Ludwigshafen, Germany.
Manuel WeinheimerQuantitative, Translational & ADME Sciences, AbbVie Deutschland GmbH & Co KG, Knollstr, 67061, Ludwigshafen, Germany. manuel.weinheimer@abbvie.com.ORCID http://orcid.org/0000-0001-8521-4283

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn previous studies, we established and validated three Madin Darby Canine Kidney MDCKII cell lines, recombinantly modified with zinc finger nuclease (ZFN) technology. Here, we investigated the applicability of seeding these three canine P-gp deficient MDCK_ZFN cell lines, directly from frozen cryopreserved stocks without previous cultivation for efflux transporter and permeability studies. This technique is referred to as "assay-ready" and allows for highly standardized conduction of cell-based assays and shorter cultivation cycles.

methodsTo obtain a rapid fitness of the cells for that purpose, a very gentle freezing and thawing protocol was applied. Assay-ready MDCK_ZFN cells were tested in bi-directional transport studies and compared to their traditionally cultured counterparts. Long-term performance robustness, human effective intestinal permeability (P

resultsEfflux ratios (ER) and apparent permeability (P

conclusionAssay-ready methodology for handling MDCK_ZFN cells allows more flexibility in assay planning and reduces performance fluctuations in assays caused by cell aging. Therefore, the assay-ready principle has proven superior over conventional cultivation for MDCK_ZFN cells and is considered as a key technology to optimize processes with other cellular systems.

Indexed as

Madin Darby Canine Kidney CellsAnimalsBiological TransportCaco-2 CellsDogsHumansReproducibility of ResultsWorkflowassay-readycell cultureefflux transport studiesmadin-darby canine kidney type II (MDCKII) cellspermeability

Identifiers

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Registered trials

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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.