Evidence map›Paper›PMID 36986751›Full record

ArticlePharmaceutics2023

Evaluation of Pharmacobezoar Formation from Suspensions of Spray-Dried Amorphous Solid Dispersions: An MRI Study in Rats.

Hannes Gierke, Susan Mouchantat, Sabine Berg, Michael Grimm, Stefan Hadlich, Marie-Luise Kromrey, Thomas Nolte, Teresa Pfrommer, Vincent Rönnpagel, Adrian Rump and 3 more

Abstract read
In one paragraph

Article in Pharmaceutics, 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
–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

0 citing papers in PubMed.

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

13 authors.

Hannes GierkeDepartment of Biopharmaceutics and Pharmaceutical Technology, Center of Drug Absorption and Transport, University of Greifswald, 17489 Greifswald, Germany.ORCID 0000-0002-4639-0425
Susan MouchantatDepartment of Diagnostic Radiology and Neuroradiology, University Medicine Greifswald, 17475 Greifswald, Germany.
Sabine BergCentral Core & Research Facility of Laboratory Animals, University Medicine Greifswald, 17489 Greifswald, Germany.
Michael GrimmDepartment of Biopharmaceutics and Pharmaceutical Technology, Center of Drug Absorption and Transport, University of Greifswald, 17489 Greifswald, Germany.ORCID 0000-0002-1310-7435
Stefan HadlichDepartment of Diagnostic Radiology and Neuroradiology, University Medicine Greifswald, 17475 Greifswald, Germany.
Marie-Luise KromreyDepartment of Diagnostic Radiology and Neuroradiology, University Medicine Greifswald, 17475 Greifswald, Germany.ORCID 0000-0002-0420-7303
Thomas NolteBoehringer Ingelheim Pharma GmbH & Co. KG, 88400 Biberach, Germany.ORCID 0000-0001-9722-0146
Teresa PfrommerBoehringer Ingelheim Pharma GmbH & Co. KG, 88400 Biberach, Germany.
Vincent RönnpagelDepartment of General Pharmacology, University Medicine Greifswald, 17487 Greifswald, Germany.
Adrian RumpDepartment of Biopharmaceutics and Pharmaceutical Technology, Center of Drug Absorption and Transport, University of Greifswald, 17489 Greifswald, Germany.ORCID 0000-0003-1335-2809
Kerstin SchaeferBoehringer Ingelheim Pharma GmbH & Co. KG, 88400 Biberach, Germany.
Ann-Cathrin WillmannBoehringer Ingelheim Pharma GmbH & Co. KG, 88400 Biberach, Germany.ORCID 0000-0001-5859-1315
Werner WeitschiesDepartment of Biopharmaceutics and Pharmaceutical Technology, Center of Drug Absorption and Transport, University of Greifswald, 17489 Greifswald, Germany.ORCID 0000-0003-3492-7747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spray-dried amorphous solid dispersions of new chemical entities and pH-dependent soluble polymer hydroxypropyl methylcellulose acetate succinate (HPMC-AS) were found to form solid agglomerates in the gastrointestinal tract of rodents after oral administration. These agglomerates, referring to descriptions of intra-gastrointestinal aggregated oral dosage forms termed pharmacobezoars, represent a potential risk for animal welfare. Previously, we introduced an in vitro model to assess the agglomeration potential of amorphous solid dispersions from suspensions and how it can be reduced. In this work, we investigated if the in vitro effective approach of viscosity enhancement of the vehicle used to prepare suspensions of amorphous solid dispersions could reduce the pharmacobezoar formation potential following repeated daily oral dosing to rats as well. The dose level of 2400 mg/kg/day used in the main study was determined in a dose finding study carried out in advance. In the dose finding study, MRI investigations were carried out at short time intervals to gain insights into the process of pharmacobezoar formation. Whereas MRI investigations underlined the importance of the forestomach for the formation of pharmacobezoars, viscosity enhancement of the vehicle reduced the incidence of pharmacobezoars, delayed the onset of pharmacobezoar formation and reduced the overall mass of pharmacobezoars found at necropsy.

Indexed as

MRI studypharmacobezoarspreclinical testingrodent stomachspray-dried amorphous solid dispersionsviscosity

Identifiers

PMID36986751
PMCPMC10052685

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