Evidence map›Paper›PMID 39005761›Full record

ArticleACS omega2024

Screening, Synthesis, and Characterization of a More Rapidly Dissolving Celecoxib Crystal Form.

Aaron O'Sullivan, Enrico Spoletti, Steven A Ross, Matteo Lusi, Dennis Douroumis, Kevin M Ryan, Luis Padrela

Abstract read
In one paragraph

Article in ACS omega, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

7 authors.

Aaron O'SullivanSSPC Research Centre, University of Limerick, Limerick V94 T9PX, Ireland.ORCID https://orcid.org/0000-0002-5070-161X
Enrico SpolettiDepartment of Chemical Sciences, Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.
Steven A RossCustom Pharma Services, Brighton and Hove, East Sussex BN3 3LW, U.K.ORCID https://orcid.org/0000-0002-9275-2028
Matteo LusiDepartment of Chemical Sciences, Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.
Dennis DouroumisCIPERinitio Centre for Innovation and Process Engineering Research, University of Greenwich, Chatham, Maritime Kent ME4 4TB, U.K.
Kevin M RyanSSPC Research Centre, University of Limerick, Limerick V94 T9PX, Ireland.ORCID https://orcid.org/0000-0003-3670-8505
Luis PadrelaSSPC Research Centre, University of Limerick, Limerick V94 T9PX, Ireland.ORCID https://orcid.org/0000-0002-8632-2320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence of poor solubility in active pharmaceutical ingredients (APIs) such as celecoxib (CEL) is a major bottleneck in the pharmaceutical industry, leading to a low concentration gradient, poor passive diffusion, and in vivo failure. This study presents the synthesis and characterization of a new cocrystal of the API CEL. CEL is a nonsteroidal anti-inflammatory drug used for the treatment of osteoarthritis and rheumatoid arthritis. Computational screening was completed for CEL against a large library of generally recognized as safe (GRAS) coformers, based on molecular complementarity and hydrogen bond propensity (HBP). The generated list of 17 coformers with a likelihood for cocrystallization with CEL were experimentally screened using four techniques: liquid-assisted grinding (LAG), solvent evaporation (SE), gas antisolvent crystallization (GAS), and supercritical enhanced atomization (SEA). One new crystalline form was isolated, employing the liquid coformer

Identifiers

PMID39005761
PMCPMC11238285

What OpenQuestion holds

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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.