Evidence map›Paper›PMID 42199632›Full record

ArticleJournal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques2026

Dissolution-permeation approach for biopharmaceutical evaluation: a feasibility study using naproxen.

Andrejs Sitovs, Katarina Gurkina, Liga Petersone, Valentyn Mohylyuk

Abstract read
In one paragraph

Article in Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 2026. 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

4 authors.

Andrejs SitovsLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, Riga, Latvia.
Katarina GurkinaLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, Riga, Latvia.
Liga PetersoneLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, Riga, Latvia.
Valentyn MohylyukLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, Riga, Latvia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Dissolution and/or release profile alone are insufficient to predict the Methods: The assembled dissolution-permeation system evaluated the effect of 5% and 10% soy L-α-phosphatidylcholine in dodecane (LiDo) and permeable membrane material on apparent permeability coefficients of naproxen, a BCS II class drug. Results: Naproxen release from the tablets reached approximately 100% within 30 min. Naproxen P Conclusion: The proposed compendial dissolution-permeation system with an Ussing chamber allowed for the simultaneous determination of dissolution and permeability of naproxen. All P

Indexed as

Anti-Inflammatory Agents, Non-SteroidalNaproxenDrug LiberationFeasibility StudiesMembranes, ArtificialPermeabilityPhosphatidylcholinesSolubilityTabletsAnti-Inflammatory Agents, Non-SteroidalMembranes, ArtificialNaproxenPhosphatidylcholinesTabletsBCSdissolutionnaproxenpermeabilitypermeation

Identifiers

PMID42199632
PMCPMC13199132

What OpenQuestion holds

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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.