Evidence map›Paper›PMID 40731208›Full record

ArticleAAPS PharmSciTech2025

Fast-Dissolving Pullulan Film as a Solid Dosage Form for Sublingual Administration of Nifedipine-Loaded Nanocapsules.

Bárbara Felin Osmari, Giovana Aime Medeiros, Lucas Saldanha da Rosa, Nadine Lysyk Funk, Paulo Ricardo de Souza, Ruy Carlos Ruver Beck, Letícia Cruz

Abstract read
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In one paragraph

Article in AAPS PharmSciTech, 2025. 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. Article
  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.

Bárbara Felin OsmariLaboratório de Tecnologia Farmacêutica, Programa de Pós-Graduação Em Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal de Santa Maria, Santa Maria, Brazil.
Giovana Aime MedeirosLaboratório de Tecnologia Farmacêutica, Programa de Pós-Graduação Em Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal de Santa Maria, Santa Maria, Brazil.
Lucas Saldanha da RosaLaboratório de Biomateriais, Centro de Ciências da Saúde, Departamento de Odontologia Restauradora, Universidade Federal de Santa Maria, Santa Maria, Brazil.
Nadine Lysyk FunkLaboratório de Nanocarreadores E Impressão 3D Em Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brazil.
Paulo Ricardo de SouzaLaboratório de Superfícies E Macromoléculas, Departamento de Física, Centro de Ciências Naturais E Exatas, Universidade Federal de Santa Maria, Santa Maria, Brazil.
Ruy Carlos Ruver BeckLaboratório de Nanocarreadores E Impressão 3D Em Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brazil.
Letícia CruzLaboratório de Tecnologia Farmacêutica, Programa de Pós-Graduação Em Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal de Santa Maria, Santa Maria, Brazil. leticia.cruz@ufsm.br.ORCID http://orcid.org/0000-0001-6230-4577

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fast-dissolving pullulan films were developed as a final dosage form for the sublingual administration of nanocapsules containing nifedipine (NIFE). Eudragit® RS100 nanocapsule suspensions presenting 1 mg/mL of NIFE, 150 nm in size, and positive zeta potential were converted into films using pullulan through the solvent-casting method. The films retained the nanometric size profile of the original suspension and NIFE homogeneity content. The conversion of the nanocapsule suspension into films improved the stability of NIFE. SEM analysis identified smooth, uniform surfaces, while AFM revealed increased surface roughness in films containing nanocapsules. All films exhibited high deformability and flexibility, ensuring comfortable sublingual administration. The contact angle of the films was less than 90º, indicating a hydrophilic surface, corroborating the high swelling index (> 200%). Moreover, the films disintegrated and dispersed quickly, with values less than 3 min and 30 s, respectively, confirming their fast-dissolving nature. The in vitro release showed NIFE maintained its controlled release, reaching 66.95 ± 4.18% in 24 h. The porcine mucosa study demonstrated NIFE's ability to permeate sublingual tissue in 3.12 ± 0.89%.cm

Indexed as

GlucansNanocapsulesNifedipineAdministration, SublingualAnimalsChemistry, PharmaceuticalDelayed-Action PreparationsDrug LiberationParticle SizeSolubilitySwineDelayed-Action PreparationsGlucansNanocapsulesNifedipinepullulanbioadhesioncalcium-channel blockersEudragit® RS100nanoparticlessublingual route

Identifiers

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.