Evidence map›Paper›PMID 33467593›Full record

ArticleMolecules (Basel, Switzerland)2021

Pectin-Based Formulations for Controlled Release of an Ellagic Acid Salt with High Solubility Profile in Physiological Media.

Marco Aldo Ortenzi, Stefano Antenucci, Stefania Marzorati, Lucia Panzella, Silvia Molino, José Ángel Rufián-Henares, Alessandra Napolitano, Luisella Verotta

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 29% of its field
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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Microbiota and gastric cancer: from molecular mechanisms to therapeutic strategies.Frontiers in cellular and infection microbiology · 2025
    Review
  3. Article
  4. Review
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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

8 authors at 3 institutions in 2 countries.

Marco Aldo OrtenziLaboratory of Materials and Polymers (LaMPo), Dipartimento di Chimica, via Golgi 19, University of Milan, 20133 Milano, Italy.ORCID 0000-0001-6206-9589
Stefano AntenucciLaboratory of Materials and Polymers (LaMPo), Dipartimento di Chimica, via Golgi 19, University of Milan, 20133 Milano, Italy.
Stefania MarzoratiDepartment of Environmental Science and Policy, via Celoria 2, University of Milan, 20133 Milano, Italy.ORCID 0000-0002-9080-1973
Lucia PanzellaDepartment of Chemical Sciences, University of Naples "Federico II", via Cintia 4, 80126 Naples, Italy.ORCID 0000-0002-2662-8205
Silvia MolinoDepartamento de Nutrición y Bromatología, Instituto de Nutrición y Tecnología de Alimentos, Centro de Investigación Biomédica, Universidad de Granada, 18071 Granada, Spain.ORCID 0000-0001-9405-5085
José Ángel Rufián-HenaresDepartamento de Nutrición y Bromatología, Instituto de Nutrición y Tecnología de Alimentos, Centro de Investigación Biomédica, Universidad de Granada, 18071 Granada, Spain.ORCID 0000-0002-1428-4353
Alessandra NapolitanoDepartment of Chemical Sciences, University of Naples "Federico II", via Cintia 4, 80126 Naples, Italy.ORCID 0000-0003-0507-5370
Luisella VerottaDepartment of Environmental Science and Policy, via Celoria 2, University of Milan, 20133 Milano, Italy.ORCID 0000-0002-5739-6291
University of Milan · ITUniversidad de Granada · ESUniversity of Naples Federico II · IT

Funding

European Union's Horizon 2020 816303
6 · The paper itself

Abstract

Among bioactive phytochemicals, ellagic acid (EA) is one of the most controversial because its high antioxidant and cancer-preventing effects are strongly inhibited by low gastrointestinal absorption and rapid excretion. Strategies toward an increase of solubility in water and bioavailability, while preserving its structural integrity and warranting its controlled release at the physiological targets, are therefore largely pursued. In this work, EA lysine salt at 1:4 molar ratio (EALYS), exhibiting a more than 400 times increase of water solubility with respect to literature reports, was incorporated at 10% in low methoxylated (LM) and high methoxylated (HM) pectin films. The release of EA in PBS at pH 7.4 from both film preparations was comparable and reached 15% of the loaded compound over 2 h. Under simulated gastric conditions, release of EA from HM and LM pectin films was minimal at gastric pH, whereas higher concentrations-up to 300 μM, corresponding to ca. 50% of the overall content-were obtained in the case of the HM pectin film after 2 h incubation at the slightly alkaline pH of small intestine environment, with the enzyme and bile salt components enhancing the release. EALYS pectin films showed a good prebiotic activity as evaluated by determination of short chain fatty acids (SCFAs) levels following microbial fermentation, with a low but significant increase of the effects produced by the pectins themselves. Overall, these results highlight pectin films loaded with EALYS salt as a promising formulation to improve administration and controlled release of the compound.

Indexed as

Biological AvailabilityDelayed-Action PreparationsDrug CompoundingEllagic AcidFecesFermentationGastrointestinal MicrobiomeHumansHydroxylationIntestinal AbsorptionPectinsSolubilityDelayed-Action PreparationsEllagic AcidPectinscontrolled releaseellagic acid lysine saltgastrointestinal digestiongut microbiotapectin-based formulations

Identifiers

PMID33467593
PMCPMC7829853
OpenAlexW3120708752

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.