Evidence map›Paper›PMID 35566392›Full record

ArticleMolecules (Basel, Switzerland)2022

Solubility and Permeability Enhancement of Oleanolic Acid by Solid Dispersion in Poloxamers and γ-CD.

Chiara De Stefani, Jessika Lodovichi, Laura Albonetti, Maria Cristina Salvatici, José Carlos Quintela, Anna Rita Bilia, Maria Camilla Bergonzi

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  8. Reducing hydrophobic drug adsorption in an in-vitro extracorporeal membrane oxygenation model.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2024
    Article
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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

7 authors at 2 institutions in 1 country.

Chiara De StefaniDepartment of Chemistry, University of Florence, Via U Schiff 6, 50519 Sesto Fiorentino, Florence, Italy.ORCID 0000-0001-8165-6607
Jessika LodovichiDepartment of Chemistry, University of Florence, Via U Schiff 6, 50519 Sesto Fiorentino, Florence, Italy.
Laura AlbonettiDepartment of Chemistry, University of Florence, Via U Schiff 6, 50519 Sesto Fiorentino, Florence, Italy.
Maria Cristina SalvaticiNational Research Council (CNR), Institute of Chemistry of Organometallic Compounds (ICCOM)-Electron Microscopy Centre (Ce.M.E.), Via Madonna del Piano 10, 50019 Sesto Fiorentino, Florence, Italy.
José Carlos QuintelaNATAC BIOTECH, Electronica 7, Alcorcón, 28923 Madrid, Spain.
Anna Rita BiliaDepartment of Chemistry, University of Florence, Via U Schiff 6, 50519 Sesto Fiorentino, Florence, Italy.ORCID 0000-0001-8772-1895
Maria Camilla BergonziDepartment of Chemistry, University of Florence, Via U Schiff 6, 50519 Sesto Fiorentino, Florence, Italy.ORCID 0000-0001-5144-1330
University of Florence · ITInstitute for the Chemistry of OrganoMetallic Compounds · IT

Funding

European Union 101023256
6 · The paper itself

Abstract

Oleanolic acid (OA) is a pentacyclic triterpenoid widely found in the Oleaceae family, and it represents 3.5% of the dry weight of olive leaves. OA has many pharmacological activities, such as hepatoprotection, anti-inflammatory, anti-oxidant, anti-diabetic, anti-tumor, and anti-microbic activities. Its therapeutic application is limited by its poor water solubility, bioavailability, and permeability. In this study, solid dispersions (SDs) were developed to overcome these OA limitations. Solubility studies were conducted to evaluate different hydrophilic polymers, drug-to-polymer ratios, and preparation methods. Poloxamer 188, Poloxamer 407, and γ-CD exhibited the highest increases in terms of OA solubility, regardless of the method of preparation. Binary systems were characterized using differential scanning calorimetry (DSC), X-ray diffraction (XRPD), and Fourier transform infrared spectroscopy (FTIR). In addition, pure compounds and SDs were analyzed using scanning electron microscopy (SEM) in order to observe both the morphology and the particle surface. In vitro dissolution studies were performed for P407, P188, and γ-CD SDs. Preparation using the solvent evaporation method (SEM) produced the highest increase in the dissolution profiles of all three polymers with respect to the OA solution. Finally, the effect of SDs on OA permeability was evaluated with an in vitro parallel artificial membrane permeability assay (PAMPA). The formulation improved passive permeation across the simulated barrier due to OA increased solubility. The dissolution and PAMPA results indicate that the amorphization of OA by SD preparation could be a useful method to enhance its oral absorption, and it is also applicable on an industrial scale.

Indexed as

Oleanolic AcidPoloxamerCalorimetry, Differential ScanningPermeabilityPolymersSolubilitySpectroscopy, Fourier Transform InfraredX-Ray DiffractionOleanolic AcidPoloxamerPolymersoleanolic acidPAMPA assaypoloxamerssolid dispersionsγ-CD

Identifiers

PMID35566392
PMCPMC9101807
OpenAlexW4229439721

What OpenQuestion holds

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LicenceCC BY
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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.