Evidence map›Paper›PMID 34563196›Full record

ArticleBMC veterinary research2021

An in vivo pharmacokinetic study of metformin microparticles as an oral sustained release formulation in rabbits.

Sihem Bouriche, Angela Alonso-García, Carlos M Cárceles-Rodríguez, Farouk Rezgui, Emilio Fernández-Varón

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

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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

5 authors at 3 institutions in 2 countries.

Sihem BouricheLaboratoire des Matériaux Organiques (LMO), Faculté de Technologie, Département de Génie des Procédés, Université de Bejaia, 06000, Bejaia, Algeria.
Angela Alonso-GarcíaDepartment of Pharmacology, Faculty of Veterinary Medicine, Universidad de Murcia, Murcia, Spain.
Carlos M Cárceles-RodríguezDepartment of Pharmacology, Faculty of Veterinary Medicine, Universidad de Murcia, Murcia, Spain. carceles@um.es.
Farouk RezguiLaboratoire des Matériaux Organiques (LMO), Faculté de Technologie, Département de Génie des Procédés, Université de Bejaia, 06000, Bejaia, Algeria.
Emilio Fernández-VarónDepartment of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, 18071, Granada, Spain.
Universidad de Murcia · ESUniversidad de Granada · ESUniversity of Béjaïa · DZ

Funding

Fundación Séneca 20950/PI/18
6 · The paper itself

Abstract

backgroundMetformin hydrochloride is a biguanide derivative that has been widely used to treat type 2 diabetes in humans. In veterinary medicine, metformin has shown increasing potential for diabetes treatment in different species, such as equids, dogs, cats and rabbits. It is highly hydrophilic, with incomplete gastrointestinal absorption and very large variability in absolute bioavailability between species, ranging from 4% in equids to 60% in humans. Metformin also shows a short half-life of approximately 2 h in dogs, cats, horses and humans. The objectives of this study were to evaluate a poly (lactic acid) (PLA) metformin microparticle formulation to test in rabbits and conduct a pharmacokinetics study of intravenous (S

resultsMetformin-loaded PLA microparticles were characterized by a spherical shape and high encapsulation efficiency. The results from Fourier transform infrared (FTIR) spectroscopy suggested the presence of interactions between metformin and PLA. X-Ray diffraction (XRD) analysis corroborated the results from the differential scanning calorimetry (DSC) studies, showing that metformin is present in an amorphous state within the microparticles. Physicochemical characterization suggested that PLA and metformin hydrochloride interacted within the microparticles via hydrogen bonding interactions. The pharmacokinetic study in rabbits showed sustained-release characteristics from the prepared microparticles with a delay in the time needed to reach the maximum concentration (T

conclusionsMetformin-loaded PLA microparticles showed optimal and beneficial properties in terms of their physicochemical characteristics, making them suitable for use in an in vivo pharmacokinetic study. The pharmacokinetic parameters of the metformin microparticles from the in vivo study showed a shorter T

Indexed as

Administration, IntravenousAdministration, OralAnimalsDelayed-Action PreparationsHalf-LifeMetforminParticle SizePolyestersRabbitsDelayed-Action PreparationsMetforminPolyesterspoly(lactide)Controlled-releaseMetforminMicroparticlesPharmacokineticsPolymeric-based formulations

Identifiers

PMID34563196
PMCPMC8467142
OpenAlexW3203507278

What Socratic holds

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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 Socratic graph.