Evidence map›Paper›PMID 36678827›Full record

ArticlePharmaceutics2023

Development and Characterization of Pharmaceutical Systems Containing Rifampicin.

Antonella V Dan Córdoba, Virginia Aiassa, Jesica A Dimmer, Camila N Barrionuevo, Mario A Quevedo, Marcela R Longhi, Ariana Zoppi

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Cyclodextrins and Their Derivatives as Drug Stability Modifiers.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Article
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.

Antonella V Dan CórdobaUnidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Facultad Ciencias Químicas, Departamento de Ciencias Farmacéuticas, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.ORCID 0000-0003-4865-9034
Virginia AiassaUnidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Facultad Ciencias Químicas, Departamento de Ciencias Farmacéuticas, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.
Jesica A DimmerCentro de Investigaciones y Transferencia de Villa María (CIT-VM), Universidad de Villa María, Villa María, Córdoba 5900, Argentina.ORCID 0000-0003-2040-7038
Camila N BarrionuevoCentro de Estudios e Investigación de la Enfermedad de Chagas y Leishmaniasis, Facultad Ciencias Médicas, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.
Mario A QuevedoUnidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Facultad Ciencias Químicas, Departamento de Ciencias Farmacéuticas, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.
Marcela R LonghiUnidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Facultad Ciencias Químicas, Departamento de Ciencias Farmacéuticas, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.ORCID 0000-0002-3189-9886
Ariana ZoppiUnidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Facultad Ciencias Químicas, Departamento de Ciencias Farmacéuticas, Universidad Nacional de Córdoba, Córdoba 5000, Argentina.ORCID 0000-0002-2968-7737
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad Nacional de Córdoba · AR

Funding

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) 112 202001 02912Fondo para la Investigación Científica y Tecnológica Préstamo BID PICT 2019-2664
6 · The paper itself

Abstract

Rifampicin is a potent antimicrobial drug with some suboptimal properties, such as poor stability, low solubility, and variable bioavailability. Therefore, in the current study, a multicomponent complex between rifampicin, γ-cyclodextrin, and arginine was prepared with the aim of improving drug properties. Solubility was evaluated by phase-solubility studies. The mechanism of interaction was established through proton nuclear magnetic resonance spectroscopy and molecular modeling. Physicochemical characterization was investigated using Fourier transform-infrared spectroscopy, powder X-ray diffraction, and scanning electron microscopy. The dissolution properties, antimicrobial activity (antibacterial, antibiofilm, and antileishmanial), and stability of the different samples were studied. The results obtained in this investigation demonstrate that multicomponent complexes can improve the water solubility and dissolution rate of rifampicin, as well as its antibacterial and antileishmanial action, and present suitable stability. In conclusion, rifampicin complexed with γ-cyclodextrin and arginine is an attractive approach for developing pharmaceutical dosage forms of rifampicin with increased antimicrobial activities.

Indexed as

antibiofilm activityantileishmanial activityargininerifampicinsolubilitystabilityγ-cyclodextrin

Identifiers

PMID36678827
PMCPMC9864009
OpenAlexW4313648560

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.