Evidence map›Paper›PMID 30682086›Full record

ArticlePloS one2019

Cyclodextrins as multifunctional excipients: Influence of inclusion into β-cyclodextrin on physicochemical and biological properties of tebipenem pivoxil.

Magdalena Paczkowska, Daria Szymanowska-Powałowska, Mikołaj Mizera, Dominika Siąkowska, Wioletta Błaszczak, Hanna Piotrowska-Kempisty, Judyta Cielecka-Piontek

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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 3 institutions in 1 country.

Magdalena PaczkowskaDepartment of Pharmacognosy, Poznan University of Medical Sciences, Święcickiego, Poznan, Poland.
Daria Szymanowska-PowałowskaDepartment of Biotechnology and Food Microbiology, Poznan University of Life Sciences, Wojska Polskiego, Poznan, Poland.
Mikołaj MizeraDepartment of Pharmacognosy, Poznan University of Medical Sciences, Święcickiego, Poznan, Poland.
Dominika SiąkowskaDepartment of Pharmacognosy, Poznan University of Medical Sciences, Święcickiego, Poznan, Poland.
Wioletta BłaszczakInstitute of Animal Reproduction and Food Research of Polish Academy of Sciences, Tuwima, Olsztyn, Poland.
Hanna Piotrowska-KempistyDepartment of Toxicology, Faculty of Pharmacy, Poznan University of Medical Sciences, Dojazd, Poznan, Poland.
Judyta Cielecka-PiontekDepartment of Pharmacognosy, Poznan University of Medical Sciences, Święcickiego, Poznan, Poland.ORCID 0000-0003-0891-5419
Poznan University of Medical Sciences · PLInLife Institute of Animal Reproduction and Food Research, Polish Academy of Sciences · PLUniversity of Life Sciences in Poznań · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel approach for drug design based on the oral carbapenem analog tebipenem pivoxil (TP) has been proposed. The formation of the tebipenem pivoxil-β-cyclodextrin (TP-β-CD) complex resulted in changes concerning physicochemical properties of TP, which is significant for planning the development of an innovative pharmaceutical formulation as well as in the modifications of biological activity profile of the studied delivery system. The inclusion of TP into β-cyclodextrin (β-CD) was confirmed by spectral (infrared and Raman spectroscopies) and thermal method (differential scanning calorimetry). Precise indications of TP domains responsible for interaction with β-CD were possible through a theoretical approach. The most important physicochemical modifications obtained as an effect of TP inclusion were changes in solubility and its rate depending on acceptor fluids, and an increase in chemical stability in the solid state. Biologically essential effects of TP and β-CD interactions were decreased TP permeability through Caco-2 cell monolayers with the use of efflux effect inhibition and increased antibacterial activity. The proposed approach is an opportunity for development of the treatment in resistant bacterial infections, in which along with physicochemical modifications induced by a drug carrier impact, a carrier synergy with a pharmacological potential of an active pharmaceutical substance could be used.

Indexed as

Anti-Bacterial Agentsbeta-CyclodextrinsCaco-2 CellsCalorimetry, Differential ScanningCarbapenemsCell Membrane PermeabilityHumansModels, TheoreticalSolubilitySpectroscopy, Fourier Transform InfraredSpectrum Analysis, RamanAnti-Bacterial Agentsbeta-CyclodextrinsCarbapenemstebipenem

Identifiers

PMID30682086
PMCPMC6347292
OpenAlexW2912720741

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.