Evidence map›Paper›PMID 27620838›Full record

ArticleScientific reports2016

Molecular organization, localization and orientation of antifungal antibiotic amphotericin B in a single lipid bilayer.

Wojciech Grudzinski, Joanna Sagan, Renata Welc, Rafal Luchowski, Wieslaw I Gruszecki

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 56 citations in OpenAlex.

  1. Flipper dendrimers.Chemical science · 2026
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  6. An Overview of Lutein in the Lipid Membrane.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Quest for the Molecular Basis of Improved Selective Toxicity ofInternational journal of molecular sciences · 2021
    Article
  13. Review
  14. Review
  15. ABCA1 transporter reduces amphotericin B cytotoxicity in mammalian cells.Cellular and molecular life sciences : CMLS · 2019
    Article
  16. Article
  17. Preclinical Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Antifungal Activity of Liposomal Amphotericin B.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Review
  18. Pharmacology of Liposomal Amphotericin B: An Introduction to Preclinical and Clinical Advances for Treatment of Life-threatening Invasive Fungal Infections.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019
    Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Wojciech GrudzinskiDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Joanna SaganDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Renata WelcDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Rafal LuchowskiDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Wieslaw I GruszeckiDepartment of Biophysics, Institute of Physics, Maria Curie-Skłodowska University, Lublin, Poland.
Maria Curie-Skłodowska University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amphotericin B is a popular antifungal antibiotic, a gold standard in treatment of systemic mycotic infections, due to its high effectiveness. On the other hand, applicability of the drug is limited by its considerable toxicity to patients. Biomembranes are a primary target of physiological activity of amphotericin B and both the pharmacologically desired and toxic side effects of the drug relay on its molecular organization in the lipid phase. In the present work, molecular organization, localization and orientation of amphotericin B, in a single lipid bilayer system, was analysed simultaneously, thanks to application of a confocal fluorescence lifetime imaging microscopy of giant unilamellar vesicles. The results show that the presence of sterols, in the lipid phase, promotes formation of supramolecular structures of amphotericin B and their penetration into the membrane hydrophobic core. The fact that such an effect is substantially less pronounced in the case of cholesterol than ergosterol, the sterol of fungal membranes, provides molecular insight into the selectivity of the drug.

Indexed as

Amphotericin BAnisotropyAntifungal AgentsCholesterolErgosterolHydrophobic and Hydrophilic InteractionsLipid BilayersLipidsLiposomesMembranes, ArtificialMicroscopy, ConfocalMicroscopy, FluorescenceModels, TheoreticalSpectrophotometrySterolsAmphotericin BAntifungal AgentsCholesterolErgosterolLipid BilayersLipidsLiposomesMembranes, ArtificialSterols

Identifiers

PMID27620838
PMCPMC5020354
OpenAlexW2518877851

What OpenQuestion holds

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LicenceCC BY
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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.