Evidence map›Paper›PMID 24482779›Full record

ArticleScientia pharmaceutica

Liposomes for topical use: a physico-chemical comparison of vesicles prepared from egg or soy lecithin.

Lívia Budai, Nóra Kaszás, Pál Gróf, Katalin Lenti, Katayoon Maghami, István Antal, Imre Klebovich, Ilona Petrikovics, Marianna Budai

Open access · goldAbstract read
In one paragraph

Article in Scientia pharmaceutica. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Viscoelasticity of Liposomal Dispersions.Nanomaterials (Basel, Switzerland) · 2023
    Article
  7. Article
  8. Interaction of Caffeine with Model Lipid Membranes.The journal of physical chemistry. B · 2021
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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

9 authors at 1 institution in 1 country.

Lívia BudaiSemmelweis University, Department of Pharmaceutics, Hőgyes E. u. 7., H-1092, Budapest, Hungary.
Nóra KaszásSemmelweis University, Department of Pharmaceutics, Hőgyes E. u. 7., H-1092, Budapest, Hungary.
Pál GrófSemmelweis University, Department of Biophysics and Radiation Biology, Tűzoltó u. 37-47., H-1094, Budapest, Hungary.
Katalin LentiSemmelweis University, Faculty of Health Sciences, Department of Morphology and Physiology, Vas u. 17, H-1088, Budapest, Hungary.
Katayoon MaghamiSemmelweis University, Department of Pharmaceutics, Hőgyes E. u. 7., H-1092, Budapest, Hungary.
István AntalSemmelweis University, Department of Pharmaceutics, Hőgyes E. u. 7., H-1092, Budapest, Hungary.
Imre KlebovichSemmelweis University, Department of Pharmaceutics, Hőgyes E. u. 7., H-1092, Budapest, Hungary.
Ilona PetrikovicsSam Houston State University, Department of Chemistry, TX-77340, Huntsville, USA.
Marianna BudaiSemmelweis University, Department of Pharmaceutics, Hőgyes E. u. 7., H-1092, Budapest, Hungary.
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developments in nanotechnology and in the formulation of liposomal systems provide the opportunity for cosmetic dermatology to design novel delivery systems. Determination of their physico-chemical parameters has importance when developing a nano-delivery system. The present study highlights some technological aspects/characteristics of liposomes formulated from egg or soy lecithins for topical use. Alterations in the pH, viscosity, surface tension, and microscopic/macroscopic appearance of these vesicular systems were investigated. The chemical composition of the two types of lecithin was checked by mass spectrometry. Caffeine, as a model molecule, was encapsulated into multilamellar vesicles prepared from the two types of lecithin: then zeta potential, membrane fluidity, and encapsulation efficiency were compared. According to our observations, samples prepared from the two lecithins altered the pH in opposite directions: egg lecithin increased it while soy lecithin decreased it with increased lipid concentration. Our EPR spectroscopic results showed that the binding of caffeine did not change the membrane fluidity in the temperature range of possible topical use (measured between 2 and 50 °C). Combining our results on encapsulation efficiency for caffeine (about 30% for both lecithins) with those on membrane fluidity data, we concluded that the interaction of caffeine with the liposomal membrane does not change the rotational motion of the lipid molecules close to the head group region. In conclusion, topical use of egg lecithin for liposomal formulations can be preferred if there are no differences in the physico-chemical properties due to the encapsulated drugs, because the physiological effects of egg lecithin vesicles on skin are significantly better than that of soy lecithin liposomes.

Indexed as

Macroscopic/microscopic AppearanceMultilamellar vesicleNatural lipidTopical drug delivery

Identifiers

PMID24482779
PMCPMC3867246
OpenAlexW2157394588

What OpenQuestion 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 OpenQuestion graph.