Evidence map›Paper›PMID 37630925›Full record

ArticleNanomaterials (Basel, Switzerland)2023

Viscoelasticity of Liposomal Dispersions.

Lívia Budai, Marianna Budai, Zsófia Edit Fülöpné Pápay, Petra Szalkai, Noémi Anna Niczinger, Shosho Kijima, Kenji Sugibayashi, István Antal, Nikolett Kállai-Szabó

Open access · goldAbstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

7 citing papers in PubMed, 5 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

9 authors at 2 institutions in 2 countries.

Lívia BudaiDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.ORCID 0000-0002-6720-5989
Marianna BudaiDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.
Zsófia Edit Fülöpné PápayDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.ORCID 0000-0002-7653-1065
Petra SzalkaiDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.
Noémi Anna NiczingerDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.
Shosho KijimaFaculty of Pharmacy and Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado 350-0295, Saitama, Japan.
Kenji SugibayashiFaculty of Pharmacy and Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado 350-0295, Saitama, Japan.ORCID 0000-0003-1332-2001
István AntalDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.
Nikolett Kállai-SzabóDepartment of Pharmaceutics, Semmelweis University, Hőgyes Str. 7, 1092 Budapest, Hungary.ORCID 0000-0002-8164-3993
Semmelweis University · HUJosai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Janus-faced viscoelastic gelling agents-possessing both elastic and viscous characteristics-provide materials with unique features including strengthening ability under stress and a liquid-like character with lower viscosities under relaxed conditions. The mentioned multifunctional character is manifested in several body fluids such as human tears, synovial liquids, skin tissues and mucins, endowing the fluids with a special physical resistance property that can be analyzed by dynamic oscillatory rheology. Therefore, during the development of pharmaceutical or cosmetical formulations-with the intention of mimicking the physiological conditions-rheological studies on viscoelasticity are strongly recommended and the selection of viscoelastic preparations is highlighted. In our study, we aimed to determine the viscoelasticity of various liposomal dispersions. We intended to evaluate the impact of lipid concentration, the presence of cholesterol or 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) and the gelling agents polyvinyl alcohol (PVA) and hydroxyethylcellulose (HEC) on the viscoelasticity of vesicular systems. Furthermore, the effect of two model drugs (phenyl salicylate and caffeine) on the viscoelastic behavior of liposomal systems was studied. Based on our measurements, the oscillation rheological properties of the liposomal formulations were influenced both by the composition and the lamellarity/size of the lipid vesicles.

Indexed as

drug delivery systemliposomenanotechnologyoscillation rheologyviscoelasticity

Identifiers

PMID37630925
PMCPMC10459094
OpenAlexW4385840436

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.