Evidence map›Paper›PMID 22275830›Full record

ArticleInternational journal of nanomedicine2012

How can micelle systems be rebuilt by a heating process?

Miguel Adelino da Silva-Filho, Scheyla Daniela Vieira da Silva Siqueira, Larissa Bandeira Freire, Ivonete Batista de Araújo, Káttya Gyselle de Holanda e Silva, Aldo da Cunha Medeiros, Irami Araújo-Filho, Anselmo Gomes de Oliveira, Eryvaldo Sócrates Tabosa do Egito

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2012. 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
0.8field-weighted citation impact, top 31% 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, 18 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 3 institutions in 1 country.

Miguel Adelino da Silva-FilhoDispersed Systems Laboratory, Federal University of Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil.
Scheyla Daniela Vieira da Silva Siqueira
Larissa Bandeira Freire
Ivonete Batista de Araújo
Káttya Gyselle de Holanda e Silva
Aldo da Cunha Medeiros
Irami Araújo-Filho
Anselmo Gomes de Oliveira
Eryvaldo Sócrates Tabosa do Egito
Universidade Federal do Rio Grande do Norte · BRCentro Universitário do Rio Grande do Norte · BRUniversidade Estadual Paulista (Unesp) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this work was to evaluate how an aqueous micellar system containing Amphotericin B (AmB) and sodium deoxycholate (DOC) can be rebuilt after heating treatment. Also, a review of the literature on the physicochemical and biological properties of this new system was conducted. Heated (AmB-DOC-H) and unheated (AmB-DOC) micelles were then diluted at four different concentrations (50 mg · L(-1), 5 mg · L(-1), 0.5 mg · L(-1), and 0.05 mg · L(-1)) to perform physicochemical studies and a pharmacotoxicity assay, in which two cell models were used for the in vitro experiments: red blood cells (RBC) from human donors and Candida parapsilosis (Cp). While potassium (K(+)) and hemoglobin leakage from RBC were the parameters used to evaluate acute and chronic toxicity, respectively, the efficacy of AmB-DOC and AmB-DOC-H were assessed by K(+) leakage and cell survival rate from Cp. The spectral study revealed a slight change in the AmB-DOC aggregate peak from 327 nm to 323 nm, which is the peak for AmB-DOC-H. Although AmB-DOC and AmB-DOC-H exhibited different behavior for hemoglobin leakage, AmB-DOC produced higher leakage than AmB-DOC-H at high concentrations (from 5 mg · L(-1)). For K(+) leakage, both AmB-DOC and AmB-DOC-H showed a similar profile for both cell models, RBC and Cp (P < 0.05). AmB-DOC-H and AmB-DOC also revealed a similar profile of activity against Cp with an equivalent survival rate. In short, AmB-DOC-H showed much less toxicity than AmB-DOC, but remained as active as AmB-DOC against fungal cells. The results highlight the importance of this new procedure as a simple, inexpensive, and safe way to produce a new kind of micelle system for the treatment of systemic fungal infections.

Indexed as

MicellesAmphotericin BAnalysis of VarianceCandidaDeoxycholic AcidDose-Response Relationship, DrugErythrocytesHemoglobinsHemolysisHot TemperatureHumansMicrobial ViabilityModels, BiologicalNanotechnologyPotassiumSpectrophotometry, UltravioletAmphotericin BDeoxycholic AcidHemoglobinsMicellesPotassiummicellesnanotechnologypre-heated amphotericin Bsuper-aggregates

Identifiers

PMID22275830
PMCPMC3263407
OpenAlexW1967242786

What OpenQuestion holds

Textmetadata
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.