Evidence map›Paper›PMID 27316742›Full record

ArticleNanoscale research letters2016

Polymeric Nanoparticles of Brazilian Red Propolis Extract: Preparation, Characterization, Antioxidant and Leishmanicidal Activity.

Ticiano Gomes do Nascimento, Priscilla Fonseca da Silva, Lais Farias Azevedo, Louisianny Guerra da Rocha, Isabel Cristina Celerino de Moraes Porto, Túlio Flávio Accioly Lima E Moura, Irinaldo Diniz Basílio-Júnior, Luciano Aparecido Meireles Grillo, Camila Braga Dornelas, Eduardo Jorge da Silva Fonseca and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nanoscale research letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
15.0field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 154 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

13 authors at 4 institutions in 2 countries.

Ticiano Gomes do NascimentoQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil. ticianogn@yahoo.com.br.
Priscilla Fonseca da SilvaQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Lais Farias AzevedoQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Louisianny Guerra da RochaQuality Control of Drugs Laboratory (LCQMed), Postgraduate Program of Pharmaceutical Science, Department of Pharmacy, Federal University of Rio Grande do Norte, Rua General Cordeiro de Farias S/N, Petrópolis, Natal, RN, 59010-180, Brazil.
Isabel Cristina Celerino de Moraes PortoQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Túlio Flávio Accioly Lima E MouraQuality Control of Drugs Laboratory (LCQMed), Postgraduate Program of Pharmaceutical Science, Department of Pharmacy, Federal University of Rio Grande do Norte, Rua General Cordeiro de Farias S/N, Petrópolis, Natal, RN, 59010-180, Brazil.
Irinaldo Diniz Basílio-JúniorQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Luciano Aparecido Meireles GrilloQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Camila Braga DornelasQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Eduardo Jorge da Silva FonsecaQuality Control Laboratory of Drugs and Medicines, Postgraduate Program in Pharmaceutical Sciences, School of Nursing and Pharmacy, Federal University of Alagoas, Alagoas, Avenida Lourival Melo Mota, s/n Campus A. C. Simões, University City, Tabuleiro dos Martins, 57072-900, Maceió, Alagoas, Brazil.
Eduardo de Jesus OliveiraLaboratory of Pharmaceutical analysis, Postgraduate Program of Pharmaceutical Science, Pharmacy College, Federal University of Vales do Jequitinhonha e Mucuri, Campus JK, Rodovia MGT 367 Km 583, n° 5000, Alto da Jacuba, Diamantina, Minas Gerais, 39100-000, Brazil.
Alex Tong ZhangDepartment of Pharmaceutical Science, Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, UK.
David G WatsonDepartment of Pharmaceutical Science, Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, UK.
Universidade Federal de Alagoas · BRUniversidade Federal do Rio Grande do Norte · BRUniversity of Strathclyde · GBUniversidade Federal dos Vales do Jequitinhonha e Mucuri · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ever-increasing demand for natural products and biotechnology derived from bees and ultra-modernization of various analytical devices has facilitated the rational and planned development of biotechnology products with a focus on human health to treat chronic and neglected diseases. The aim of the present study was to prepare and characterize polymeric nanoparticles loaded with Brazilian red propolis extract and evaluate the cytotoxic activity of "multiple-constituent extract in co-delivery system" for antileishmanial therapies. The polymeric nanoparticles loaded with red propolis extract were prepared with a combination of poly-ε-caprolactone and pluronic using nanoprecipitation method and characterized by different analytical techniques, antioxidant and leishmanicidal assay. The red propolis nanoparticles in aqueous medium presented particle size (200-280 nm) in nanometric scale and zeta analysis (-20 to -26 mV) revealed stability of the nanoparticles without aggregation phenomenon during 1 month. After freeze-drying method using cryoprotectant (sodium starch glycolate), it was possible to observe particles with smooth and spherical shape and apparent size of 200 to 400 nm. Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and thermal analysis revealed the encapsulation of the flavonoids from the red propolis extract into the polymeric matrix. Ultra performance liquid chromatography coupled with diode array detector (UPLC-DAD) identified the flavonoids liquiritigenin, pinobanksin, isoliquiritigenin, formononetin and biochanin A in ethanolic extract of propolis (EEP) and nanoparticles of red propolis extract (NRPE). The efficiency of encapsulation was determinate, and median values (75.0 %) were calculated using UPLC-DAD. 2,2-Diphenyl-1-picryhydrazyl method showed antioxidant activity to EEP and red propolis nanoparticles. Compared to negative control, EEP and NRPE exhibited leishmanicidal activity with an IC50 value of ≅38.0 μg/mL and 31.3 μg/mL, 47.2 μg/mL, 154.2μg/mL and 193.2 μg/mL for NRPE A1, NRPE A2, NRPE A3 and NRPE A4, respectively. Nanoparticles loaded with red propolis extract in co-delivery system and EEP presented cytotoxic activity on Leishmania (V.) braziliensis. Red propolis extract loaded in nanoparticles has shown to be potential candidates as intermediate products for preparation of various pharmaceutical dosage forms containing red propolis extract in the therapy against negligible diseases such as leishmaniasis. Graphical Abstract Some biochemical mechanisms of cellular debridement of Leishmania (V.) braziliensis species by the flavonoids of red propolis extract (EEP) or NRPE loaded with red propolis extract.

Indexed as

Antioxidant activityATR-FTIRLeishmanicidal activityPCL-pluronic nanoparticlesRed propolis extractSEM analysisThermal analysisUPLC-DAD

Identifiers

PMID27316742
PMCPMC4912519
OpenAlexW2431426158

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.