Evidence map›Paper›PMID 29785109›Full record

ArticleInternational journal of nanomedicine2018

Development and characterization of a nanoemulsion containing propranolol for topical delivery.

Tatiana Zanela da Silva Marques, Ralph Santos-Oliveira, Luciana Betzler de Oliveira de Siqueira, Verônica da Silva Cardoso, Zaida Maria Faria de Freitas, Rita de Cássia da Silva Ascenção Barros, Ana Lúcia Vazquez Villa, Mariana Sato de Souza de Bustamante Monteiro, Elisabete Pereira Dos Santos, Eduardo Ricci-Junior

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 68 citations in OpenAlex.

  1. Bioadhesive Eudragit RLPharmaceutics · 2025
    Article
  2. Nanotechnology in Infantile Hemangioma Management.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article
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  13. Design and characterization of propolis extract loaded self-nano emulsifying drug delivery system as immunostimulant.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2021
    Article
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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

10 authors at 2 institutions in 4 countries.

Tatiana Zanela da Silva MarquesDepartment of Drugs and Medicines, Faculty of Pharmacy.
Ralph Santos-OliveiraInstitute of Nuclear Energy.
Luciana Betzler de Oliveira de SiqueiraDepartment of Drugs and Medicines, Faculty of Pharmacy.
Verônica da Silva CardosoUnit of Biocatalysis, Bioproducts and Bioenergy (Bioinivar), Institute of Microbiology Paulo de Góes, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Zaida Maria Faria de FreitasDepartment of Drugs and Medicines, Faculty of Pharmacy.
Rita de Cássia da Silva Ascenção BarrosDepartment of Drugs and Medicines, Faculty of Pharmacy.
Ana Lúcia Vazquez VillaDepartment of Drugs and Medicines, Faculty of Pharmacy.
Mariana Sato de Souza de Bustamante MonteiroDepartment of Drugs and Medicines, Faculty of Pharmacy.
Elisabete Pereira Dos SantosDepartment of Drugs and Medicines, Faculty of Pharmacy.
Eduardo Ricci-JuniorDepartment of Drugs and Medicines, Faculty of Pharmacy.
Universidade Federal do Rio de Janeiro · BRCenter for Drug Evaluation and Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPropranolol (PPN) is a therapeutic option for the treatment of infantile hemangiomas. This study aimed at the development of nanoemulsion (NE) containing 1% PPN, characterization of the system, and safety studies based on ex vivo permeation, cytotoxicity, and biodistribution in vivo.

methodsThe formulation was developed and characterized in relation to the droplet size, polydispersity index (PDI), pH, zeta potential, and electronic microscopy. Ex vivo permeation studies were used to evaluate the cutaneous retention of PPN in the epidermis and dermis. Cytotoxicity studies were performed in fibroblasts, macrophages, and keratinocytes. In vivo biodistribution assay of the formulations was performed by means of labeling with technetium-99m.

resultsNE1 exhibited droplet size of 26 nm, PDI <0.4, pH compatible with the skin, and zeta potential of -20 mV, which possibly contributes to the stability. Electron microscopy showed that the NE presented droplets of nanometric size and spherical shape. NE1 provided excellent stability for PPN. In the ex vivo cutaneous permeation assay, the NE provided satisfactory PPN retention particularly in the dermis, which is the site of drug action. In addition, NE1 promoted cutaneous permeation of the PPN in small amount. In vivo biodistribution showed that the radiolabeled formulation remained in the skin and a small amount reached the bloodstream. NE1 presented low cytotoxicity to fibroblasts, macrophages, and keratinocytes in the concentrations evaluated in the cytotoxicity assay.

conclusionWe concluded that the formulation is safe for skin administration; however, cutaneous irritation studies should be performed to confirm the safety of the formulation before clinical studies in patients with infantile hemangiomas.

Indexed as

Administration, CutaneousAdministration, TopicalAnimalsCells, CulturedDrug Delivery SystemsEmulsionsEpidermisHumansHydrogen-Ion ConcentrationMaleNanostructuresPropranololRats, WistarSkinSkin AbsorptionSus scrofaEmulsionsPropranololTechnetiumcytotoxicityex vivo permeation studiesinfantile hemangiomasnanoemulsionpropranolol

Identifiers

PMID29785109
PMCPMC5957063
OpenAlexW2799323837

What OpenQuestion holds

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LicenceCC BY-NC
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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.