Evidence map›Paper›PMID 29063342›Full record

ArticlePharmaceutical research2017

Microradiopharmaceutical for Metastatic Melanoma.

Thiago Goulart Rosa, Sofia Nascimento Dos Santos, Terezina de Jesus Andreoli Pinto, Daniele Dal Molim Ghisleni, Thereza Christina Barja-Fidalgo, Eduardo Ricci-Junior, Mohammed Al-Qahtani, Jan Kozempel, Emerson Soares Bernardes, Ralph Santos-Oliveira

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Article in Pharmaceutical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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.

Thiago Goulart RosaBrazilian Nuclear Energy Commission, Nuclear Engineering Institute, Rio de Janeiro, Brazil.
Sofia Nascimento Dos SantosBrazilian Nuclear Energy Commission, Nuclear Engineering Institute, Rio de Janeiro, Brazil.
Terezina de Jesus Andreoli PintoFaculty of Pharmaceutical Sciences,, University of São Paulo, São Paulo, SP, Brazil.
Daniele Dal Molim GhisleniFaculty of Pharmaceutical Sciences,, University of São Paulo, São Paulo, SP, Brazil.
Thereza Christina Barja-FidalgoLaboratory of Molecular and Cellular Pharmacology; Department of Cell Biology, Institute of Biology Roberto Alcântara Gomes, Biomedical Center, State University of Rio de Janeiro,, Rio de Janeiro, RJ, Brazil.
Eduardo Ricci-JuniorFaculty of Pharmacy, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Mohammed Al-QahtaniCyclotron and Radiopharmaceuticals Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Jan KozempelKatedra jaderné chemie, FJFI ČVUT v Praze, Prague, Czech Republic.
Emerson Soares BernardesCentro de Radiofarmácia, Instituto de Pesquisas Energéticas e Nucleares, São Paulo, Brazil.
Ralph Santos-OliveiraBrazilian Nuclear Energy Commission, Nuclear Engineering Institute, Rio de Janeiro, Brazil. presidenciaradiofarmacia@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of this article was to develop, characterize and test (in vivo) dacarbazine microparticles that may be labeled with 99mTc and Ra-223 for both use: diagnostic and therapy of metastatic melanoma.

methodsWe developed by double emulsion solvent evaporation methodology the microparticle. The characterization has been done using, Dynamic Light Scattering (DLS) and Scanning Electron Microscopy (SEM). The labeling with 99mTc and Ra-223 has been done by the direct labeling process. Also the formulation has been tested pre-clinically using Balb/c mice inducted with melanoma, performing the the biodistribution and planar imaging. Cytotoxicity evaluation was also done in M3 V cell line. In order to understand the safety aspects of the microparticles, microbiological study (endotoxin and sterility) has been done. Finally, planar imaging was performed to evaluate the diagnosing aspect.

resultsThe results showed that a 559 nm microparticles was obtained with a spherical shape. The labeling process with 99mTc reached over 90% of efficacy. On the other hand, the labeling process with Ra-223 showed a 70% efficacy. The results in inducted animals demonstrated that the microparticles were able to reach the tumor with a high rate (20%). Also demonstrated a low recognition by the Mononuclear Phagocytic System. The cytotoxicity and the microbiological control, corroborates the safety aspect of these microparticles.

conclusionThe planar image and the possible labeling with Ra-223, corroborates the use as a theragnostic agent for imaging and therapy of Metastatic Melanoma.

Indexed as

AnimalsAntineoplastic Agents, AlkylatingCell Line, TumorCell SurvivalDacarbazineDrug Delivery SystemsFemaleMelanomaMice, Inbred BALB CMice, NudeRadiumTechnetiumTissue DistributionAntineoplastic Agents, AlkylatingDacarbazineRadiumRadium-223Technetiumcancermicroparticlesnuclear medicineradiopharmaceuticals

Identifiers

What OpenQuestion holds

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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.