Evidence map›Paper›PMID 31102112›Full record

ArticleNanoscale research letters2019

Environmentally compatible bioconjugated gold nanoparticles as efficient contrast agents for inflammation-induced cancer imaging.

Vinícius Barreto Garcia, Thaís Gomes de Carvalho, Luiz Henrique da Silva Gasparotto, Heloiza Fernanda Oliveira da Silva, Aurigena Antunes de Araújo, Gerlane Coelho Bernardo Guerra, Timo Schomann, Luis J Cruz, Alan B Chan, Raimundo Fernandes de Araújo Júnior

Open access · goldAbstract read
In one paragraph

Article in Nanoscale research letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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 3 institutions in 2 countries.

Vinícius Barreto GarciaDepartment of Morphology, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil.
Thaís Gomes de CarvalhoDepartment of Morphology, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil.
Luiz Henrique da Silva GasparottoGroup of Biological Chemistry and Chemometrics, Institute of Chemistry, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil.
Heloiza Fernanda Oliveira da SilvaGroup of Biological Chemistry and Chemometrics, Institute of Chemistry, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil.
Aurigena Antunes de AraújoDepartment of Biophysics and Pharmacology, Post-Graduation Programme in Public Health, Post-Graduation Programme in Pharmaceutical Science, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil.
Gerlane Coelho Bernardo GuerraDepartment of Biophysics and Pharmacology, Post-Graduation Programme in Public Health, Post-Graduation Programme in Pharmaceutical Science, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil.
Timo SchomannTranslational Nanobiomaterials and Imaging, Department of Radiology, Leiden University Medical Center, 2333, ZA, Leiden, the Netherlands.
Luis J CruzTranslational Nanobiomaterials and Imaging, Department of Radiology, Leiden University Medical Center, 2333, ZA, Leiden, the Netherlands.
Alan B ChanPercuros B.V, 2333, CL, Leiden, the Netherlands.
Raimundo Fernandes de Araújo JúniorDepartment of Morphology, Federal University of Rio Grande do Norte, Natal, RN, 59072-970, Brazil. araujojr@cb.ufrn.br.ORCID http://orcid.org/0000-0003-2349-2354
Universidade Federal do Rio Grande do Norte · BRLeiden University Medical Center · NLPercuros (Netherlands) · NL

Funding

European Commission/ MSCA-ITN-2015-ETN 675743UNIVERSAL/CNPq 2016 425786/2016-1
6 · The paper itself

Abstract

For many cancers, early detection is the key to improve survival and reduce the morbidity, which is associated with radical resections due to late diagnosis. Here, we describe the efficiency of primary antibody-conjugated gold nanoparticles (AuNPs) to specifically target chronic inflammatory processes, specially M2 macrophages, in tissue sections of ulcerative colitis (UC) and steatohepatitis in rats which may lead to colorectal cancer and liver carcinoma, respectively. In this study, we demonstrate that AuNPs synthesized by a simple, inexpensive, and environmentally compatible method can be easily conjugated with the antibodies anti-COX-2, anti-MIF, and Alexa Fluor® 488 (ALEXA) to perform immunofluorescence staining in inflamed tissues. Moreover, we showed that primary antibody-conjugated gold nanoparticles (AuNPs) can be used to target M2 macrophages by flow cytometry. We designed three immunofluorescence staining protocols of tissue section with AuNPs for 30 min and overnight incubation, as well as one flow cytometry protocol of M2 macrophage labeling with AuNPs for 30 min. Immunofluorescence and flow cytometry results suggest that conjugation was achieved by direct adsorption of antibodies on the AuNPs surface. When compared to the standard ALEXA protocol in immunofluorescence (IF) and flow cytometry (FC), our 30-min incubation protocol using AuNPs instead of ALEXA decreased from approximately 23 h to 5 h for IF and from 4 h to 1 h for FC, proving to be less laborious, which makes the method eligible for inflammation-induced cancer diagnostic.

Indexed as

Cancer diagnosticsGolden nanoparticlesImmunofluorescenceInflammatory processesM2 macrophagesUlcerative colitis

Identifiers

PMID31102112
PMCPMC6525234
OpenAlexW2946226371

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.