Evidence map›Paper›PMID 30116897›Full record

ArticleMikrochimica acta2018

Impedimetric gene assay for BCR/ABL transcripts in plasmids of patients with chronic myeloid leukemia.

Karen Yasmim Pereira Dos Santos Avelino, Isaac Aarón Morales Frías, Norma Lucena-Silva, César Augusto Souza de Andrade, Maria Danielly Lima de Oliveira

Abstract read
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In one paragraph

Article in Mikrochimica acta, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 10 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 2 institutions in 1 country.

Karen Yasmim Pereira Dos Santos AvelinoPrograma de Pós-Graduação em Bioquímica e Fisiologia, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Isaac Aarón Morales FríasPrograma de Pós-Graduação em Inovação Terapêutica, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Norma Lucena-SilvaFundação Oswaldo Cruz (Fiocruz), Instituto Aggeu Magalhães, Recife, PE, 50670-420, Brazil.
César Augusto Souza de AndradePrograma de Pós-Graduação em Bioquímica e Fisiologia, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil.
Maria Danielly Lima de OliveiraPrograma de Pós-Graduação em Bioquímica e Fisiologia, Universidade Federal de Pernambuco, Recife, PE, 50670-901, Brazil. m_danielly@yahoo.com.br.
Universidade Federal de Pernambuco · BRFundação Oswaldo Cruz · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 302885/2015-3Conselho Nacional de Desenvolvimento Científico e Tecnológico (BR) 310364/2015-9FACEPE 0040-4.00/13Ministério da Saúde (BR) 401700/2015-1
6 · The paper itself

Abstract

A label-free impedimetric biosensor was developed for determination of BCR/ABL transcripts. Specific DNA primers were covalently immobilized on a gold electrode modified with carboxylated multiwalled carbon nanotubes (cMWCNTs) and zinc oxide nanoparticles (ZnO-NPs). Aggregation of the ZnO-NPs is prevented by the introduction of an amino-modified silica coating, which also allows a subsequent covalent linkage to cMWCNTs. The impedimetric biosensor was typically operated at a working voltage of +10 mV vs. Ag/AgCl, in a frequency range from 100 mHz to 100 kHz. Studies on the surface morphology and electrochemical properties of the electrode demonstrated improved bioactivity. Amperometric currents and impedimetric parameters, such as charge transfer resistance, varied significantly throughout the construction of the biosensor. The hybridization process was also evidenced by changes in the topography of the surface after exposure to samples containing BCR/ABL. The gene sensor has a linear concentration range for the target gene of 6.94 aM to 694 fM with a limit of detection as low as 0.039 aM. Also, the biosensor is selective and reproducible with a standard deviation of 4.1%. Three replicates for each experimental condition were used. Hence, it is perceived to be a viable tool for early-stage diagnosis of the BCR/ABL fusion gene and monitoring of major molecular remission in clinical samples. Graphical abstract Schematic of a highly sensitive hybridization assay for the BCR/ABL fusion gene. It is based on ZnO nanoparticle functionalized with 3-(aminopropyl)triethoxysilane.

Indexed as

Biological AssayElectrochemical TechniquesElectrodesFusion Proteins, bcr-ablGoldHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMetal NanoparticlesNanotubes, CarbonPlasmidsFusion Proteins, bcr-ablGoldNanotubes, CarbonBiosensorCarbon nanotubesCyclic voltammetryElectrochemistryImpedance spectroscopyMajor molecular remissionZinc oxide

Identifiers

PMID30116897
OpenAlexW2887844372

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.