Evidence map›Paper›PMID 39866618›Full record

ArticleACS omega2025

Optimized Synthesis and Stabilization of Superparamagnetic Iron Oxide Nanoparticles for Enhanced Biomolecule Adsorption.

Wanderson Juvencio Keijok, Luis Alberto Contreras Alvarez, Angelo Marcio de Souza Gomes, Fabiana Vasconcelos Campos, Jairo Pinto de Oliveira, Marco Cesar Cunegundes Guimarães

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. 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

6 authors.

Wanderson Juvencio KeijokFederal University of Espírito Santo, Av Marechal Campos 1468, Vitória, ES 29.040 090, Brazil.ORCID https://orcid.org/0000-0001-6352-7182
Luis Alberto Contreras AlvarezFederal University of Espírito Santo, Av Marechal Campos 1468, Vitória, ES 29.040 090, Brazil.
Angelo Marcio de Souza GomesPhysics Institute, Federal University of Rio de Janeiro, Rio de Janeiro, Cidade Universitária, Rio de Janeiro 21941 972, Brazil.
Fabiana Vasconcelos CamposFederal University of Espírito Santo, Av Marechal Campos 1468, Vitória, ES 29.040 090, Brazil.
Jairo Pinto de OliveiraFederal University of Espírito Santo, Av Marechal Campos 1468, Vitória, ES 29.040 090, Brazil.ORCID https://orcid.org/0000-0001-7595-1183
Marco Cesar Cunegundes GuimarãesFederal University of Espírito Santo, Av Marechal Campos 1468, Vitória, ES 29.040 090, Brazil.ORCID https://orcid.org/0000-0003-2146-0180

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monodisperse and colloidally stable magnetic iron oxide nanoparticles have been developed for diverse biotechnology applications. Although promising for the adsorption of organic molecules, the low density of adsorption sites in these nanoparticles has been a significant challenge. In this study, an optimized factorial design with response surface methodology (RSM) was employed to produce small Superparamagnetic Iron Oxide Nanoparticles (SPIONs) stabilized with tetraethoxysilane (TEOS). Bovine Serum Albumin (BSA) was selected for immobilization on the surface of SPIONs to test adsorption capacity. The model was validated by correlating significant factors with experimental responses, enabling the prediction of the smallest nanoparticle size. We obtained superparamagnetic SPIONs (75.12 emu/g) with high surface area and an average diameter of 11.06 ± 0.84 nm, with stability improved by the adsorption of TEOS (-46.24 mV) and suitable for pH values from 2 to 10 and salt concentrations up to 1 M. The maximum adsorption capacity of the nanoparticles was 87.8 ± 1.79 mg of BSA per gram of nanoparticles. The nanomaterial synthesized here presents a favorable platform for anchoring protein molecules via silanol groups on its electrostatically charged surface. This study introduces an effective strategy for the synthesis and stabilization of SPIONs with potential biotechnology applications.

Identifiers

PMID39866618
PMCPMC11755185

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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.