Evidence map›Paper›PMID 27013873›Full record

ArticleInternational journal of nanomedicine2016

Degradation of the electrospun silica nanofiber in a biological medium for primary hippocampal neuron - effect of surface modification.

Z Vivian Feng, Wen Shuo Chen, Khomson Keratithamkul, Michael Stoick, Brittany Kapala, Eryn Johnson, An-Chi Huang, Ting Yu Chin, Yui Whei Chen-Yang, Mong-Lin Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Impact of nanoparticles on neuron biology: current research trends.International journal of nanomedicine · 2018
    Review
  6. Review
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.

Z Vivian FengChemistry Department, Augsburg College, Minneapolis, MN, USA.
Wen Shuo ChenDepartment of Chemistry, Center for Nanotechnology, Center for Biomedical Technology, Chung Yuan Christian University, Chung Li, Taiwan, Republic of China.
Khomson KeratithamkulChemistry Department, Augsburg College, Minneapolis, MN, USA.
Michael StoickChemistry Department, Augsburg College, Minneapolis, MN, USA.
Brittany KapalaDepartment of Science, Concordia University Saint Paul, Saint Paul, MN, USA.
Eryn JohnsonDepartment of Science, Concordia University Saint Paul, Saint Paul, MN, USA.
An-Chi HuangDepartment of Chemistry, Center for Nanotechnology, Center for Biomedical Technology, Chung Yuan Christian University, Chung Li, Taiwan, Republic of China.
Ting Yu ChinDepartment of Bioscience Technology, Chung Yuan Christian University, Chung Li, Taiwan, Republic of China.
Yui Whei Chen-YangDepartment of Chemistry, Center for Nanotechnology, Center for Biomedical Technology, Chung Yuan Christian University, Chung Li, Taiwan, Republic of China.
Mong-Lin YangDepartment of Science, Concordia University Saint Paul, Saint Paul, MN, USA.
Chung Yuan Christian University · TWAugsburg University · USConcordia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, silica nanofibers (SNFs) were prepared by an electrospinning method and modified with poly-d-lysine (PDL) or (3-aminopropyl) trimethoxysilane (APTS) making biocompatible and degradable substrates for neuronal growth. The as-prepared SNF, modified SNF-PDL, and SNF-APTS were evaluated using scanning electron microscopy, nitrogen adsorption/desorption isotherms, contact angle measurements, and inductively coupled plasma atomic emission spectroscopy. Herein, the scanning electron microscopic images revealed that dissolution occurred in a corrosion-like manner by enlarging porous structures, which led to loss of structural integrity. In addition, covalently modified SNF-APTS with more hydrophobic surfaces and smaller surface areas resulted in significantly slower dissolution compared to SNF and physically modified SNF-PDL, revealing that different surface modifications can be used to tune the dissolution rate. Growth of primary hippocampal neuron on all substrates led to a slower dissolution rate. The three-dimensional SNF with larger surface area and higher surface density of the amino group promoted better cell attachment and resulted in an increased neurite density. This is the first known work addressing the degradability of SNF substrate in physiological conditions with neuron growth in vitro, suggesting a strong potential for the applications of the material in controlled drug release.

Indexed as

ElectrochemistryAnimalsBiocompatible MaterialsCell DifferentiationCell ProliferationCells, CulturedEmbryo, MammalianHippocampusMicroscopy, Electron, ScanningNanofibersNeuronsPorosityRatsSilanesSilicon DioxideSurface PropertiesBiocompatible MaterialsSilanesSilicon Dioxidetrimethoxysilanedissolutionelectrospinningneurite densitysilica nanofiberssurface modification

Identifiers

PMID27013873
PMCPMC4777233
OpenAlexW2291038936

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.